Variant report

Variant	rs9539055
Chromosome Location	chr13:61755041-61755042
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs1384853	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17833594	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2175953	0.87[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3127277	0.81[EUR][1000 genomes]
rs7324266	0.88[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7997602	1.00[ASN][1000 genomes]
rs9317162	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9539057	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9598241	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832627	chr13:61642811-61829217	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	1 gene(s)	inside rSNPs	diseases
2	esv3444432	chr13:61665252-61781081	Enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	1 gene(s)	inside rSNPs	diseases
3	nsv900243	chr13:61711163-61799269	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:61753000-61755200	Enhancers	HUES64 Cell Line	embryonic stem cell
2	chr13:61753800-61759200	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr13:61754200-61755400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
4	chr13:61754800-61755400	Enhancers	iPS-20b Cell Line	embryonic stem cell
5	chr13:61754800-61757200	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr13:61755000-61756600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr13:61755000-61756800	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr13:61755000-61757000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr13:61755000-61757000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
10	chr13:61755000-61758800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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

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