Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:149885788-149885980 | Rare:41 | ||||
chr1:150160435-150160739 | Common:2; Rare:57 | ||||
chr1:150553283-150553569 | Common:1; Rare:77; Clinvar:2; Clinvar (benign):1 | ||||
chr1:150564927-150565176 | Rare:41 | ||||
chr1:150604799-150605023 | Common:1; Rare:39 | ||||
chr1:150611528-150611849 | Common:1; Rare:46 | ||||
chr1:150613549-150613892 | Common:2; Rare:69 | ||||
chr1:150620026-150620192 | Rare:31 | ||||
chr1:151941469-151941694 | Rare:26 | ||||
chr1:151945773-151946059 | Common:3; Rare:55 | ||||
chr1:151946482-151946710 | Common:1; Rare:38 | ||||
chr1:151982666-151983025 | Common:2; Rare:55 | ||||
chr1:151989578-151989780 | Common:3; Rare:41 | ||||
chr1:154251269-154251565 | Common:1; Rare:74 | ||||
chr1:154407374-154407573 | Common:2; Rare:38 |