Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:107240597-107240724 | Rare:52 | ||||
chr3:131072302-131072408 | Common:1; Rare:15 | ||||
chr3:139373314-139373775 | Rare:84 | ||||
chr3:153164039-153164056 | Rare:3 | ||||
chr3:169765032-169765274 | Rare:89; Clinvar:2; Clinvar (pathogenic):2 | ||||
chr4:121669637-121669973 | Common:3; Rare:94 | ||||
chr4:147637412-147637439 | Rare:4 | ||||
chr5:1633944-1634048 | Common:2; Rare:32 | ||||
chr5:128083053-128083171 | Common:8; Rare:38 | ||||
chr5:137752761-137753036 | Rare:70 | ||||
chr5:159100310-159100523 | Common:3; Rare:67 | ||||
chr5:177939442-177939539 | Common:1; Rare:21 | ||||
chr6:28136819-28136883 | Common:1; Rare:18 | ||||
chr6:30684092-30684223 | Rare:21 | ||||
chr6:31400629-31400722 | Common:3; Rare:21 |