| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:22544410-22544780 | Common:2; Rare:87 | ||||
| chr12:22624988-22625250 | Common:1; Rare:122 | ||||
| chr12:23895670-23896150 | Common:1; Rare:127 | ||||
| chr12:23949641-23949920 | Common:5; Rare:50 | ||||
| chr12:23950243-23950436 | Common:3; Rare:51 | ||||
| chr12:23951027-23951127 | Rare:27 | ||||
| chr12:24948860-24949470 | Common:5; Rare:141 | ||||
| chr12:25195086-25195328 | Common:2; Rare:78 | ||||
| chr12:25250821-25251305 | Rare:147; Clinvar:5; Clinvar (benign):4 | ||||
| chr12:25958435-25958695 | Common:1; Rare:100 | ||||
| chr12:25959377-25959660 | Common:3; Rare:49 | ||||
| chr12:26125094-26125504 | Common:2; Rare:87 | ||||
| chr12:26195230-26195630 | Common:5; Rare:76 | ||||
| chr12:26195650-26196000 | Common:7; Rare:97 | ||||
| chr12:26196020-26196400 | Common:2; Rare:79 |