| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:62574743-62575166 | Common:1; Rare:129 | ||||
| chr11:65422678-65422885 | Common:1; Rare:67 | ||||
| chr11:65499253-65499859 | Common:2; Rare:333 | ||||
| chr11:65500797-65501245 | Common:3; Rare:227 | ||||
| chr11:65501844-65502060 | Common:1; Rare:88 | ||||
| chr11:73718672-73718815 | Rare:38 | ||||
| chr11:82689839-82689889 | Rare:6 | ||||
| chr11:118791734-118792028 | Rare:75 | ||||
| chr11:119308302-119308629 | Common:4; Rare:85 | ||||
| chr13:76884833-76884851 | Rare:5 | ||||
| chr13:113817727-113817863 | Common:2; Rare:27 | ||||
| chr14:22771021-22771347 | Common:2; Rare:114 | ||||
| chr14:49633953-49634046 | Common:1; Rare:41; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr14:76761381-76761534 | Common:2; Rare:64 | ||||
| chr14:98972843-98973036 | Rare:40 |