Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:16647340-16647413 | Rare:1 | ||||
chr1:21983507-21983634 | Common:4; Rare:32 | ||||
chr1:22005404-22005803 | Common:4; Rare:161 | ||||
chr1:22006782-22006801 | Rare:3 | ||||
chr1:22009667-22010141 | Common:6; Rare:123 | ||||
chr1:22012499-22012782 | Common:6; Rare:29 | ||||
chr1:28581866-28582027 | Common:1; Rare:45 | ||||
chr1:28648297-28648622 | Common:4; Rare:108 | ||||
chr1:32240272-32240518 | Common:1; Rare:52 | ||||
chr1:44776358-44776492 | Rare:31 | ||||
chr1:58575660-58575736 | Rare:15 | ||||
chr1:58576066-58576124 | Common:1; Rare:8; Clinvar:1; Clinvar (benign):1 | ||||
chr1:58576314-58576511 | Common:2; Rare:93; Clinvar:2; Clinvar (benign):2 | ||||
chr1:58781150-58781168 | Rare:5 | ||||
chr1:58782017-58782236 | Rare:69 |