Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:225777700-225777879 | Common:3; Rare:49 | ||||
chr1:225924128-225924545 | Common:11; Rare:136 | ||||
chr1:225999308-225999616 | Common:2; Rare:104 | ||||
chr1:226186430-226186748 | Common:1; Rare:88 | ||||
chr1:227735273-227735465 | Common:2; Rare:110 | ||||
chr1:228103061-228103489 | Common:2; Rare:174 | ||||
chr1:228139860-228140078 | Common:1; Rare:53 | ||||
chr1:228457865-228458113 | Common:1; Rare:78 | ||||
chr1:229271034-229271293 | Rare:87 | ||||
chr1:229508296-229508443 | Common:1; Rare:57 | ||||
chr1:231241107-231241262 | Rare:87; Clinvar:3 | ||||
chr1:231528495-231528738 | Common:2; Rare:82 | ||||
chr1:234373326-234373539 | Common:1; Rare:106; Clinvar (benign):3 | ||||
chr1:234373645-234373775 | Rare:49; Clinvar (benign):3 | ||||
chr1:234608194-234608351 | Rare:54 |