| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:535418-535732 | Common:5; Rare:126; Clinvar (benign):1 | ||||
| chr11:537314-537533 | Common:5; Rare:69 | ||||
| chr11:559738-560020 | Common:2; Rare:63 | ||||
| chr11:560690-561046 | Common:7; Rare:167 | ||||
| chr11:575883-576189 | Common:2; Rare:53 | ||||
| chr11:576412-576538 | Rare:52 | ||||
| chr11:627172-627395 | Common:2; Rare:102 | ||||
| chr11:627409-627438 | Rare:6 | ||||
| chr11:637012-637317 | Common:5; Rare:123 | ||||
| chr11:694918-695388 | Common:1; Rare:175; Clinvar:3; Clinvar (benign):2 | ||||
| chr11:695605-695675 | Common:1; Rare:13 | ||||
| chr11:695715-695827 | Rare:38 | ||||
| chr11:706945-707024 | Rare:25 | ||||
| chr11:707049-707084 | Rare:7 | ||||
| chr11:720731-721072 | Common:11; Rare:173 |