Proximal

H1(Human) | 12287 records |
Coordinate Validation Epigenomic status Core promoter element(s) Mutation TF registry
chr17:9162688-9162846 K27ac K4me3 CTCF I DPR TATA I DPR TATA Common:2; Rare:50
chr17:9576551-9576682 K27ac K4me3 CTCF I DPR TATA I DPR TATA Common:1; Rare:34
chr17:9645367-9645553 K27ac K4me3 CTCF I DPR TATA I DPR TATA Rare:48
chr17:10697477-10697654 K27ac K4me3 CTCF I DPR TATA I DPR TATA Common:3; Rare:82; Clinvar:5; Clinvar (benign):3
chr17:10729696-10729857 K27ac K4me3 CTCF I DPR TATA I DPR TATA Rare:74
chr17:10729982-10730133 K27ac K4me3 CTCF I DPR TATA I DPR TATA Common:3; Rare:33
chr17:11997362-11997588 K27ac K4me3 CTCF I DPR TATA I DPR TATA Rare:88
chr17:12020693-12020880 K27ac K4me3 CTCF I DPR TATA I DPR TATA Common:1; Rare:82
chr17:12021339-12021628 K27ac K4me3 CTCF I DPR TATA I DPR TATA Rare:85
chr17:12789383-12789564 K27ac K4me3 CTCF I DPR TATA I DPR TATA Rare:65
chr17:13017618-13017768 K27ac K4me3 CTCF I DPR TATA I DPR TATA Rare:62; Clinvar (benign):1
chr17:13017944-13018339 K27ac K4me3 CTCF I DPR TATA I DPR TATA Common:7; Rare:132; Clinvar (benign):2
chr17:13601951-13602184 K27ac K4me3 CTCF I DPR TATA I DPR TATA Common:1; Rare:69
chr17:14069349-14069620 K27ac K4me3 CTCF I DPR TATA I DPR TATA Common:2; Rare:99; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1
chr17:14300804-14301105 K27ac K4me3 CTCF I DPR TATA I DPR TATA Common:2; Rare:81
  • 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