| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:72080425-72080867 | Common:2; Rare:106; Clinvar:9 | ||||
| chr11:72112216-72112508 | Rare:76 | ||||
| chr11:72752382-72752529 | Common:2; Rare:44 | ||||
| chr11:72793597-72793839 | Common:1; Rare:62 | ||||
| chr11:73307955-73308330 | Common:3; Rare:110 | ||||
| chr11:73598063-73598158 | Common:1; Rare:29 | ||||
| chr11:73598169-73598260 | Common:1; Rare:17 | ||||
| chr11:73760196-73760340 | Rare:29 | ||||
| chr11:73760570-73760637 | Rare:13 | ||||
| chr11:73760654-73760764 | Common:2; Rare:25 | ||||
| chr11:73760772-73760816 | Rare:6 | ||||
| chr11:73787875-73787978 | Common:1; Rare:36 | ||||
| chr11:73876784-73877054 | Common:5; Rare:75 | ||||
| chr11:74170842-74171424 | Common:3; Rare:186 | ||||
| chr11:74493277-74493395 | Rare:55; Clinvar (pathogenic):1 |