| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:308078-308435 | Common:8; Rare:121 | ||||
| chr11:320751-321012 | Common:10; Rare:78; Clinvar:1 | ||||
| chr11:506733-507001 | Common:3; Rare:92 | ||||
| chr11:560710-561003 | Common:5; Rare:137 | ||||
| chr11:576431-576531 | Rare:40 | ||||
| chr11:695756-695830 | Rare:28 | ||||
| chr11:747329-747514 | Rare:78; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:764236-764339 | Rare:30 | ||||
| chr11:777460-777637 | Common:1; Rare:80 | ||||
| chr11:790043-790163 | Common:1; Rare:28 | ||||
| chr11:798262-798484 | Rare:64 | ||||
| chr11:809525-809595 | Rare:21 | ||||
| chr11:832858-833018 | Common:7; Rare:58 | ||||
| chr11:842439-842895 | Common:7; Rare:191 | ||||
| chr11:1763837-1764274 | Common:4; Rare:169; Clinvar:8; Clinvar (benign):7 |