| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:69675324-69675491 | Rare:45 | ||||
| chr11:70398425-70398596 | Common:2; Rare:61 | ||||
| chr11:71448321-71448791 | Common:5; Rare:119; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:71452871-71453212 | Common:4; Rare:81 | ||||
| chr11:71928930-71929089 | Common:1; Rare:51 | ||||
| chr11:72080432-72080824 | Common:2; Rare:92; Clinvar:7 | ||||
| chr11:72103220-72103518 | Rare:88 | ||||
| chr11:72814063-72814440 | Common:4; Rare:111 | ||||
| chr11:73598063-73598281 | Common:2; Rare:58 | ||||
| chr11:73760919-73761248 | Common:3; Rare:101 | ||||
| chr11:73876809-73877024 | Common:3; Rare:53 | ||||
| chr11:74170853-74171445 | Common:3; Rare:186 | ||||
| chr11:74949055-74949294 | Common:6; Rare:64 | ||||
| chr11:75351603-75351878 | Common:3; Rare:82 | ||||
| chr11:76444660-76444806 | Rare:34 |