Variant report

Variant	rs9789704
Chromosome Location	chr2:187588184-187588185
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:187586395..187588666-chr2:187589274..187592197,2	K562	blood:
2	chr2:187586601..187588975-chr2:187605009..187606836,2	MCF-7	breast:

Extended variants
information (count: 34 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10165992	0.90[EUR][1000 genomes]
rs1072901	0.80[ASN][1000 genomes]
rs10755000	0.81[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10931253	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12471718	0.80[ASN][1000 genomes]
rs12618322	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12620821	0.92[ASN][1000 genomes]
rs13028008	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1448427	0.84[ASN][1000 genomes]
rs17406229	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17406346	0.82[ASN][1000 genomes]
rs2012128	0.87[EUR][1000 genomes]
rs2121975	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2121976	0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2460766	0.85[EUR][1000 genomes]
rs2595383	0.86[EUR][1000 genomes]
rs2595386	0.87[EUR][1000 genomes]
rs2595395	0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2682863	0.88[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2682868	0.96[EUR][1000 genomes]
rs2682873	0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs3213964	0.85[ASN][1000 genomes]
rs34056045	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs34840521	0.84[ASN][1000 genomes]
rs35348196	0.84[ASN][1000 genomes]
rs3816375	0.81[ASN][1000 genomes]
rs4667108	0.81[ASN][1000 genomes]
rs55961288	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs56222785	0.80[ASN][1000 genomes]
rs62173041	0.82[ASN][1000 genomes]
rs62196185	0.81[ASN][1000 genomes]
rs6705757	0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs930657	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv428069	chr2:187575692-187766209	ZNF genes & repeats Weak transcription Active TSS Strong transcription Enhancers Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:187583800-187588600	Weak transcription	Brain Substantia Nigra	brain
2	chr2:187583800-187588800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr2:187584400-187589000	Weak transcription	Brain Angular Gyrus	brain
4	chr2:187584400-187590400	Weak transcription	Brain Hippocampus Middle	brain
5	chr2:187584600-187588400	Weak transcription	Fetal Brain Male	brain
6	chr2:187584600-187590200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr2:187584600-187590600	Weak transcription	Fetal Brain Female	brain
8	chr2:187584600-187591600	Weak transcription	HUES48 Cell Line	embryonic stem cell
9	chr2:187584600-187591800	Weak transcription	H1 Cell Line	embryonic stem cell
10	chr2:187584600-187596000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr2:187587600-187588800	Weak transcription	Cortex derived primary cultured neurospheres	brain
12	chr2:187587600-187589200	Weak transcription	Brain Anterior Caudate	brain
13	chr2:187587600-187590400	Weak transcription	Brain Cingulate Gyrus	brain
14	chr2:187588000-187590400	Weak transcription	Brain Inferior Temporal Lobe	brain

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