Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:102845749-102846084 | Common:8; Rare:87; Clinvar:2; Clinvar (benign):4 | ||||
chr13:108218313-108218520 | Rare:80 | ||||
chr13:110914887-110915242 | Common:3; Rare:152 | ||||
chr13:113208621-113208751 | Rare:77 | ||||
chr13:113490679-113491021 | Common:1; Rare:124 | ||||
chr13:113759108-113759260 | Common:1; Rare:45 | ||||
chr13:114281318-114281654 | Common:5; Rare:133 | ||||
chr13:114281811-114282061 | Common:6; Rare:124 | ||||
chr14:20343174-20343655 | Common:12; Rare:280 | ||||
chr14:20413420-20413527 | Common:2; Rare:30 | ||||
chr14:20455041-20455303 | Common:2; Rare:77 | ||||
chr14:20684438-20684622 | Common:2; Rare:30; Clinvar (benign):2 | ||||
chr14:21025028-21025309 | Rare:90 | ||||
chr14:21025494-21025615 | Common:1; Rare:29 | ||||
chr14:21025661-21025927 | Common:2; Rare:50 |