Variant report

Variant	rs473968
Chromosome Location	chr11:85010582-85010583
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:85010195..85012743-chr11:85014676..85016678,2	K562	blood:

Extended variants
information (count: 59 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs10792810	0.87[MEX][hapmap]
rs10898380	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs10898382	0.89[CHB][hapmap];0.95[JPT][hapmap]
rs11234316	0.84[CHB][hapmap];0.83[CHD][hapmap];0.89[JPT][hapmap]
rs12419394	0.85[CHB][hapmap];0.95[JPT][hapmap];0.86[ASN][1000 genomes]
rs1517308	0.91[MEX][hapmap]
rs1517311	0.94[ASW][hapmap];0.90[CHB][hapmap];0.83[CHD][hapmap];0.89[GIH][hapmap];0.95[JPT][hapmap]
rs1682383	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17810088	0.84[CHB][hapmap]
rs1793210	0.86[ASN][1000 genomes]
rs1826612	0.88[CHB][hapmap];0.95[JPT][hapmap];0.84[ASN][1000 genomes]
rs1914373	0.90[CHB][hapmap];0.95[JPT][hapmap]
rs1914376	0.89[ASN][1000 genomes]
rs2138748	0.95[CHB][hapmap];1.00[JPT][hapmap]
rs286044	0.84[ASN][1000 genomes]
rs286499	0.89[CHB][hapmap];0.89[JPT][hapmap]
rs286513	0.89[CHB][hapmap];0.89[JPT][hapmap]
rs286515	0.88[CEU][hapmap];0.89[CHB][hapmap];0.91[CHD][hapmap];0.89[JPT][hapmap];0.85[TSI][hapmap]
rs2930575	0.85[ASN][1000 genomes]
rs35167573	0.83[ASN][1000 genomes]
rs471786	0.91[MEX][hapmap]
rs474992	0.89[ASN][1000 genomes]
rs475164	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs476781	0.94[ASN][1000 genomes]
rs488668	0.90[ASN][1000 genomes]
rs4943918	0.89[CHB][hapmap];0.84[JPT][hapmap]
rs4944513	0.84[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs495905	0.94[AFR][1000 genomes];0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs496814	0.95[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs497607	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs500307	0.90[ASN][1000 genomes]
rs508177	0.91[ASN][1000 genomes]
rs512775	0.81[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs512910	0.81[AFR][1000 genomes];0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs514639	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs516080	0.90[ASN][1000 genomes]
rs516620	0.90[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs519429	0.86[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs526990	0.85[ASN][1000 genomes]
rs527928	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs530293	0.94[ASN][1000 genomes]
rs531331	0.88[ASW][hapmap];0.95[CHB][hapmap];0.94[CHD][hapmap];1.00[JPT][hapmap];0.82[MEX][hapmap];0.97[ASN][1000 genomes]
rs534604	0.85[AFR][1000 genomes];0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs539551	0.98[ASN][1000 genomes]
rs550981	1.00[CHB][hapmap];0.93[JPT][hapmap];0.98[ASN][1000 genomes]
rs601857	0.87[MEX][hapmap]
rs603170	0.89[CHB][hapmap];0.95[JPT][hapmap]
rs680675	0.81[ASN][1000 genomes]
rs7106588	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs7110363	0.89[CHB][hapmap];0.84[JPT][hapmap]
rs7111281	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs789599	0.96[ASN][1000 genomes]
rs938728	0.90[CHB][hapmap];0.95[JPT][hapmap];0.86[ASN][1000 genomes]
rs951729	0.94[ASW][hapmap];0.84[CHB][hapmap];0.89[GIH][hapmap];0.89[JPT][hapmap];0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1044370	chr11:84748993-85293233	Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
2	nsv898043	chr11:84895033-85148689	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv898044	chr11:84895033-85220773	ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
4	nsv1051155	chr11:85006564-85721261	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
5	nsv541110	chr11:85006564-85721261	Enhancers Strong transcription Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:84967800-85019400	Weak transcription	Ovary	ovary
2	chr11:85009600-85011200	Enhancers	A549	lung
3	chr11:85010000-85010600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr11:85010200-85010600	Enhancers	Primary hematopoietic stem cells short term culture	blood
5	chr11:85010200-85010800	Enhancers	Fetal Intestine Large	intestine
6	chr11:85010400-85010600	Enhancers	Psoas Muscle	Psoas
7	chr11:85010400-85010600	Enhancers	HSMMtube	muscle
8	chr11:85010400-85011200	Enhancers	Colon Smooth Muscle	Colon

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