Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:211578009-211578119 | Rare:36 | ||||
chr1:211829250-211829477 | Common:1; Rare:48 | ||||
chr1:212052044-212052070 | Rare:2 | ||||
chr1:212286171-212286277 | Common:1; Rare:33 | ||||
chr1:212309512-212309533 | Rare:4 | ||||
chr1:212824362-212824624 | Common:2; Rare:44 | ||||
chr1:215586092-215586375 | Rare:43 | ||||
chr1:218345205-218345673 | Common:3; Rare:92; Clinvar:3; Clinvar (benign):1 | ||||
chr1:218348103-218348205 | Rare:22 | ||||
chr1:218369296-218369455 | Rare:25 | ||||
chr1:218380595-218380791 | Rare:31 | ||||
chr1:219208006-219208115 | Common:1; Rare:18 | ||||
chr1:222654276-222654476 | Common:1; Rare:48 | ||||
chr1:223783905-223784155 | Rare:68 | ||||
chr1:223992541-223992760 | Common:3; Rare:86 |