Variant report

Variant	rs5749394
Chromosome Location	chr22:32706221-32706222
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	22:32694902-32708216..22:33452523-33459358	K562	blood:

Variant related genes	Relation type
ENSG00000185666	Chromatin interaction

Extended variants
information (count: 61 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs12484711	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1807684	0.94[ASN][1000 genomes]
rs1807690	0.89[ASN][1000 genomes]
rs1810415	0.81[ASN][1000 genomes]
rs1883135	0.90[CHB][hapmap];0.80[ASN][1000 genomes]
rs1961908	0.93[ASN][1000 genomes]
rs2049912	0.81[ASN][1000 genomes]
rs2072808	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2072811	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2281032	0.83[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs2413091	0.80[CHB][hapmap];1.00[JPT][hapmap]
rs2413094	0.92[ASN][1000 genomes]
rs2413095	0.92[ASN][1000 genomes]
rs2413096	0.93[ASN][1000 genomes]
rs2413097	0.91[ASN][1000 genomes]
rs2413098	0.93[ASN][1000 genomes]
rs2413099	0.82[CHB][hapmap]
rs2899179	0.85[ASN][1000 genomes]
rs2899180	0.81[ASN][1000 genomes]
rs4302308	0.90[CHB][hapmap];0.80[ASN][1000 genomes]
rs4435548	0.90[CHB][hapmap];0.80[ASN][1000 genomes]
rs4820073	0.81[CHB][hapmap]
rs5749384	0.81[CHB][hapmap]
rs5749387	0.80[ASN][1000 genomes]
rs5749391	0.80[ASN][1000 genomes]
rs5749393	0.94[CHB][hapmap];0.82[ASN][1000 genomes]
rs5749400	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs5753904	0.82[JPT][hapmap]
rs5753908	1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs5753909	0.86[JPT][hapmap];0.85[ASN][1000 genomes]
rs5753911	0.89[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs5753912	0.89[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs5753916	0.93[ASN][1000 genomes]
rs5753917	0.93[ASN][1000 genomes]
rs5753945	0.82[CHB][hapmap]
rs5753948	0.95[ASN][1000 genomes]
rs5753950	0.81[CHB][hapmap]
rs5753956	0.90[CHB][hapmap];0.80[ASN][1000 genomes]
rs5753957	0.89[ASN][1000 genomes]
rs5753972	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs5753973	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs5753977	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs5994524	0.93[ASN][1000 genomes]
rs5994538	0.86[AFR][1000 genomes];0.98[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs5998384	0.84[ASN][1000 genomes]
rs5998403	0.81[CHB][hapmap]
rs713764	0.93[ASN][1000 genomes]
rs7288282	0.94[ASN][1000 genomes]
rs7291431	0.94[ASN][1000 genomes]
rs9609493	0.95[ASN][1000 genomes]
rs9609498	0.90[CHB][hapmap];0.87[JPT][hapmap];0.86[ASN][1000 genomes]
rs9609504	0.84[CHB][hapmap];0.83[ASN][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	nsv948789	chr22:32462505-32764760	Enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
2	nsv1065175	chr22:32467617-32761093	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
3	nsv544680	chr22:32467617-32761093	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
4	esv2830423	chr22:32477718-32767825	Enhancers Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
5	esv2422247	chr22:32486448-32788258	Strong transcription Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	44 gene(s)	inside rSNPs	diseases
6	nsv459874	chr22:32574274-32866934	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
7	nsv588895	chr22:32574274-32866934	Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
8	esv2753006	chr22:32592120-32719481	Enhancers Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
9	nsv1064737	chr22:32603912-32829725	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	38 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	chr22:32702000-32707000	Weak transcription	Spleen	Spleen
2	chr22:32705800-32706600	Enhancers	H1 Cell Line	embryonic stem cell
3	chr22:32706200-32706400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr22:32706200-32706400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr22:32706200-32706800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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