Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:171781381-171781718 | Common:4; Rare:86 | ||||
chr1:172444011-172444168 | Rare:51 | ||||
chr1:173477050-173477442 | Common:5; Rare:140 | ||||
chr1:173824348-173824684 | Rare:61 | ||||
chr1:173824866-173825004 | Rare:30 | ||||
chr1:173867969-173868196 | Common:1; Rare:82 | ||||
chr1:174022313-174022508 | Rare:51 | ||||
chr1:174159338-174159549 | Common:2; Rare:80 | ||||
chr1:174999617-175000152 | Common:3; Rare:175 | ||||
chr1:178725123-178725341 | Common:10; Rare:80 | ||||
chr1:179293672-179293837 | Common:1; Rare:60 | ||||
chr1:179877770-179877866 | Rare:20 | ||||
chr1:179882505-179882878 | Rare:182; Clinvar:8; Clinvar (benign):2 | ||||
chr1:180502329-180502651 | Common:1; Rare:112 | ||||
chr1:180502814-180502989 | Rare:67 |