| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:109999093-109999211 | Rare:19 | ||||
| chr12:110450242-110450437 | Common:2; Rare:73 | ||||
| chr12:110468715-110468923 | Rare:58 | ||||
| chr12:110502058-110502244 | Common:1; Rare:66 | ||||
| chr12:110613991-110614195 | Rare:60; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:111685786-111686127 | Rare:131 | ||||
| chr12:111766814-111766977 | Rare:51 | ||||
| chr12:111841887-111841998 | Common:2; Rare:36 | ||||
| chr12:112013123-112013468 | Common:1; Rare:122 | ||||
| chr12:112108748-112108876 | Common:1; Rare:34 | ||||
| chr12:112409554-112409707 | Common:1; Rare:52 | ||||
| chr12:113185447-113185777 | Common:8; Rare:115 | ||||
| chr12:113966315-113966462 | Common:3; Rare:47 | ||||
| chr12:116276669-116276815 | Common:1; Rare:47 | ||||
| chr12:118135955-118136201 | Common:2; Rare:76 |