Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr12:80937659-80937832 | Common:1; Rare:56 | ||||
chr12:80937918-80938099 | Common:1; Rare:30 | ||||
chr12:82358224-82358554 | Common:2; Rare:161 | ||||
chr12:82358743-82358896 | Common:3; Rare:80 | ||||
chr12:88141901-88142418 | Common:1; Rare:137; Clinvar:8; Clinvar (benign):1 | ||||
chr12:88580375-88580561 | Common:2; Rare:60 | ||||
chr12:89524745-89524874 | Common:1; Rare:23 | ||||
chr12:89525911-89526083 | Common:1; Rare:69 | ||||
chr12:89708796-89708969 | Rare:68 | ||||
chr12:92929208-92929517 | Common:1; Rare:98 | ||||
chr12:93377606-93377929 | Rare:101 | ||||
chr12:93441880-93442103 | Common:2; Rare:77 | ||||
chr12:93570826-93571092 | Rare:67 | ||||
chr12:93571394-93571700 | Common:1; Rare:78 | ||||
chr12:93571738-93571912 | Common:7; Rare:67 |