Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:39738790-39738903 | Common:1; Rare:21 | ||||
chr1:39954963-39955281 | Common:1; Rare:86 | ||||
chr1:40040444-40040801 | Common:3; Rare:108 | ||||
chr1:40069971-40070234 | Common:2; Rare:70 | ||||
chr1:40161265-40161432 | Rare:52 | ||||
chr1:40257903-40258282 | Common:4; Rare:103; Clinvar:7; Clinvar (benign):1 | ||||
chr1:40508674-40508822 | Common:4; Rare:43 | ||||
chr1:40531514-40531586 | Rare:21 | ||||
chr1:40691504-40691860 | Common:2; Rare:159 | ||||
chr1:40692027-40692111 | Rare:34 | ||||
chr1:42335114-42335349 | Common:4; Rare:125 | ||||
chr1:42335853-42336108 | Rare:53 | ||||
chr1:42456010-42456107 | Rare:32 | ||||
chr1:42682158-42682448 | Common:2; Rare:71 | ||||
chr1:42682606-42682731 | Common:1; Rare:52 |