Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:31665799-31666163 | Common:3; Rare:100 | ||||
chr6:31730148-31730376 | Common:2; Rare:67 | ||||
chr6:31736372-31736641 | Common:2; Rare:52 | ||||
chr6:31739727-31740021 | Common:3; Rare:68 | ||||
chr6:31792775-31793039 | Common:1; Rare:80 | ||||
chr6:31806760-31807036 | Common:1; Rare:113 | ||||
chr6:31815285-31815546 | Common:1; Rare:77 | ||||
chr6:31862781-31862982 | Common:2; Rare:51; Clinvar:3; Clinvar (benign):1 | ||||
chr6:31897649-31897782 | Rare:27 | ||||
chr6:31958891-31959198 | Rare:102; Clinvar:8 | ||||
chr6:32178084-32178458 | Common:3; Rare:56 | ||||
chr6:32190171-32190253 | Rare:14 | ||||
chr6:32838219-32838338 | Rare:33; Clinvar (benign):1 | ||||
chr6:32843961-32844119 | Common:1; Rare:39; Clinvar:1; Clinvar (benign):1 | ||||
chr6:32844328-32844405 | Rare:19 |