Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:8797631-8797867 | Rare:89; Clinvar:2; Clinvar (benign):1 | ||||
chr16:10580581-10580781 | Rare:64 | ||||
chr16:11851506-11851635 | Rare:62 | ||||
chr16:11915900-11916206 | Common:2; Rare:122 | ||||
chr16:14630200-14630433 | Rare:100 | ||||
chr16:15094247-15094442 | Rare:91 | ||||
chr16:18801429-18801830 | Common:4; Rare:140; Clinvar:1 | ||||
chr16:21953024-21953408 | Common:1; Rare:96; Clinvar (benign):3 | ||||
chr16:23641278-23641525 | Common:2; Rare:69; Clinvar:1; Clinvar (benign):2 | ||||
chr16:23678710-23678935 | Common:4; Rare:70 | ||||
chr16:24729604-24729727 | Common:6; Rare:68 | ||||
chr16:25111573-25111735 | Common:1; Rare:31 | ||||
chr16:27549880-27550167 | Common:2; Rare:109 | ||||
chr16:28846265-28846646 | Common:2; Rare:128; Clinvar:6; Clinvar (benign):5 | ||||
chr16:29995609-29995693 | Rare:42 |