Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:154974853-154975155 | Common:3; Rare:103 | ||||
chr1:154975205-154975312 | Rare:15 | ||||
chr1:154975512-154975570 | Rare:13 | ||||
chr1:154975599-154975829 | Rare:58 | ||||
chr1:154983048-154983426 | Common:2; Rare:79; Clinvar (benign):2 | ||||
chr1:155002022-155002263 | Common:1; Rare:69 | ||||
chr1:155002476-155002866 | Common:2; Rare:63 | ||||
chr1:155003302-155003443 | Common:3; Rare:31 | ||||
chr1:155050518-155050776 | Rare:79 | ||||
chr1:155050893-155050941 | Rare:16 | ||||
chr1:155051107-155051402 | Common:2; Rare:99 | ||||
chr1:155063581-155063817 | Rare:73 | ||||
chr1:155063843-155064096 | Rare:77 | ||||
chr1:155064233-155064316 | Rare:17 | ||||
chr1:155078685-155078923 | Rare:81 |