| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:106301620-106302020 | Common:4; Rare:126 | ||||
| chr12:106302724-106302888 | Common:4; Rare:49 | ||||
| chr12:106357580-106357826 | Common:6; Rare:90; Clinvar:4; Clinvar (benign):2 | ||||
| chr12:106357939-106358158 | Common:7; Rare:151 | ||||
| chr12:106774020-106774400 | Common:6; Rare:173 | ||||
| chr12:106774420-106774725 | Common:2; Rare:123 | ||||
| chr12:106955387-106955963 | Common:6; Rare:418 | ||||
| chr12:106956447-106956983 | Common:2; Rare:263 | ||||
| chr12:106987026-106987286 | Common:8; Rare:125 | ||||
| chr12:107093500-107093643 | Rare:93 | ||||
| chr12:107093787-107094087 | Common:4; Rare:154 | ||||
| chr12:107685666-107685929 | Common:2; Rare:136 | ||||
| chr12:107761068-107761282 | Common:6; Rare:163 | ||||
| chr12:108515017-108515336 | Common:2; Rare:188 | ||||
| chr12:108561137-108561488 | Common:8; Rare:166 |