Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:8878578-8878874 | Rare:157 | ||||
chr1:8879127-8879310 | Common:2; Rare:68 | ||||
chr1:9071685-9071780 | Rare:28 | ||||
chr1:9651396-9651788 | Common:8; Rare:69 | ||||
chr1:9943063-9943507 | Common:6; Rare:118 | ||||
chr1:10032722-10033077 | Common:2; Rare:95 | ||||
chr1:10033300-10033527 | Common:3; Rare:37 | ||||
chr1:10210324-10210460 | Common:5; Rare:27 | ||||
chr1:10210667-10210867 | Common:2; Rare:57; Clinvar:2; Clinvar (benign):3 | ||||
chr1:10398649-10399125 | Common:3; Rare:164 | ||||
chr1:10399392-10399508 | Common:2; Rare:25 | ||||
chr1:10430340-10430567 | Common:3; Rare:65 | ||||
chr1:10430665-10431049 | Common:6; Rare:99 | ||||
chr1:10472454-10472588 | Rare:43 | ||||
chr1:10796634-10796820 | Common:1; Rare:55 |