Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:216781425-216781611 | Rare:40 | ||||
chr1:218345200-218345405 | Common:1; Rare:37; Clinvar (benign):1 | ||||
chr1:218348124-218348321 | Common:1; Rare:47 | ||||
chr1:222814982-222815141 | Common:1; Rare:58 | ||||
chr1:223992547-223992818 | Common:4; Rare:102 | ||||
chr1:228464587-228464887 | Common:2; Rare:70 | ||||
chr1:230807094-230807330 | Common:1; Rare:50 | ||||
chr1:234602667-234602958 | Common:2; Rare:60 | ||||
chr1:234724017-234724236 | Common:3; Rare:48 | ||||
chr1:243473431-243473584 | Rare:24 | ||||
chr1:244052184-244052263 | Common:1; Rare:12 | ||||
chr1:244863695-244863789 | Rare:30; Clinvar:1; Clinvar (benign):1 | ||||
chr1:244970945-244971078 | Rare:34 | ||||
chr1:247126138-247126433 | Common:3; Rare:43 | ||||
chr1:247210802-247210971 | Common:2; Rare:54 |