| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:128522239-128522574 | Common:2; Rare:181 | ||||
| chr11:129279420-129279840 | Common:8; Rare:266 | ||||
| chr11:129815712-129815902 | Common:2; Rare:85 | ||||
| chr11:129895516-129895698 | Common:4; Rare:137 | ||||
| chr11:130002710-130003460 | Common:8; Rare:385 | ||||
| chr11:130069617-130070020 | Common:4; Rare:252 | ||||
| chr11:130314390-130314590 | Common:3; Rare:104 | ||||
| chr11:130314732-130315070 | Common:6; Rare:172 | ||||
| chr11:130916374-130916658 | Common:12; Rare:152 | ||||
| chr11:134223907-134224134 | Common:4; Rare:142 | ||||
| chr11:134224515-134224722 | Rare:160 | ||||
| chr11:134225441-134225576 | Rare:71 | ||||
| chr11:134253301-134253608 | Common:4; Rare:211; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr12:214537-214649 | Common:2; Rare:25 | ||||
| chr12:388850-389160 | Common:6; Rare:192 |