Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:40161272-40161436 | Rare:50 | ||||
chr1:40257908-40258265 | Common:4; Rare:96; Clinvar:7 | ||||
chr1:40508649-40508789 | Common:3; Rare:38 | ||||
chr1:40531514-40531653 | Rare:31 | ||||
chr1:40691457-40691831 | Common:3; Rare:174 | ||||
chr1:40692039-40692331 | Common:1; Rare:88 | ||||
chr1:40979459-40979797 | Common:4; Rare:112 | ||||
chr1:41242104-41242398 | Rare:88 | ||||
chr1:41484681-41484831 | Common:2; Rare:38 | ||||
chr1:42335134-42335280 | Common:2; Rare:67 | ||||
chr1:42455993-42456397 | Common:1; Rare:107 | ||||
chr1:42456481-42456583 | Rare:50 | ||||
chr1:42463002-42463354 | Common:4; Rare:112 | ||||
chr1:42658265-42658447 | Common:2; Rare:51 | ||||
chr1:42683255-42683465 | Common:3; Rare:86 |