Variant report

Variant	rs2185871
Chromosome Location	chr20:23259064-23259065
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1110402	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11697315	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11700168	0.94[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13043798	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2185870	0.81[ASN][1000 genomes]
rs2405001	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs34877072	0.99[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs35327803	0.98[ASN][1000 genomes]
rs4815183	0.98[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4815186	0.98[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4815188	0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6048657	0.87[ASN][1000 genomes]
rs6048658	0.87[ASN][1000 genomes]
rs6048661	0.85[AFR][1000 genomes]
rs6083070	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1066734	chr20:23170094-23277628	Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Bivalent/Poised TSS Strong transcription	Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv458948	chr20:23234699-23292849	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Strong transcription	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv585721	chr20:23234699-23292849	Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:23253200-23274400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr20:23253800-23267000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr20:23257600-23259200	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr20:23257600-23259200	Enhancers	Monocytes-CD14+_RO01746	blood

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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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