| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:66616357-66616684 | Common:2; Rare:105 | ||||
| chr11:66616850-66616989 | Rare:34 | ||||
| chr11:66638647-66638757 | Common:1; Rare:46 | ||||
| chr11:66677765-66677912 | Common:1; Rare:57 | ||||
| chr11:66687054-66687371 | Common:2; Rare:87; Clinvar:7; Clinvar (benign):2 | ||||
| chr11:66689081-66689455 | Common:1; Rare:89; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:66744650-66744933 | Common:4; Rare:106 | ||||
| chr11:66842451-66842712 | Common:1; Rare:53 | ||||
| chr11:67056762-67056929 | Common:1; Rare:49 | ||||
| chr11:67289919-67290161 | Common:1; Rare:66 | ||||
| chr11:67303343-67303628 | Rare:78 | ||||
| chr11:67307295-67307629 | Rare:100 | ||||
| chr11:67317758-67317877 | Rare:22 | ||||
| chr11:67353510-67353631 | Rare:36 | ||||
| chr11:67373583-67373787 | Rare:38 |