Variant report

Variant	rs7905396
Chromosome Location	chr10:44962376-44962377
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:44959846..44962752-chr10:44965575..44968477,3	K562	blood:

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:57)

rs_ID	r²[population]
rs10793540	0.90[ASN][1000 genomes]
rs10900036	0.93[ASN][1000 genomes]
rs10900037	0.93[ASN][1000 genomes]
rs10900042	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10900043	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10900048	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11239036	0.90[ASN][1000 genomes]
rs11239038	0.80[ASN][1000 genomes]
rs11239039	0.80[ASN][1000 genomes]
rs11239043	0.93[ASN][1000 genomes]
rs11239053	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11239061	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11239062	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11239063	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1147941	0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1147949	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1147950	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11523862	0.93[ASN][1000 genomes]
rs11598951	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1253716	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12763241	0.90[ASN][1000 genomes]
rs12764958	0.90[ASN][1000 genomes]
rs12770922	0.90[ASN][1000 genomes]
rs1419281	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1572204	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1599985	0.90[ASN][1000 genomes]
rs2225819	0.93[ASN][1000 genomes]
rs35213189	0.90[ASN][1000 genomes]
rs3897796	0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3961908	0.90[ASN][1000 genomes]
rs3980045	0.90[ASN][1000 genomes]
rs4948636	0.86[ASN][1000 genomes]
rs4948637	0.86[ASN][1000 genomes]
rs4948881	0.87[ASN][1000 genomes]
rs4948889	0.93[ASN][1000 genomes]
rs4948893	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4948901	0.86[ASN][1000 genomes]
rs6593415	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6593416	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6593417	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6593418	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6593419	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6593420	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7067631	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7070870	0.93[ASN][1000 genomes]
rs7071025	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7074207	0.93[ASN][1000 genomes]
rs7075418	0.93[ASN][1000 genomes]
rs7086409	0.93[ASN][1000 genomes]
rs7087908	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7899455	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7909036	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7909184	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7911230	0.90[ASN][1000 genomes]
rs7916506	0.92[ASN][1000 genomes]
rs7917412	0.93[ASN][1000 genomes]
rs7920634	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv895101	chr10:44909081-45007131	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr10:44955800-44968400	Weak transcription	Psoas Muscle	Psoas
2	chr10:44955800-44971800	Weak transcription	Right Atrium	heart
3	chr10:44956600-44970400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr10:44960000-44966200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr10:44961000-44962400	Enhancers	NH-A	brain
6	chr10:44961200-44965200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr10:44961400-44963200	Weak transcription	Fetal Muscle Leg	muscle
8	chr10:44962200-44965400	Weak transcription	Osteobl	bone
9	chr10:44962200-44965600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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