Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:37690487-37690740 | Common:6; Rare:67 | ||||
chr1:37692204-37692496 | Common:3; Rare:61 | ||||
chr1:37859569-37859764 | Common:3; Rare:64 | ||||
chr1:38012501-38012805 | Common:1; Rare:92 | ||||
chr1:38859686-38860033 | Rare:134 | ||||
chr1:38873294-38873573 | Common:3; Rare:96 | ||||
chr1:39026109-39026390 | Common:1; Rare:65 | ||||
chr1:39738781-39738910 | Common:1; Rare:27 | ||||
chr1:40040444-40040801 | Common:3; Rare:108 | ||||
chr1:40161255-40161402 | Rare:38 | ||||
chr1:40257903-40258292 | Common:4; Rare:108; Clinvar:7; Clinvar (benign):1 | ||||
chr1:40450067-40450159 | Common:2; Rare:36 | ||||
chr1:40508626-40508781 | Common:5; Rare:47 | ||||
chr1:40531550-40531597 | Rare:12 | ||||
chr1:40691342-40691805 | Common:3; Rare:194 |