Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:179264535-179264857 | Common:4; Rare:119 | ||||
chr2:180980246-180980545 | Common:1; Rare:94 | ||||
chr2:180980827-180980964 | Rare:31 | ||||
chr2:182715935-182716391 | Common:3; Rare:149 | ||||
chr2:183124252-183124460 | Common:4; Rare:71 | ||||
chr2:186485966-186486364 | Common:3; Rare:114 | ||||
chr2:186589881-186590029 | Rare:43 | ||||
chr2:186590113-186590460 | Rare:117 | ||||
chr2:186693908-186694149 | Rare:94 | ||||
chr2:188291595-188292066 | Common:6; Rare:133 | ||||
chr2:188292072-188292083 | Common:1; Rare:2 | ||||
chr2:188293005-188293064 | Rare:7 | ||||
chr2:188974441-188974555 | Rare:38; Clinvar:1; Clinvar (pathogenic):1 | ||||
chr2:189441054-189441511 | Common:3; Rare:147 | ||||
chr2:189580637-189580896 | Common:1; Rare:58; Clinvar:2; Clinvar (benign):2 |