| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67401754-67402076 | Common:3; Rare:116 | ||||
| chr11:67428301-67428537 | Rare:82 | ||||
| chr11:67443451-67443734 | Common:2; Rare:91 | ||||
| chr11:67469205-67469340 | Rare:47 | ||||
| chr11:67482906-67483192 | Rare:63; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr11:67508044-67508468 | Common:1; Rare:97 | ||||
| chr11:67508627-67508768 | Common:3; Rare:52 | ||||
| chr11:67583581-67583876 | Common:2; Rare:96 | ||||
| chr11:68004051-68004193 | Rare:39 | ||||
| chr11:68030367-68030764 | Common:3; Rare:110; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:68038860-68039073 | Rare:63; Clinvar:1 | ||||
| chr11:68121389-68121656 | Common:1; Rare:87 | ||||
| chr11:68213528-68213979 | Common:1; Rare:259 | ||||
| chr11:68271891-68272115 | Common:2; Rare:95 | ||||
| chr11:68460223-68460320 | Common:2; Rare:49 |