Variant report

Variant	rs9662096
Chromosome Location	chr1:85283089-85283090
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs11161462	0.91[ASW][hapmap];0.88[CEU][hapmap];0.90[CHD][hapmap];0.84[GIH][hapmap];0.93[MKK][hapmap];0.82[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs11161464	0.86[GIH][hapmap];0.85[LWK][hapmap];0.82[MKK][hapmap];0.92[TSI][hapmap];0.91[EUR][1000 genomes]
rs1325272	0.92[CHB][hapmap];0.94[MEX][hapmap];0.82[AMR][1000 genomes]
rs2389786	0.85[CHB][hapmap];0.84[CHD][hapmap]
rs4256829	0.83[EUR][1000 genomes]
rs9727725	0.88[CEU][hapmap];1.00[CHB][hapmap];0.90[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.90[LWK][hapmap];0.94[MEX][hapmap];0.91[MKK][hapmap];0.96[TSI][hapmap];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9729018	0.88[CEU][hapmap];0.92[CHD][hapmap];0.97[GIH][hapmap];0.95[LWK][hapmap];0.85[MEX][hapmap];0.93[MKK][hapmap];0.96[TSI][hapmap];0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:85264000-85295600	Weak transcription	NHEK	skin
2	chr1:85266400-85287200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr1:85277000-85285400	Weak transcription	Left Ventricle	heart
4	chr1:85277200-85284800	Weak transcription	Fetal Heart	heart
5	chr1:85278200-85287200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr1:85281200-85289200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr1:85282400-85295800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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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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