Variant report

Variant	rs10797083
Chromosome Location	chr1:160571958-160571959
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 65 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:61)

rs_ID	r²[population]
rs1061217	1.00[CEU][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10752638	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10908789	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10908792	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10908794	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10908796	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11265442	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11265443	0.82[ASN][1000 genomes]
rs11265444	0.92[ASN][1000 genomes]
rs11265449	0.81[CHB][hapmap];0.83[JPT][hapmap];0.91[ASN][1000 genomes]
rs11265451	0.88[ASN][1000 genomes]
rs11265452	0.84[CEU][hapmap]
rs1138323	0.84[EUR][1000 genomes]
rs11583402	0.80[CEU][hapmap]
rs11585738	0.80[CEU][hapmap]
rs11590035	0.81[CEU][hapmap]
rs12048466	0.86[JPT][hapmap];0.88[ASN][1000 genomes]
rs12144628	0.96[CEU][hapmap];0.82[EUR][1000 genomes]
rs12402879	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.91[YRI][hapmap];0.92[AFR][1000 genomes];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12728784	1.00[CEU][hapmap];0.92[CHB][hapmap];0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12736781	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1394079	0.93[CHB][hapmap];0.91[JPT][hapmap];0.96[ASN][1000 genomes]
rs151607	0.88[CEU][hapmap]
rs1572382	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1604783	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16832283	0.84[CEU][hapmap]
rs17381453	0.80[CEU][hapmap]
rs17385407	0.80[CEU][hapmap]
rs1809963	0.81[CEU][hapmap]
rs1998651	1.00[CEU][hapmap];0.94[CHB][hapmap];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2025516	0.88[CEU][hapmap]
rs2025517	0.84[CEU][hapmap]
rs2083128	0.92[CEU][hapmap]
rs2089088	0.86[JPT][hapmap];0.88[ASN][1000 genomes]
rs2099604	0.95[CEU][hapmap];0.87[CHB][hapmap];0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2102225	0.88[ASN][1000 genomes]
rs2102226	0.88[ASN][1000 genomes]
rs2369725	0.88[ASN][1000 genomes]
rs2369726	0.88[ASN][1000 genomes]
rs2753260	0.92[CEU][hapmap]
rs349249	0.80[ASN][1000 genomes]
rs3733264	0.80[CEU][hapmap]
rs3733265	0.80[CEU][hapmap]
rs3733266	0.80[CEU][hapmap]
rs3766387	0.84[CEU][hapmap]
rs3766388	0.84[CEU][hapmap]
rs3766389	0.80[CEU][hapmap]
rs3816146	0.96[CEU][hapmap];0.93[CHB][hapmap];0.82[EUR][1000 genomes]
rs5002947	0.84[CEU][hapmap]
rs6427535	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6660233	0.80[CEU][hapmap]
rs6668760	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6670721	0.84[CEU][hapmap]
rs6687641	0.92[CEU][hapmap]
rs6692382	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7526815	0.98[ASN][1000 genomes]
rs7534679	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7547054	0.92[CEU][hapmap]
rs7550771	0.92[CEU][hapmap]
rs927202	0.86[JPT][hapmap];0.88[ASN][1000 genomes]
rs977019	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1829614	chr1:160465291-160595000	Strong transcription Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	nsv872491	chr1:160470258-160580549	Weak transcription Flanking Active TSS Enhancers Strong transcription Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	nsv831703	chr1:160496124-160643024	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	esv1822379	chr1:160545332-160831143	Enhancers Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs10797083	CD84	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:160555600-160575200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
2	chr1:160558000-160575400	Weak transcription	Primary T helper naive cells from peripheral blood	blood

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