Variant report

Variant	rs9986911
Chromosome Location	chr7:3950767-3950768
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 163 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:152)

rs_ID	r²[population]
rs10085400	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs10085568	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs1013880	0.83[CEU][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs10215004	0.93[CEU][hapmap];0.88[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10215340	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10228397	0.80[ASN][1000 genomes]
rs10241703	0.81[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap]
rs10242459	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs10243770	0.89[CHB][hapmap]
rs10244636	0.81[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap]
rs10245389	1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.80[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs10246449	0.81[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap]
rs10249255	0.92[ASN][1000 genomes]
rs10250659	0.88[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10252169	0.85[JPT][hapmap]
rs10254099	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs10256741	0.87[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap]
rs10262942	0.88[CEU][hapmap];0.85[CHB][hapmap];0.85[JPT][hapmap];0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10263496	1.00[JPT][hapmap]
rs10267786	0.89[CHB][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs10273444	0.89[CHB][hapmap];1.00[JPT][hapmap];0.80[ASN][1000 genomes]
rs10479833	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs10479834	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs10485864	0.80[ASN][1000 genomes]
rs10951315	0.82[JPT][hapmap]
rs10951322	0.89[CHB][hapmap];0.85[JPT][hapmap]
rs10951336	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs10951368	0.92[ASN][1000 genomes]
rs10951374	0.94[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs11514766	1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11971293	0.81[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs11973380	0.93[ASN][1000 genomes]
rs11974190	0.81[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap]
rs11974357	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11976915	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs11977993	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs11980947	1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11982345	0.83[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs11983563	0.83[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs12112335	0.89[CHB][hapmap]
rs12531046	1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs12531980	0.89[CHB][hapmap];0.85[JPT][hapmap]
rs12531984	0.82[JPT][hapmap]
rs12532040	0.89[CHB][hapmap];0.85[JPT][hapmap]
rs12532171	0.94[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs12532903	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs12532912	1.00[JPT][hapmap]
rs12533946	0.92[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs12536445	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs12537696	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs12538997	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs12539695	0.82[JPT][hapmap]
rs12540101	0.88[CHB][hapmap];1.00[JPT][hapmap]
rs12690803	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs12690804	0.86[CEU][hapmap];1.00[JPT][hapmap]
rs12701219	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs12701221	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs12701229	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs12701262	0.88[CEU][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs12701271	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12701272	0.91[AMR][1000 genomes];0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13221624	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs13236653	0.88[CHB][hapmap];1.00[JPT][hapmap]
rs13236719	0.89[CHB][hapmap];0.85[JPT][hapmap]
rs13245096	0.88[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs1476644	1.00[JPT][hapmap]
rs1548612	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs1548613	0.82[JPT][hapmap]
rs1548614	0.82[JPT][hapmap]
rs17133859	0.84[JPT][hapmap]
rs17259867	0.82[JPT][hapmap]
rs17259924	0.82[JPT][hapmap]
rs17261199	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs17325709	0.82[JPT][hapmap]
rs1962783	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs1962784	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs1962785	0.81[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap]
rs2007554	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs2057920	0.88[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap]
rs2057921	0.81[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap]
rs2079376	1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2341959	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs2880159	0.93[CEU][hapmap];0.88[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs2880204	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs34730154	0.80[ASN][1000 genomes]
rs41873	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs4431501	0.81[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap]
rs6462361	0.89[CHB][hapmap];0.85[JPT][hapmap]
rs6462401	0.87[CEU][hapmap]
rs6462407	0.81[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap]
rs6462411	0.82[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap]
rs6462413	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs6462423	0.80[ASN][1000 genomes]
rs6462447	0.94[CEU][hapmap]
rs6943646	0.82[JPT][hapmap]
rs6944393	0.83[CEU][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs6945778	0.89[CHB][hapmap];0.85[JPT][hapmap]
rs6948552	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs6952864	0.81[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap]
