Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:68232281-68232320 | Rare:10 | ||||
chr1:68497025-68497225 | Common:2; Rare:68 | ||||
chr1:70205398-70205650 | Rare:102 | ||||
chr1:70205652-70205770 | Rare:32 | ||||
chr1:70221307-70221603 | Rare:121 | ||||
chr1:70227726-70227950 | Common:2; Rare:43 | ||||
chr1:70228757-70229335 | Common:1; Rare:92 | ||||
chr1:70229416-70229731 | Rare:43 | ||||
chr1:70229776-70230114 | Rare:47 | ||||
chr1:70230151-70230518 | Common:2; Rare:66 | ||||
chr1:70230918-70231313 | Rare:49 | ||||
chr1:70246828-70247077 | Rare:52 | ||||
chr1:70354677-70354925 | Rare:81 | ||||
chr1:70411096-70411283 | Common:1; Rare:44; Clinvar:1; Clinvar (benign):1 | ||||
chr1:71066697-71066877 | Rare:62 |