Variant report

Variant	rs4916210
Chromosome Location	chr1:173146732-173146733
allele	G/T
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]
rs10465507	1.00[ASN][1000 genomes]
rs10489266	1.00[ASN][1000 genomes]
rs10489268	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10798264	1.00[ASN][1000 genomes]
rs10912558	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10912561	1.00[ASN][1000 genomes]
rs11587348	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11801818	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11806687	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11807031	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11808060	1.00[ASN][1000 genomes]
rs12120808	0.82[ASN][1000 genomes]
rs12125395	0.82[ASN][1000 genomes]
rs12138547	0.82[ASN][1000 genomes]
rs12141186	0.82[ASN][1000 genomes]
rs12144635	0.82[ASN][1000 genomes]
rs12144665	0.82[ASN][1000 genomes]
rs17300347	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17300677	0.82[ASN][1000 genomes]
rs17300754	0.82[ASN][1000 genomes]
rs17346501	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17372309	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4090392	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4113832	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4916314	1.00[ASN][1000 genomes]
rs56074681	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57928823	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61826345	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61828261	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61828267	0.82[ASN][1000 genomes]
rs72722845	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72722865	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	chr1:173132200-173158800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr1:173142400-173150800	Weak transcription	HSMMtube	muscle
3	chr1:173143000-173150600	Weak transcription	HSMM	muscle
4	chr1:173143000-173159000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr1:173145400-173147400	Weak transcription	Primary hematopoietic stem cells	blood
6	chr1:173145400-173152400	Weak transcription	HUVEC	blood vessel
7	chr1:173146200-173147200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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