Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:38873327-38873554 | Common:3; Rare:75 | ||||
chr1:39026223-39026397 | Common:1; Rare:45 | ||||
chr1:39738793-39738921 | Common:1; Rare:34 | ||||
chr1:39883454-39883570 | Common:1; Rare:48; Clinvar (pathogenic):1 | ||||
chr1:40040444-40040835 | Common:3; Rare:118 | ||||
chr1:40161272-40161399 | Rare:32 | ||||
chr1:40257915-40258304 | Common:4; Rare:107; Clinvar:7; Clinvar (benign):1 | ||||
chr1:40508674-40508807 | Common:4; Rare:37 | ||||
chr1:40531497-40531653 | Rare:38 | ||||
chr1:40979383-40979826 | Common:5; Rare:136 | ||||
chr1:42335164-42335386 | Common:5; Rare:106 | ||||
chr1:42455987-42456752 | Common:3; Rare:245 | ||||
chr1:42658275-42658482 | Common:2; Rare:62 | ||||
chr1:42682158-42682436 | Common:2; Rare:70 | ||||
chr1:42682606-42682731 | Common:1; Rare:52 |