Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:66924808-66925031 | Rare:96 | ||||
chr1:67053941-67054211 | Common:1; Rare:92 | ||||
chr1:67684934-67685247 | Common:3; Rare:83 | ||||
chr1:68232201-68232219 | Rare:4 | ||||
chr1:70205542-70205764 | Rare:72 | ||||
chr1:70354656-70354862 | Rare:69 | ||||
chr1:71066700-71066869 | Rare:60 | ||||
chr1:71080992-71081364 | Rare:100 | ||||
chr1:72282844-72282906 | Common:2; Rare:15 | ||||
chr1:74198141-74198356 | Common:2; Rare:119 | ||||
chr1:74732966-74733323 | Common:6; Rare:120 | ||||
chr1:77219400-77219520 | Rare:54 | ||||
chr1:77682629-77682723 | Rare:26 | ||||
chr1:77759665-77759891 | Common:2; Rare:88 | ||||
chr1:77888078-77888756 | Common:3; Rare:157; Clinvar:2; Clinvar (benign):1 |