Variant report

Variant	rs10472030
Chromosome Location	chr5:57311558-57311559
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 79 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:61)

rs_ID	r²[population]
rs1027164	0.81[CEU][hapmap]
rs11738952	0.87[ASN][1000 genomes]
rs11740997	1.00[ASN][1000 genomes]
rs11741208	1.00[ASN][1000 genomes]
rs11741819	1.00[ASN][1000 genomes]
rs11742445	0.95[ASN][1000 genomes]
rs11744663	0.83[ASN][1000 genomes]
rs11749915	1.00[ASN][1000 genomes]
rs13160441	0.84[ASN][1000 genomes]
rs1349957	0.92[ASN][1000 genomes]
rs1352609	0.82[ASN][1000 genomes]
rs1352610	0.84[ASN][1000 genomes]
rs1378248	0.95[ASN][1000 genomes]
rs1387641	0.84[ASN][1000 genomes]
rs1454908	0.81[CEU][hapmap]
rs1454918	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs1454920	0.84[ASN][1000 genomes]
rs1454924	0.84[ASN][1000 genomes]
rs1454925	0.82[CHB][hapmap];0.84[ASN][1000 genomes]
rs1454926	0.83[ASN][1000 genomes]
rs1489791	0.92[ASN][1000 genomes]
rs1489797	0.84[ASN][1000 genomes]
rs17749982	1.00[CHB][hapmap];0.95[ASN][1000 genomes]
rs1826101	0.84[ASN][1000 genomes]
rs1826106	0.84[ASN][1000 genomes]
rs1844437	0.84[ASN][1000 genomes]
rs4699920	0.85[ASN][1000 genomes]
rs4700243	0.84[ASN][1000 genomes]
rs4700244	0.84[ASN][1000 genomes]
rs4700245	0.84[ASN][1000 genomes]
rs56976559	0.92[ASN][1000 genomes]
rs60707702	1.00[ASN][1000 genomes]
rs62359146	0.92[ASN][1000 genomes]
rs62359148	0.89[ASN][1000 genomes]
rs62360186	0.90[ASN][1000 genomes]
rs62360187	0.95[ASN][1000 genomes]
rs62360200	0.98[ASN][1000 genomes]
rs62368373	1.00[ASN][1000 genomes]
rs62368399	0.95[ASN][1000 genomes]
rs62368400	1.00[ASN][1000 genomes]
rs62368401	1.00[ASN][1000 genomes]
rs62368402	1.00[ASN][1000 genomes]
rs62368403	0.87[ASN][1000 genomes]
rs62368405	1.00[ASN][1000 genomes]
rs62368406	1.00[ASN][1000 genomes]
rs62368407	1.00[ASN][1000 genomes]
rs62368408	1.00[ASN][1000 genomes]
rs62368409	1.00[ASN][1000 genomes]
rs62368410	0.96[ASN][1000 genomes]
rs62368411	0.96[ASN][1000 genomes]
rs62368412	0.96[ASN][1000 genomes]
rs62368413	0.96[ASN][1000 genomes]
rs62368414	0.96[ASN][1000 genomes]
rs62368415	0.96[ASN][1000 genomes]
rs6450456	0.92[YRI][hapmap]
rs6450458	0.84[ASN][1000 genomes]
rs6884729	1.00[ASN][1000 genomes]
rs6886096	0.99[ASN][1000 genomes]
rs7713227	0.88[ASN][1000 genomes]
rs7736576	0.89[ASN][1000 genomes]
rs984926	0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv525330	chr5:56931673-57320343	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	esv1792273	chr5:57214817-57320343	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	nsv10700	chr5:57277483-57313710	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	esv1817904	chr5:57277522-57359476	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	esv1829717	chr5:57277522-57359476	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	esv1830976	chr5:57277522-57359476	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
7	esv1837615	chr5:57277522-57359476	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
8	esv1846984	chr5:57277522-57359476	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
9	esv1850205	chr5:57277522-57359476	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
10	nsv508357	chr5:57304472-57360187	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
11	nsv1020936	chr5:57309031-57333521	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	n/a
12	nsv1015769	chr5:57309031-57338357	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	n/a
13	nsv598229	chr5:57309072-57345166	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
14	nsv1018119	chr5:57309406-57332632	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	n/a
15	nsv1019152	chr5:57310368-57332632	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	n/a
16	nsv1016557	chr5:57310368-57332943	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	n/a
17	nsv1021803	chr5:57310368-57333521	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	n/a
18	nsv4840	chr5:57311002-57352746	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	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	chr5:57302600-57315600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr5:57307200-57312600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr5:57308200-57311800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr5:57308400-57311800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr5:57309600-57314400	Weak transcription	Fetal Heart	heart
6	chr5:57310800-57312400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr5:57311200-57312400	Enhancers	Hela-S3	cervix
8	chr5:57311400-57312200	Enhancers	Pancreatic Islets	Pancreatic Islet
9	chr5:57311400-57315400	Weak transcription	Left Ventricle	heart

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