| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:121802915-121803109 | Common:1; Rare:49 | ||||
| chr12:122078970-122079266 | Common:1; Rare:62 | ||||
| chr12:122266404-122266547 | Common:2; Rare:60 | ||||
| chr12:122526537-122526735 | Common:3; Rare:72 | ||||
| chr12:122526864-122527282 | Common:4; Rare:147 | ||||
| chr12:122859341-122859536 | Common:2; Rare:81 | ||||
| chr12:122872023-122872122 | Rare:14 | ||||
| chr12:122975143-122975264 | Common:1; Rare:38 | ||||
| chr12:122980568-122980915 | Common:2; Rare:103 | ||||
| chr12:123233093-123233506 | Common:2; Rare:140; Clinvar:1 | ||||
| chr12:123364807-123364995 | Common:3; Rare:72 | ||||
| chr12:123436437-123436581 | Rare:28 | ||||
| chr12:123584330-123584789 | Common:8; Rare:154 | ||||
| chr12:123601846-123602151 | Common:6; Rare:82 | ||||
| chr12:123633597-123633868 | Common:2; Rare:135; Clinvar:8; Clinvar (benign):1 |