Variant report

Variant	rs61735169
Chromosome Location	chr13:49281679-49281680
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs7329349	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9331979	1.00[AMR][1000 genomes]
rs9331993	1.00[AMR][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	nsv832604	chr13:49061081-49281807	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv1049117	chr13:49089476-49928945	Enhancers Strong transcription Weak transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
3	nsv832605	chr13:49171305-49344970	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:49252000-49283600	Weak transcription	Primary T cells from cord blood	blood
2	chr13:49259000-49302200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr13:49264000-49283800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
4	chr13:49269400-49282000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
5	chr13:49278600-49283800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr13:49279200-49284200	Weak transcription	Primary T helper cells fromperipheralblood	blood
7	chr13:49279400-49282600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
8	chr13:49279600-49284600	Weak transcription	Primary T cells fromperipheralblood	blood
9	chr13:49281000-49282000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr13:49281000-49283000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr13:49281200-49281800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
12	chr13:49281200-49282000	Strong transcription	Left Ventricle	heart
13	chr13:49281200-49283200	ZNF genes & repeats	Primary hematopoietic stem cells	blood
14	chr13:49281200-49283400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
15	chr13:49281400-49281800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr13:49281600-49281800	Strong transcription	Primary T helper cells PMA-I stimulated	--
17	chr13:49281600-49282400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr13:49281600-49284000	Strong transcription	Dnd41	blood

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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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