| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:79934932-79935255 | Common:1; Rare:125 | ||||
| chr12:82358381-82358546 | Rare:65 | ||||
| chr12:88142086-88142350 | Rare:69; Clinvar:2 | ||||
| chr12:102120070-102120217 | Rare:55 | ||||
| chr12:104064470-104064536 | Rare:19 | ||||
| chr12:107685709-107685820 | Rare:35 | ||||
| chr12:109573488-109573783 | Common:3; Rare:84; Clinvar:3; Clinvar (benign):3 | ||||
| chr12:110502060-110502231 | Common:1; Rare:60 | ||||
| chr12:112013140-112013460 | Common:1; Rare:111 | ||||
| chr12:113185449-113185560 | Common:6; Rare:44 | ||||
| chr12:113966323-113966520 | Common:8; Rare:67 | ||||
| chr12:118135941-118136175 | Common:2; Rare:75 | ||||
| chr12:120201085-120201311 | Common:2; Rare:74 | ||||
| chr12:120446346-120446470 | Common:1; Rare:54 | ||||
| chr12:120469635-120469889 | Common:3; Rare:91 |