| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:5685005-5685210 | Common:5; Rare:50 | ||||
| chr11:5937967-5938228 | Common:6; Rare:67 | ||||
| chr11:5938536-5938751 | Common:8; Rare:57 | ||||
| chr11:6234284-6235288 | Common:9; Rare:392 | ||||
| chr11:6390138-6390573 | Common:7; Rare:273; Clinvar (benign):1 | ||||
| chr11:6418925-6419233 | Common:3; Rare:67 | ||||
| chr11:6473079-6473533 | Common:9; Rare:181 | ||||
| chr11:6473659-6474304 | Common:4; Rare:378 | ||||
| chr11:6481172-6481668 | Common:15; Rare:471 | ||||
| chr11:6603522-6603862 | Common:12; Rare:290; Clinvar (benign):9 | ||||
| chr11:6612116-6612383 | Common:8; Rare:231 | ||||
| chr11:6612534-6612934 | Common:4; Rare:114; Clinvar:5; Clinvar (benign):1 | ||||
| chr11:6619356-6619632 | Common:4; Rare:85; Clinvar:2; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr11:6683214-6683686 | Common:18; Rare:463 | ||||
| chr11:6926263-6926480 | Common:4; Rare:61 |