| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:29944133-29944616 | Common:37; Rare:122 | ||||
| chr6:29964771-29965073 | Common:11; Rare:54 | ||||
| chr6:30655254-30655399 | Common:1; Rare:39 | ||||
| chr6:31185436-31185515 | Common:1; Rare:11 | ||||
| chr6:31185926-31185999 | Common:1; Rare:14 | ||||
| chr6:31186046-31186188 | Common:5; Rare:30 | ||||
| chr6:31400608-31400732 | Common:5; Rare:25 | ||||
| chr6:31410195-31410490 | Common:13; Rare:52 | ||||
| chr6:31411747-31412049 | Common:10; Rare:57; Clinvar (benign):1 | ||||
| chr6:31863697-31863823 | Rare:39 | ||||
| chr6:31865313-31865581 | Rare:75 | ||||
| chr6:31869204-31869582 | Common:3; Rare:64 | ||||
| chr6:31889618-31889627 | Rare:1 | ||||
| chr6:32853221-32853444 | Rare:77; Clinvar:3; Clinvar (benign):2 | ||||
| chr6:32894576-32894945 | Common:16; Rare:114 |