| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:76348371-76348561 | Common:2; Rare:63; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:77065530-77065706 | Rare:58 | ||||
| chr12:82358358-82358547 | Rare:80 | ||||
| chr12:88142043-88142367 | Rare:89; Clinvar:3 | ||||
| chr12:88580440-88580552 | Common:1; Rare:40 | ||||
| chr12:89524737-89524869 | Common:1; Rare:26 | ||||
| chr12:89708815-89708981 | Rare:68 | ||||
| chr12:93441901-93442139 | Common:2; Rare:76 | ||||
| chr12:98601254-98601386 | Rare:40; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:100267079-100267279 | Common:1; Rare:93 | ||||
| chr12:101407659-101408049 | Common:3; Rare:95 | ||||
| chr12:102120060-102120256 | Rare:78 | ||||
| chr12:103841224-103841438 | Common:3; Rare:79 | ||||
| chr12:103965705-103965910 | Common:2; Rare:53 | ||||
| chr12:104064445-104064556 | Rare:27 |