Variant report

Variant	rs10208150
Chromosome Location	chr2:178237170-178237171
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs10165785	0.80[ASN][1000 genomes]
rs10170546	0.87[ASN][1000 genomes]
rs10176632	0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11893448	0.82[ASN][1000 genomes]
rs12104588	0.87[ASN][1000 genomes]
rs12620035	0.80[ASN][1000 genomes]
rs12693120	0.82[ASN][1000 genomes]
rs1453371	0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1453373	0.82[ASN][1000 genomes]
rs1901824	0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1901825	0.87[AFR][1000 genomes];0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1901826	0.84[AFR][1000 genomes];0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1901829	0.91[AFR][1000 genomes];0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2060929	0.82[ASN][1000 genomes]
rs2364845	0.87[AFR][1000 genomes];0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3813259	0.87[ASN][1000 genomes]
rs3902850	0.80[ASN][1000 genomes]
rs4243388	0.82[ASN][1000 genomes]
rs4893821	0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4893823	0.81[ASN][1000 genomes]
rs4893824	0.80[ASN][1000 genomes]
rs4893825	0.80[ASN][1000 genomes]
rs4893931	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4893932	0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4893934	0.91[AFR][1000 genomes];0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4893935	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4893936	0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4893938	0.87[ASN][1000 genomes]
rs4893941	0.82[ASN][1000 genomes]
rs4893945	0.81[ASN][1000 genomes]
rs59208652	0.80[ASN][1000 genomes]
rs7573763	0.87[ASN][1000 genomes]
rs7586051	0.82[ASN][1000 genomes]
rs7591807	0.87[ASN][1000 genomes]
rs9679607	0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv3051	chr2:178193436-178239394	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:178203400-178244400	Weak transcription	HSMM	muscle
2	chr2:178218000-178256200	Weak transcription	HepG2	liver
3	chr2:178221600-178240600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr2:178232800-178244400	Weak transcription	Dnd41	blood
5	chr2:178235400-178256600	Weak transcription	Primary T cells from cord blood	blood
6	chr2:178235800-178244600	Weak transcription	Monocytes-CD14+_RO01746	blood

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