| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:32130168-32130495 | Common:4; Rare:56 | ||||
| chr6:32153316-32153581 | Rare:44 | ||||
| chr6:32154328-32154493 | Rare:23 | ||||
| chr6:32176018-32176264 | Common:1; Rare:54 | ||||
| chr6:32177019-32177444 | Common:2; Rare:71 | ||||
| chr6:32178085-32178466 | Common:3; Rare:59 | ||||
| chr6:32188644-32189354 | Common:5; Rare:132 | ||||
| chr6:32189784-32189923 | Common:3; Rare:47 | ||||
| chr6:32190171-32190235 | Rare:13 | ||||
| chr6:32192623-32192686 | Rare:7 | ||||
| chr6:32832442-32832694 | Common:8; Rare:57; Clinvar (benign):5 | ||||
| chr6:32843851-32844119 | Common:2; Rare:76; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:32844280-32844802 | Common:1; Rare:114 | ||||
| chr6:32853654-32853802 | Common:1; Rare:71; Clinvar:2; Clinvar (benign):3 | ||||
| chr6:32854015-32854225 | Common:2; Rare:54 |