Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:216206284-216206556 | Common:1; Rare:46 | ||||
chr2:226796085-226796309 | Common:1; Rare:90; Clinvar (benign):1 | ||||
chr2:226796840-226797047 | Rare:61; Clinvar (pathogenic):1 | ||||
chr2:226801779-226802105 | Common:1; Rare:70 | ||||
chr2:227548966-227548988 | Rare:2 | ||||
chr2:230469812-230470096 | Common:3; Rare:75 | ||||
chr2:232844161-232844439 | Common:2; Rare:73 | ||||
chr2:237213625-237213873 | Common:2; Rare:37 | ||||
chr2:237378440-237378703 | Common:1; Rare:51; Clinvar:1; Clinvar (benign):4 | ||||
chr2:237384747-237384811 | Rare:11 | ||||
chr2:237385501-237385555 | Rare:7 | ||||
chr2:237392818-237393017 | Common:1; Rare:40 | ||||
chr2:237393371-237393402 | Common:1; Rare:8 | ||||
chr20:327166-327525 | Common:4; Rare:125 | ||||
chr20:327541-327761 | Common:5; Rare:56 |