| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:6481299-6481524 | Common:4; Rare:89 | ||||
| chr11:6603542-6603822 | Common:4; Rare:86; Clinvar (benign):3 | ||||
| chr11:6683263-6683634 | Common:6; Rare:142 | ||||
| chr11:6926254-6926540 | Common:5; Rare:84 | ||||
| chr11:7020305-7020462 | Rare:50 | ||||
| chr11:7513626-7513958 | Common:5; Rare:99 | ||||
| chr11:7673448-7673575 | Common:1; Rare:44 | ||||
| chr11:8169000-8169074 | Common:1; Rare:25 | ||||
| chr11:8682684-8682816 | Common:1; Rare:60 | ||||
| chr11:8910935-8911265 | Common:6; Rare:90 | ||||
| chr11:8964372-8964558 | Common:3; Rare:58 | ||||
| chr11:9003996-9004091 | Rare:37 | ||||
| chr11:9460697-9461050 | Common:3; Rare:97 | ||||
| chr11:9575486-9575554 | Common:1; Rare:9 | ||||
| chr11:9663898-9664203 | Common:4; Rare:101 |