| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:68011507-68012554 | Common:6; Rare:253 | ||||
| chr11:68013248-68013494 | Rare:42 | ||||
| chr11:69122870-69123280 | Common:6; Rare:170 | ||||
| chr11:69636420-69636840 | Common:1; Rare:219 | ||||
| chr11:69691540-69691820 | Common:6; Rare:85 | ||||
| chr11:69697020-69697500 | Common:5; Rare:110 | ||||
| chr11:69700710-69701190 | Common:5; Rare:130 | ||||
| chr11:70404951-70405442 | Common:4; Rare:122 | ||||
| chr11:71299370-71299610 | Common:1; Rare:41 | ||||
| chr11:72195060-72195743 | Common:8; Rare:297; Clinvar:14; Clinvar (benign):20; Clinvar (pathogenic):2 | ||||
| chr11:72471290-72471690 | Common:7; Rare:126 | ||||
| chr11:72472720-72473211 | Common:7; Rare:112 | ||||
| chr11:72534991-72535175 | Common:1; Rare:28 | ||||
| chr11:72536125-72536343 | Common:1; Rare:39 | ||||
| chr11:72548510-72548800 | Common:10; Rare:87 |