Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:1231970-1232296 | Rare:124; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
chr1:1273811-1273999 | Rare:76 | ||||
chr1:1324624-1324809 | Common:2; Rare:100 | ||||
chr1:1375154-1375617 | Common:7; Rare:135 | ||||
chr1:1399286-1399597 | Common:1; Rare:139 | ||||
chr1:1407218-1407435 | Common:1; Rare:96 | ||||
chr1:1435559-1435725 | Rare:62 | ||||
chr1:1574503-1574947 | Common:1; Rare:191 | ||||
chr1:1658919-1659060 | Common:2; Rare:56 | ||||
chr1:1692450-1692535 | Rare:11 | ||||
chr1:1692539-1692821 | Common:1; Rare:43 | ||||
chr1:1724273-1724504 | Common:4; Rare:85 | ||||
chr1:2194698-2194830 | Rare:46 | ||||
chr1:2195059-2195225 | Rare:32 | ||||
chr1:2391484-2391927 | Common:2; Rare:158 |