Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:129249525-129249710 | Common:2; Rare:57 | ||||
chr3:129439856-129440264 | Common:1; Rare:121; Clinvar:1; Clinvar (benign):1 | ||||
chr3:130746764-130746921 | Common:3; Rare:51 | ||||
chr3:131381467-131381792 | Common:2; Rare:81 | ||||
chr3:131502876-131503013 | Common:1; Rare:58 | ||||
chr3:132659785-132659989 | Common:3; Rare:46 | ||||
chr3:134485696-134485749 | Rare:23 | ||||
chr3:134485969-134486045 | Common:2; Rare:32 | ||||
chr3:136861936-136862275 | Common:1; Rare:102 | ||||
chr3:139389557-139389828 | Common:1; Rare:89 | ||||
chr3:141368441-141368530 | Rare:18 | ||||
chr3:143001444-143001641 | Common:3; Rare:70 | ||||
chr3:146161129-146161386 | Common:2; Rare:63; Clinvar:2; Clinvar (benign):1 | ||||
chr3:150603176-150603309 | Common:1; Rare:43 | ||||
chr3:152268889-152268965 | Rare:30 |