Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:226186683-226186835 | Rare:57 | ||||
chr1:227735226-227735488 | Common:3; Rare:152 | ||||
chr1:228103298-228103502 | Common:1; Rare:69 | ||||
chr1:228109239-228109455 | Rare:72 | ||||
chr1:229626080-229626250 | Rare:58 | ||||
chr1:230978833-230979102 | Common:1; Rare:95 | ||||
chr1:231241087-231241304 | Common:1; Rare:113; Clinvar:3; Clinvar (benign):1 | ||||
chr1:231337795-231338065 | Common:2; Rare:97 | ||||
chr1:231528598-231528741 | Common:1; Rare:55 | ||||
chr1:234373649-234373775 | Rare:46; Clinvar (benign):3 | ||||
chr1:243255729-243256150 | Common:1; Rare:120; Clinvar:4; Clinvar (benign):1 | ||||
chr1:246566147-246566584 | Common:2; Rare:150 | ||||
chr10:1048872-1049065 | Common:2; Rare:108 | ||||
chr10:3067428-3067604 | Common:2; Rare:78 | ||||
chr10:3785139-3785552 | Common:4; Rare:156 |