| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:752327-752614 | Common:1; Rare:83 | ||||
| chr12:990452-990562 | Common:1; Rare:31 | ||||
| chr12:990759-990902 | Rare:44 | ||||
| chr12:991101-991322 | Common:3; Rare:100 | ||||
| chr12:1970558-1970834 | Rare:42 | ||||
| chr12:2004345-2004631 | Common:1; Rare:111 | ||||
| chr12:2053156-2053352 | Common:2; Rare:46; Clinvar:1 | ||||
| chr12:2053454-2053609 | Common:1; Rare:46; Clinvar:1; Clinvar (benign):2 | ||||
| chr12:2795016-2795216 | Rare:82 | ||||
| chr12:2812522-2812727 | Common:1; Rare:53 | ||||
| chr12:2812885-2813013 | Rare:38 | ||||
| chr12:2877042-2877253 | Rare:63 | ||||
| chr12:2959824-2959903 | Common:1; Rare:20 | ||||
| chr12:3077277-3077439 | Common:5; Rare:73 | ||||
| chr12:4273881-4273955 | Rare:14 |