| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:705872-706284 | Common:2; Rare:126 | ||||
| chr11:707046-707420 | Common:2; Rare:80 | ||||
| chr11:721125-721346 | Rare:96 | ||||
| chr11:722376-722751 | Common:1; Rare:150 | ||||
| chr11:747329-747599 | Rare:112; Clinvar:5; Clinvar (benign):1 | ||||
| chr11:763097-763850 | Common:24; Rare:343; Clinvar:4; Clinvar (pathogenic):3 | ||||
| chr11:763986-764430 | Common:4; Rare:119; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr11:764706-764845 | Common:1; Rare:48; Clinvar:1 | ||||
| chr11:777447-777619 | Common:1; Rare:78 | ||||
| chr11:798262-798589 | Rare:103 | ||||
| chr11:809486-809615 | Common:1; Rare:41 | ||||
| chr11:809812-810040 | Common:2; Rare:105 | ||||
| chr11:832883-833014 | Common:7; Rare:49 | ||||
| chr11:842413-842978 | Common:8; Rare:231 | ||||
| chr11:1257986-1258138 | Common:2; Rare:54; Clinvar (benign):1 |