| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:61361835-61362051 | Common:2; Rare:52; Clinvar:2 | ||||
| chr11:61362255-61362397 | Common:1; Rare:40; Clinvar:6 | ||||
| chr11:61392357-61392655 | Common:2; Rare:72; Clinvar:5; Clinvar (benign):2 | ||||
| chr11:61429231-61429349 | Common:2; Rare:48 | ||||
| chr11:61429912-61430149 | Common:1; Rare:105; Clinvar:1; Clinvar (benign):3 | ||||
| chr11:61792573-61792943 | Common:5; Rare:97 | ||||
| chr11:61967313-61967790 | Common:3; Rare:179; Clinvar:4 | ||||
| chr11:62123757-62124065 | Common:7; Rare:79 | ||||
| chr11:62545620-62545987 | Common:1; Rare:80 | ||||
| chr11:62601210-62601294 | Rare:18 | ||||
| chr11:62611595-62611817 | Rare:53 | ||||
| chr11:62621943-62622209 | Common:2; Rare:85 | ||||
| chr11:62653268-62653504 | Common:1; Rare:67 | ||||
| chr11:62665156-62665452 | Common:6; Rare:136 | ||||
| chr11:62671632-62672059 | Common:2; Rare:160; Clinvar (benign):3 |