Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:1809808-1810022 | Rare:36 | ||||
chr20:2837021-2837403 | Rare:68 | ||||
chr20:2886712-2886993 | Common:1; Rare:55 | ||||
chr20:3035595-3035886 | Rare:92 | ||||
chr20:3048213-3048543 | Rare:46 | ||||
chr20:3784377-3784858 | Common:2; Rare:110 | ||||
chr20:3785110-3785530 | Common:2; Rare:144 | ||||
chr20:4134386-4134446 | Rare:11 | ||||
chr20:4134585-4135233 | Common:4; Rare:125 | ||||
chr20:4135297-4135334 | Common:1; Rare:11 | ||||
chr20:4135667-4135833 | Common:1; Rare:22 | ||||
chr20:4685694-4685730 | Rare:8 | ||||
chr20:5115322-5115550 | Rare:49; Clinvar (pathogenic):1 | ||||
chr20:5117813-5117962 | Rare:32 | ||||
chr20:5189801-5190121 | Common:1; Rare:70 |