| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:45422174-45422363 | Common:1; Rare:44 | ||||
| chr6:45422421-45422724 | Common:2; Rare:110; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr6:46652779-46653008 | Rare:60 | ||||
| chr6:49463180-49463438 | Common:1; Rare:76; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:52420108-52420422 | Common:3; Rare:133; Clinvar:1; Clinvar (benign):3 | ||||
| chr6:52576806-52576883 | Rare:32 | ||||
| chr6:52576888-52577307 | Common:7; Rare:151 | ||||
| chr6:52671066-52671242 | Rare:40 | ||||
| chr6:52995071-52995354 | Rare:61 | ||||
| chr6:53065369-53065789 | Common:1; Rare:121 | ||||
| chr6:53348905-53349204 | Common:2; Rare:108 | ||||
| chr6:56462470-56462710 | Rare:42 | ||||
| chr6:56541898-56542358 | Common:1; Rare:67 | ||||
| chr6:56542779-56543118 | Common:2; Rare:57 | ||||
| chr6:56843061-56843113 | Rare:11 |