Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:150010692-150010879 | Common:1; Rare:48 | ||||
chr1:150067593-150067864 | Common:1; Rare:78 | ||||
chr1:150364595-150364724 | Rare:42 | ||||
chr1:150487273-150487459 | Common:3; Rare:48; Clinvar (benign):3 | ||||
chr1:150549214-150549410 | Rare:48 | ||||
chr1:150578674-150578742 | Rare:14 | ||||
chr1:150579574-150579901 | Common:10; Rare:105 | ||||
chr1:150629112-150629374 | Common:1; Rare:76 | ||||
chr1:150629430-150629853 | Common:1; Rare:101 | ||||
chr1:150808240-150808369 | Rare:34; Clinvar:2 | ||||
chr1:150876544-150876985 | Common:5; Rare:155 | ||||
chr1:151006687-151006930 | Rare:50 | ||||
chr1:151156589-151156677 | Rare:21 | ||||
chr1:151165851-151166158 | Common:3; Rare:86 | ||||
chr1:151281933-151282318 | Rare:114 |