| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:85036275-85036362 | Rare:24 | ||||
| chr12:85279917-85280399 | Common:2; Rare:141 | ||||
| chr12:85280400-85280516 | Common:1; Rare:48; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:88035435-88035640 | Common:1; Rare:66 | ||||
| chr12:88141992-88142392 | Rare:112; Clinvar:4 | ||||
| chr12:88580471-88580588 | Common:1; Rare:35 | ||||
| chr12:89352241-89352711 | Common:1; Rare:132 | ||||
| chr12:89353647-89353721 | Common:1; Rare:14 | ||||
| chr12:89524748-89524901 | Common:2; Rare:28 | ||||
| chr12:89525456-89525665 | Common:1; Rare:53 | ||||
| chr12:89525891-89526081 | Common:1; Rare:75 | ||||
| chr12:89708813-89709097 | Common:1; Rare:111 | ||||
| chr12:91111377-91111664 | Common:5; Rare:64 | ||||
| chr12:92145836-92146250 | Common:2; Rare:127 | ||||
| chr12:92929042-92929517 | Common:3; Rare:142 |