Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:39026223-39026398 | Common:1; Rare:45 | ||||
chr1:39268324-39268496 | Rare:27 | ||||
chr1:39284163-39284355 | Common:1; Rare:43 | ||||
chr1:39883467-39883575 | Rare:42; Clinvar (pathogenic):1 | ||||
chr1:40039936-40040242 | Common:2; Rare:68 | ||||
chr1:40040444-40040807 | Common:3; Rare:111 | ||||
chr1:40161279-40161402 | Rare:32 | ||||
chr1:40257903-40258265 | Common:4; Rare:98; Clinvar:7 | ||||
chr1:40373513-40373821 | Common:1; Rare:71 | ||||
chr1:40508626-40508816 | Common:6; Rare:57 | ||||
chr1:40531497-40531675 | Rare:43 | ||||
chr1:40691586-40691850 | Common:1; Rare:120 | ||||
chr1:40692039-40692284 | Common:1; Rare:77 | ||||
chr1:40979621-40979822 | Common:1; Rare:64 | ||||
chr1:41005983-41006094 | Rare:25 |