Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:89508262-89508410 | Common:1; Rare:84 | ||||
chr16:89560540-89560709 | Rare:71 | ||||
chr16:89657647-89658053 | Common:3; Rare:212 | ||||
chr16:89686567-89686702 | Common:6; Rare:59 | ||||
chr16:89720872-89720981 | Common:1; Rare:28 | ||||
chr16:89816640-89816775 | Common:2; Rare:59; Clinvar:2 | ||||
chr16:89923160-89923395 | Rare:103 | ||||
chr16:89972521-89972614 | Rare:30 | ||||
chr16:90019390-90019660 | Common:5; Rare:82 | ||||
chr16:90022551-90022709 | Rare:63 | ||||
chr17:714785-714874 | Common:2; Rare:33 | ||||
chr17:1400046-1400342 | Common:2; Rare:123 | ||||
chr17:1516628-1516958 | Common:1; Rare:117 | ||||
chr17:1684790-1685038 | Common:2; Rare:81; Clinvar:5; Clinvar (benign):1 | ||||
chr17:1829832-1830051 | Common:7; Rare:91 |