Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:160343217-160343410 | Rare:73 | ||||
chr1:161045929-161046042 | Rare:25 | ||||
chr1:161118011-161118155 | Rare:75 | ||||
chr1:161132420-161132674 | Common:1; Rare:90 | ||||
chr1:161153745-161153933 | Common:1; Rare:41 | ||||
chr1:161314264-161314404 | Common:3; Rare:50; Clinvar:2; Clinvar (benign):2 | ||||
chr1:161749653-161749829 | Rare:61 | ||||
chr1:162497718-162497855 | Common:2; Rare:39 | ||||
chr1:163321723-163322057 | Common:1; Rare:91 | ||||
chr1:165698556-165698818 | Common:4; Rare:78 | ||||
chr1:165768796-165769052 | Common:2; Rare:111 | ||||
chr1:166839252-166839522 | Rare:84 | ||||
chr1:167220663-167220918 | Common:1; Rare:62 | ||||
chr1:167935974-167936261 | Common:1; Rare:87 | ||||
chr1:167936549-167936706 | Rare:51 |