Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:40161247-40161399 | Rare:39 | ||||
chr1:40257908-40258332 | Common:4; Rare:123; Clinvar:7; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr1:40344734-40344850 | Rare:17 | ||||
chr1:40508649-40508812 | Common:4; Rare:46 | ||||
chr1:40531506-40531579 | Rare:23 | ||||
chr1:40691460-40691641 | Common:2; Rare:84 | ||||
chr1:40691652-40691810 | Common:1; Rare:71 | ||||
chr1:40692051-40692384 | Common:2; Rare:94 | ||||
chr1:40979388-40979803 | Common:5; Rare:131 | ||||
chr1:42335157-42335369 | Common:5; Rare:105 | ||||
chr1:42456232-42456571 | Common:1; Rare:100 | ||||
chr1:42658121-42658447 | Common:3; Rare:81 | ||||
chr1:42682605-42682731 | Common:1; Rare:52 | ||||
chr1:42766978-42767303 | Common:4; Rare:110; Clinvar (benign):1 | ||||
chr1:42816961-42817136 | Common:1; Rare:49 |