Variant report

Variant	rs35293990
Chromosome Location	chr5:118781456-118781457
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs2262888	1.00[ASN][1000 genomes]
rs2560715	1.00[ASN][1000 genomes]
rs2560716	1.00[ASN][1000 genomes]
rs2560723	1.00[ASN][1000 genomes]
rs2678068	1.00[ASN][1000 genomes]
rs34935918	1.00[ASN][1000 genomes]
rs61460721	1.00[ASN][1000 genomes]
rs72547237	1.00[ASN][1000 genomes]
rs73236735	1.00[ASN][1000 genomes]
rs73251677	1.00[ASN][1000 genomes]
rs73790879	1.00[ASN][1000 genomes]
rs7708761	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1030717	chr5:118709310-118836951	Active TSS Strong transcription Enhancers Genic enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv427732	chr5:118730999-119034741	Strong transcription Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
3	nsv4974	chr5:118750259-118795376	Genic enhancers Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
4	nsv1024455	chr5:118770429-119487982	Strong transcription Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 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	chr5:118775400-118787600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
2	chr5:118781000-118781600	Active TSS	ES-I3 Cell Line	embryonic stem cell
3	chr5:118781200-118781600	Active TSS	H9 Cell Line	embryonic stem cell
4	chr5:118781200-118781600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr5:118781200-118781600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr5:118781200-118781600	Enhancers	Lung	lung
7	chr5:118781200-118782000	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr5:118781200-118782400	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr5:118781400-118781600	Enhancers	H1 Cell Line	embryonic stem cell
10	chr5:118781400-118782800	Weak transcription	iPS-15b 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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