Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:185156675-185156748 | Rare:39 | ||||
chr1:185156922-185157300 | Common:1; Rare:104 | ||||
chr1:185157422-185157540 | Common:1; Rare:38 | ||||
chr1:185301135-185301409 | Common:1; Rare:59 | ||||
chr1:186375104-186375491 | Rare:112 | ||||
chr1:186375671-186375932 | Common:1; Rare:70 | ||||
chr1:192808905-192809079 | Common:3; Rare:79 | ||||
chr1:193059321-193059677 | Rare:167 | ||||
chr1:193186608-193186689 | Rare:16 | ||||
chr1:196608539-196608840 | Rare:62 | ||||
chr1:196608859-196609027 | Rare:32 | ||||
chr1:196651904-196652172 | Common:2; Rare:69; Clinvar:2; Clinvar (benign):4 | ||||
chr1:196887746-196888109 | Common:1; Rare:61 | ||||
chr1:200027388-200027737 | Common:2; Rare:49 | ||||
chr1:200042423-200042670 | Common:1; Rare:54 |