Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:87818137-87818359 | Common:2; Rare:78 | ||||
chr10:87864203-87864538 | Common:1; Rare:92; Clinvar:17; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
chr10:88583196-88583245 | Rare:23 | ||||
chr10:88583257-88583402 | Rare:38 | ||||
chr10:88952731-88952960 | Rare:35; Clinvar:1 | ||||
chr10:88990380-88990914 | Common:6; Rare:133; Clinvar:1; Clinvar (benign):5 | ||||
chr10:88991330-88991451 | Common:2; Rare:21 | ||||
chr10:89327953-89328022 | Common:1; Rare:8 | ||||
chr10:89332169-89332543 | Common:3; Rare:69 | ||||
chr10:89377733-89378070 | Common:3; Rare:53 | ||||
chr10:89414524-89414619 | Common:1; Rare:24 | ||||
chr10:89414654-89414785 | Common:3; Rare:61 | ||||
chr10:89556673-89556849 | Common:2; Rare:33 | ||||
chr10:89643803-89644119 | Rare:60 | ||||
chr10:89644990-89645285 | Common:2; Rare:132 |