Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:230104784-230104973 | Rare:46 | ||||
chr1:230327900-230328340 | Common:4; Rare:81 | ||||
chr1:230824867-230825267 | Rare:143 | ||||
chr1:231091930-231092350 | Common:1; Rare:84 | ||||
chr1:231211376-231211666 | Common:2; Rare:76 | ||||
chr1:231216606-231216718 | Rare:16 | ||||
chr1:231407900-231408380 | Common:6; Rare:72 | ||||
chr1:231422225-231422492 | Common:5; Rare:124; Clinvar:5; Clinvar (benign):5 | ||||
chr1:231422547-231422658 | Common:1; Rare:37; Clinvar:2; Clinvar (benign):1 | ||||
chr1:231422682-231422831 | Rare:37; Clinvar:2 | ||||
chr1:231508497-231508897 | Rare:82 | ||||
chr1:231512433-231512597 | Rare:24 | ||||
chr1:231918260-231918610 | Common:3; Rare:63 | ||||
chr1:232376963-232377363 | Common:2; Rare:83 | ||||
chr1:232630105-232630334 | Rare:92 |