Variant report

Variant	rs73075798
Chromosome Location	chr5:35326155-35326156
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs16873529	0.93[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs16873766	0.85[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs17585046	0.92[ASN][1000 genomes]
rs56967971	0.93[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs58975450	0.93[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs59862556	0.93[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs61687847	0.93[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs73087009	0.93[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73087012	0.93[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73087013	0.93[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73087019	0.93[AMR][1000 genomes];1.00[ASN][1000 genomes]

No data

Chromatin state (count:1 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:35325200-35334200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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