| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:132962186-132962479 | Rare:70 | ||||
| chr10:133472828-133473014 | Common:3; Rare:27 | ||||
| chr10:133505417-133505696 | Common:1; Rare:39 | ||||
| chr10:133523638-133523977 | Common:4; Rare:52 | ||||
| chr10:133528840-133529020 | Rare:44 | ||||
| chr11:319951-320130 | Common:1; Rare:56 | ||||
| chr11:698044-698184 | Common:3; Rare:24 | ||||
| chr11:840465-840755 | Common:7; Rare:88 | ||||
| chr11:1227221-1227394 | Common:1; Rare:45 | ||||
| chr11:1229772-1230113 | Common:2; Rare:89; Clinvar (benign):1 | ||||
| chr11:1230220-1230543 | Common:2; Rare:79 | ||||
| chr11:1234291-1234628 | Common:1; Rare:79; Clinvar (benign):2 | ||||
| chr11:1254833-1255129 | Common:2; Rare:89; Clinvar (benign):1 | ||||
| chr11:1753512-1753913 | Common:3; Rare:163; Clinvar:12; Clinvar (benign):14; Clinvar (pathogenic):2 | ||||
| chr11:1836816-1837079 | Common:1; Rare:103 |