Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:222922523-222922841 | Common:2; Rare:82 | ||||
chr2:226796833-226797120 | Rare:86; Clinvar (pathogenic):1 | ||||
chr2:227816910-227817201 | Rare:44 | ||||
chr2:228840379-228840628 | Common:2; Rare:33 | ||||
chr2:228841866-228842240 | Common:1; Rare:47 | ||||
chr2:230498768-230499106 | Common:1; Rare:64 | ||||
chr2:230512900-230513016 | Common:2; Rare:21 | ||||
chr2:230513233-230513336 | Common:2; Rare:12 | ||||
chr2:230520764-230520951 | Rare:23 | ||||
chr2:233012352-233012663 | Common:5; Rare:56 | ||||
chr2:233760847-233761146 | Common:1; Rare:93; Clinvar:9; Clinvar (pathogenic):4 | ||||
chr2:233761418-233761668 | Common:1; Rare:35 | ||||
chr2:233976306-233976360 | Rare:8 | ||||
chr2:234998677-234998873 | Common:1; Rare:35 | ||||
chr2:236828855-236829063 | Common:1; Rare:31 |