| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:31827474-31827941 | Common:8; Rare:198 | ||||
| chr6:31834618-31834937 | Common:3; Rare:73 | ||||
| chr6:31958902-31959214 | Rare:104; Clinvar:8 | ||||
| chr6:32153843-32154200 | Common:2; Rare:60 | ||||
| chr6:32154364-32154487 | Rare:15 | ||||
| chr6:32154749-32155047 | Rare:60 | ||||
| chr6:32164486-32164656 | Rare:23 | ||||
| chr6:32176054-32176282 | Common:1; Rare:47 | ||||
| chr6:32844002-32844146 | Rare:31; Clinvar:1 | ||||
| chr6:32844622-32844840 | Common:1; Rare:47 | ||||
| chr6:32853685-32853799 | Rare:56; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:32853985-32854204 | Common:2; Rare:51 | ||||
| chr6:32968770-32968923 | Common:4; Rare:54 | ||||
| chr6:32970739-32970952 | Common:1; Rare:59 | ||||
| chr6:33200656-33200932 | Common:2; Rare:83 |