Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:52355653-52355853 | Rare:70 | ||||
chr1:52404390-52404629 | Common:1; Rare:67 | ||||
chr1:52553050-52553206 | Common:3; Rare:51 | ||||
chr1:52698056-52698162 | Rare:21 | ||||
chr1:52913098-52913345 | Common:1; Rare:36 | ||||
chr1:53220561-53220728 | Common:2; Rare:82 | ||||
chr1:53238378-53238639 | Common:2; Rare:83 | ||||
chr1:53328056-53328233 | Rare:45 | ||||
chr1:53946259-53946739 | Common:3; Rare:146 | ||||
chr1:54053136-54053645 | Common:6; Rare:170 | ||||
chr1:54199995-54200283 | Rare:89 | ||||
chr1:54335832-54336166 | Common:1; Rare:80 | ||||
chr1:54886442-54886860 | Common:1; Rare:137 | ||||
chr1:54886892-54887271 | Common:2; Rare:130; Clinvar:6; Clinvar (benign):2 | ||||
chr1:55039367-55039641 | Common:2; Rare:65; Clinvar:4; Clinvar (benign):1 |