| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:126211634-126211825 | Rare:86 | ||||
| chr11:126266207-126266524 | Rare:109 | ||||
| chr11:126268510-126268649 | Common:2; Rare:35 | ||||
| chr11:126268779-126269207 | Common:2; Rare:165; Clinvar:2; Clinvar (benign):4 | ||||
| chr11:126303868-126304141 | Rare:132 | ||||
| chr11:126304207-126304336 | Common:1; Rare:52 | ||||
| chr11:126355486-126355783 | Common:2; Rare:82 | ||||
| chr11:128522186-128522572 | Common:1; Rare:112 | ||||
| chr11:128692827-128692963 | Rare:34 | ||||
| chr11:128693204-128693269 | Common:1; Rare:21 | ||||
| chr11:128693956-128694234 | Rare:50 | ||||
| chr11:130069653-130069960 | Common:2; Rare:111 | ||||
| chr11:130314394-130314524 | Common:1; Rare:44 | ||||
| chr11:130448403-130448645 | Rare:58 | ||||
| chr11:131909909-131909924 | Rare:2 |