Variant report

Variant	rs13190420
Chromosome Location	chr5:166170905-166170906
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:10)

rs_ID	r²[population]
rs10475800	0.97[ASN][1000 genomes]
rs11958937	0.96[ASN][1000 genomes]
rs13164829	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2194152	0.96[ASN][1000 genomes]
rs34795507	0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs34881947	0.99[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs35139258	0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs62390565	0.82[ASN][1000 genomes]
rs6555706	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6860339	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[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	nsv830543	chr5:166146858-166314761	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:166169200-166171000	Active TSS	H9 Cell Line	embryonic stem cell
2	chr5:166170600-166171200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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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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