rs6953282	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs6953604	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs6953707	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6955650	0.82[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap]
rs6956020	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6956479	0.87[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap]
rs6957166	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs6958535	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs6959492	0.83[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs6959674	0.83[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs6959835	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs6961230	0.89[CHB][hapmap];0.85[JPT][hapmap]
rs6961561	0.81[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap]
rs6962058	1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs6962389	1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs6962750	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6963674	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs6966030	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs6968948	0.84[CHB][hapmap];1.00[JPT][hapmap]
rs6969052	0.82[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap]
rs6970116	0.84[CHB][hapmap];1.00[JPT][hapmap]
rs6971803	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs6971828	1.00[JPT][hapmap]
rs6971873	0.94[CEU][hapmap];0.88[CHB][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6971953	0.88[CHB][hapmap];1.00[JPT][hapmap]
rs6972806	0.82[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap]
rs6973944	0.89[CHB][hapmap];0.82[JPT][hapmap]
rs6975313	0.89[CHB][hapmap];0.82[JPT][hapmap]
rs6975723	0.81[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap]
rs6977305	0.94[CEU][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6977844	0.88[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap]
rs6978964	0.89[CHB][hapmap];0.85[JPT][hapmap]
rs6979937	0.89[CHB][hapmap];0.85[JPT][hapmap]
rs6980085	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs768721	0.82[JPT][hapmap]
rs7778705	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs7783415	0.88[CHB][hapmap];1.00[JPT][hapmap];0.80[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7786556	1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs7791274	0.82[JPT][hapmap]
rs7794504	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs7800775	1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs7804166	0.89[CHB][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs7807003	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs7809616	0.82[ASN][1000 genomes]
rs874344	0.93[ASN][1000 genomes]
rs917168	0.89[CHB][hapmap];1.00[JPT][hapmap];0.80[ASN][1000 genomes]
rs917198	0.89[CHB][hapmap];0.85[JPT][hapmap]
rs9655007	0.81[CEU][hapmap];1.00[JPT][hapmap]
rs9655343	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs9655347	0.80[ASN][1000 genomes]
rs9655348	1.00[JPT][hapmap];0.80[ASN][1000 genomes]
rs9886069	0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9886234	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1021650	chr7:3665232-4577439	Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1029406	chr7:3860894-4477095	Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv538685	chr7:3860894-4477095	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv1026410	chr7:3869104-4383606	Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv1025497	chr7:3905444-4176032	Enhancers Strong transcription ZNF genes & repeats Genic enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv538686	chr7:3905444-4176032	Enhancers Weak transcription Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv433014	chr7:3910039-4054769	Strong transcription Enhancers Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv518377	chr7:3939055-3978342	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
9	nsv1030082	chr7:3941203-3986403	Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
10	nsv1020222	chr7:3946655-3985756	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
11	nsv1027500	chr7:3949954-3986403	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:3901200-3959600	Weak transcription	Pancreas	Pancrea
2	chr7:3936800-3974200	Weak transcription	Aorta	Aorta
3	chr7:3940600-3953800	Weak transcription	Fetal Brain Male	brain
4	chr7:3947200-3951600	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr7:3948200-3951400	Weak transcription	Fetal Lung	lung
6	chr7:3948200-3955000	Weak transcription	Spleen	Spleen
7	chr7:3948800-3951000	Enhancers	Brain Inferior Temporal Lobe	brain
8	chr7:3948800-3953000	Enhancers	Cortex derived primary cultured neurospheres	brain
9	chr7:3949000-3951000	Enhancers	Brain Hippocampus Middle	brain
10	chr7:3949000-3951200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr7:3949200-3952200	Weak transcription	Fetal Muscle Trunk	muscle
12	chr7:3950200-3952200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr7:3950200-3953600	Weak transcription	Fetal Brain Female	brain
14	chr7:3950400-3951000	Enhancers	Brain Substantia Nigra	brain
15	chr7:3950400-3951400	Weak transcription	NH-A	brain
16	chr7:3950400-3951600	Weak transcription	Brain Germinal Matrix	brain
17	chr7:3950400-3952400	Enhancers	Brain Anterior Caudate	brain
18	chr7:3950400-3952600	Enhancers	Brain Cingulate Gyrus	brain
19	chr7:3950600-3950800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr7:3950600-3951000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr7:3950600-3951200	Enhancers	Esophagus	oesophagus
22	chr7:3950600-3952200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr7:3950600-3952800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr7:3950600-3953000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr7:3950600-3955600	Weak transcription	Brain Angular Gyrus	brain
26	chr7:3950600-3955800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin

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