Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:34961423-34961569 | Common:1; Rare:74 | ||||
chr17:35242901-35243081 | Rare:59 | ||||
chr17:35578551-35578719 | Common:1; Rare:45; Clinvar (benign):1 | ||||
chr17:35587226-35587547 | Rare:81 | ||||
chr17:35809307-35809543 | Rare:97 | ||||
chr17:36534799-36535029 | Common:3; Rare:98 | ||||
chr17:36544787-36544942 | Common:2; Rare:50 | ||||
chr17:36936635-36936801 | Common:1; Rare:32 | ||||
chr17:37406762-37406929 | Rare:71 | ||||
chr17:37489678-37489911 | Rare:92 | ||||
chr17:37609362-37609562 | Common:1; Rare:87 | ||||
chr17:37745065-37745200 | Rare:34; Clinvar (benign):1 | ||||
chr17:38825287-38825427 | Common:1; Rare:43 | ||||
chr17:38853685-38853895 | Common:3; Rare:83 | ||||
chr17:39637024-39637182 | Common:2; Rare:49 |