Variant report

Variant	rs10192634
Chromosome Location	chr2:180500950-180500951
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10172379	0.95[AFR][1000 genomes]
rs10930879	0.83[CEU][hapmap];0.91[CHB][hapmap];0.84[ASN][1000 genomes]
rs12476520	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1515269	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs1515276	0.91[JPT][hapmap]
rs1515279	0.84[CEU][hapmap];0.91[CHB][hapmap];0.84[ASN][1000 genomes]
rs1588848	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs2222030	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3106708	0.95[CHB][hapmap];0.85[ASN][1000 genomes]
rs3112943	0.87[JPT][hapmap]
rs3112960	0.95[CHB][hapmap];0.97[ASN][1000 genomes]
rs3112963	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs3112965	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs35667895	0.84[ASN][1000 genomes]
rs6718154	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6739057	0.88[ASN][1000 genomes]
rs872162	0.95[CHB][hapmap];0.91[JPT][hapmap];0.83[ASN][1000 genomes]
rs925751	0.91[CHB][hapmap];0.90[JPT][hapmap];0.97[ASN][1000 genomes]
rs925753	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:180495000-180502200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr2:180500800-180501200	Enhancers	Fetal Heart	heart
3	chr2:180500800-180501600	Enhancers	Fetal Kidney	kidney
4	chr2:180500800-180501600	Flanking Active TSS	HepG2	liver
5	chr2:180500800-180502400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr2:180500800-180502400	Enhancers	Liver	Liver

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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