Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:160407935-160408047 | Common:1; Rare:24 | ||||
chr1:160408060-160408305 | Common:1; Rare:45 | ||||
chr1:160896346-160896537 | Rare:46 | ||||
chr1:160986122-160986162 | Rare:3 | ||||
chr1:160986888-160987221 | Common:2; Rare:60 | ||||
chr1:160999394-160999674 | Rare:68 | ||||
chr1:161018723-161018771 | Rare:10 | ||||
chr1:161020096-161020423 | Common:1; Rare:57 | ||||
chr1:161074775-161075086 | Common:1; Rare:73 | ||||
chr1:161105098-161105266 | Rare:25 | ||||
chr1:161109631-161109656 | |||||
chr1:161363072-161363319 | Common:1; Rare:42; Clinvar (benign):2 | ||||
chr1:161365844-161365961 | Rare:19 | ||||
chr1:161750353-161750449 | Rare:14 | ||||
chr1:162600391-162600634 | Common:3; Rare:42 |