Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:47795725-47795991 | Common:4; Rare:73; Clinvar:16; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
chr2:47801981-47802281 | Common:1; Rare:84; Clinvar (benign):1 | ||||
chr2:47802577-47802623 | Rare:13 | ||||
chr2:47832658-47832806 | Rare:47 | ||||
chr2:47906462-47906820 | Common:2; Rare:132 | ||||
chr2:48315700-48315788 | Rare:30 | ||||
chr2:53771724-53771942 | Common:1; Rare:56 | ||||
chr2:53969999-53970192 | Rare:57 | ||||
chr2:54457892-54458028 | Rare:38 | ||||
chr2:54533139-54533191 | Rare:7 | ||||
chr2:54579942-54580159 | Common:3; Rare:42 | ||||
chr2:54623484-54623801 | Common:2; Rare:80 | ||||
chr2:54664450-54664917 | Common:2; Rare:127 | ||||
chr2:55023360-55023425 | Rare:11 | ||||
chr2:55023435-55023597 | Rare:26 |