Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:153634243-153634380 | Common:1; Rare:36 | ||||
chr1:153634401-153634512 | Rare:38 | ||||
chr1:153664028-153664473 | Common:2; Rare:93 | ||||
chr1:153670904-153671246 | Rare:117 | ||||
chr1:153727746-153728082 | Common:1; Rare:102 | ||||
chr1:153766810-153766946 | Rare:28 | ||||
chr1:153922786-153923284 | Common:2; Rare:136 | ||||
chr1:153923369-153923390 | Rare:8 | ||||
chr1:153963269-153963355 | Rare:18 | ||||
chr1:153963484-153963760 | Common:2; Rare:77 | ||||
chr1:153967434-153967517 | Common:1; Rare:12 | ||||
chr1:153967624-153967954 | Common:1; Rare:59 | ||||
chr1:153986264-153986455 | Rare:44 | ||||
chr1:153990652-153990809 | Common:2; Rare:73 | ||||
chr1:154170398-154170771 | Rare:86; Clinvar (benign):2 |