| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:47257540-47257745 | Common:1; Rare:27 | ||||
| chr11:47269545-47269721 | Common:1; Rare:62 | ||||
| chr11:47269966-47270184 | Common:1; Rare:71 | ||||
| chr11:47378361-47378645 | Rare:79 | ||||
| chr11:47426412-47426725 | Rare:69 | ||||
| chr11:47553008-47553317 | Common:3; Rare:111 | ||||
| chr11:47565490-47565650 | Common:3; Rare:33 | ||||
| chr11:47578943-47579136 | Rare:103; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr11:47586493-47586691 | Rare:38 | ||||
| chr11:47642443-47642705 | Rare:106 | ||||
| chr11:47767269-47767428 | Rare:74 | ||||
| chr11:47848315-47848658 | Common:3; Rare:121 | ||||
| chr11:57311443-57311724 | Common:1; Rare:71 | ||||
| chr11:57324877-57325183 | Common:1; Rare:101 | ||||
| chr11:57426885-57427200 | Common:1; Rare:86 |