Variant report

Variant	rs61990261
Chromosome Location	chr14:77728825-77728826
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs10130630	0.84[ASN][1000 genomes]
rs11159254	0.85[ASN][1000 genomes]
rs11547794	0.85[ASN][1000 genomes]
rs11624564	0.85[ASN][1000 genomes]
rs1600005	0.91[ASN][1000 genomes]
rs4903565	0.85[ASN][1000 genomes]
rs59730492	0.97[ASN][1000 genomes]
rs7158951	0.85[ASN][1000 genomes]
rs7159558	0.85[ASN][1000 genomes]
rs747273	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs8009261	0.85[ASN][1000 genomes]
rs8009733	0.85[ASN][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:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:77709800-77729600	Weak transcription	Fetal Brain Male	brain
2	chr14:77711200-77731000	Weak transcription	Spleen	Spleen
3	chr14:77723000-77734000	Weak transcription	Gastric	stomach
4	chr14:77725000-77730400	Weak transcription	Fetal Brain Female	brain
5	chr14:77727200-77732000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr14:77727400-77731800	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr14:77727800-77731400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
8	chr14:77728000-77731200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr14:77728000-77731400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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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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