| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:6390243-6390512 | Common:2; Rare:77 | ||||
| chr11:6419058-6419190 | Common:2; Rare:32 | ||||
| chr11:6481285-6481527 | Common:4; Rare:98 | ||||
| chr11:6603597-6603831 | Common:2; Rare:73; Clinvar (benign):3 | ||||
| chr11:6612179-6612348 | Common:2; Rare:54 | ||||
| chr11:6619379-6619570 | Common:3; Rare:60; Clinvar:2; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr11:6683279-6683650 | Common:6; Rare:136 | ||||
| chr11:6926475-6926522 | Rare:13 | ||||
| chr11:8682636-8682816 | Common:2; Rare:81 | ||||
| chr11:8683011-8683260 | Common:2; Rare:80 | ||||
| chr11:8964364-8964511 | Common:4; Rare:49 | ||||
| chr11:8964926-8965024 | Common:1; Rare:24 | ||||
| chr11:9314439-9314848 | Common:5; Rare:143 | ||||
| chr11:9384335-9384654 | Common:3; Rare:84 | ||||
| chr11:9663945-9664164 | Common:4; Rare:70 |