| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65859643-65859748 | Rare:18 | ||||
| chr11:65860275-65860521 | Common:2; Rare:88 | ||||
| chr11:65873480-65873840 | Common:3; Rare:111 | ||||
| chr11:65888392-65888703 | Common:1; Rare:108 | ||||
| chr11:65888894-65889294 | Common:2; Rare:97 | ||||
| chr11:65890436-65890703 | Common:5; Rare:83 | ||||
| chr11:65900381-65900554 | Common:1; Rare:34 | ||||
| chr11:65919026-65919274 | Rare:89 | ||||
| chr11:65945585-65945775 | Common:1; Rare:72 | ||||
| chr11:65961472-65961758 | Common:1; Rare:93 | ||||
| chr11:66002097-66002563 | Common:3; Rare:134; Clinvar:7; Clinvar (benign):3 | ||||
| chr11:66002568-66002968 | Common:5; Rare:150 | ||||
| chr11:66045120-66045400 | Common:4; Rare:78 | ||||
| chr11:66049110-66049360 | Common:2; Rare:46 | ||||
| chr11:66051129-66051927 | Common:4; Rare:182 |