Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:44960362-44960487 | Common:1; Rare:52 | ||||
chr20:44966370-44966571 | Common:1; Rare:78 | ||||
chr20:45115001-45115306 | Common:4; Rare:65 | ||||
chr20:45124458-45124565 | Rare:25 | ||||
chr20:45363115-45363208 | Rare:31 | ||||
chr20:45405831-45406098 | Common:2; Rare:68 | ||||
chr20:45406541-45406723 | Rare:46 | ||||
chr20:45791844-45792017 | Common:1; Rare:65 | ||||
chr20:45833729-45833940 | Common:7; Rare:50 | ||||
chr20:45857311-45857562 | Common:4; Rare:72 | ||||
chr20:45891010-45891413 | Common:3; Rare:121; Clinvar:8; Clinvar (benign):3 | ||||
chr20:45971846-45971946 | Rare:31 | ||||
chr20:46364386-46364551 | Rare:63 | ||||
chr20:47356661-47356847 | Rare:40 | ||||
chr20:49278020-49278263 | Rare:63 |