| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67353294-67353340 | Rare:16 | ||||
| chr11:67353473-67353909 | Common:2; Rare:103 | ||||
| chr11:67401778-67402075 | Common:3; Rare:111 | ||||
| chr11:67428140-67428531 | Rare:115 | ||||
| chr11:67443451-67443598 | Common:1; Rare:51 | ||||
| chr11:67464804-67465005 | Rare:76 | ||||
| chr11:67469188-67469346 | Common:2; Rare:59 | ||||
| chr11:67482820-67483119 | Common:1; Rare:67; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr11:67507782-67508113 | Rare:96 | ||||
| chr11:67508627-67508811 | Common:3; Rare:73 | ||||
| chr11:68030467-68030744 | Common:3; Rare:70; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:68038919-68039093 | Rare:50; Clinvar:1 | ||||
| chr11:68271869-68272104 | Common:2; Rare:98 | ||||
| chr11:68460546-68460806 | Common:3; Rare:91 | ||||
| chr11:68903784-68903943 | Common:4; Rare:76; Clinvar (benign):6 |