| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:75511588-75511665 | Rare:33 | ||||
| chr12:76084568-76084878 | Common:1; Rare:103 | ||||
| chr12:76348351-76348460 | Common:1; Rare:45; Clinvar:3; Clinvar (benign):1 | ||||
| chr12:76559719-76559914 | Rare:75 | ||||
| chr12:76764051-76764261 | Common:1; Rare:87 | ||||
| chr12:79690511-79690630 | Rare:28 | ||||
| chr12:79934918-79935278 | Common:1; Rare:142 | ||||
| chr12:82358361-82358510 | Rare:60 | ||||
| chr12:82358742-82358906 | Common:3; Rare:81 | ||||
| chr12:88035419-88035563 | Common:1; Rare:39 | ||||
| chr12:88142009-88142368 | Rare:101; Clinvar:4 | ||||
| chr12:89352458-89352711 | Rare:74 | ||||
| chr12:89524756-89524883 | Common:1; Rare:23 | ||||
| chr12:91178507-91179011 | Common:4; Rare:89; Clinvar (benign):1 | ||||
| chr12:91182673-91182916 | Rare:47; Clinvar:2; Clinvar (benign):1 |