Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:244451816-244452103 | Common:1; Rare:109 | ||||
chr1:244461221-244461316 | Common:1; Rare:28 | ||||
chr1:244835215-244835333 | Rare:43 | ||||
chr1:244835575-244835723 | Common:2; Rare:65; Clinvar (benign):4 | ||||
chr1:244856459-244856857 | Common:1; Rare:80; Clinvar (benign):2 | ||||
chr1:244863001-244863276 | Common:4; Rare:116 | ||||
chr1:244863802-244864254 | Common:1; Rare:142; Clinvar:6; Clinvar (benign):8 | ||||
chr1:244864258-244864354 | Rare:29 | ||||
chr1:244864364-244864716 | Common:1; Rare:138 | ||||
chr1:244970017-244970424 | Common:5; Rare:174 | ||||
chr1:246507245-246507375 | Common:1; Rare:51 | ||||
chr1:246566160-246566596 | Common:3; Rare:147 | ||||
chr1:246724279-246724568 | Common:2; Rare:100 | ||||
chr1:247104301-247104550 | Common:2; Rare:77 | ||||
chr1:247416150-247416179 | Rare:7 |