Proximal

HT1080(Human) | 6819 records |
Coordinate Validation Epigenomic status Core promoter element(s) Mutation TF registry
chr21:25735129-25735502 K27ac K4me3 CTCF I DPR TATA I DPR TATA Common:3; Rare:112
chr21:25735527-25735721 K27ac K4me3 CTCF I DPR TATA I DPR TATA Rare:54
chr21:25735725-25735765 K27ac K4me3 CTCF I DPR TATA I DPR TATA Common:1; Rare:1
chr21:26170655-26170926 K27ac K4me3 CTCF I DPR TATA I DPR TATA Common:5; Rare:91; Clinvar:5; Clinvar (benign):2
chr21:28885336-28885413 K27ac K4me3 CTCF I DPR TATA I DPR TATA Common:2; Rare:60
chr21:28992781-28993075 K27ac K4me3 CTCF I DPR TATA I DPR TATA Common:2; Rare:124
chr21:29019273-29019434 K27ac K4me3 CTCF I DPR TATA I DPR TATA Common:5; Rare:63
chr21:29024520-29024753 K27ac K4me3 CTCF I DPR TATA I DPR TATA Common:2; Rare:100
chr21:29024858-29024997 K27ac K4me3 CTCF I DPR TATA I DPR TATA Rare:30
chr21:29073573-29073798 K27ac K4me3 CTCF I DPR TATA I DPR TATA Common:2; Rare:68
chr21:29145415-29145639 K27ac K4me3 CTCF I DPR TATA I DPR TATA Rare:37
chr21:29298738-29298937 K27ac K4me3 CTCF I DPR TATA I DPR TATA Common:1; Rare:85
chr21:29299009-29299436 K27ac K4me3 CTCF I DPR TATA I DPR TATA Common:2; Rare:134
chr21:31659502-31659838 K27ac K4me3 CTCF I DPR TATA I DPR TATA Common:2; Rare:151; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):7
chr21:31732069-31732319 K27ac K4me3 CTCF I DPR TATA I DPR TATA Common:4; Rare:116
  • 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