| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:16754689-16754949 | Rare:66 | ||||
| chr11:16997758-16997915 | Common:2; Rare:33 | ||||
| chr11:17501054-17501357 | Common:3; Rare:86; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr11:17522832-17523192 | Common:1; Rare:116; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr11:17529202-17529330 | Rare:21 | ||||
| chr11:17531045-17531225 | Common:1; Rare:48; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:17543033-17543346 | Common:2; Rare:44 | ||||
| chr11:35663562-35663658 | Rare:31; Clinvar (pathogenic):1 | ||||
| chr11:46383202-46383477 | Common:1; Rare:56 | ||||
| chr11:46680269-46680438 | Common:1; Rare:34 | ||||
| chr11:46762494-46762673 | Rare:39 | ||||
| chr11:47173460-47173751 | Rare:62 | ||||
| chr11:57780176-57780244 | Rare:9 | ||||
| chr11:57784041-57784262 | Common:1; Rare:24 | ||||
| chr11:57787911-57788245 | Rare:51 |