Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:47318972-47319077 | Rare:28 | ||||
chr20:47356666-47356887 | Rare:51 | ||||
chr20:47501770-47501950 | Common:1; Rare:62 | ||||
chr20:49046219-49046367 | Common:3; Rare:48 | ||||
chr20:49915462-49915578 | Common:3; Rare:46 | ||||
chr20:50191177-50191406 | Common:1; Rare:75 | ||||
chr20:50958488-50958860 | Common:1; Rare:132; Clinvar:1; Clinvar (benign):3 | ||||
chr20:56392188-56392542 | Common:3; Rare:96 | ||||
chr20:56468423-56468757 | Rare:109 | ||||
chr20:58309418-58309736 | Common:2; Rare:121 | ||||
chr20:58515360-58515534 | Common:3; Rare:32 | ||||
chr20:58909204-58909423 | Common:2; Rare:52; Clinvar:1; Clinvar (pathogenic):2 | ||||
chr20:59006989-59007115 | Rare:40 | ||||
chr20:62143299-62143808 | Common:6; Rare:217 | ||||
chr20:62182954-62183049 | Rare:23 |