| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:110346060-110346388 | Common:2; Rare:88; Clinvar (benign):3 | ||||
| chr12:110450267-110450468 | Common:2; Rare:71 | ||||
| chr12:110502069-110502331 | Common:1; Rare:94 | ||||
| chr12:111685989-111686110 | Rare:41 | ||||
| chr12:111766813-111766988 | Rare:54 | ||||
| chr12:111841892-111842260 | Common:3; Rare:103 | ||||
| chr12:112013129-112013468 | Common:1; Rare:119 | ||||
| chr12:113185438-113185623 | Common:7; Rare:73 | ||||
| chr12:116737983-116738336 | Common:5; Rare:121 | ||||
| chr12:118061078-118061289 | Common:1; Rare:57 | ||||
| chr12:118135962-118136272 | Common:2; Rare:89 | ||||
| chr12:120116725-120116797 | Rare:17 | ||||
| chr12:120201076-120201354 | Common:2; Rare:89 | ||||
| chr12:120446331-120446478 | Common:1; Rare:65 | ||||
| chr12:120469621-120469868 | Common:2; Rare:88 |