Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:2087723-2087886 | Common:1; Rare:69; Clinvar:3; Clinvar (benign):7 | ||||
chr16:2562731-2562957 | Rare:36 | ||||
chr16:2603382-2603498 | Rare:52 | ||||
chr16:2673302-2673736 | Common:10; Rare:151 | ||||
chr16:2955208-2955450 | Common:2; Rare:68 | ||||
chr16:3033751-3033787 | Rare:4 | ||||
chr16:3144059-3144264 | Common:1; Rare:40 | ||||
chr16:4253777-4253880 | Common:2; Rare:34 | ||||
chr16:4677517-4677685 | Rare:61 | ||||
chr16:5249073-5249125 | Rare:7 | ||||
chr16:8843614-8843823 | Common:4; Rare:58 | ||||
chr16:8847523-8847957 | Common:2; Rare:183; Clinvar:12; Clinvar (benign):7; Clinvar (pathogenic):8 | ||||
chr16:11887730-11887839 | Rare:25 | ||||
chr16:12041686-12041798 | Common:1; Rare:30 | ||||
chr16:15028656-15028932 | Rare:58 |