| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:73598020-73598347 | Common:3; Rare:85 | ||||
| chr11:73598521-73598759 | Common:5; Rare:47 | ||||
| chr11:73760162-73760645 | Common:2; Rare:120 | ||||
| chr11:73760779-73761434 | Common:5; Rare:171 | ||||
| chr11:73787748-73788395 | Common:9; Rare:159 | ||||
| chr11:73788427-73788610 | Common:2; Rare:33 | ||||
| chr11:73876481-73876904 | Common:3; Rare:109 | ||||
| chr11:73876949-73877107 | Common:3; Rare:52 | ||||
| chr11:73877233-73877327 | Rare:12 | ||||
| chr11:74170811-74171027 | Common:1; Rare:57 | ||||
| chr11:74171108-74171443 | Common:2; Rare:110 | ||||
| chr11:74311533-74311795 | Common:1; Rare:84 | ||||
| chr11:74398337-74398605 | Common:3; Rare:71 | ||||
| chr11:74398717-74398997 | Rare:81 | ||||
| chr11:74493098-74493520 | Common:1; Rare:150; Clinvar (pathogenic):1 |