| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:41057056-41057304 | Rare:33 | ||||
| chr6:41584897-41585186 | Common:1; Rare:62 | ||||
| chr6:43277560-43277755 | Common:1; Rare:33 | ||||
| chr6:43502089-43502212 | Rare:21 | ||||
| chr6:43624587-43624901 | Common:1; Rare:77 | ||||
| chr6:44249412-44250262 | Common:5; Rare:263 | ||||
| chr6:44251126-44251434 | Common:2; Rare:96 | ||||
| chr6:44251466-44252107 | Common:2; Rare:222 | ||||
| chr6:44253187-44253537 | Common:3; Rare:121 | ||||
| chr6:52362980-52363247 | Common:2; Rare:48 | ||||
| chr6:52363652-52363684 | Rare:5 | ||||
| chr6:56640517-56640867 | Common:1; Rare:75; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:57961347-57961643 | Common:2; Rare:93 | ||||
| chr6:70394845-70394902 | Rare:11 | ||||
| chr6:79233633-79233723 | Common:2; Rare:23 |