| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:6390214-6390502 | Common:2; Rare:82 | ||||
| chr11:6390680-6390913 | Common:6; Rare:110; Clinvar:13; Clinvar (benign):8; Clinvar (pathogenic):4 | ||||
| chr11:6473789-6474109 | Rare:92 | ||||
| chr11:6481276-6481581 | Common:5; Rare:133 | ||||
| chr11:6603553-6603822 | Common:4; Rare:83; Clinvar (benign):3 | ||||
| chr11:6926251-6926436 | Common:1; Rare:44 | ||||
| chr11:7020303-7020489 | Rare:64 | ||||
| chr11:7513604-7513983 | Common:6; Rare:116 | ||||
| chr11:7577182-7577257 | Rare:12 | ||||
| chr11:8682630-8682832 | Common:2; Rare:88 | ||||
| chr11:8682955-8683264 | Common:2; Rare:104 | ||||
| chr11:8964366-8964589 | Common:4; Rare:73 | ||||
| chr11:9460623-9461048 | Common:4; Rare:109 | ||||
| chr11:9573784-9573921 | Rare:31 | ||||
| chr11:9663893-9664157 | Common:4; Rare:77 |