Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:229625938-229626284 | Rare:113 | ||||
chr1:230978663-230979222 | Common:5; Rare:208; Clinvar (benign):1 | ||||
chr1:231241094-231241292 | Rare:106; Clinvar:3 | ||||
chr1:231337786-231338056 | Common:2; Rare:101 | ||||
chr1:231338217-231338343 | Rare:27 | ||||
chr1:231528515-231528763 | Common:2; Rare:85 | ||||
chr1:232805318-232805438 | Common:2; Rare:68 | ||||
chr1:232950488-232950678 | Common:3; Rare:62 | ||||
chr1:234373342-234373768 | Common:1; Rare:198; Clinvar (benign):7 | ||||
chr1:235128641-235128708 | Rare:20 | ||||
chr1:235128722-235129090 | Common:1; Rare:157 | ||||
chr1:235328108-235328659 | Common:5; Rare:169 | ||||
chr1:235328778-235329046 | Common:1; Rare:89 | ||||
chr1:235650576-235650658 | Rare:23 | ||||
chr1:235866842-235867193 | Common:3; Rare:109 |