Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:91021374-91021759 | Common:2; Rare:94 | ||||
chr1:91021771-91022418 | Common:1; Rare:165 | ||||
chr1:91022600-91022629 | Rare:6 | ||||
chr1:91022631-91022737 | Rare:23 | ||||
chr1:91500705-91500941 | Common:2; Rare:78 | ||||
chr1:91501002-91501165 | Rare:49 | ||||
chr1:91501269-91501451 | Rare:50 | ||||
chr1:91886148-91886385 | Rare:93 | ||||
chr1:92298639-92299149 | Common:2; Rare:176; Clinvar:2; Clinvar (benign):2 | ||||
chr1:92483642-92484184 | Common:2; Rare:107 | ||||
chr1:92484524-92485038 | Common:4; Rare:100 | ||||
chr1:92485787-92486264 | Common:1; Rare:106 | ||||
chr1:92486548-92486642 | Rare:24 | ||||
chr1:92486644-92487068 | Common:5; Rare:96; Clinvar:1; Clinvar (benign):1 | ||||
chr1:92785125-92785376 | Common:5; Rare:68 |