Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:173415390-173415704 | Common:2; Rare:62 | ||||
chr1:173838107-173838243 | Rare:29; Clinvar (pathogenic):2 | ||||
chr1:174968922-174969085 | Rare:33 | ||||
chr1:174978741-174978890 | Rare:22 | ||||
chr1:177351331-177351646 | Common:2; Rare:59 | ||||
chr1:178006510-178006692 | Rare:40 | ||||
chr1:178579679-178579814 | Rare:25 | ||||
chr1:179825289-179825428 | Rare:25 | ||||
chr1:181135010-181135109 | Rare:13 | ||||
chr1:182149347-182149708 | Common:1; Rare:52 | ||||
chr1:182790573-182790790 | Common:12; Rare:50 | ||||
chr1:182791046-182791142 | Rare:23 | ||||
chr1:182794914-182794956 | Rare:8 | ||||
chr1:183471128-183471458 | Common:2; Rare:59 | ||||
chr1:183538105-183538410 | Common:1; Rare:60 |