Variant report

Variant	rs56348595
Chromosome Location	chr15:73512648-73512649
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 78 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:74)

rs_ID	r²[population]
rs1023924	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1038137	0.80[ASN][1000 genomes]
rs11072403	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11072406	0.96[ASN][1000 genomes]
rs1116880	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11634084	0.83[EUR][1000 genomes]
rs11634147	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12050658	0.87[EUR][1000 genomes]
rs12050685	0.87[EUR][1000 genomes]
rs12050774	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12902768	0.95[ASN][1000 genomes]
rs1479338	0.94[AFR][1000 genomes];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1479339	0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1479340	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1564345	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs17762516	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs17762600	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17829830	0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17829836	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs17829957	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1812835	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1871385	0.89[ASN][1000 genomes]
rs2127277	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2169951	0.81[EUR][1000 genomes]
rs2415147	0.88[ASN][1000 genomes]
rs2415148	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2899784	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs34013312	0.84[ASN][1000 genomes]
rs35450875	0.88[ASN][1000 genomes]
rs3736510	0.88[ASN][1000 genomes]
rs3784801	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs3985587	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs3985588	0.92[AFR][1000 genomes];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4545783	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4777598	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs55646651	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs55836604	0.81[EUR][1000 genomes]
rs55853625	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs55868723	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs55939596	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs56215298	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs56377702	0.80[EUR][1000 genomes]
rs58060856	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs59066156	0.90[AFR][1000 genomes];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs62015460	0.94[EUR][1000 genomes]
rs62015484	0.86[EUR][1000 genomes]
rs62015499	0.85[EUR][1000 genomes]
rs62015500	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs62015502	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs62015504	0.83[EUR][1000 genomes]
rs62016806	0.80[EUR][1000 genomes]
rs62016811	0.81[EUR][1000 genomes]
rs62016849	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs62016851	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs62016853	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs62016854	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs62016856	0.92[EUR][1000 genomes]
rs62016857	0.87[EUR][1000 genomes]
rs62016858	0.92[EUR][1000 genomes]
rs62017774	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs62017776	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7169083	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7172021	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7172396	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs74022925	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs74025262	0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs747872	0.89[ASN][1000 genomes]
rs747873	0.89[ASN][1000 genomes]
rs7497992	0.87[EUR][1000 genomes]
rs8024575	0.96[ASN][1000 genomes]
rs8035925	0.84[ASN][1000 genomes]
rs8042700	0.96[ASN][1000 genomes]
rs9806496	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs9972347	0.81[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv525462	chr15:73349633-73563495	Genic enhancers Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv904340	chr15:73375847-73524629	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv904342	chr15:73390790-73524629	Enhancers ZNF genes & repeats Strong transcription Weak transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv904343	chr15:73396760-73775043	Strong transcription Bivalent Enhancer Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Genic enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:73474200-73523800	Weak transcription	Esophagus	oesophagus
2	chr15:73475200-73517600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr15:73487200-73519800	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr15:73492200-73518000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr15:73492400-73516200	Weak transcription	Fetal Brain Male	brain
6	chr15:73493400-73528600	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr15:73497000-73517600	Weak transcription	Brain Hippocampus Middle	brain
8	chr15:73497800-73541800	Weak transcription	Fetal Kidney	kidney
9	chr15:73498000-73515200	Weak transcription	Fetal Lung	lung
10	chr15:73502800-73517200	Weak transcription	Rectal Mucosa Donor 31	rectum
11	chr15:73509400-73525000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
12	chr15:73509600-73528800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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