Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:45687017-45687357 | Common:2; Rare:89 | ||||
chr1:45688042-45688243 | Common:1; Rare:56 | ||||
chr1:45750615-45750839 | Rare:81 | ||||
chr1:45913464-45913651 | Rare:32 | ||||
chr1:46198331-46198546 | Common:2; Rare:97; Clinvar:1; Clinvar (benign):1 | ||||
chr1:46203259-46203376 | Rare:27 | ||||
chr1:46303124-46303820 | Common:3; Rare:208 | ||||
chr1:46340657-46340846 | Common:3; Rare:54 | ||||
chr1:46604199-46604400 | Common:1; Rare:56 | ||||
chr1:47314110-47314332 | Common:3; Rare:42; Clinvar:1 | ||||
chr1:47333759-47333979 | Common:3; Rare:78 | ||||
chr1:48472129-48472419 | Common:4; Rare:82 | ||||
chr1:50960231-50960395 | Rare:43 | ||||
chr1:51236209-51236536 | Common:4; Rare:104 | ||||
chr1:51518935-51518970 | Rare:9 |