| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:124983041-124983247 | Common:1; Rare:31 | ||||
| chr10:130110456-130110579 | Common:2; Rare:43 | ||||
| chr10:131970932-131971039 | Rare:32 | ||||
| chr11:319967-320149 | Common:1; Rare:51 | ||||
| chr11:1934577-1934898 | Common:1; Rare:96; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:1995874-1996247 | Common:4; Rare:119 | ||||
| chr11:2644485-2644742 | Common:1; Rare:52 | ||||
| chr11:2681309-2681380 | Rare:10 | ||||
| chr11:2682704-2682762 | Rare:10 | ||||
| chr11:3477036-3477079 | Common:1; Rare:13 | ||||
| chr11:9758165-9758356 | Rare:53 | ||||
| chr11:16604273-16604487 | Common:1; Rare:46 | ||||
| chr11:20024435-20024763 | Common:2; Rare:60 | ||||
| chr11:27202033-27202243 | Common:3; Rare:38 | ||||
| chr11:45355391-45355510 | Rare:30 |