Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:39268385-39268494 | Rare:19 | ||||
chr1:39284162-39284361 | Common:1; Rare:44 | ||||
chr1:39408794-39409083 | Common:5; Rare:100 | ||||
chr1:39491507-39491662 | Common:2; Rare:61 | ||||
chr1:39672094-39672192 | Common:1; Rare:33 | ||||
chr1:39738762-39738930 | Common:1; Rare:41 | ||||
chr1:39883406-39883570 | Common:1; Rare:69; Clinvar (pathogenic):1 | ||||
chr1:40040094-40040262 | Common:2; Rare:30 | ||||
chr1:40040444-40040858 | Common:3; Rare:130 | ||||
chr1:40161276-40161436 | Rare:49 | ||||
chr1:40257895-40258282 | Common:4; Rare:107; Clinvar:8; Clinvar (benign):1 | ||||
chr1:40316650-40316993 | Common:2; Rare:77 | ||||
chr1:40374613-40374674 | Common:6; Rare:13 | ||||
chr1:40508619-40508793 | Common:5; Rare:55 | ||||
chr1:40531514-40531715 | Rare:53 |