Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:44651687-44651831 | Common:1; Rare:39; Clinvar (benign):1 | ||||
chr20:44966383-44966571 | Common:1; Rare:70 | ||||
chr20:45416305-45416603 | Rare:91; Clinvar (pathogenic):2 | ||||
chr20:45791852-45792014 | Common:1; Rare:61 | ||||
chr20:45812296-45812698 | Common:4; Rare:118 | ||||
chr20:45857326-45857655 | Common:3; Rare:97 | ||||
chr20:45891013-45891387 | Common:3; Rare:114; Clinvar:8; Clinvar (benign):3 | ||||
chr20:46363954-46364099 | Common:1; Rare:30 | ||||
chr20:47318970-47319114 | Common:1; Rare:38 | ||||
chr20:47356664-47356887 | Rare:51 | ||||
chr20:47501720-47502009 | Common:1; Rare:101 | ||||
chr20:47659397-47659509 | Rare:31 | ||||
chr20:47786345-47786672 | Common:4; Rare:60 | ||||
chr20:49046162-49046358 | Common:3; Rare:58 | ||||
chr20:49219275-49219538 | Rare:118 |