Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:45687059-45687353 | Common:1; Rare:77 | ||||
chr1:45688079-45688237 | Common:1; Rare:48 | ||||
chr1:45750621-45750816 | Rare:71 | ||||
chr1:46198338-46198500 | Common:1; Rare:69; Clinvar:1; Clinvar (benign):1 | ||||
chr1:46203200-46203374 | Rare:38 | ||||
chr1:46303131-46303747 | Common:3; Rare:181 | ||||
chr1:48472001-48472082 | Common:1; Rare:24 | ||||
chr1:50023862-50023951 | Rare:25 | ||||
chr1:50960212-50960267 | Rare:26 | ||||
chr1:50970152-50970268 | Rare:18 | ||||
chr1:51236209-51236536 | Common:4; Rare:104 | ||||
chr1:51325921-51326069 | Common:1; Rare:32 | ||||
chr1:51330473-51330698 | Common:2; Rare:69 | ||||
chr1:51345074-51345112 | Rare:9 | ||||
chr1:52055089-52055256 | Common:1; Rare:48 |