Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:40709191-40709369 | Rare:44 | ||||
chr1:42335181-42335355 | Common:3; Rare:90 | ||||
chr1:42456473-42456595 | Rare:62 | ||||
chr1:42682145-42682424 | Common:2; Rare:74 | ||||
chr1:42682680-42682723 | Common:1; Rare:13 | ||||
chr1:42767023-42767316 | Common:5; Rare:92 | ||||
chr1:42816975-42817136 | Common:1; Rare:44 | ||||
chr1:42817198-42817625 | Rare:130 | ||||
chr1:42846392-42846640 | Common:1; Rare:68 | ||||
chr1:42958817-42959106 | Common:4; Rare:77; Clinvar:6; Clinvar (benign):4 | ||||
chr1:43270924-43271034 | Rare:28 | ||||
chr1:43358671-43358986 | Common:7; Rare:97 | ||||
chr1:43367945-43368212 | Rare:68 | ||||
chr1:43389781-43389945 | Common:3; Rare:62 | ||||
chr1:43707352-43707571 | Common:2; Rare:63 |