| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:32434903-32435107 | Common:1; Rare:71; Clinvar:16; Clinvar (benign):5 | ||||
| chr11:32435260-32435440 | Rare:51; Clinvar:7; Clinvar (benign):2 | ||||
| chr11:32435500-32435627 | Common:1; Rare:19 | ||||
| chr11:32583580-32583956 | Rare:136 | ||||
| chr11:32584040-32584179 | Common:1; Rare:33 | ||||
| chr11:32829616-32829954 | Common:6; Rare:71 | ||||
| chr11:32892633-32892908 | Common:1; Rare:103 | ||||
| chr11:32892938-32893156 | Common:1; Rare:48 | ||||
| chr11:32893275-32893538 | Rare:64 | ||||
| chr11:32893585-32893802 | Rare:38 | ||||
| chr11:33015715-33015956 | Common:3; Rare:99 | ||||
| chr11:33039128-33040014 | Common:6; Rare:233 | ||||
| chr11:33040176-33040274 | Common:2; Rare:22 | ||||
| chr11:33040434-33040551 | Common:1; Rare:17 | ||||
| chr11:33161194-33161269 | Rare:22 |