| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:6419379-6419478 | Rare:35 | ||||
| chr11:6441051-6441140 | Rare:11 | ||||
| chr11:6473819-6474161 | Common:1; Rare:101 | ||||
| chr11:6474319-6474409 | Common:1; Rare:17 | ||||
| chr11:6481220-6481674 | Common:5; Rare:165 | ||||
| chr11:6603372-6603430 | Common:1; Rare:29 | ||||
| chr11:6603536-6603880 | Common:4; Rare:100; Clinvar (benign):3 | ||||
| chr11:6607052-6607211 | Rare:46 | ||||
| chr11:6612163-6612513 | Common:4; Rare:103 | ||||
| chr11:6612645-6612756 | Common:1; Rare:22 | ||||
| chr11:6619219-6619612 | Common:3; Rare:127; Clinvar:3; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr11:6683017-6683103 | Rare:23 | ||||
| chr11:6683263-6683700 | Common:6; Rare:162 | ||||
| chr11:7020309-7020536 | Common:1; Rare:82 | ||||
| chr11:7513260-7513294 | Rare:2 |