Variant report

Variant	rs7938610
Chromosome Location	chr11:5187079-5187080
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:5186471..5188336-chr11:5192337..5194748,2	K562	blood:
2	11:5181580-5190487..11:5527719-5533869	GM12878	blood:
3	11:5181580-5190487..11:5714465-5718134	K562	blood:
4	11:5181580-5190487..11:5533869-5541626	K562	blood:
5	11:5181580-5190487..11:5700314-5707362	GM12878	blood:
6	11:5181580-5190487..11:5250847-5268367	Hela-S3	cervix:

Variant related genes	Relation type
ENSG00000132256	Chromatin interaction
ENSG00000229988	Chromatin interaction
ENSG00000132274	Chromatin interaction
ENSG00000260629	Chromatin interaction
ENSG00000176752	Chromatin interaction
ENSG00000175520	Chromatin interaction
ENSG00000175518	Chromatin interaction
ENSG00000223609	Chromatin interaction

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

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

rs_ID	r²[population]
rs10734487	0.91[EUR][1000 genomes]
rs10768638	0.92[EUR][1000 genomes]
rs10768640	0.92[EUR][1000 genomes]
rs10837513	0.92[EUR][1000 genomes]
rs11603140	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs11606639	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11823559	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11825768	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11826290	0.83[EUR][1000 genomes]
rs4128714	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4910717	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs4910718	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs4910719	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs4910720	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs4910726	1.00[EUR][1000 genomes]
rs55658554	0.81[EUR][1000 genomes]
rs61880375	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6578562	0.89[EUR][1000 genomes]
rs6578563	0.91[EUR][1000 genomes]
rs7102118	0.88[EUR][1000 genomes]
rs7114182	0.91[EUR][1000 genomes]
rs7120612	0.81[EUR][1000 genomes]
rs72879626	0.81[EUR][1000 genomes]
rs72879629	0.85[EUR][1000 genomes]
rs73396873	0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73396875	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73396878	0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74051367	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74051386	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs74051388	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs74051390	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7479400	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7480442	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7480988	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7481293	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7482238	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7924390	0.92[EUR][1000 genomes]
rs7926026	0.82[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7927539	0.92[EUR][1000 genomes]
rs7938958	0.82[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7948322	0.92[EUR][1000 genomes]
rs7948470	0.90[EUR][1000 genomes]
rs7948698	0.92[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1054847	chr11:4642875-5200656	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	72 gene(s)	inside rSNPs	diseases
2	esv2760169	chr11:4961518-5233821	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	54 gene(s)	inside rSNPs	diseases
3	nsv553219	chr11:5026200-5214413	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	44 gene(s)	inside rSNPs	diseases
4	nsv896920	chr11:5068137-5221825	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
5	nsv896923	chr11:5091882-5199208	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
6	nsv896924	chr11:5098714-5221825	Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
7	nsv467668	chr11:5138733-5207389	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	27 gene(s)	inside rSNPs	diseases
8	nsv553224	chr11:5138733-5207389	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	27 gene(s)	inside rSNPs	diseases
9	nsv896925	chr11:5140977-5221825	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	25 gene(s)	inside rSNPs	diseases
10	nsv896927	chr11:5154157-5199208	Enhancers Genic enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	19 gene(s)	inside rSNPs	diseases
11	nsv896928	chr11:5154157-5207389	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	19 gene(s)	inside rSNPs	diseases
12	nsv1042613	chr11:5173410-5336839	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
13	nsv1051488	chr11:5175477-5258490	Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
14	nsv1048593	chr11:5183176-5261470	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
15	nsv1045187	chr11:5183176-5262622	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
16	nsv1052798	chr11:5184546-5269330	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:5181600-5187400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr11:5185200-5187200	Enhancers	K562	blood
3	chr11:5185400-5187400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr11:5186600-5192200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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