Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:92833321-92833624 | Rare:84; Clinvar (pathogenic):1 | ||||
chr1:93575700-93575918 | Rare:43 | ||||
chr1:93591842-93592012 | Rare:28 | ||||
chr1:93592457-93592524 | Rare:9 | ||||
chr1:93598687-93598814 | Rare:18 | ||||
chr1:94530528-94530814 | Common:1; Rare:60 | ||||
chr1:108901631-108901874 | Common:4; Rare:62; Clinvar:1; Clinvar (benign):1 | ||||
chr1:109100344-109100392 | Rare:16 | ||||
chr1:109100420-109100476 | Rare:18 | ||||
chr1:109100506-109100509 | Rare:1 | ||||
chr1:109750369-109750686 | Rare:82 | ||||
chr1:109757935-109758387 | Common:1; Rare:110 | ||||
chr1:109760995-109761150 | Rare:40 | ||||
chr1:110336581-110336886 | Rare:56 | ||||
chr1:110340352-110340522 | Rare:53 |