Proximal

MCF-7(Human) | 20727 records |
Coordinate Validation Epigenomic status Core promoter element(s) Mutation TF registry
chr13:36920164-36920431 K27ac K4me3 CTCF I DPR TATA I DPR TATA Common:8; Rare:178; Clinvar:7; Clinvar (benign):2
chr13:36998125-36999086 K27ac K4me3 CTCF I DPR TATA I DPR TATA Common:3; Rare:259
chr13:36999175-36999478 K27ac K4me3 CTCF I DPR TATA I DPR TATA Rare:272
chr13:37000217-37000416 K27ac K4me3 CTCF I DPR TATA I DPR TATA Common:6; Rare:94
chr13:37000485-37001430 K27ac K4me3 CTCF I DPR TATA I DPR TATA Common:10; Rare:501; Clinvar (pathogenic):3
chr13:37059429-37059889 K27ac K4me3 CTCF I DPR TATA I DPR TATA Common:4; Rare:225
chr13:38349247-38350273 K27ac K4me3 CTCF I DPR TATA I DPR TATA Common:13; Rare:557; Clinvar (pathogenic):2
chr13:38350184-38350299 K27ac K4me3 CTCF I DPR TATA I DPR TATA Rare:105
chr13:38686732-38687228 K27ac K4me3 CTCF I DPR TATA I DPR TATA Common:15; Rare:353; Clinvar:11; Clinvar (benign):3
chr13:39023921-39024030 K27ac K4me3 CTCF I DPR TATA I DPR TATA Rare:18
chr13:39037720-39038641 K27ac K4me3 CTCF I DPR TATA I DPR TATA Common:7; Rare:649
chr13:39603083-39603400 K27ac K4me3 CTCF I DPR TATA I DPR TATA Common:3; Rare:155
chr13:39655490-39655845 K27ac K4me3 CTCF I DPR TATA I DPR TATA Common:11; Rare:356; Clinvar:9; Clinvar (benign):18; Clinvar (pathogenic):3
chr13:39656101-39656278 K27ac K4me3 CTCF I DPR TATA I DPR TATA Common:3; Rare:53
chr13:40666531-40666813 K27ac K4me3 CTCF I DPR TATA I DPR TATA Common:4; Rare:192
  • Legend for epigenomic status:
  • K27ac K4me3 CTCF : Enriched for H3K27ac and DNaseI signal
  • K27ac K4me3 CTCF : Enriched for H3K4me3 and DNaseI signal
  • K27ac K4me3 CTCF : Enriched for CTCF binding signal
  • Legend for core promoter element:
  • I DPR TATA I DPR TATA : Found Initiator
  • I DPR TATA I DPR TATA : Found DPR
  • I DPR TATA I DPR TATA : Enriched TATA box