Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:110764405-110764788 | Common:1; Rare:71 | ||||
chr10:114043094-114043231 | Rare:28 | ||||
chr10:114547649-114547936 | Common:1; Rare:67 | ||||
chr10:114631986-114632198 | Rare:51 | ||||
chr10:121998416-121998512 | Rare:14 | ||||
chr10:124703889-124704066 | Rare:25 | ||||
chr11:319860-320122 | Common:1; Rare:80 | ||||
chr11:1996081-1996105 | Rare:6 | ||||
chr11:2138254-2138391 | Common:1; Rare:22 | ||||
chr11:9758160-9758366 | Rare:57 | ||||
chr11:9759139-9759242 | Rare:26 | ||||
chr11:16604288-16604482 | Common:1; Rare:41 | ||||
chr11:19209716-19209871 | Common:1; Rare:36 | ||||
chr11:43943346-43943543 | Common:2; Rare:74 | ||||
chr11:47332564-47332846 | Rare:82; Clinvar:9; Clinvar (benign):6; Clinvar (pathogenic):6 |