Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:154172905-154173203 | Common:1; Rare:54; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
chr1:154182917-154183304 | Rare:122 | ||||
chr1:154219842-154220220 | Common:5; Rare:107 | ||||
chr1:154220340-154221001 | Common:1; Rare:221 | ||||
chr1:154221248-154221390 | Rare:31 | ||||
chr1:154272503-154272776 | Common:4; Rare:77; Clinvar:3; Clinvar (benign):3 | ||||
chr1:154558878-154559089 | Common:1; Rare:71 | ||||
chr1:154627870-154628057 | Common:4; Rare:94 | ||||
chr1:154936627-154936783 | Common:2; Rare:54 | ||||
chr1:154936842-154937291 | Common:1; Rare:95 | ||||
chr1:154956089-154956270 | Common:1; Rare:54 | ||||
chr1:154961451-154961549 | Rare:28 | ||||
chr1:154961676-154962029 | Common:1; Rare:120 | ||||
chr1:154965626-154965983 | Common:3; Rare:118 | ||||
chr1:154966160-154966440 | Common:2; Rare:86 |