| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:112108755-112108888 | Common:1; Rare:34 | ||||
| chr12:113185399-113185769 | Common:10; Rare:143 | ||||
| chr12:113221019-113221319 | Common:2; Rare:86 | ||||
| chr12:114683964-114684051 | Rare:15 | ||||
| chr12:114684518-114684622 | Rare:26 | ||||
| chr12:118103876-118104099 | Common:1; Rare:53 | ||||
| chr12:118135955-118136183 | Common:2; Rare:69 | ||||
| chr12:118372846-118373192 | Common:2; Rare:93 | ||||
| chr12:119178654-119178950 | Common:1; Rare:49; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:120116747-120116907 | Rare:48 | ||||
| chr12:120201081-120201366 | Common:2; Rare:90 | ||||
| chr12:120437850-120438165 | Common:2; Rare:111; Clinvar (benign):2 | ||||
| chr12:120446353-120446478 | Common:1; Rare:57 | ||||
| chr12:120469490-120469895 | Common:5; Rare:136 | ||||
| chr12:120495859-120496177 | Common:7; Rare:110 |