| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:11621967-11622237 | Common:4; Rare:108 | ||||
| chr11:11841898-11842091 | Common:1; Rare:56 | ||||
| chr11:12377472-12377630 | Rare:61 | ||||
| chr11:13463134-13463351 | Common:1; Rare:76 | ||||
| chr11:14499782-14499973 | Common:3; Rare:58 | ||||
| chr11:14520318-14520549 | Rare:74 | ||||
| chr11:16607810-16607950 | Rare:19 | ||||
| chr11:16738432-16738729 | Common:3; Rare:68 | ||||
| chr11:17077607-17077899 | Common:2; Rare:123 | ||||
| chr11:17207916-17208111 | Common:2; Rare:72 | ||||
| chr11:17276557-17276804 | Common:3; Rare:66; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr11:17351937-17352022 | Rare:20 | ||||
| chr11:18012925-18013180 | Common:6; Rare:92 | ||||
| chr11:18322131-18322306 | Common:3; Rare:60; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:18322499-18322613 | Common:2; Rare:50 |