Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:44618039-44618352 | Common:4; Rare:58 | ||||
chr20:44939272-44939391 | Rare:18 | ||||
chr20:44959086-44959390 | Common:2; Rare:52 | ||||
chr20:45421777-45422014 | Rare:34 | ||||
chr20:45894649-45895423 | Common:5; Rare:231; Clinvar:6; Clinvar (benign):3 | ||||
chr20:45902298-45902571 | Common:1; Rare:90 | ||||
chr20:45950089-45950369 | Common:5; Rare:102; Clinvar:4; Clinvar (benign):1 | ||||
chr20:45971527-45971616 | Rare:21 | ||||
chr20:46060894-46061074 | Common:3; Rare:35 | ||||
chr20:46361638-46361951 | Common:1; Rare:49 | ||||
chr20:46595675-46595927 | Common:2; Rare:49 | ||||
chr20:47210917-47211179 | Common:2; Rare:60 | ||||
chr20:47357699-47357890 | Rare:32 | ||||
chr20:47358853-47358977 | Rare:27 | ||||
chr20:47639692-47639966 | Common:1; Rare:77 |