| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:60699101-60699788 | Common:4; Rare:111 | ||||
| chr11:60785097-60785419 | Common:2; Rare:65 | ||||
| chr11:60841893-60842147 | Common:2; Rare:88 | ||||
| chr11:60855937-60856277 | Common:2; Rare:59 | ||||
| chr11:60906414-60906800 | Rare:96 | ||||
| chr11:61161393-61161754 | Common:1; Rare:105 | ||||
| chr11:61333051-61333266 | Rare:74 | ||||
| chr11:61333280-61333399 | Rare:45 | ||||
| chr11:61341719-61341912 | Common:2; Rare:47 | ||||
| chr11:61345374-61345565 | Common:2; Rare:57 | ||||
| chr11:61361833-61362049 | Common:2; Rare:52; Clinvar:2 | ||||
| chr11:61362239-61362429 | Common:2; Rare:54; Clinvar:8; Clinvar (benign):1 | ||||
| chr11:61392527-61392649 | Common:2; Rare:41; Clinvar:3; Clinvar (benign):2 | ||||
| chr11:61429182-61429496 | Common:3; Rare:100 | ||||
| chr11:61429906-61430164 | Common:1; Rare:116; Clinvar:3; Clinvar (benign):5 |