| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:101127120-101127531 | Common:13; Rare:274 | ||||
| chr11:101129641-101130041 | Common:3; Rare:180 | ||||
| chr11:101914888-101915031 | Common:2; Rare:34 | ||||
| chr11:102317247-102317647 | Common:2; Rare:173 | ||||
| chr11:102346406-102347463 | Common:39; Rare:770 | ||||
| chr11:102451753-102452980 | Common:16; Rare:1018 | ||||
| chr11:102452990-102453330 | Rare:202 | ||||
| chr11:103091108-103091508 | Common:2; Rare:67 | ||||
| chr11:103091440-103091631 | Rare:64 | ||||
| chr11:103091920-103092460 | Common:13; Rare:667 | ||||
| chr11:103109070-103109550 | Common:1; Rare:227; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:106021672-106021786 | Common:1; Rare:29 | ||||
| chr11:106022122-106022666 | Common:16; Rare:602 | ||||
| chr11:106076326-106077746 | Common:16; Rare:1119 | ||||
| chr11:106077866-106078427 | Common:4; Rare:164 |