| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:6603462-6603861 | Common:4; Rare:128; Clinvar (benign):3 | ||||
| chr11:6683241-6683634 | Common:6; Rare:153 | ||||
| chr11:7020305-7020502 | Rare:68 | ||||
| chr11:7485251-7485533 | Rare:52 | ||||
| chr11:7513616-7514026 | Common:6; Rare:124 | ||||
| chr11:7597147-7597224 | Common:2; Rare:13 | ||||
| chr11:7597245-7597368 | Common:1; Rare:33 | ||||
| chr11:8593974-8594309 | Common:1; Rare:107 | ||||
| chr11:8682628-8683021 | Common:2; Rare:168 | ||||
| chr11:8718014-8718184 | Common:6; Rare:38 | ||||
| chr11:8910939-8911252 | Common:5; Rare:87 | ||||
| chr11:8932934-8932992 | Common:1; Rare:11 | ||||
| chr11:8932995-8933112 | Rare:31 | ||||
| chr11:8964366-8964575 | Common:4; Rare:71 | ||||
| chr11:8964920-8965044 | Common:2; Rare:31 |