| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:118376243-118376600 | Common:2; Rare:209 | ||||
| chr12:119667850-119668208 | Common:3; Rare:88 | ||||
| chr12:119877250-119877569 | Common:5; Rare:129 | ||||
| chr12:120116643-120117005 | Common:14; Rare:228 | ||||
| chr12:120117090-120117600 | Common:6; Rare:238 | ||||
| chr12:120194649-120194804 | Rare:99 | ||||
| chr12:120201069-120201394 | Common:4; Rare:199 | ||||
| chr12:120265684-120266034 | Common:2; Rare:217 | ||||
| chr12:120437837-120438225 | Common:4; Rare:223; Clinvar (benign):3 | ||||
| chr12:120446321-120446501 | Common:3; Rare:147 | ||||
| chr12:120469511-120469878 | Common:6; Rare:230 | ||||
| chr12:120495847-120496201 | Common:12; Rare:211 | ||||
| chr12:120529111-120529240 | Common:3; Rare:76 | ||||
| chr12:120581334-120581574 | Common:2; Rare:163 | ||||
| chr12:120686936-120687210 | Common:4; Rare:186 |