Proximal

SK-N-SH(Human) | 7944 records |

Coordinate Validation Epigenomic status Core promoter element(s) Mutation TF registry
chr7:56106350-56106682 K27ac K4me3 CTCF I DPR TATA I DPR TATA Common:8; Rare:123
chr7:64307268-64307593 K27ac K4me3 CTCF I DPR TATA I DPR TATA Common:2; Rare:72
chr7:65006640-65006878 K27ac K4me3 CTCF I DPR TATA I DPR TATA Common:3; Rare:72
chr7:65982174-65982328 K27ac K4me3 CTCF I DPR TATA I DPR TATA Common:2; Rare:51; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1
chr7:66075570-66075934 K27ac K4me3 CTCF I DPR TATA I DPR TATA Rare:98; Clinvar (benign):1
chr7:66114762-66114895 K27ac K4me3 CTCF I DPR TATA I DPR TATA Common:1; Rare:66
chr7:66115179-66115403 K27ac K4me3 CTCF I DPR TATA I DPR TATA Rare:53
chr7:66628640-66628958 K27ac K4me3 CTCF I DPR TATA I DPR TATA Common:2; Rare:113; Clinvar:3
chr7:66681969-66682216 K27ac K4me3 CTCF I DPR TATA I DPR TATA Common:6; Rare:108
chr7:66921049-66921482 K27ac K4me3 CTCF I DPR TATA I DPR TATA Common:1; Rare:125
chr7:66994213-66994474 K27ac K4me3 CTCF I DPR TATA I DPR TATA Common:3; Rare:82; Clinvar (benign):3; Clinvar (pathogenic):1
chr7:66995289-66995322 K27ac K4me3 CTCF I DPR TATA I DPR TATA Common:1; Rare:12; Clinvar (benign):2; Clinvar (pathogenic):2
chr7:66995332-66995373 K27ac K4me3 CTCF I DPR TATA I DPR TATA Rare:19
chr7:66996554-66996933 K27ac K4me3 CTCF I DPR TATA I DPR TATA Common:2; Rare:92
chr7:72828139-72828484 K27ac K4me3 CTCF I DPR TATA I DPR TATA Common:1; Rare:97
  • 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