Variant report

Variant	rs10737035
Chromosome Location	chr10:6049494-6049495
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	chr10:6048901..6050580-chr10:6243022..6245407,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000170525	Chromatin interaction
ENSG00000213994	Chromatin interaction

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs12251926	1.00[MEX][hapmap]
rs12722622	1.00[MEX][hapmap]
rs1359134	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1408014	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2246034	1.00[AMR][1000 genomes]
rs2478142	1.00[AMR][1000 genomes]
rs4405212	1.00[AMR][1000 genomes]
rs4607966	1.00[MEX][hapmap];1.00[AMR][1000 genomes]
rs4749891	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7078547	1.00[AMR][1000 genomes]
rs73616444	1.00[AMR][1000 genomes]
rs73618322	1.00[AMR][1000 genomes]
rs73618331	1.00[AMR][1000 genomes]
rs7896802	1.00[AMR][1000 genomes]
rs7911218	1.00[AMR][1000 genomes]
rs791594	1.00[AMR][1000 genomes]
rs7917819	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7922099	1.00[AMR][1000 genomes]
rs8177588	1.00[AMR][1000 genomes]
rs8177595	1.00[AMR][1000 genomes]
rs8177615	1.00[AMR][1000 genomes]
rs8177629	1.00[AMR][1000 genomes]
rs8177632	1.00[AMR][1000 genomes]
rs8177687	1.00[AMR][1000 genomes]
rs8177718	1.00[AMR][1000 genomes]
rs8177739	1.00[AMR][1000 genomes]
rs942198	1.00[MEX][hapmap]
rs942199	1.00[MEX][hapmap]
rs942200	1.00[MEX][hapmap]
rs9804284	1.00[AMR][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	esv34147	chr10:5726821-6105717	Strong transcription Weak transcription Genic enhancers Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
2	esv34061	chr10:5726821-6225187	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
3	nsv1042286	chr10:5795129-6578445	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	76 gene(s)	inside rSNPs	diseases
4	nsv1041261	chr10:5962635-6052196	Weak transcription Active TSS Genic enhancers Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
5	nsv1050983	chr10:5963921-6052196	Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Strong transcription Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 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	chr10:6044000-6053000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
2	chr10:6044000-6055800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
3	chr10:6048200-6050400	Weak transcription	Ovary	ovary
4	chr10:6048400-6055800	Weak transcription	K562	blood

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