Variant report

Variant	rs338702
Chromosome Location	chr13:89114905-89114906
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs234992	0.89[AFR][1000 genomes];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs338699	0.83[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs338700	0.82[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs338703	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs364426	0.81[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs379772	0.83[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs424909	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs425828	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs429851	0.81[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs431739	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs435253	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs439699	0.81[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs474389	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs496605	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs499266	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes];0.86[ASN][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	nsv1037729	chr13:88728499-89127873	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv541864	chr13:88728499-89127873	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv900809	chr13:88963676-89135721	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	nsv900810	chr13:88963676-89189142	Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv900814	chr13:89098616-89189142	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv900815	chr13:89098616-89216190	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:89111400-89116000	Enhancers	iPS-15b Cell Line	embryonic stem cell
2	chr13:89111600-89115600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
3	chr13:89111800-89115400	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr13:89113200-89116600	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr13:89113800-89115000	Weak transcription	Fetal Heart	heart
6	chr13:89114200-89116600	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr13:89114400-89115000	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr13:89114400-89115400	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr13:89114600-89115000	Weak transcription	HUES6 Cell Line	embryonic stem cell
10	chr13:89114800-89115800	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr13:89114800-89117200	Weak transcription	H1 Cell Line	embryonic stem cell

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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