Variant report

Variant	rs16884157
Chromosome Location	chr6:63079372-63079373
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 70 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:62)

rs_ID	r²[population]
rs10945156	0.87[ASN][1000 genomes]
rs10945226	0.98[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11758619	0.99[ASN][1000 genomes]
rs12528424	0.85[ASN][1000 genomes]
rs12662273	0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12663464	0.98[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs16884023	0.83[ASN][1000 genomes]
rs16884169	0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2260966	0.81[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs2345330	0.86[ASN][1000 genomes]
rs2345331	0.98[AFR][1000 genomes];0.85[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs2492796	0.87[ASN][1000 genomes]
rs2495266	0.96[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs2495267	0.87[ASN][1000 genomes]
rs2639412	0.85[ASN][1000 genomes]
rs2639413	0.99[ASN][1000 genomes]
rs2639414	0.99[ASN][1000 genomes]
rs2639415	0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2639419	0.81[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs2639446	0.83[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs2639447	0.84[ASN][1000 genomes]
rs2639448	0.83[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs2639450	0.83[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs2814648	0.96[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs2814649	0.96[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs2814650	0.85[ASN][1000 genomes]
rs2814651	0.99[ASN][1000 genomes]
rs2814652	0.85[ASN][1000 genomes]
rs2814654	0.85[ASN][1000 genomes]
rs2814655	0.96[ASN][1000 genomes]
rs2814658	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2814659	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2814660	0.87[ASN][1000 genomes]
rs2814680	0.87[ASN][1000 genomes]
rs2814681	0.98[AFR][1000 genomes];0.85[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs2842798	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2842799	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2842802	0.88[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2842809	0.85[ASN][1000 genomes]
rs2842810	0.99[ASN][1000 genomes]
rs2842812	0.85[ASN][1000 genomes]
rs494833	0.81[ASN][1000 genomes]
rs549603	0.84[ASN][1000 genomes]
rs590059	0.81[ASN][1000 genomes]
rs62416568	0.99[ASN][1000 genomes]
rs62416569	0.98[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs62416570	0.87[ASN][1000 genomes]
rs62416571	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs62416572	0.87[ASN][1000 genomes]
rs6908177	0.84[ASN][1000 genomes]
rs7742126	0.87[ASN][1000 genomes]
rs7750698	0.88[ASN][1000 genomes]
rs7772645	0.88[ASN][1000 genomes]
rs855409	0.84[ASN][1000 genomes]
rs855413	0.84[ASN][1000 genomes]
rs855414	0.84[ASN][1000 genomes]
rs876854	0.87[ASN][1000 genomes]
rs9446139	0.88[ASN][1000 genomes]
rs9446154	0.91[CHB][hapmap]
rs9454832	0.88[ASN][1000 genomes]
rs9454834	0.88[ASN][1000 genomes]
rs9454859	0.91[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1017249	chr6:62906813-63317382	Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent Enhancer Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv1020677	chr6:62911584-63309663	Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv532025	chr6:62944349-63571677	Enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	nsv916760	chr6:62944661-63290986	Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv1029503	chr6:63033365-63698355	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
6	nsv603350	chr6:63066240-63152724	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
7	nsv462967	chr6:63069063-63173293	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv603351	chr6:63069063-63173293	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island lncRNA	1 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs16884157	KHDRBS2	cis	brain	BrainEAC

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:63066600-63081600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr6:63078600-63081400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr6:63079000-63083400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr6:63079200-63079600	Weak transcription	Primary hematopoietic stem cells	blood

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