Variant report

Variant	rs16905726
Chromosome Location	chr10:38432993-38432994
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF37A-8	chr10:38426265-38433327	ENSG00000272983.1

Extended variants
information (count: 72 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:65)

rs_ID	r²[population]
rs11011445	0.94[AFR][1000 genomes]
rs11011447	0.88[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs11011448	0.83[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs11011455	0.83[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs11011456	0.83[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs11011457	0.91[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs11011492	1.00[ASN][1000 genomes]
rs12240841	1.00[ASN][1000 genomes]
rs12243715	0.88[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs12244294	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12244439	0.93[ASN][1000 genomes]
rs12244661	0.94[AFR][1000 genomes]
rs12245632	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12245792	0.83[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs12246341	0.83[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs12246875	0.97[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs12247832	0.83[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs12248050	0.83[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs12254726	1.00[ASN][1000 genomes]
rs12258247	0.88[AFR][1000 genomes]
rs12258703	0.86[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs12260759	0.83[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs12260877	0.83[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs12261570	0.83[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs12266231	0.83[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs12266460	0.94[AFR][1000 genomes]
rs12268280	0.94[AFR][1000 genomes]
rs12268465	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12772607	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12775500	0.97[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs12782054	0.83[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs12784488	0.97[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs16937696	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16937701	0.97[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs17587699	0.88[EUR][1000 genomes]
rs17587939	0.88[EUR][1000 genomes]
rs17588142	0.91[EUR][1000 genomes]
rs17664698	0.88[EUR][1000 genomes]
rs2178961	0.88[EUR][1000 genomes]
rs28448364	0.97[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs28607758	0.97[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs28719516	0.94[AFR][1000 genomes]
rs3207878	0.83[EUR][1000 genomes]
rs34067956	0.83[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs34522767	0.83[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs34571803	0.97[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs34759610	0.83[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs34908048	0.91[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs36010363	0.91[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs36091737	0.83[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs36114117	0.97[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs58217854	0.83[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs7085204	0.88[EUR][1000 genomes]
rs7086341	0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7095460	0.88[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs7100316	1.00[ASN][1000 genomes]
rs71491237	0.88[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs71491238	0.83[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs71491239	0.81[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs71491241	0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7895219	0.83[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs7897675	0.88[EUR][1000 genomes]
rs7900878	0.94[AFR][1000 genomes]
rs7901183	0.91[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs7903054	0.84[EUR][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	nsv895030	chr10:37715737-38674609	Weak transcription Active TSS Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
2	nsv1040704	chr10:37940024-38451917	Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
3	nsv540566	chr10:38301001-38680127	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
4	nsv550419	chr10:38311777-38501654	Enhancers Strong transcription Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
5	nsv895031	chr10:38402789-38464886	ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv895032	chr10:38427708-38498909	Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS	TF binding region CpG island lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv895033	chr10:38432348-38537070	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	TF binding region CpG island lncRNA	6 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:38424000-38433400	Weak transcription	Dnd41	blood
2	chr10:38425400-38435600	Weak transcription	Brain Hippocampus Middle	brain
3	chr10:38426200-38433000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr10:38426200-38437000	Weak transcription	Brain Anterior Caudate	brain
5	chr10:38426800-38435800	Weak transcription	Brain Substantia Nigra	brain
6	chr10:38427600-38436000	Weak transcription	Brain Cingulate Gyrus	brain
7	chr10:38428000-38439600	Weak transcription	HSMMtube	muscle
8	chr10:38429000-38434600	Weak transcription	Ovary	ovary
9	chr10:38429200-38436000	Weak transcription	Brain Angular Gyrus	brain
10	chr10:38429400-38433000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr10:38431800-38435200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr10:38432000-38433200	Enhancers	HepG2	liver
13	chr10:38432600-38433000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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