Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:58783416-58783681 | Rare:58 | ||||
chr1:63487738-63488078 | Common:2; Rare:74 | ||||
chr1:65067713-65067862 | Rare:38 | ||||
chr1:67831931-67832224 | Common:1; Rare:65 | ||||
chr1:85582173-85582829 | Common:1; Rare:196 | ||||
chr1:90851576-90851787 | Common:2; Rare:57 | ||||
chr1:108901559-108901867 | Common:4; Rare:68; Clinvar:1; Clinvar (benign):1 | ||||
chr1:109100434-109100451 | Rare:4 | ||||
chr1:111709011-111709193 | Rare:39 | ||||
chr1:112849786-112849878 | Common:1; Rare:15 | ||||
chr1:115717846-115717932 | Common:2; Rare:25; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr1:120464391-120464468 | Rare:14 | ||||
chr1:120850982-120851265 | Rare:18 | ||||
chr1:121117289-121117530 | Rare:63 | ||||
chr1:143904650-143904840 | Rare:63 |