Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:11654421-11654493 | Rare:22 | ||||
chr1:11654716-11654930 | Common:4; Rare:58 | ||||
chr1:11805935-11806191 | Common:2; Rare:69; Clinvar:1 | ||||
chr1:11934485-11934754 | Common:5; Rare:88; Clinvar:5; Clinvar (benign):1 | ||||
chr1:11980086-11980473 | Common:6; Rare:125; Clinvar:1; Clinvar (benign):4 | ||||
chr1:13749136-13749445 | Common:2; Rare:103 | ||||
chr1:16155928-16156201 | Rare:63; Clinvar:2 | ||||
chr1:16352420-16352606 | Common:3; Rare:99 | ||||
chr1:16613514-16613703 | Common:2; Rare:1 | ||||
chr1:17439669-17439968 | Rare:95 | ||||
chr1:19210071-19210410 | Rare:120 | ||||
chr1:19251479-19251857 | Common:6; Rare:132 | ||||
chr1:19311988-19312346 | Common:8; Rare:167 | ||||
chr1:19596874-19597080 | Common:2; Rare:100 | ||||
chr1:20508079-20508250 | Common:3; Rare:59 |