Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:68527371-68527580 | Common:2; Rare:66 | ||||
chr10:68956053-68956440 | Common:3; Rare:117 | ||||
chr10:69087927-69088236 | Rare:67 | ||||
chr10:69179927-69180301 | Common:2; Rare:116 | ||||
chr10:69315638-69315895 | Rare:35 | ||||
chr10:70170425-70170670 | Common:4; Rare:83 | ||||
chr10:70887867-70887983 | Common:1; Rare:23 | ||||
chr10:71773494-71773751 | Common:3; Rare:74 | ||||
chr10:71819484-71819894 | Common:1; Rare:164; Clinvar:5; Clinvar (benign):3 | ||||
chr10:71851187-71851344 | Common:4; Rare:76; Clinvar:4; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
chr10:72216215-72216562 | Common:3; Rare:98 | ||||
chr10:72273775-72273937 | Rare:44 | ||||
chr10:72354869-72355022 | Common:2; Rare:74 | ||||
chr10:72355084-72355196 | Rare:26 | ||||
chr10:72523896-72524146 | Common:1; Rare:44 |