Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:87864030-87864538 | Common:2; Rare:147; Clinvar:18; Clinvar (benign):12; Clinvar (pathogenic):1 | ||||
chr10:88583180-88583240 | Rare:27 | ||||
chr10:88583242-88583348 | Rare:25 | ||||
chr10:88880130-88880307 | Rare:46 | ||||
chr10:88880402-88880557 | Common:1; Rare:28 | ||||
chr10:88952731-88953041 | Common:2; Rare:55; Clinvar:1 | ||||
chr10:88990183-88990300 | Common:2; Rare:14 | ||||
chr10:88990451-88990906 | Common:5; Rare:124; Clinvar:1; Clinvar (benign):5 | ||||
chr10:88990939-88990990 | Rare:15 | ||||
chr10:88991197-88991496 | Common:4; Rare:63 | ||||
chr10:89207303-89207392 | Common:1; Rare:23 | ||||
chr10:89301676-89302079 | Rare:77 | ||||
chr10:89332261-89332537 | Common:3; Rare:45 | ||||
chr10:89392521-89392709 | Common:1; Rare:39 | ||||
chr10:89414677-89414793 | Common:3; Rare:57 |