Variant report

Variant	rs73107771
Chromosome Location	chr3:78395692-78395693
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs1512477	0.81[EUR][1000 genomes]
rs1512497	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs35887088	0.85[EUR][1000 genomes]
rs6548559	0.81[EUR][1000 genomes]
rs73107724	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs73107725	0.86[EUR][1000 genomes]
rs73107731	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs73107735	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs73107737	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs73109909	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs73109978	0.81[EUR][1000 genomes]
rs73111843	0.81[EUR][1000 genomes]
rs73846442	0.84[EUR][1000 genomes]
rs7646569	0.81[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv877017	chr3:77881397-78670654	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv529995	chr3:78188643-78739698	Enhancers Weak transcription Strong transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
3	nsv460726	chr3:78295664-78455767	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv590733	chr3:78295664-78455767	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	nsv470661	chr3:78322882-78459350	Strong transcription Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers	Chromatin interactive region lncRNA	5 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	chr3:78380000-78398000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr3:78392200-78396200	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr3:78393000-78397400	Enhancers	iPS-15b Cell Line	embryonic stem cell
4	chr3:78393400-78397400	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr3:78393600-78397200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr3:78393800-78396200	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr3:78393800-78396400	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr3:78393800-78397200	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr3:78393800-78397200	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr3:78394000-78396200	Enhancers	Brain Germinal Matrix	brain
11	chr3:78394200-78396000	Enhancers	H9 Cell Line	embryonic stem cell
12	chr3:78394400-78399000	Weak transcription	Stomach Mucosa	stomach
13	chr3:78394800-78396600	Weak transcription	H1 Cell Line	embryonic stem cell
14	chr3:78395000-78396800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr3:78395000-78397200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr3:78395200-78396400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr3:78395400-78396600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr3:78395600-78398000	Enhancers	Cortex derived primary cultured neurospheres	brain

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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