Variant report

Variant	rs883708
Chromosome Location	chr6:70976538-70976539
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:70970616..70973250-chr6:70975727..70977681,2	K562	blood:

Variant related genes	Relation type
ENSG00000112280	Chromatin interaction

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs1023034	0.89[CEU][hapmap];0.85[MEX][hapmap];0.87[TSI][hapmap];0.84[EUR][1000 genomes]
rs10945208	0.89[CEU][hapmap];0.85[MEX][hapmap];0.87[TSI][hapmap];0.87[EUR][1000 genomes]
rs11754328	0.85[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs12153933	0.84[EUR][1000 genomes]
rs12194091	0.94[CEU][hapmap];0.85[MEX][hapmap];0.90[TSI][hapmap];0.90[EUR][1000 genomes]
rs12194189	0.89[CEU][hapmap];0.84[TSI][hapmap];0.84[EUR][1000 genomes]
rs12194415	0.89[CEU][hapmap];0.84[EUR][1000 genomes]
rs12197487	0.89[CEU][hapmap];0.84[EUR][1000 genomes]
rs12197540	0.94[CEU][hapmap];0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12203351	0.85[EUR][1000 genomes]
rs13201224	0.89[CEU][hapmap];0.82[EUR][1000 genomes]
rs13201660	0.84[EUR][1000 genomes]
rs13202029	0.89[CEU][hapmap];0.87[TSI][hapmap];0.84[EUR][1000 genomes]
rs1321059	0.85[JPT][hapmap]
rs13212724	0.89[CEU][hapmap];0.87[TSI][hapmap];0.87[EUR][1000 genomes]
rs13216129	0.89[CEU][hapmap];0.85[MEX][hapmap];0.87[TSI][hapmap];0.84[EUR][1000 genomes]
rs16868814	0.92[JPT][hapmap];0.93[ASN][1000 genomes]
rs16868815	1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs16868818	0.83[CHD][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs16868820	1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs16868822	1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs2025995	0.90[EUR][1000 genomes]
rs2072650	0.92[JPT][hapmap]
rs2138659	0.89[CEU][hapmap];0.85[EUR][1000 genomes]
rs2274584	0.85[JPT][hapmap]
rs34506690	0.87[EUR][1000 genomes]
rs35970582	0.85[EUR][1000 genomes]
rs3737010	0.88[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs3806074	0.92[JPT][hapmap]
rs3806076	1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs3806089	0.88[CHB][hapmap];0.84[CHD][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs3828778	0.92[JPT][hapmap]
rs549742	0.98[ASN][1000 genomes]
rs6455358	0.89[CEU][hapmap];0.85[EUR][1000 genomes]
rs6913123	0.92[CHD][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs6914074	0.97[ASN][1000 genomes]
rs6935778	1.00[CEU][hapmap];0.85[MEX][hapmap];0.90[TSI][hapmap];0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6936355	0.97[ASN][1000 genomes]
rs7755873	0.89[CEU][hapmap];0.84[EUR][1000 genomes]
rs9446215	0.89[CEU][hapmap];0.85[MEX][hapmap];0.87[TSI][hapmap];0.85[EUR][1000 genomes]
rs9455015	0.89[CEU][hapmap];0.84[EUR][1000 genomes]
rs9455017	0.89[CEU][hapmap];0.85[MEX][hapmap];0.87[TSI][hapmap];0.85[EUR][1000 genomes]
rs9455019	0.94[CEU][hapmap];0.90[TSI][hapmap];0.90[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv932111	chr6:70736835-71633094	Enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
2	nsv886142	chr6:70741209-71251421	Weak transcription Strong transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
3	nsv1027049	chr6:70961610-71561488	Strong transcription Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh 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	29 gene(s)	inside rSNPs	diseases
4	nsv524328	chr6:70961833-71558805	Flanking Bivalent TSS/Enh Active TSS Weak transcription Strong transcription ZNF genes & repeats Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
5	nsv917312	chr6:70961903-71601688	Enhancers Genic enhancers Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
6	nsv886143	chr6:70968276-70984436	Strong transcription Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:70952200-70980400	Weak transcription	Fetal Stomach	stomach
2	chr6:70952200-70990000	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr6:70952600-70980400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
4	chr6:70952800-70989800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
5	chr6:70962000-70983600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr6:70965200-70991600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr6:70972800-70978200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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