Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:101576975-101577224 | Common:3; Rare:63 | ||||
chr3:101676256-101676509 | Common:2; Rare:86 | ||||
chr3:107240593-107240811 | Rare:80 | ||||
chr3:128859776-128859960 | Rare:30 | ||||
chr3:130111485-130111760 | Common:3; Rare:66 | ||||
chr3:150408869-150408988 | Rare:37 | ||||
chr3:155293640-155293733 | Common:2; Rare:14 | ||||
chr3:167811067-167811142 | Rare:12 | ||||
chr3:167864705-167864871 | Rare:32 | ||||
chr3:169764853-169765144 | Common:1; Rare:98; Clinvar:17; Clinvar (pathogenic):5 | ||||
chr3:172319679-172319914 | Common:1; Rare:44 | ||||
chr3:194583872-194584026 | Common:11; Rare:55 | ||||
chr3:195657927-195658136 | Common:11; Rare:37 | ||||
chr3:195990216-195990421 | Rare:25 | ||||
chr3:197627826-197628040 | Common:7; Rare:82 |