| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:130916179-130916253 | Common:1; Rare:12 | ||||
| chr11:130916387-130916672 | Common:7; Rare:88 | ||||
| chr11:133956951-133957125 | Common:1; Rare:56 | ||||
| chr11:133957306-133957398 | Common:1; Rare:21 | ||||
| chr11:134223904-134224178 | Common:2; Rare:100 | ||||
| chr11:134224468-134224712 | Common:2; Rare:101 | ||||
| chr11:134225041-134225180 | Rare:48 | ||||
| chr11:134252844-134252945 | Rare:34 | ||||
| chr11:134253297-134253623 | Common:3; Rare:119; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr11:134331645-134332139 | Common:10; Rare:124 | ||||
| chr11:134332314-134332349 | Rare:11 | ||||
| chr12:203787-203917 | Common:2; Rare:42 | ||||
| chr12:388469-388707 | Common:1; Rare:56 | ||||
| chr12:388910-388978 | Rare:24 | ||||
| chr12:388997-389054 | Rare:21 |