Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:40477163-40477393 | Common:3; Rare:66 | ||||
chr1:40508643-40508792 | Common:3; Rare:40 | ||||
chr1:40531497-40531721 | Common:1; Rare:60 | ||||
chr1:40691486-40691860 | Common:3; Rare:166 | ||||
chr1:40692016-40692318 | Common:2; Rare:93 | ||||
chr1:40709184-40709327 | Rare:34 | ||||
chr1:40862350-40862613 | Common:5; Rare:87 | ||||
chr1:40979383-40979811 | Common:5; Rare:134 | ||||
chr1:41242098-41242377 | Rare:79 | ||||
chr1:42335149-42335395 | Common:5; Rare:121 | ||||
chr1:42456010-42456349 | Common:1; Rare:90 | ||||
chr1:42456446-42456600 | Rare:72 | ||||
chr1:42456656-42456973 | Common:1; Rare:112; Clinvar (pathogenic):1 | ||||
chr1:42658261-42658477 | Common:2; Rare:61 | ||||
chr1:42682134-42682472 | Common:2; Rare:95 |