Variant report

Variant	rs10270202
Chromosome Location	chr7:118647271-118647272
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	chr7:118646033..118648474-chr7:118650936..118653090,2	K562	blood:

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs1320850	1.00[EUR][1000 genomes]
rs1881868	1.00[EUR][1000 genomes]
rs1881869	1.00[EUR][1000 genomes]
rs1919918	1.00[EUR][1000 genomes]
rs2222814	1.00[EUR][1000 genomes]
rs2222815	1.00[EUR][1000 genomes]
rs2590583	1.00[EUR][1000 genomes]
rs2590586	1.00[EUR][1000 genomes]
rs2590587	1.00[EUR][1000 genomes]
rs2590601	1.00[EUR][1000 genomes]
rs2590620	1.00[EUR][1000 genomes]
rs2590642	1.00[EUR][1000 genomes]
rs2590643	1.00[EUR][1000 genomes]
rs2699733	1.00[EUR][1000 genomes]
rs2699735	1.00[EUR][1000 genomes]
rs2699737	1.00[EUR][1000 genomes]
rs2699749	1.00[EUR][1000 genomes]
rs2699754	1.00[EUR][1000 genomes]
rs2699758	1.00[EUR][1000 genomes]
rs2699760	1.00[EUR][1000 genomes]
rs2699766	1.00[EUR][1000 genomes]
rs2699767	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv889093	chr7:117977091-118709754	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv889096	chr7:118438184-118709754	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv1021902	chr7:118452600-118719244	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv831110	chr7:118543340-118739362	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv889098	chr7:118590050-118896639	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv1016543	chr7:118626169-118660614	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv967471	chr7:118635494-118653086	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
8	esv1825159	chr7:118640865-118842361	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:118646600-118647800	Enhancers	Fetal Brain Male	brain
2	chr7:118646600-118648400	Enhancers	Fetal Lung	lung

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