| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:86068659-86068873 | Rare:64 | ||||
| chr11:86244971-86245268 | Common:1; Rare:131 | ||||
| chr11:86955340-86955623 | Common:1; Rare:91; Clinvar (benign):1 | ||||
| chr11:87037769-87038040 | Common:3; Rare:127 | ||||
| chr11:88175360-88175579 | Common:2; Rare:90 | ||||
| chr11:88337670-88337856 | Common:4; Rare:95; Clinvar:6; Clinvar (benign):3 | ||||
| chr11:90222989-90223128 | Common:1; Rare:55 | ||||
| chr11:93741381-93741719 | Common:7; Rare:136 | ||||
| chr11:93784189-93784367 | Common:3; Rare:55 | ||||
| chr11:94129052-94129191 | Common:2; Rare:38 | ||||
| chr11:94493779-94494075 | Common:6; Rare:88; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:94706435-94706571 | Common:2; Rare:31 | ||||
| chr11:94973528-94973719 | Rare:58 | ||||
| chr11:95066778-95066952 | Rare:31 | ||||
| chr11:95067124-95067210 | Rare:28 |