| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:109573383-109573852 | Common:5; Rare:159; Clinvar:8; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr12:109880371-109880651 | Common:1; Rare:88 | ||||
| chr12:109900159-109900360 | Rare:67 | ||||
| chr12:109999093-109999231 | Rare:24 | ||||
| chr12:110281012-110281264 | Rare:92 | ||||
| chr12:110450253-110450412 | Common:2; Rare:60 | ||||
| chr12:110468715-110468909 | Rare:52 | ||||
| chr12:110502051-110502331 | Common:1; Rare:101 | ||||
| chr12:110613996-110614193 | Rare:57; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:111369025-111369212 | Common:1; Rare:52 | ||||
| chr12:111597989-111598039 | Rare:21 | ||||
| chr12:111685724-111686127 | Rare:144 | ||||
| chr12:111766810-111766992 | Rare:58 | ||||
| chr12:111841854-111842224 | Common:3; Rare:103 | ||||
| chr12:112013119-112013603 | Common:1; Rare:184 |