Variant report

Variant	rs7912367
Chromosome Location	chr10:54728522-54728523
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 121 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:111)

rs_ID	r²[population]
rs10508979	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10508980	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10824851	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11003297	0.81[AMR][1000 genomes]
rs11003298	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11003300	0.88[EUR][1000 genomes]
rs11003301	0.81[YRI][hapmap];0.85[EUR][1000 genomes]
rs11003305	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11003306	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11003307	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11003308	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11003309	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11003311	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11003313	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11003314	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11003316	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11003317	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11003318	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11003319	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11003320	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11003321	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11003322	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11003323	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11003324	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11003325	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11003326	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11003327	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11003328	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11592153	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11594477	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11594875	0.94[EUR][1000 genomes]
rs11594930	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11596013	0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11596708	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs11598902	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12354890	0.80[CEU][hapmap];0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12355649	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12356355	0.88[EUR][1000 genomes]
rs12358058	0.80[CEU][hapmap];0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12359301	0.88[EUR][1000 genomes]
rs1343049	0.80[CEU][hapmap];0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1343050	0.80[CEU][hapmap];0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1573146	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1573148	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs16936072	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs16936083	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs16936094	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs16936097	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs16936108	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs16936179	0.96[EUR][1000 genomes]
rs16936282	0.94[EUR][1000 genomes]
rs16936283	0.94[EUR][1000 genomes]
rs2091176	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2384101	0.82[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs2384102	0.81[AMR][1000 genomes]
rs2891424	0.81[AMR][1000 genomes]
rs35747583	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4083148	0.80[CEU][hapmap];0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4258288	0.81[AMR][1000 genomes]
rs4294491	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4403716	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4564234	0.80[CEU][hapmap];0.88[EUR][1000 genomes]
rs4589197	0.80[CEU][hapmap];0.88[EUR][1000 genomes]
rs4611108	0.88[EUR][1000 genomes]
rs4622164	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4636566	0.88[EUR][1000 genomes]
rs56667843	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs56999418	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs59171053	0.88[EUR][1000 genomes]
rs59605539	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs59993736	0.85[EUR][1000 genomes]
rs60635951	0.85[EUR][1000 genomes]
rs61134451	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs61387465	0.85[EUR][1000 genomes]
rs61844531	0.85[EUR][1000 genomes]
rs7074652	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7084055	0.92[EUR][1000 genomes]
rs7086840	0.83[EUR][1000 genomes]
rs7475455	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7893356	0.81[AMR][1000 genomes]
rs7893527	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7894017	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7894623	0.81[AMR][1000 genomes]
rs7894718	0.96[EUR][1000 genomes]
rs7896118	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7899425	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7899454	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7899582	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7900326	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7903815	0.94[EUR][1000 genomes]
rs7905190	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7905634	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7906006	0.96[EUR][1000 genomes]
rs7906107	0.96[EUR][1000 genomes]
rs7907039	0.88[AFR][1000 genomes];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7910673	0.81[AMR][1000 genomes]
rs7912023	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7912728	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7914381	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7914999	0.96[EUR][1000 genomes]
rs7915183	0.96[EUR][1000 genomes]
rs7915769	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7917355	0.96[EUR][1000 genomes]
rs7918032	0.96[EUR][1000 genomes]
rs7918282	0.96[EUR][1000 genomes]
rs7921542	0.96[EUR][1000 genomes]
rs7921965	0.82[EUR][1000 genomes]
rs7923744	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9787467	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs9787531	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9787652	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532194	chr10:53746620-54735550	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
2	nsv895404	chr10:54545590-54850707	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	nsv831877	chr10:54565135-54764638	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	nsv1041940	chr10:54621342-54737528	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
5	nsv1043809	chr10:54645158-54860817	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
6	nsv540627	chr10:54645158-54860817	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
7	nsv467201	chr10:54697623-54929003	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
8	nsv550906	chr10:54697623-54929003	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
9	nsv470939	chr10:54700783-54917339	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
10	nsv508584	chr10:54704765-54747382	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:54724800-54729000	Enhancers	Fetal Intestine Small	intestine
2	chr10:54725000-54730200	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr10:54725000-54730400	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr10:54725200-54730200	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr10:54725200-54730200	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr10:54725400-54729800	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr10:54725600-54730400	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr10:54725800-54733200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr10:54726200-54730000	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr10:54726800-54729000	Enhancers	Fetal Intestine Large	intestine
11	chr10:54726800-54729800	Enhancers	H1 Cell Line	embryonic stem cell
12	chr10:54727000-54730000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr10:54727000-54730000	Enhancers	HepG2	liver
14	chr10:54727400-54729600	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr10:54727600-54729400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr10:54727800-54729200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr10:54728000-54730200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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