Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:228213164-228213209 | Rare:7 | ||||
chr1:228406751-228407162 | Common:5; Rare:84 | ||||
chr1:228457860-228458116 | Common:1; Rare:85 | ||||
chr1:228487074-228487439 | Common:4; Rare:106 | ||||
chr1:228487545-228487645 | Rare:24 | ||||
chr1:229271007-229271355 | Rare:110 | ||||
chr1:229508253-229508448 | Common:1; Rare:78 | ||||
chr1:229626049-229626296 | Rare:94 | ||||
chr1:230978791-230979153 | Common:2; Rare:138 | ||||
chr1:230995534-230995981 | Common:5; Rare:106; Clinvar:1; Clinvar (pathogenic):1 | ||||
chr1:231241070-231241395 | Common:2; Rare:155; Clinvar:5; Clinvar (benign):2 | ||||
chr1:231337795-231338114 | Common:4; Rare:111 | ||||
chr1:231528485-231528758 | Common:2; Rare:91 | ||||
chr1:232950453-232950664 | Common:3; Rare:78 | ||||
chr1:233613453-233613570 | Rare:24 |