| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:95067630-95067910 | Common:2; Rare:104 | ||||
| chr11:95089673-95089888 | Common:3; Rare:92 | ||||
| chr11:95231195-95231402 | Rare:63 | ||||
| chr11:95789468-95789914 | Common:4; Rare:202 | ||||
| chr11:95790030-95790208 | Common:1; Rare:51 | ||||
| chr11:95790338-95790714 | Common:3; Rare:148 | ||||
| chr11:95791035-95791146 | Rare:32 | ||||
| chr11:95923776-95923897 | Common:1; Rare:44; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:95923947-95924196 | Rare:108; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:96343221-96343426 | Common:3; Rare:51 | ||||
| chr11:96389707-96390074 | Common:3; Rare:138 | ||||
| chr11:100687222-100687340 | Common:1; Rare:35 | ||||
| chr11:100687684-100688068 | Common:1; Rare:82 | ||||
| chr11:101914846-101915034 | Common:2; Rare:51 | ||||
| chr11:101915106-101915228 | Rare:23 |