Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:149917810-149917948 | Common:1; Rare:36 | ||||
chr1:149927738-149927922 | Common:1; Rare:71; Clinvar (benign):5 | ||||
chr1:149928229-149928361 | Rare:25 | ||||
chr1:150010510-150010906 | Common:4; Rare:98 | ||||
chr1:150067079-150067457 | Common:4; Rare:69 | ||||
chr1:150067625-150067899 | Rare:77 | ||||
chr1:150235906-150236374 | Common:1; Rare:108 | ||||
chr1:150256903-150257322 | Common:3; Rare:63 | ||||
chr1:150257719-150257915 | Rare:40 | ||||
chr1:150257958-150258155 | Common:2; Rare:51 | ||||
chr1:150268356-150268516 | Rare:33 | ||||
chr1:150282149-150282237 | Rare:22 | ||||
chr1:150293803-150293927 | Common:1; Rare:44 | ||||
chr1:150321404-150321590 | Rare:59; Clinvar:3; Clinvar (benign):1 | ||||
chr1:150363919-150364206 | Common:4; Rare:101 |