Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:178725029-178725309 | Common:10; Rare:102 | ||||
chr1:179877766-179877926 | Rare:31 | ||||
chr1:179882488-179882945 | Common:1; Rare:227; Clinvar:9; Clinvar (benign):4 | ||||
chr1:180502347-180502647 | Common:1; Rare:102 | ||||
chr1:182391744-182392016 | Common:3; Rare:92; Clinvar:4; Clinvar (benign):3 | ||||
chr1:182604381-182604509 | Rare:27 | ||||
chr1:182789622-182789792 | Common:2; Rare:61 | ||||
chr1:182839213-182839752 | Common:4; Rare:210 | ||||
chr1:183185761-183186084 | Common:1; Rare:60; Clinvar:1 | ||||
chr1:183635655-183636114 | Common:5; Rare:128 | ||||
chr1:184051653-184051793 | Common:2; Rare:57 | ||||
chr1:184386732-184387082 | Common:3; Rare:108 | ||||
chr1:184754812-184755160 | Common:1; Rare:85 | ||||
chr1:184974415-184974587 | Rare:45 | ||||
chr1:185156941-185157243 | Common:1; Rare:77 |