Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:241847885-241848019 | Common:1; Rare:30 | ||||
chr1:241848048-241848310 | Common:4; Rare:100 | ||||
chr1:243255019-243255517 | Common:1; Rare:137 | ||||
chr1:243255726-243256162 | Common:2; Rare:238; Clinvar:8; Clinvar (benign):2 | ||||
chr1:244451823-244452340 | Common:4; Rare:283 | ||||
chr1:244652958-244653313 | Common:4; Rare:216 | ||||
chr1:244834943-244835386 | Rare:277 | ||||
chr1:244835545-244835739 | Common:5; Rare:154; Clinvar (benign):7 | ||||
chr1:244862999-244863202 | Common:3; Rare:84 | ||||
chr1:244863660-244864103 | Common:2; Rare:200; Clinvar:11; Clinvar (benign):13 | ||||
chr1:244864385-244864724 | Common:2; Rare:255 | ||||
chr1:244969706-244969859 | Rare:46 | ||||
chr1:244969850-244970219 | Common:1; Rare:189 | ||||
chr1:244970226-244970431 | Common:8; Rare:195 | ||||
chr1:244970555-244970860 | Common:7; Rare:88 |