Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:3916925-3917161 | Rare:63; Clinvar:2; Clinvar (pathogenic):2 | ||||
chr20:3918293-3918521 | Common:4; Rare:37 | ||||
chr20:4090835-4090979 | Common:1; Rare:15 | ||||
chr20:5115300-5115532 | Rare:49; Clinvar (pathogenic):1 | ||||
chr20:5189783-5190075 | Common:1; Rare:63 | ||||
chr20:5589309-5589375 | Rare:14 | ||||
chr20:5601983-5602029 | Rare:10 | ||||
chr20:5609861-5610135 | Common:1; Rare:52 | ||||
chr20:5943410-5943682 | Rare:80 | ||||
chr20:8408094-8408337 | Common:3; Rare:40 | ||||
chr20:9310670-9310771 | Common:1; Rare:25 | ||||
chr20:9472513-9472843 | Common:1; Rare:48 | ||||
chr20:10660582-10660649 | Rare:10 | ||||
chr20:11229831-11230130 | Common:1; Rare:54 | ||||
chr20:17498948-17499221 | Common:3; Rare:60; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 |