Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:32901245-32901544 | Common:1; Rare:77 | ||||
chr1:32964093-32964194 | Rare:19 | ||||
chr1:33021369-33021656 | Rare:68; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr1:35031663-35031780 | Rare:36 | ||||
chr1:35079317-35079422 | Common:3; Rare:30 | ||||
chr1:35192670-35192693 | Rare:7 | ||||
chr1:35193014-35193175 | Rare:68 | ||||
chr1:35268655-35269007 | Rare:121 | ||||
chr1:35557350-35557842 | Common:3; Rare:150 | ||||
chr1:35641486-35641626 | Rare:30 | ||||
chr1:35931198-35931235 | Rare:10 | ||||
chr1:36155858-36156174 | Rare:121 | ||||
chr1:36178116-36178519 | Common:2; Rare:124 | ||||
chr1:36178958-36179152 | Common:1; Rare:70 | ||||
chr1:36224236-36224498 | Rare:76 |