Variant report

Variant	rs2891842
Chromosome Location	chr8:127681578-127681579
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10105909	0.85[EUR][1000 genomes]
rs10106191	0.88[EUR][1000 genomes]
rs10106433	0.99[EUR][1000 genomes]
rs10505497	0.85[CEU][hapmap]
rs12334974	0.98[EUR][1000 genomes]
rs13249816	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13264085	1.00[CEU][hapmap];0.85[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs16901632	0.85[CEU][hapmap]
rs6470455	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs7813452	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7828002	1.00[CEU][hapmap];0.99[EUR][1000 genomes]
rs7831824	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7831850	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv917354	chr8:127545903-127728374	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
2	nsv891438	chr8:127670339-127845702	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 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	chr8:127613200-127686800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
2	chr8:127680800-127703800	Weak transcription	Pancreas	Pancrea
3	chr8:127681400-127682000	Enhancers	Cortex derived primary cultured neurospheres	brain
4	chr8:127681400-127682200	Enhancers	Fetal Kidney	kidney

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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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