Variant report

Variant	rs1591746
Chromosome Location	chr1:211336356-211336357
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs1338352	0.89[ASN][1000 genomes]
rs1338354	0.87[ASN][1000 genomes]
rs1338355	0.87[ASN][1000 genomes]
rs1416066	0.87[ASN][1000 genomes]
rs1577986	0.91[ASN][1000 genomes]
rs2066025	0.81[ASN][1000 genomes]
rs2211040	0.91[ASN][1000 genomes]
rs3111222	0.89[ASN][1000 genomes]
rs3111223	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3120779	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3811393	0.81[ASN][1000 genomes]
rs6665927	0.85[ASN][1000 genomes]
rs7548416	0.89[ASN][1000 genomes]

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:211334200-211340400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr1:211334400-211336400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell

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

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