Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:31730143-31730402 | Common:2; Rare:73 | ||||
chr6:31736260-31736595 | Common:2; Rare:84 | ||||
chr6:31739706-31740051 | Common:3; Rare:93 | ||||
chr6:31815284-31815550 | Common:1; Rare:80 | ||||
chr6:31897673-31897782 | Rare:20 | ||||
chr6:31958895-31959190 | Rare:93; Clinvar:8 | ||||
chr6:32130205-32130389 | Common:1; Rare:35 | ||||
chr6:32192509-32192555 | Rare:15 | ||||
chr6:32192558-32192736 | Rare:27 | ||||
chr6:32838196-32838321 | Rare:33; Clinvar (benign):1 | ||||
chr6:32843967-32844148 | Common:1; Rare:42; Clinvar:1; Clinvar (benign):1 | ||||
chr6:32844324-32844848 | Common:1; Rare:114 | ||||
chr6:32853664-32854287 | Common:5; Rare:184; Clinvar:2; Clinvar (benign):3 | ||||
chr6:32976396-32976633 | Rare:95 | ||||
chr6:33200356-33200432 | Rare:18 |