Variant report

Variant	rs13385783
Chromosome Location	chr2:142589230-142589231
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	chr2:142588077..142589694-chr2:142590092..142592138,2	MCF-7	breast:

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10166169	0.84[CEU][hapmap];1.00[CHB][hapmap]
rs10167034	0.84[CEU][hapmap];1.00[CHB][hapmap];0.81[AMR][1000 genomes]
rs10167533	0.85[CEU][hapmap];1.00[CHB][hapmap];0.81[AMR][1000 genomes]
rs10172953	0.85[CEU][hapmap];1.00[CHB][hapmap]
rs10176459	0.84[CEU][hapmap];1.00[CHB][hapmap]
rs10178875	0.92[CEU][hapmap];1.00[CHB][hapmap]
rs10179633	0.84[CEU][hapmap];1.00[CHB][hapmap];0.81[AMR][1000 genomes]
rs10181557	0.84[CEU][hapmap];1.00[CHB][hapmap]
rs10192543	1.00[CHB][hapmap]
rs10193124	0.84[CEU][hapmap];1.00[CHB][hapmap]
rs10203168	1.00[CHB][hapmap]
rs10203777	1.00[CHB][hapmap]
rs10439174	0.85[CEU][hapmap];1.00[CHB][hapmap];0.81[AMR][1000 genomes]
rs10439185	0.81[AMR][1000 genomes]
rs10439186	0.84[CEU][hapmap];1.00[CHB][hapmap];0.81[AMR][1000 genomes]
rs10439187	0.84[CEU][hapmap];1.00[CHB][hapmap];0.81[AMR][1000 genomes]
rs10439188	0.85[CEU][hapmap];1.00[CHB][hapmap];0.81[AMR][1000 genomes]
rs10439189	0.85[CEU][hapmap];1.00[CHB][hapmap];0.81[AMR][1000 genomes]
rs13387675	1.00[CHB][hapmap]
rs13389827	0.84[CEU][hapmap];1.00[CHB][hapmap]
rs13400934	0.84[CEU][hapmap];1.00[CHB][hapmap];0.84[EUR][1000 genomes]
rs1435596	0.90[CEU][hapmap];1.00[CHB][hapmap]
rs17816590	0.85[CEU][hapmap];1.00[CHB][hapmap]
rs17817209	1.00[CHB][hapmap];0.86[EUR][1000 genomes]
rs2053172	0.88[CEU][hapmap];1.00[CHB][hapmap]
rs2053173	0.84[CEU][hapmap];1.00[CHB][hapmap]
rs2053174	1.00[CHB][hapmap]
rs2053175	0.84[CEU][hapmap];1.00[CHB][hapmap]
rs7557907	1.00[CHB][hapmap]
rs7558288	1.00[CHB][hapmap]
rs7598735	1.00[CHB][hapmap]
rs7602631	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs9287325	0.84[CEU][hapmap];1.00[CHB][hapmap];0.81[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv834394	chr2:142430225-142593264	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv530398	chr2:142474842-142843839	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv875249	chr2:142527100-142614345	Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	n/a
4	nsv875250	chr2:142540240-142614345	Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	n/a
5	nsv1010008	chr2:142574406-142606021	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
6	nsv1009893	chr2:142585905-142662116	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:0 , 50 per page) page:

No data

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