| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:111879147-111879551 | Common:1; Rare:125 | ||||
| chr11:111911957-111912212 | Common:3; Rare:46 | ||||
| chr11:111912712-111913119 | Common:3; Rare:84 | ||||
| chr11:111913128-111913300 | Rare:46 | ||||
| chr11:111923728-111923774 | Common:1; Rare:6 | ||||
| chr11:112025323-112025515 | Rare:53; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:112074150-112074349 | Common:1; Rare:45 | ||||
| chr11:112086656-112086928 | Rare:126; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr11:112163968-112164203 | Common:2; Rare:48 | ||||
| chr11:112226487-112226650 | Common:1; Rare:63; Clinvar:1; Clinvar (pathogenic):3 | ||||
| chr11:112961409-112961624 | Common:4; Rare:101 | ||||
| chr11:113314411-113314602 | Rare:66 | ||||
| chr11:113875461-113875765 | Common:4; Rare:110 | ||||
| chr11:114059399-114059833 | Common:1; Rare:88 | ||||
| chr11:114059842-114059904 | Rare:9 |