Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:231337422-231337508 | Rare:22 | ||||
chr1:231337760-231338319 | Common:5; Rare:181 | ||||
chr1:231420307-231420343 | Rare:7 | ||||
chr1:231420381-231420520 | Rare:40 | ||||
chr1:231528482-231528805 | Common:2; Rare:110 | ||||
chr1:234373288-234373800 | Common:1; Rare:218; Clinvar (benign):7 | ||||
chr1:234608071-234608247 | Common:1; Rare:55 | ||||
chr1:235128787-235129025 | Rare:92 | ||||
chr1:235328149-235328611 | Common:4; Rare:141 | ||||
chr1:235866869-235867180 | Common:3; Rare:99 | ||||
chr1:236065037-236065356 | Common:3; Rare:120; Clinvar (pathogenic):1 | ||||
chr1:243255047-243255344 | Common:1; Rare:64 | ||||
chr1:243255776-243256135 | Common:1; Rare:105; Clinvar:4; Clinvar (benign):1 | ||||
chr1:244451879-244452219 | Common:1; Rare:112 | ||||
chr1:244835580-244835756 | Common:2; Rare:82; Clinvar:1; Clinvar (benign):5 |