Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:111449185-111449531 | Common:4; Rare:174 | ||||
chr1:111619550-111619870 | Common:2; Rare:103 | ||||
chr1:111739367-111739707 | Common:3; Rare:96 | ||||
chr1:111739756-111739995 | Common:4; Rare:51 | ||||
chr1:111755390-111755710 | Common:4; Rare:97 | ||||
chr1:111755789-111755969 | Common:1; Rare:64 | ||||
chr1:112395918-112396262 | Common:2; Rare:109 | ||||
chr1:112619067-112619245 | Rare:67 | ||||
chr1:112619637-112619877 | Common:2; Rare:85 | ||||
chr1:112674570-112674746 | Common:1; Rare:28 | ||||
chr1:112705115-112705343 | Common:2; Rare:60 | ||||
chr1:112707094-112707246 | Rare:56 | ||||
chr1:112707320-112707590 | Rare:67 | ||||
chr1:112956141-112956470 | Common:5; Rare:137; Clinvar:10; Clinvar (benign):3 | ||||
chr1:113072698-113072855 | Common:1; Rare:38 |