Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:244461221-244461334 | Common:2; Rare:30 | ||||
chr1:244652965-244653212 | Common:2; Rare:100 | ||||
chr1:244835197-244835333 | Rare:58 | ||||
chr1:244835574-244835752 | Common:2; Rare:80; Clinvar (benign):5 | ||||
chr1:244863931-244864686 | Common:1; Rare:257; Clinvar:3; Clinvar (benign):6 | ||||
chr1:244969461-244970001 | Common:1; Rare:149 | ||||
chr1:244970017-244970442 | Common:5; Rare:184 | ||||
chr1:244970916-244971110 | Common:1; Rare:57 | ||||
chr1:246507213-246507359 | Common:1; Rare:61 | ||||
chr1:246566140-246566596 | Common:3; Rare:153 | ||||
chr1:247078733-247078902 | Rare:53 | ||||
chr1:247104304-247104550 | Common:2; Rare:77 | ||||
chr1:247171924-247172067 | Common:2; Rare:17 | ||||
chr1:247331226-247331318 | Rare:29 | ||||
chr1:247331590-247332054 | Rare:119 |