Variant report

Variant	rs10497592
Chromosome Location	chr2:182928801-182928802
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:18)

rs_ID	r²[population]
rs10497591	1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs10497593	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12105839	1.00[MEX][hapmap]
rs16822346	1.00[MEX][hapmap]
rs16822397	1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16822446	0.95[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs16822453	1.00[MEX][hapmap]
rs16822454	1.00[ASW][hapmap];1.00[MEX][hapmap];0.88[YRI][hapmap];0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16822458	1.00[ASW][hapmap];1.00[MEX][hapmap];0.89[YRI][hapmap];0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16822460	0.82[YRI][hapmap];0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16822482	1.00[MEX][hapmap]
rs58836112	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61711545	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6750153	1.00[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7569843	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7578135	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7588817	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7608147	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:182918800-182937400	Weak transcription	Thymus	Thymus
2	chr2:182926800-182929600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr2:182927200-182929400	Enhancers	Fetal Intestine Small	intestine
4	chr2:182928200-182929200	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr2:182928400-182929400	Enhancers	Left Ventricle	heart
6	chr2:182928400-182929600	Enhancers	Fetal Intestine Large	intestine
7	chr2:182928400-182929600	Enhancers	Skeletal Muscle Male	skeletal muscle
8	chr2:182928400-182930600	Enhancers	Fetal Lung	lung
9	chr2:182928400-182930600	Strong transcription	Fetal Thymus	thymus
10	chr2:182928600-182931600	Weak transcription	Liver	Liver
11	chr2:182928800-182929600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr2:182928800-182929600	Enhancers	Fetal Heart	heart

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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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