Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:49278421-49278669 | Common:8; Rare:85 | ||||
chr20:49568041-49568159 | Common:6; Rare:33 | ||||
chr20:49915487-49915596 | Common:3; Rare:37 | ||||
chr20:50113106-50113244 | Common:5; Rare:69 | ||||
chr20:50153641-50153928 | Common:2; Rare:116 | ||||
chr20:50190620-50190833 | Rare:59 | ||||
chr20:50958361-50958896 | Common:1; Rare:207; Clinvar:5; Clinvar (benign):5 | ||||
chr20:51562784-51563027 | Common:3; Rare:50 | ||||
chr20:52972666-52972781 | Common:2; Rare:28 | ||||
chr20:53593763-53593914 | Common:1; Rare:56 | ||||
chr20:56392199-56392695 | Common:6; Rare:131 | ||||
chr20:56468432-56468734 | Rare:101 | ||||
chr20:58309431-58309715 | Common:2; Rare:111 | ||||
chr20:58651131-58651305 | Common:2; Rare:38; Clinvar:1; Clinvar (benign):1 | ||||
chr20:58991066-58991311 | Common:1; Rare:53 |