Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:54542100-54542540 | Common:8; Rare:234 | ||||
chr1:54542546-54542990 | Common:3; Rare:243 | ||||
chr1:54715585-54715985 | Common:15; Rare:321 | ||||
chr1:54716260-54716729 | Common:8; Rare:219 | ||||
chr1:54763831-54764236 | Common:4; Rare:190 | ||||
chr1:54764404-54764896 | Common:24; Rare:437; Clinvar (benign):2 | ||||
chr1:54886312-54886732 | Common:4; Rare:209 | ||||
chr1:54886776-54887580 | Common:22; Rare:1074; Clinvar:27; Clinvar (benign):11 | ||||
chr1:55039150-55039645 | Common:12; Rare:436; Clinvar:23; Clinvar (benign):6 | ||||
chr1:55214277-55215559 | Common:19; Rare:1670 | ||||
chr1:55215566-55215966 | Common:4; Rare:146 | ||||
chr1:56516399-56516799 | Common:2; Rare:91 | ||||
chr1:56516835-56517235 | Common:4; Rare:112 | ||||
chr1:58545742-58546483 | Common:9; Rare:192 | ||||
chr1:58546443-58546575 | Rare:29 |