| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:110613991-110614168 | Rare:54; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:110742816-110743179 | Common:3; Rare:139 | ||||
| chr12:111099465-111099485 | Rare:5 | ||||
| chr12:111685752-111686085 | Rare:125 | ||||
| chr12:111841887-111842266 | Common:3; Rare:107 | ||||
| chr12:112013119-112013475 | Common:1; Rare:127 | ||||
| chr12:112108755-112108806 | Rare:16 | ||||
| chr12:112109404-112109614 | Common:1; Rare:36 | ||||
| chr12:112907060-112907142 | Rare:27 | ||||
| chr12:112978316-112978539 | Common:1; Rare:36 | ||||
| chr12:113056622-113056754 | Rare:33 | ||||
| chr12:113135685-113135949 | Common:1; Rare:41 | ||||
| chr12:113184907-113185076 | Common:1; Rare:48 | ||||
| chr12:113185415-113185783 | Common:9; Rare:137 | ||||
| chr12:113221019-113221322 | Common:2; Rare:87 |