Variant report

Variant	rs16869032
Chromosome Location	chr5:90016871-90016872
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr5:90011449..90014347-chr5:90016654..90019207,2	K562	blood:
2	chr5:90005181..90006888-chr5:90015330..90017702,2	K562	blood:
3	chr5:90007247..90014347-chr5:90014590..90019207,8	K562	blood:
4	chr5:90009460..90011230-chr5:90014685..90016873,2	K562	blood:

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs10044044	0.82[MEX][hapmap]
rs10514331	0.89[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10514334	1.00[ASW][hapmap];0.81[LWK][hapmap];0.86[YRI][hapmap]
rs11951632	0.89[CEU][hapmap];0.85[JPT][hapmap];0.91[EUR][1000 genomes]
rs11952742	0.82[MEX][hapmap];0.86[TSI][hapmap]
rs11955565	0.83[ASN][1000 genomes]
rs11959270	0.83[ASW][hapmap];0.89[CEU][hapmap];0.86[CHB][hapmap];0.98[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.94[MKK][hapmap];1.00[TSI][hapmap];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11960887	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1344030	0.82[MEX][hapmap];0.86[TSI][hapmap]
rs154557	0.82[MEX][hapmap]
rs16868901	0.82[MEX][hapmap];0.82[TSI][hapmap]
rs16868906	0.91[EUR][1000 genomes]
rs16868924	0.91[EUR][1000 genomes]
rs16868927	0.91[EUR][1000 genomes]
rs16868932	0.91[EUR][1000 genomes]
rs16868964	0.89[CEU][hapmap];0.81[CHB][hapmap];1.00[JPT][hapmap];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs16868970	0.86[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs16868972	0.82[CHB][hapmap];0.98[CHD][hapmap];0.82[GIH][hapmap];1.00[JPT][hapmap];0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs16868985	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs16869013	0.89[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs16869043	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1878881	0.89[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1996551	0.83[ASW][hapmap];0.89[CEU][hapmap];0.86[CHB][hapmap];0.98[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.94[MKK][hapmap];1.00[TSI][hapmap];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2366776	0.91[MEX][hapmap];0.84[MKK][hapmap];0.83[TSI][hapmap]
rs41303352	0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs41308295	0.91[EUR][1000 genomes]
rs4916687	1.00[ASW][hapmap];0.87[YRI][hapmap];0.84[AFR][1000 genomes]
rs4916690	0.87[AFR][1000 genomes]
rs4916809	0.87[GIH][hapmap];0.87[MKK][hapmap];0.88[TSI][hapmap];0.85[EUR][1000 genomes]
rs4916810	0.85[EUR][1000 genomes]
rs4916818	1.00[ASW][hapmap];0.85[LWK][hapmap];0.87[YRI][hapmap];0.82[AFR][1000 genomes]
rs55720814	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs58582125	0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs60562826	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs61525440	0.80[EUR][1000 genomes]
rs6452908	1.00[ASW][hapmap];0.82[LWK][hapmap];0.87[YRI][hapmap];0.87[AFR][1000 genomes]
rs6867004	0.86[CHB][hapmap];1.00[JPT][hapmap];0.84[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6875517	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6880570	0.89[CEU][hapmap];0.86[CHB][hapmap];0.93[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.83[MEX][hapmap];1.00[TSI][hapmap];0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs72656677	0.91[EUR][1000 genomes]
rs73772469	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7707357	0.82[MEX][hapmap];0.86[TSI][hapmap]
rs7709691	0.82[MEX][hapmap];0.82[TSI][hapmap]
rs7721027	0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7729205	0.81[EUR][1000 genomes]
rs7729644	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7730204	1.00[ASW][hapmap];0.88[LWK][hapmap];0.86[YRI][hapmap];0.93[AFR][1000 genomes]
rs9293546	0.82[MEX][hapmap];0.82[TSI][hapmap]
rs950692	0.89[CEU][hapmap];0.85[JPT][hapmap];1.00[MEX][hapmap];0.86[MKK][hapmap];0.96[TSI][hapmap];0.91[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv432750	chr5:89410113-90137144	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
2	nsv432751	chr5:89457044-90090444	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
3	nsv529544	chr5:89523963-90412409	Weak transcription Enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
4	nsv531965	chr5:89886550-90145002	Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
5	nsv882367	chr5:89956991-90209824	Enhancers Strong transcription Weak transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
6	nsv934323	chr5:89968158-90111853	Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Enhancers Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
7	nsv1015449	chr5:89968626-90219398	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
8	nsv1031718	chr5:89999033-90099868	Weak transcription Strong transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
9	nsv517049	chr5:90003131-90262475	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:89950400-90033400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr5:89995000-90025800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr5:89997800-90017600	Strong transcription	HUES48 Cell Line	embryonic stem cell
4	chr5:89998800-90018000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr5:90002200-90022000	Weak transcription	Brain Germinal Matrix	brain
6	chr5:90002200-90023200	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr5:90008200-90021600	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr5:90008200-90022000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr5:90010600-90035200	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr5:90011200-90027200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr5:90011800-90017800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr5:90013000-90021200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
13	chr5:90015200-90017000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
14	chr5:90015200-90018200	Strong transcription	K562	blood
15	chr5:90015400-90017200	Strong transcription	HUES64 Cell Line	embryonic stem cell
16	chr5:90016200-90021000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr5:90016800-90017000	Strong transcription	H1 Cell Line	embryonic stem cell

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