Variant report

Variant	rs28909971
Chromosome Location	chr14:77732123-77732124
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:16)

rs_ID	r²[population]
rs10138606	1.00[AMR][1000 genomes]
rs10140162	1.00[AMR][1000 genomes]
rs10145195	1.00[AMR][1000 genomes]
rs10147727	1.00[AMR][1000 genomes]
rs10438171	1.00[MEX][hapmap];1.00[AMR][1000 genomes]
rs11845206	1.00[MEX][hapmap]
rs1508299	1.00[MEX][hapmap]
rs17105786	1.00[MEX][hapmap];1.00[AMR][1000 genomes]
rs2655976	1.00[ASW][hapmap]
rs28587702	1.00[AMR][1000 genomes]
rs28834759	1.00[AMR][1000 genomes]
rs7141831	1.00[AMR][1000 genomes]
rs8177541	1.00[MEX][hapmap]
rs877895	1.00[AMR][1000 genomes]
rs994223	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9944157	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	nsv431017	chr14:76938089-77854647	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	107 gene(s)	inside rSNPs	diseases
2	nsv1361	chr14:77707417-77753024	Flanking Bivalent TSS/Enh Weak transcription Strong transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Enhancers Genic enhancers ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	12 gene(s)	inside rSNPs	diseases
3	nsv902104	chr14:77720741-77756321	Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:77723000-77734000	Weak transcription	Gastric	stomach
2	chr14:77729600-77732600	Enhancers	Fetal Brain Male	brain
3	chr14:77730400-77732200	Enhancers	Fetal Brain Female	brain
4	chr14:77731200-77732400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr14:77731400-77732200	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr14:77731400-77732400	Enhancers	Brain Hippocampus Middle	brain
7	chr14:77732000-77732200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
8	chr14:77732000-77732400	Enhancers	iPS DF 19.11 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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