Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:174439751-174440043 | Rare:62 | ||||
chr3:174468626-174468714 | Rare:16 | ||||
chr3:174839187-174839247 | Rare:10 | ||||
chr3:175718673-175718957 | Common:3; Rare:56 | ||||
chr3:177013246-177013459 | Common:1; Rare:34 | ||||
chr3:177026370-177026620 | Rare:44; Clinvar:1; Clinvar (benign):1 | ||||
chr3:177032769-177033121 | Common:2; Rare:68; Clinvar:1; Clinvar (benign):1 | ||||
chr3:179027479-179027796 | Rare:88 | ||||
chr3:180948366-180948809 | Common:2; Rare:90 | ||||
chr3:180972601-180972649 | Rare:10 | ||||
chr3:180973119-180973180 | Rare:9 | ||||
chr3:183812585-183812894 | Common:2; Rare:48 | ||||
chr3:184187141-184187523 | Common:5; Rare:111 | ||||
chr3:184308468-184308981 | Common:2; Rare:130 | ||||
chr3:184317396-184317718 | Common:2; Rare:83 |