Variant report

Variant	rs17718694
Chromosome Location	chr2:209355947-209355948
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10193961	1.00[ASN][1000 genomes]
rs10206991	1.00[ASN][1000 genomes]
rs1080646	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11897777	1.00[ASN][1000 genomes]
rs11902124	1.00[ASN][1000 genomes]
rs1259699	1.00[ASN][1000 genomes]
rs1259700	1.00[ASN][1000 genomes]
rs13397965	1.00[ASN][1000 genomes]
rs16841239	1.00[ASN][1000 genomes]
rs16841294	1.00[ASN][1000 genomes]
rs34259292	1.00[ASN][1000 genomes]
rs61082488	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61193569	1.00[ASN][1000 genomes]
rs66521274	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66700780	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6716615	1.00[ASN][1000 genomes]
rs67168689	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6717082	1.00[ASN][1000 genomes]
rs67393765	1.00[ASN][1000 genomes]
rs67757182	1.00[ASN][1000 genomes]
rs67984155	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs68112042	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72981015	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72981030	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72981046	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72981047	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72986744	1.00[ASN][1000 genomes]
rs72990613	0.87[AMR][1000 genomes]
rs7563597	1.00[ASN][1000 genomes]
rs7570304	1.00[ASN][1000 genomes]
rs7586219	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7608913	1.00[ASN][1000 genomes]

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:209353200-209356600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr2:209354400-209357400	Enhancers	K562	blood
3	chr2:209354600-209357600	Weak transcription	Pancreas	Pancrea
4	chr2:209355200-209361000	Weak transcription	Stomach Mucosa	stomach
5	chr2:209355200-209366000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr2:209355800-209356400	Enhancers	Primary hematopoietic stem cells	blood
7	chr2:209355800-209357200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr2:209355800-209357200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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