Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:207529739-207530119 | Common:3; Rare:107 | ||||
chr2:208266023-208266286 | Common:9; Rare:92; Clinvar:1; Clinvar (benign):2 | ||||
chr2:210477535-210477720 | Rare:53 | ||||
chr2:215435656-215435804 | Common:2; Rare:41 | ||||
chr2:215435826-215435949 | Rare:19 | ||||
chr2:215435955-215436307 | Common:2; Rare:112 | ||||
chr2:216081765-216081882 | Rare:34 | ||||
chr2:216498715-216498893 | Common:7; Rare:73 | ||||
chr2:216694768-216694803 | Rare:9 | ||||
chr2:216694878-216694927 | Rare:4 | ||||
chr2:216694942-216695306 | Common:2; Rare:69 | ||||
chr2:218002853-218002889 | Rare:9 | ||||
chr2:218217058-218217282 | Common:2; Rare:76 | ||||
chr2:218270096-218270532 | Common:5; Rare:134; Clinvar:2; Clinvar (benign):1 | ||||
chr2:218568297-218568702 | Common:4; Rare:103 |