Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:97438737-97439037 | Common:1; Rare:48 | ||||
chr1:97529796-97530096 | Rare:71 | ||||
chr1:97658992-97659054 | Rare:12 | ||||
chr1:97827875-97828155 | Rare:63; Clinvar:1; Clinvar (pathogenic):2 | ||||
chr1:97967671-97967854 | Common:1; Rare:36 | ||||
chr1:98028963-98029111 | Common:1; Rare:19 | ||||
chr1:98046210-98046459 | Common:2; Rare:54 | ||||
chr1:98054259-98054459 | Common:1; Rare:57 | ||||
chr1:108696086-108696424 | Common:1; Rare:72 | ||||
chr1:108925322-108925557 | Common:2; Rare:31 | ||||
chr1:109237106-109237369 | Rare:57 | ||||
chr1:109409789-109409932 | Rare:34 | ||||
chr1:109592019-109592457 | Rare:97 | ||||
chr1:112671527-112671796 | Common:2; Rare:49 | ||||
chr1:113020524-113020750 | Common:6; Rare:28 |