| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:6603542-6603822 | Common:4; Rare:86; Clinvar (benign):3 | ||||
| chr11:6683137-6683458 | Common:4; Rare:142 | ||||
| chr11:6926249-6926555 | Common:5; Rare:87 | ||||
| chr11:7020312-7020476 | Rare:55 | ||||
| chr11:7673443-7673576 | Common:1; Rare:45 | ||||
| chr11:8168963-8169074 | Common:2; Rare:44 | ||||
| chr11:8594184-8594310 | Rare:42 | ||||
| chr11:8682628-8682820 | Common:2; Rare:85 | ||||
| chr11:8910921-8911263 | Common:6; Rare:94 | ||||
| chr11:8964376-8964518 | Common:3; Rare:43 | ||||
| chr11:9460650-9461044 | Common:4; Rare:103 | ||||
| chr11:9575469-9575535 | Rare:9 | ||||
| chr11:9663893-9664241 | Common:4; Rare:116 | ||||
| chr11:10304881-10305088 | Common:1; Rare:48 | ||||
| chr11:10541128-10541477 | Common:3; Rare:102 |