Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:36481609-36481729 | Common:2; Rare:29 | ||||
chr22:37849316-37849452 | Rare:79 | ||||
chr22:38681817-38682003 | Common:1; Rare:78 | ||||
chr22:41621018-41621360 | Common:7; Rare:129 | ||||
chr22:42614940-42615248 | Common:3; Rare:128 | ||||
chr22:45413571-45413720 | Rare:58 | ||||
chr22:46762524-46762659 | Common:3; Rare:44 | ||||
chr22:50783628-50783846 | Common:1; Rare:64 | ||||
chr3:9792990-9793112 | Common:2; Rare:56 | ||||
chr3:10026307-10026434 | Rare:44 | ||||
chr3:10141660-10141813 | Common:1; Rare:56; Clinvar:4; Clinvar (benign):7 | ||||
chr3:12664096-12664315 | Common:1; Rare:60; Clinvar:1; Clinvar (benign):2 | ||||
chr3:14124713-14125093 | Common:4; Rare:114; Clinvar:4; Clinvar (benign):1 | ||||
chr3:14178593-14178857 | Common:1; Rare:133; Clinvar:3; Clinvar (benign):1 | ||||
chr3:15427501-15427623 | Rare:42 |