| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:112409554-112409707 | Common:1; Rare:52 | ||||
| chr12:113165668-113165952 | Rare:103 | ||||
| chr12:113185429-113185794 | Common:9; Rare:132 | ||||
| chr12:113221039-113221319 | Common:2; Rare:79 | ||||
| chr12:118135947-118136315 | Common:2; Rare:113 | ||||
| chr12:119178571-119179171 | Common:3; Rare:108; Clinvar:3; Clinvar (benign):2 | ||||
| chr12:119179175-119179569 | Rare:122; Clinvar:8; Clinvar (benign):4 | ||||
| chr12:119179573-119179679 | Rare:27; Clinvar:2 | ||||
| chr12:120116655-120116935 | Common:5; Rare:82 | ||||
| chr12:120201081-120201354 | Common:2; Rare:88 | ||||
| chr12:120446344-120446478 | Common:1; Rare:60 | ||||
| chr12:120469589-120469906 | Common:3; Rare:112 | ||||
| chr12:120495856-120496158 | Common:6; Rare:102 | ||||
| chr12:120581353-120581458 | Rare:46 | ||||
| chr12:121210059-121210152 | Common:2; Rare:33 |