Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:108449071-108449271 | Rare:82 | ||||
chr2:108534199-108534491 | Common:7; Rare:119 | ||||
chr2:108654710-108655055 | Rare:68 | ||||
chr2:108719372-108719577 | Common:3; Rare:84; Clinvar (benign):2 | ||||
chr2:108786646-108786800 | Common:5; Rare:87 | ||||
chr2:109613834-109613998 | Common:1; Rare:60 | ||||
chr2:110678027-110678232 | Rare:61 | ||||
chr2:111884151-111884255 | Rare:30 | ||||
chr2:112275366-112275615 | Common:1; Rare:88 | ||||
chr2:112584283-112584641 | Common:2; Rare:99 | ||||
chr2:112584785-112584854 | Rare:17 | ||||
chr2:112645707-112645945 | Common:1; Rare:87 | ||||
chr2:112764594-112764803 | Common:2; Rare:67; Clinvar (pathogenic):1 | ||||
chr2:113627041-113627312 | Common:4; Rare:79 | ||||
chr2:113756477-113756695 | Common:1; Rare:62 |