Variant report

Variant	rs73837314
Chromosome Location	chr4:93421656-93421657
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 26 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10022969	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs55705165	1.00[AMR][1000 genomes]
rs56022555	0.85[AMR][1000 genomes]
rs56410156	1.00[AMR][1000 genomes]
rs60005779	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73837303	0.83[AMR][1000 genomes]
rs73837306	1.00[AMR][1000 genomes]
rs73837307	1.00[AMR][1000 genomes]
rs73837308	1.00[AMR][1000 genomes]
rs73837309	1.00[AMR][1000 genomes]
rs73837311	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73837312	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73837313	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73837315	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9991929	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948712	chr4:93007985-93740409	Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv1000700	chr4:93270083-93425831	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	nsv537182	chr4:93270083-93425831	Enhancers Weak transcription ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	nsv997925	chr4:93270083-93464386	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
5	nsv537183	chr4:93270083-93464386	Enhancers Genic enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
6	nsv1005500	chr4:93359923-93590452	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
7	nsv537184	chr4:93359923-93590452	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
8	nsv879605	chr4:93376231-93740409	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Active TSS Strong transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
9	nsv1006957	chr4:93389054-93511561	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
10	nsv879606	chr4:93391251-93479275	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
11	nsv1013199	chr4:93395509-93511052	ZNF genes & repeats Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:93414600-93421800	Weak transcription	HUES6 Cell Line	embryonic stem cell
2	chr4:93414800-93434400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr4:93420800-93423000	Enhancers	H1 Cell Line	embryonic stem cell
4	chr4:93420800-93429800	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr4:93421000-93422800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr4:93421000-93424000	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr4:93421400-93422600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr4:93421400-93423000	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr4:93421600-93422200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr4:93421600-93422200	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr4:93421600-93422600	Enhancers	Cortex derived primary cultured neurospheres	brain
12	chr4:93421600-93422800	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr4:93421600-93428800	Enhancers	HUES64 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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