Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:145707322-145707465 | Common:1; Rare:21 | ||||
chr1:145707480-145707542 | Rare:13 | ||||
chr1:145707573-145707629 | Rare:13 | ||||
chr1:145823678-145823849 | Common:1; Rare:60 | ||||
chr1:145823855-145824288 | Rare:152 | ||||
chr1:145824354-145824488 | Rare:26 | ||||
chr1:145845343-145845766 | Common:5; Rare:127 | ||||
chr1:145858929-145859219 | Rare:90 | ||||
chr1:145859731-145859955 | Common:2; Rare:70 | ||||
chr1:145918642-145919133 | Common:2; Rare:115; Clinvar:2 | ||||
chr1:145927420-145927713 | Common:1; Rare:86; Clinvar (pathogenic):1 | ||||
chr1:145957972-145958226 | Rare:62 | ||||
chr1:145964377-145964832 | Rare:82 | ||||
chr1:145996540-145996772 | Rare:93 | ||||
chr1:146938327-146938551 | Common:2; Rare:69 |