| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:535339-535359 | Rare:1 | ||||
| chr11:535518-535864 | Common:6; Rare:124 | ||||
| chr11:536661-536811 | Common:1; Rare:36 | ||||
| chr11:536908-536930 | Common:1; Rare:7 | ||||
| chr11:537188-537562 | Common:6; Rare:113 | ||||
| chr11:560676-560998 | Common:6; Rare:155 | ||||
| chr11:575790-576320 | Common:6; Rare:124 | ||||
| chr11:576365-576595 | Rare:87 | ||||
| chr11:615885-616137 | Common:2; Rare:80 | ||||
| chr11:638675-639010 | Rare:110 | ||||
| chr11:639137-639261 | Common:1; Rare:32 | ||||
| chr11:694940-695435 | Common:1; Rare:177; Clinvar:3; Clinvar (benign):2 | ||||
| chr11:695590-695941 | Common:3; Rare:100 | ||||
| chr11:696053-696124 | Common:2; Rare:17 | ||||
| chr11:746751-746865 | Rare:23 |