Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:153986114-153986449 | Rare:87 | ||||
chr1:153990655-153990968 | Common:2; Rare:130 | ||||
chr1:153991031-153991223 | Rare:53 | ||||
chr1:154172906-154173144 | Common:1; Rare:46; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
chr1:154182636-154183304 | Common:1; Rare:178 | ||||
chr1:154219834-154220221 | Common:5; Rare:110 | ||||
chr1:154220498-154221033 | Common:1; Rare:181 | ||||
chr1:154221250-154221383 | Rare:30 | ||||
chr1:154272445-154272776 | Common:4; Rare:84; Clinvar:3; Clinvar (benign):3 | ||||
chr1:154405461-154405607 | Rare:30 | ||||
chr1:154558226-154558460 | Rare:68 | ||||
chr1:154558908-154559106 | Common:1; Rare:72 | ||||
chr1:154608795-154608830 | Common:3; Rare:6 | ||||
chr1:154627862-154628057 | Common:4; Rare:95 | ||||
chr1:154936606-154936780 | Common:2; Rare:60 |