| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:31369724-31369882 | Rare:48 | ||||
| chr11:31509575-31509796 | Common:1; Rare:71 | ||||
| chr11:32435641-32435733 | Rare:30 | ||||
| chr11:32829653-32829790 | Common:1; Rare:25 | ||||
| chr11:33161449-33161648 | Common:6; Rare:52 | ||||
| chr11:33257210-33257479 | Common:3; Rare:88 | ||||
| chr11:33258095-33258539 | Common:2; Rare:152 | ||||
| chr11:33736385-33736528 | Common:2; Rare:48 | ||||
| chr11:33774456-33774650 | Common:2; Rare:73 | ||||
| chr11:34052159-34052576 | Common:4; Rare:195 | ||||
| chr11:34105386-34105724 | Common:4; Rare:105 | ||||
| chr11:34438784-34439023 | Common:2; Rare:82; Clinvar (benign):1 | ||||
| chr11:34916287-34916669 | Common:10; Rare:156; Clinvar:5; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr11:35139008-35139327 | Common:1; Rare:85 | ||||
| chr11:35943917-35944131 | Common:3; Rare:71 |