| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:110468691-110468915 | Rare:58 | ||||
| chr12:110502058-110502241 | Common:1; Rare:64 | ||||
| chr12:110613997-110614187 | Rare:55; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:111685784-111686085 | Rare:119 | ||||
| chr12:111766814-111766971 | Rare:47 | ||||
| chr12:111841887-111842058 | Common:2; Rare:48 | ||||
| chr12:112013129-112013496 | Common:1; Rare:135 | ||||
| chr12:113185435-113185777 | Common:8; Rare:124 | ||||
| chr12:113966306-113966525 | Common:8; Rare:75 | ||||
| chr12:118135941-118136226 | Common:2; Rare:92 | ||||
| chr12:118372827-118373165 | Common:2; Rare:88 | ||||
| chr12:120194683-120194796 | Rare:42 | ||||
| chr12:120201081-120201349 | Common:2; Rare:85 | ||||
| chr12:120446333-120446474 | Common:1; Rare:62 | ||||
| chr12:120469624-120469906 | Common:3; Rare:99 |