| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:6603553-6603817 | Common:4; Rare:82; Clinvar (benign):3 | ||||
| chr11:8682638-8682814 | Common:2; Rare:79 | ||||
| chr11:8964370-8964507 | Common:3; Rare:43 | ||||
| chr11:9314565-9314888 | Common:3; Rare:103 | ||||
| chr11:9460682-9461010 | Common:4; Rare:86 | ||||
| chr11:10455129-10455420 | Common:5; Rare:52; Clinvar:2; Clinvar (benign):6 | ||||
| chr11:10808877-10809122 | Common:1; Rare:105 | ||||
| chr11:10858013-10858246 | Common:3; Rare:73 | ||||
| chr11:11621997-11622241 | Common:3; Rare:92 | ||||
| chr11:13463170-13463395 | Common:1; Rare:87 | ||||
| chr11:14520300-14520543 | Rare:83 | ||||
| chr11:16738466-16738723 | Common:3; Rare:55 | ||||
| chr11:17207911-17208085 | Common:2; Rare:66 | ||||
| chr11:17276566-17276828 | Common:4; Rare:68; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr11:18106037-18106308 | Common:2; Rare:83 |