Variant report

Variant	rs1705639
Chromosome Location	chr14:84329656-84329657
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs11852069	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1698244	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1705636	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1705637	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1705640	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1705641	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1756285	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1756289	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1756290	1.00[AMR][1000 genomes]
rs937639	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2751287	chr14:84294487-84338247	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv565375	chr14:84299666-84336944	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv1054166	chr14:84299761-84338200	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv1036610	chr14:84299761-84338626	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv1051093	chr14:84303380-84338626	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv431019	chr14:84303525-84365447	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv520014	chr14:84311967-84336944	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:84329200-84330200	Enhancers	HUES6 Cell Line	embryonic stem cell
2	chr14:84329200-84330400	Enhancers	Ovary	ovary
3	chr14:84329400-84329800	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr14:84329400-84329800	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr14:84329600-84329800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr14:84329600-84329800	Enhancers	Fetal Brain Female	brain
7	chr14:84329600-84330000	Enhancers	Stomach Mucosa	stomach

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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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