| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:72228943-72229534 | Rare:150; Clinvar (pathogenic):1 | ||||
| chr11:72722079-72722359 | Common:2; Rare:57 | ||||
| chr11:72752347-72752587 | Common:3; Rare:73 | ||||
| chr11:72793535-72793825 | Common:1; Rare:63 | ||||
| chr11:72814047-72814447 | Common:4; Rare:119 | ||||
| chr11:73308738-73308927 | Rare:63 | ||||
| chr11:73597938-73598321 | Common:3; Rare:95 | ||||
| chr11:73760158-73760561 | Common:2; Rare:102 | ||||
| chr11:73760564-73760776 | Common:2; Rare:52 | ||||
| chr11:73760927-73761084 | Common:2; Rare:53 | ||||
| chr11:73787859-73787973 | Common:1; Rare:35 | ||||
| chr11:73876517-73876706 | Rare:45 | ||||
| chr11:73876774-73877066 | Common:5; Rare:82 | ||||
| chr11:74170811-74171083 | Common:2; Rare:77 | ||||
| chr11:74171125-74171522 | Common:2; Rare:132 |