Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:39026195-39026398 | Common:1; Rare:51 | ||||
chr1:39284162-39284359 | Common:1; Rare:43 | ||||
chr1:39562073-39562344 | Rare:57 | ||||
chr1:39788877-39788950 | Rare:29 | ||||
chr1:39883402-39883565 | Common:1; Rare:70; Clinvar (pathogenic):1 | ||||
chr1:39955332-39955379 | Rare:9 | ||||
chr1:40040444-40040819 | Common:3; Rare:116 | ||||
chr1:40070324-40070495 | Common:2; Rare:42 | ||||
chr1:40161276-40161402 | Rare:32 | ||||
chr1:40257895-40258288 | Common:4; Rare:109; Clinvar:8; Clinvar (benign):1 | ||||
chr1:40344734-40344861 | Rare:17 | ||||
chr1:40374115-40374163 | Rare:8 | ||||
chr1:40374614-40374669 | Common:6; Rare:11 | ||||
chr1:40508626-40508816 | Common:6; Rare:57 | ||||
chr1:40531514-40531667 | Rare:35 |