Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:108692151-108692464 | Common:3; Rare:109 | ||||
chr1:108692489-108692690 | Common:3; Rare:86 | ||||
chr1:108692775-108693065 | Rare:87 | ||||
chr1:108746421-108746810 | Common:3; Rare:134 | ||||
chr1:108746893-108747044 | Rare:39 | ||||
chr1:108876790-108877201 | Common:2; Rare:111; Clinvar:7; Clinvar (benign):1 | ||||
chr1:108963175-108963624 | Common:5; Rare:158 | ||||
chr1:109041964-109042412 | Common:5; Rare:119 | ||||
chr1:109075926-109076279 | Rare:111 | ||||
chr1:109090168-109090359 | Common:1; Rare:38 | ||||
chr1:109090413-109090802 | Common:4; Rare:86 | ||||
chr1:109090843-109090966 | Rare:38 | ||||
chr1:109091163-109091234 | Common:1; Rare:25 | ||||
chr1:109213735-109214022 | Rare:104 | ||||
chr1:109214298-109214621 | Common:1; Rare:59 |