| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:31546553-31546871 | Common:3; Rare:65 | ||||
| chr6:31547436-31547650 | Common:2; Rare:43 | ||||
| chr6:31652368-31652475 | Rare:24 | ||||
| chr6:31652642-31652773 | Common:2; Rare:26 | ||||
| chr6:31665859-31666115 | Common:3; Rare:70 | ||||
| chr6:31837255-31837404 | Rare:49 | ||||
| chr6:31897679-31897786 | Rare:21 | ||||
| chr6:31958840-31959182 | Rare:102; Clinvar:8 | ||||
| chr6:32130169-32130461 | Common:4; Rare:49 | ||||
| chr6:32154330-32154487 | Rare:22 | ||||
| chr6:32176057-32176251 | Common:1; Rare:39 | ||||
| chr6:32178078-32178466 | Common:3; Rare:59 | ||||
| chr6:32843986-32844149 | Rare:37; Clinvar:1 | ||||
| chr6:32844282-32844833 | Common:1; Rare:125 | ||||
| chr6:32853642-32854226 | Common:4; Rare:176; Clinvar:2; Clinvar (benign):4 |