Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:32291919-32292156 | Common:1; Rare:82 | ||||
chr1:32331266-32331581 | Rare:77 | ||||
chr1:32351416-32351632 | Common:1; Rare:57 | ||||
chr1:32364602-32364910 | Rare:46 | ||||
chr1:32394403-32394708 | Common:1; Rare:86 | ||||
chr1:32650908-32651321 | Common:2; Rare:151 | ||||
chr1:32651766-32652060 | Rare:64 | ||||
chr1:32741717-32742101 | Common:3; Rare:123 | ||||
chr1:32786418-32786748 | Common:2; Rare:65 | ||||
chr1:32817233-32817674 | Rare:116; Clinvar:5 | ||||
chr1:33021372-33021704 | Rare:81; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr1:33080992-33081167 | Common:2; Rare:44 | ||||
chr1:34792804-34793057 | Common:1; Rare:63 | ||||
chr1:34985292-34985393 | Common:1; Rare:37 | ||||
chr1:35031667-35031792 | Rare:41 |