Variant report

Variant	rs4691198
Chromosome Location	chr4:166369041-166369042
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs10517847	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17489060	1.00[AFR][1000 genomes]
rs17489067	1.00[AFR][1000 genomes]
rs17585655	1.00[AFR][1000 genomes]
rs17686888	1.00[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17686918	1.00[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs17687037	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs17687250	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17687429	0.82[EUR][1000 genomes]
rs2053276	0.81[AMR][1000 genomes]
rs3775313	0.82[EUR][1000 genomes]
rs4690818	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4691194	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72701627	1.00[AFR][1000 genomes]
rs72701632	1.00[AFR][1000 genomes]
rs72701634	1.00[AFR][1000 genomes]
rs72701636	1.00[AFR][1000 genomes]
rs72701637	1.00[AFR][1000 genomes]
rs72701639	1.00[AFR][1000 genomes]
rs72701642	1.00[AFR][1000 genomes]
rs72701645	1.00[AFR][1000 genomes]
rs72701652	1.00[AFR][1000 genomes]
rs72701657	1.00[AFR][1000 genomes]
rs72701659	1.00[AFR][1000 genomes]
rs72701664	1.00[AFR][1000 genomes]
rs72701670	1.00[AFR][1000 genomes]
rs72701672	1.00[AFR][1000 genomes]
rs72701673	1.00[AFR][1000 genomes]
rs72701675	1.00[AFR][1000 genomes]
rs72701694	0.87[ASN][1000 genomes]
rs72703611	0.85[ASN][1000 genomes]
rs72703619	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72703624	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72703639	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs72703653	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72703657	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72703674	0.82[EUR][1000 genomes]
rs72703686	0.82[EUR][1000 genomes]
rs7656675	1.00[AFR][1000 genomes]
rs7657847	1.00[AFR][1000 genomes]

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:166361800-166375200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr4:166362200-166381600	Weak transcription	Fetal Stomach	stomach
3	chr4:166362400-166381600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr4:166362400-166382400	Weak transcription	Aorta	Aorta
5	chr4:166362400-166384600	Weak transcription	Brain Cingulate Gyrus	brain
6	chr4:166362600-166370000	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr4:166362600-166379000	Weak transcription	Fetal Brain Female	brain
8	chr4:166362800-166379200	Weak transcription	Brain Anterior Caudate	brain
9	chr4:166364400-166374800	Weak transcription	HepG2	liver

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