Variant report

Variant	rs11963931
Chromosome Location	chr6:161343052-161343053
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:161342992..161345118-chr6:161348741..161350289,2	K562	blood:

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

rSNPs within LD-proxies of this variant (count:56)

rs_ID	r²[population]
rs11751714	1.00[ASN][1000 genomes]
rs11751813	1.00[ASN][1000 genomes]
rs11752957	1.00[ASN][1000 genomes]
rs11753115	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11754459	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs11755099	1.00[ASN][1000 genomes]
rs11758427	1.00[ASN][1000 genomes]
rs11758620	0.87[AFR][1000 genomes];0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11759366	1.00[ASN][1000 genomes]
rs13194157	1.00[JPT][hapmap]
rs1464779	1.00[JPT][hapmap]
rs1464780	1.00[JPT][hapmap]
rs1543261	1.00[JPT][hapmap]
rs1562026	1.00[JPT][hapmap]
rs1982291	1.00[JPT][hapmap]
rs2275925	0.85[CEU][hapmap];1.00[JPT][hapmap]
rs2275926	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs2872613	1.00[JPT][hapmap]
rs4472323	1.00[JPT][hapmap]
rs4708898	1.00[JPT][hapmap]
rs4709486	1.00[JPT][hapmap]
rs4709490	1.00[JPT][hapmap]
rs4709491	1.00[JPT][hapmap]
rs56160793	1.00[ASN][1000 genomes]
rs56820519	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60465142	1.00[ASN][1000 genomes]
rs615269	1.00[JPT][hapmap]
rs619393	1.00[JPT][hapmap]
rs6455701	1.00[JPT][hapmap]
rs6905942	1.00[JPT][hapmap]
rs6913706	1.00[JPT][hapmap]
rs6914092	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs6925502	1.00[JPT][hapmap]
rs6925800	1.00[JPT][hapmap]
rs6929462	1.00[JPT][hapmap]
rs6933810	1.00[JPT][hapmap]
rs705829	1.00[JPT][hapmap]
rs73019757	1.00[ASN][1000 genomes]
rs73019758	1.00[ASN][1000 genomes]
rs73019760	1.00[ASN][1000 genomes]
rs73019762	1.00[ASN][1000 genomes]
rs73019772	1.00[ASN][1000 genomes]
rs73019780	1.00[ASN][1000 genomes]
rs73019797	1.00[ASN][1000 genomes]
rs73021743	1.00[ASN][1000 genomes]
rs7738762	1.00[JPT][hapmap]
rs7750449	0.91[AFR][1000 genomes];0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7753585	1.00[JPT][hapmap]
rs7760056	1.00[JPT][hapmap]
rs9355330	1.00[JPT][hapmap]
rs9355332	1.00[JPT][hapmap]
rs9355867	1.00[JPT][hapmap]
rs9355873	1.00[JPT][hapmap]
rs9364585	1.00[JPT][hapmap]
rs9364586	1.00[JPT][hapmap]
rs9365248	1.00[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830853	chr6:161180005-161376481	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	esv2422347	chr6:161211171-161442377	Flanking Active TSS Enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:161334200-161347800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr6:161340000-161352000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr6:161340400-161343400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr6:161341400-161350800	Weak transcription	GM12878-XiMat	blood
5	chr6:161341800-161343200	Weak transcription	Osteobl	bone

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