| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:113136845-113137251 | Common:4; Rare:121 | ||||
| chr12:113206020-113206795 | Common:10; Rare:268 | ||||
| chr12:113222689-113223498 | Common:4; Rare:212 | ||||
| chr12:113233356-113233622 | Common:2; Rare:58 | ||||
| chr12:113241562-113242561 | Common:10; Rare:275 | ||||
| chr12:113245916-113246276 | Rare:134 | ||||
| chr12:113246464-113247090 | Common:3; Rare:158 | ||||
| chr12:113591360-113591800 | Common:21; Rare:121 | ||||
| chr12:113773572-113773972 | Common:3; Rare:184 | ||||
| chr12:113955137-113955415 | Common:3; Rare:73 | ||||
| chr12:113957580-113957970 | Common:7; Rare:116 | ||||
| chr12:114390322-114390501 | Rare:31 | ||||
| chr12:114394745-114395586 | Common:3; Rare:257; Clinvar:1; Clinvar (benign):2 | ||||
| chr12:114399603-114399938 | Common:2; Rare:196; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr12:114528718-114529130 | Common:8; Rare:280 |