| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:103930132-103930571 | Common:8; Rare:151 | ||||
| chr12:103965698-103965960 | Common:2; Rare:59 | ||||
| chr12:104064465-104064586 | Rare:32 | ||||
| chr12:104138170-104138387 | Common:1; Rare:57 | ||||
| chr12:104286741-104287075 | Common:3; Rare:62 | ||||
| chr12:104287216-104287411 | Rare:52 | ||||
| chr12:104958254-104958417 | Common:3; Rare:47 | ||||
| chr12:105107612-105107818 | Common:1; Rare:96; Clinvar:1 | ||||
| chr12:105176042-105176294 | Common:1; Rare:74 | ||||
| chr12:105176973-105177158 | Common:1; Rare:54 | ||||
| chr12:105235972-105236304 | Common:3; Rare:130 | ||||
| chr12:106357681-106357819 | Common:3; Rare:31; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:107685705-107685935 | Rare:76 | ||||
| chr12:108339218-108339532 | Common:3; Rare:77 | ||||
| chr12:108515024-108515305 | Common:1; Rare:84 |