Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:243255040-243255358 | Common:1; Rare:73 | ||||
chr1:243255472-243255497 | Rare:3 | ||||
chr1:243255741-243256157 | Common:1; Rare:121; Clinvar:4; Clinvar (benign):1 | ||||
chr1:244451796-244452212 | Common:1; Rare:140 | ||||
chr1:244461221-244461435 | Common:2; Rare:62 | ||||
chr1:244835025-244835333 | Rare:113 | ||||
chr1:244835575-244835736 | Common:2; Rare:69; Clinvar (benign):4 | ||||
chr1:244863922-244864614 | Common:1; Rare:228; Clinvar:5; Clinvar (benign):6 | ||||
chr1:244969885-244970229 | Common:1; Rare:114 | ||||
chr1:244970563-244970846 | Common:7; Rare:80 | ||||
chr1:246565824-246565970 | Common:1; Rare:62 | ||||
chr1:246566134-246566606 | Common:3; Rare:158 | ||||
chr1:246566971-246567182 | Common:1; Rare:47 | ||||
chr1:247104314-247104481 | Common:2; Rare:55 | ||||
chr1:248825848-248826015 | Common:2; Rare:49 |