| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:31649381-31649552 | Rare:34 | ||||
| chr6:33249235-33249629 | Rare:120 | ||||
| chr6:33425656-33425846 | Common:1; Rare:46; Clinvar (benign):1 | ||||
| chr6:33633589-33633879 | Common:5; Rare:84 | ||||
| chr6:34246202-34246416 | Common:1; Rare:43 | ||||
| chr6:34879558-34879855 | Rare:50 | ||||
| chr6:35469517-35469585 | Rare:21 | ||||
| chr6:36601776-36601929 | Common:1; Rare:51 | ||||
| chr6:37845107-37845239 | Rare:28 | ||||
| chr6:37953838-37953914 | Rare:6 | ||||
| chr6:41073833-41074106 | Common:3; Rare:65 | ||||
| chr6:41789227-41789756 | Rare:105 | ||||
| chr6:42197852-42198096 | Common:2; Rare:45 | ||||
| chr6:42200098-42200335 | Common:5; Rare:35 | ||||
| chr6:43172270-43172436 | Common:1; Rare:31 |