Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:8064485-8064876 | Common:12; Rare:120 | ||||
chr10:8072271-8072506 | Common:6; Rare:66 | ||||
chr10:8073352-8073906 | Common:5; Rare:218; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):4 | ||||
chr10:8084730-8085480 | Common:22; Rare:323 | ||||
chr10:8097690-8098120 | Common:11; Rare:148 | ||||
chr10:8103103-8103454 | Common:21; Rare:214 | ||||
chr10:8128542-8129090 | Common:12; Rare:175 | ||||
chr10:8296090-8296510 | Common:1; Rare:95 | ||||
chr10:8332283-8332512 | Common:1; Rare:46 | ||||
chr10:8366090-8366490 | Rare:81 | ||||
chr10:8407300-8408203 | Common:20; Rare:339 | ||||
chr10:8543690-8544540 | Common:12; Rare:306 | ||||
chr10:8616212-8616612 | Common:3; Rare:135 | ||||
chr10:8670040-8670740 | Common:3; Rare:109 | ||||
chr10:8703246-8704207 | Common:13; Rare:236 |