Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:14612102-14612181 | Rare:8 | ||||
chr10:14837752-14837922 | Rare:58 | ||||
chr10:14837937-14838412 | Common:4; Rare:145 | ||||
chr10:14838843-14839098 | Rare:66 | ||||
chr10:14878231-14878433 | Rare:68 | ||||
chr10:14878494-14878959 | Common:4; Rare:145 | ||||
chr10:14879035-14879152 | Rare:43 | ||||
chr10:14879473-14879756 | Rare:72 | ||||
chr10:14953477-14953785 | Common:4; Rare:78 | ||||
chr10:14953882-14954512 | Common:3; Rare:173; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr10:14959205-14959871 | Common:4; Rare:200 | ||||
chr10:14959892-14960141 | Common:1; Rare:52 | ||||
chr10:15088747-15088963 | Common:1; Rare:80 | ||||
chr10:15096991-15097452 | Common:7; Rare:191 | ||||
chr10:15097454-15097545 | Common:1; Rare:32 |