| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:119084731-119084949 | Common:1; Rare:62; Clinvar (benign):1 | ||||
| chr11:119095122-119095490 | Common:2; Rare:125 | ||||
| chr11:119101138-119101469 | Rare:80 | ||||
| chr11:119101756-119102025 | Rare:69; Clinvar:4 | ||||
| chr11:119121274-119121632 | Common:1; Rare:84 | ||||
| chr11:119168571-119168770 | Rare:36; Clinvar:1 | ||||
| chr11:119206180-119206413 | Common:5; Rare:103; Clinvar:8; Clinvar (benign):4 | ||||
| chr11:119206651-119206857 | Common:2; Rare:36 | ||||
| chr11:119317124-119317239 | Rare:42 | ||||
| chr11:119334282-119334536 | Rare:67 | ||||
| chr11:119381601-119381903 | Common:1; Rare:75 | ||||
| chr11:119423145-119423440 | Common:6; Rare:73 | ||||
| chr11:120325253-120325344 | Common:1; Rare:22 | ||||
| chr11:120857841-120857978 | Rare:28 | ||||
| chr11:121024001-121024162 | Common:1; Rare:52 |