| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:94543683-94543888 | Common:4; Rare:42 | ||||
| chr11:94544251-94544282 | Rare:10 | ||||
| chr11:94767970-94768497 | Common:3; Rare:140 | ||||
| chr11:94768843-94769017 | Common:1; Rare:43 | ||||
| chr11:94973531-94973711 | Rare:56 | ||||
| chr11:95067457-95067590 | Rare:54 | ||||
| chr11:95089660-95090015 | Common:3; Rare:136 | ||||
| chr11:95789478-95789872 | Common:4; Rare:182 | ||||
| chr11:95790359-95790598 | Common:1; Rare:91 | ||||
| chr11:95923842-95924157 | Common:2; Rare:139; Clinvar:5; Clinvar (benign):5 | ||||
| chr11:96389860-96390050 | Common:1; Rare:78 | ||||
| chr11:101127324-101127365 | Common:1; Rare:10 | ||||
| chr11:101127523-101127850 | Common:3; Rare:145 | ||||
| chr11:101583906-101584157 | Rare:64; Clinvar:1 | ||||
| chr11:101914869-101915093 | Common:4; Rare:62 |