Variant report

Variant	rs1355403
Chromosome Location	chr4:127451519-127451520
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs11098883	0.81[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs11098884	0.92[AMR][1000 genomes];0.80[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13123040	0.94[ASN][1000 genomes]
rs1355404	0.82[EUR][1000 genomes]
rs1542999	0.92[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs1543000	0.92[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs1553874	0.84[AFR][1000 genomes]
rs1606111	0.97[ASN][1000 genomes]
rs192856	0.83[YRI][hapmap]
rs313086	0.94[ASN][1000 genomes]
rs313094	0.83[ASN][1000 genomes]
rs401403	0.94[ASN][1000 genomes]
rs6810452	0.91[ASN][1000 genomes]
rs6823628	0.92[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs992181	0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv595385	chr4:127383473-127451806	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:127451400-127454400	Weak transcription	K562	blood

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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