| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:114683964-114684219 | Common:3; Rare:83; Clinvar:2 | ||||
| chr12:114684493-114684631 | Rare:40 | ||||
| chr12:116910844-116911040 | Rare:64 | ||||
| chr12:118061044-118061466 | Common:4; Rare:94 | ||||
| chr12:118103856-118104113 | Common:1; Rare:64 | ||||
| chr12:118135932-118136228 | Common:2; Rare:94 | ||||
| chr12:118359044-118359310 | Rare:48 | ||||
| chr12:118372820-118373220 | Common:2; Rare:113 | ||||
| chr12:119178603-119179033 | Common:1; Rare:74; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:120064202-120064658 | Common:1; Rare:77 | ||||
| chr12:120116621-120116938 | Common:5; Rare:90 | ||||
| chr12:120194687-120194798 | Rare:40 | ||||
| chr12:120201070-120201366 | Common:2; Rare:94 | ||||
| chr12:120249965-120250245 | Common:3; Rare:39 | ||||
| chr12:120437881-120438227 | Common:2; Rare:133; Clinvar (benign):2 |