Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:228166023-228166130 | Common:1; Rare:63; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
chr1:228457865-228458116 | Common:1; Rare:82 | ||||
chr1:228487339-228487394 | Rare:25 | ||||
chr1:229271003-229271197 | Rare:72 | ||||
chr1:229508312-229508489 | Common:1; Rare:66 | ||||
chr1:229625915-229626253 | Rare:102 | ||||
chr1:230978833-230979104 | Common:1; Rare:95 | ||||
chr1:231241087-231241295 | Rare:112; Clinvar:3 | ||||
chr1:231337746-231337994 | Common:3; Rare:97 | ||||
chr1:231528603-231528728 | Common:1; Rare:51 | ||||
chr1:234373328-234373788 | Common:1; Rare:207; Clinvar (benign):7 | ||||
chr1:234406121-234406192 | Rare:20 | ||||
chr1:234608173-234608337 | Rare:57 | ||||
chr1:234608493-234608525 | Common:1; Rare:10; Clinvar (benign):1 | ||||
chr1:234609309-234609368 | Rare:15 |