Variant report

Variant	rs1370327
Chromosome Location	chr2:142468592-142468593
allele	A/G
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:12)

rs_ID	r²[population]
rs10496892	0.94[ASW][hapmap];0.82[MEX][hapmap]
rs1191700	0.85[CEU][hapmap]
rs12622943	0.91[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs164975	0.85[CEU][hapmap];0.81[CHD][hapmap];0.84[TSI][hapmap]
rs2028130	0.85[CEU][hapmap];0.82[TSI][hapmap]
rs2118276	0.85[CEU][hapmap];0.87[TSI][hapmap]
rs2381154	0.81[YRI][hapmap]
rs355545	0.85[CEU][hapmap]
rs4427957	0.85[CEU][hapmap]
rs6747694	0.93[CEU][hapmap];0.87[TSI][hapmap]
rs6751890	0.85[CEU][hapmap];0.84[TSI][hapmap]
rs7582357	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap]

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	nsv834394	chr2:142430225-142593264	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 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	chr2:142462400-142469400	Weak transcription	Fetal Lung	lung
2	chr2:142467400-142469600	Enhancers	Liver	Liver

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

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