Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:23691669-23691934 | Common:6; Rare:100; Clinvar:2; Clinvar (benign):3 | ||||
chr1:23692154-23692308 | Rare:50 | ||||
chr1:23743013-23743190 | Common:1; Rare:35 | ||||
chr1:23743274-23743548 | Rare:96 | ||||
chr1:23744047-23744132 | Rare:21 | ||||
chr1:23744529-23744566 | Common:1; Rare:6 | ||||
chr1:23778194-23778498 | Common:9; Rare:142 | ||||
chr1:23790930-23791261 | Rare:91 | ||||
chr1:23799538-23799709 | Rare:27 | ||||
chr1:23800521-23801020 | Common:1; Rare:158 | ||||
chr1:23825316-23825627 | Common:3; Rare:97; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):4 | ||||
chr1:23825895-23826085 | Common:1; Rare:30 | ||||
chr1:23868217-23868557 | Common:6; Rare:90; Clinvar:2; Clinvar (benign):5 | ||||
chr1:23913334-23913499 | Rare:32 | ||||
chr1:23958935-23959446 | Common:4; Rare:102 |