| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:110468671-110468929 | Rare:69 | ||||
| chr12:110613991-110614203 | Rare:64; Clinvar:3; Clinvar (benign):2 | ||||
| chr12:110742825-110743177 | Common:3; Rare:136 | ||||
| chr12:111685763-111686110 | Rare:129 | ||||
| chr12:111766810-111766976 | Rare:50 | ||||
| chr12:111841854-111842219 | Common:3; Rare:103 | ||||
| chr12:112013109-112013550 | Common:1; Rare:168 | ||||
| chr12:112108725-112108965 | Common:1; Rare:62 | ||||
| chr12:112125322-112125578 | Rare:65 | ||||
| chr12:112409102-112409214 | Rare:22 | ||||
| chr12:113185435-113185739 | Common:7; Rare:116 | ||||
| chr12:113335096-113335260 | Rare:50 | ||||
| chr12:113966306-113966488 | Common:4; Rare:60 | ||||
| chr12:116910918-116911025 | Rare:43 | ||||
| chr12:118016535-118016798 | Common:2; Rare:53 |