Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:169694383-169694582 | Common:5; Rare:58 | ||||
chr2:169798793-169798916 | Rare:35 | ||||
chr2:171434018-171434234 | Common:1; Rare:54 | ||||
chr2:171688063-171688304 | Common:1; Rare:56 | ||||
chr2:173965281-173965508 | Common:1; Rare:80 | ||||
chr2:174395650-174395795 | Common:1; Rare:48 | ||||
chr2:177263441-177263520 | Rare:13 | ||||
chr2:177264643-177264797 | Common:2; Rare:51 | ||||
chr2:177392672-177392790 | Rare:30; Clinvar:1 | ||||
chr2:178451120-178451382 | Common:5; Rare:74; Clinvar:3; Clinvar (benign):3 | ||||
chr2:180980830-180980963 | Rare:30 | ||||
chr2:186486120-186486330 | Common:3; Rare:67 | ||||
chr2:189783929-189784133 | Common:4; Rare:73; Clinvar:1; Clinvar (benign):1 | ||||
chr2:189784286-189784535 | Common:4; Rare:89; Clinvar:8; Clinvar (benign):2 | ||||
chr2:190343955-190344063 | Rare:23 |