| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:59615625-59616339 | Common:4; Rare:369 | ||||
| chr11:59668956-59669363 | Rare:277 | ||||
| chr11:59755295-59755465 | Common:2; Rare:61 | ||||
| chr11:59810642-59810995 | Common:7; Rare:208 | ||||
| chr11:60841905-60842204 | Common:4; Rare:202 | ||||
| chr11:60906427-60906852 | Rare:186 | ||||
| chr11:60913835-60914238 | Common:2; Rare:164 | ||||
| chr11:60924353-60924539 | Common:2; Rare:102 | ||||
| chr11:61161370-61161510 | Rare:44 | ||||
| chr11:61161598-61161781 | Common:1; Rare:62 | ||||
| chr11:61294970-61295170 | Rare:45 | ||||
| chr11:61295234-61295482 | Common:2; Rare:101 | ||||
| chr11:61332948-61333337 | Common:2; Rare:227 | ||||
| chr11:61361835-61362056 | Common:2; Rare:52; Clinvar:2 | ||||
| chr11:61362246-61362427 | Common:4; Rare:102; Clinvar:16; Clinvar (benign):2 |