Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:7961455-7961767 | Common:4; Rare:107; Clinvar:2; Clinvar (benign):3 | ||||
chr1:8878578-8878609 | Rare:15 | ||||
chr1:8878612-8878880 | Rare:144 | ||||
chr1:9943320-9943489 | Common:2; Rare:38 | ||||
chr1:10398896-10399108 | Common:2; Rare:84 | ||||
chr1:11262495-11262860 | Common:3; Rare:107 | ||||
chr1:11805905-11806258 | Common:2; Rare:99; Clinvar:1 | ||||
chr1:13749175-13749439 | Common:2; Rare:90 | ||||
chr1:15526553-15526889 | Common:2; Rare:104 | ||||
chr1:16352420-16352570 | Common:2; Rare:83 | ||||
chr1:16613508-16613643 | |||||
chr1:17053997-17054187 | Common:3; Rare:58; Clinvar:5; Clinvar (benign):6 | ||||
chr1:19210254-19210395 | Rare:53 | ||||
chr1:19251494-19251854 | Common:6; Rare:121 | ||||
chr1:19596744-19597080 | Common:3; Rare:126 |