Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:26657484-26657625 | Common:1; Rare:26 | ||||
chr22:26672656-26672778 | Common:2; Rare:30 | ||||
chr22:42600990-42601229 | Common:1; Rare:50 | ||||
chr3:40453307-40453417 | Common:2; Rare:25 | ||||
chr3:72979690-72979977 | Common:2; Rare:40 | ||||
chr3:75435108-75435379 | Common:2; Rare:88 | ||||
chr3:101576981-101576999 | Rare:3 | ||||
chr3:101676256-101676468 | Common:2; Rare:71 | ||||
chr3:107240630-107240729 | Rare:42 | ||||
chr3:130111473-130111762 | Common:3; Rare:71 | ||||
chr3:169765053-169765181 | Rare:58; Clinvar (pathogenic):2 | ||||
chr3:197627841-197627987 | Common:6; Rare:50 | ||||
chr3:197850988-197851149 | Rare:31 | ||||
chr4:212567-212629 | Common:1; Rare:16 | ||||
chr4:38664889-38665051 | Rare:46 |