Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:153658567-153658776 | Common:2; Rare:61 | ||||
chr1:153658868-153658999 | Rare:51 | ||||
chr1:153678575-153678761 | Common:1; Rare:36 | ||||
chr1:153727754-153728097 | Common:1; Rare:103 | ||||
chr1:153728383-153728602 | Rare:41 | ||||
chr1:153775110-153775412 | Common:1; Rare:148 | ||||
chr1:153945197-153945328 | Rare:19 | ||||
chr1:153962755-153962924 | Rare:32 | ||||
chr1:153963479-153963706 | Common:2; Rare:58 | ||||
chr1:153967729-153967912 | Rare:34 | ||||
chr1:153986167-153986449 | Rare:73 | ||||
chr1:154182650-154183236 | Common:1; Rare:159 | ||||
chr1:154220476-154221181 | Common:1; Rare:228 | ||||
chr1:154272572-154272688 | Common:4; Rare:27; Clinvar:1; Clinvar (benign):3 | ||||
chr1:154405502-154405630 | Rare:23 |