Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:159925463-159925617 | Common:1; Rare:42 | ||||
chr1:160031841-160032028 | Common:2; Rare:48 | ||||
chr1:160262436-160262653 | Common:1; Rare:69 | ||||
chr1:160343181-160343399 | Rare:90 | ||||
chr1:160711781-160712008 | Common:5; Rare:52 | ||||
chr1:161045887-161046047 | Common:1; Rare:42 | ||||
chr1:161118021-161118141 | Rare:59 | ||||
chr1:161166268-161166477 | Common:2; Rare:49; Clinvar:2; Clinvar (benign):1 | ||||
chr1:161225757-161226069 | Common:10; Rare:46 | ||||
chr1:161314215-161314408 | Common:3; Rare:68; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr1:161524395-161524541 | Common:3; Rare:46 | ||||
chr1:161707108-161707293 | Common:3; Rare:55 | ||||
chr1:161707308-161707342 | Rare:8 | ||||
chr1:161721365-161721592 | Common:2; Rare:37 | ||||
chr1:161749614-161749822 | Rare:70 |