Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:99352736-99353058 | Common:1; Rare:76 | ||||
chr4:99563989-99564167 | Common:2; Rare:53; Clinvar:2; Clinvar (benign):2 | ||||
chr4:99894345-99894620 | Common:3; Rare:96 | ||||
chr4:99946558-99946799 | Rare:85 | ||||
chr4:99950266-99950488 | Rare:42 | ||||
chr4:101347581-101347822 | Common:4; Rare:75 | ||||
chr4:102826770-102826993 | Rare:66 | ||||
chr4:102827435-102827971 | Common:4; Rare:179 | ||||
chr4:102827985-102828122 | Rare:48 | ||||
chr4:102868850-102869063 | Common:2; Rare:72 | ||||
chr4:103076308-103076372 | Rare:19 | ||||
chr4:105552312-105552753 | Rare:71 | ||||
chr4:105708633-105708847 | Common:1; Rare:69 | ||||
chr4:106316179-106316601 | Common:5; Rare:136 | ||||
chr4:107720177-107720511 | Common:7; Rare:134 |