Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:74685342-74685382 | Rare:10; Clinvar (pathogenic):1 | ||||
chr5:74685503-74685521 | Rare:6 | ||||
chr5:74767047-74767355 | Common:3; Rare:98 | ||||
chr5:75336966-75337297 | Common:3; Rare:113 | ||||
chr5:75511585-75511917 | Common:1; Rare:117 | ||||
chr5:77087196-77087280 | Rare:22 | ||||
chr5:78360380-78360634 | Common:5; Rare:98 | ||||
chr5:79236018-79236142 | Common:1; Rare:47 | ||||
chr5:80256035-80256227 | Common:1; Rare:78 | ||||
chr5:80407801-80408148 | Common:1; Rare:123 | ||||
chr5:81301464-81301701 | Common:5; Rare:83 | ||||
chr5:81971789-81972075 | Common:3; Rare:115 | ||||
chr5:82278319-82278670 | Common:3; Rare:111 | ||||
chr5:83077330-83077618 | Common:1; Rare:86 | ||||
chr5:88883166-88883284 | Rare:41; Clinvar:3; Clinvar (benign):1 |