Variant report

Variant	rs7811443
Chromosome Location	chr7:38475832-38475833
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs10282062	1.00[GIH][hapmap];0.81[MEX][hapmap]
rs11977538	0.93[YRI][hapmap]
rs17171344	1.00[YRI][hapmap];0.96[AFR][1000 genomes]
rs17171348	0.93[AFR][1000 genomes]
rs41279582	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs55873909	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs55886441	0.80[AMR][1000 genomes]
rs55908594	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs56046664	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs56156710	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56905382	0.82[AFR][1000 genomes]
rs58000336	0.82[AFR][1000 genomes]
rs58110874	0.89[AFR][1000 genomes]
rs60918146	0.93[AFR][1000 genomes]
rs6462843	0.93[AFR][1000 genomes]
rs6462846	0.81[MEX][hapmap]
rs6462847	0.81[MEX][hapmap]
rs6955238	0.88[YRI][hapmap]
rs6955569	0.87[YRI][hapmap]
rs6969918	0.87[YRI][hapmap]
rs73118148	0.85[EUR][1000 genomes]
rs73118200	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs73120213	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs73120220	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs73120230	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs73120241	0.85[EUR][1000 genomes]
rs73120243	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs73120259	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs73120268	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs73120282	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs73120287	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs73122226	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs73352603	0.93[AFR][1000 genomes]
rs73352622	0.96[AFR][1000 genomes]
rs73352635	0.96[AFR][1000 genomes]
rs73352664	0.90[AFR][1000 genomes]
rs73356685	0.88[AFR][1000 genomes]
rs740066	1.00[CEU][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs741265	1.00[CEU][hapmap];0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7776921	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7778313	1.00[CEU][hapmap];0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7784259	0.91[YRI][hapmap]
rs7791817	0.82[CEU][hapmap]
rs7803476	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2758112	chr7:38218703-38523455	Enhancers Weak transcription Active TSS Genic enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
2	esv2759524	chr7:38218703-38523455	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
3	nsv427776	chr7:38218703-38523455	Genic enhancers Transcr. at gene 5' and 3' Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
4	nsv1025974	chr7:38227528-38503472	Active TSS Enhancers Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
5	nsv538819	chr7:38227528-38503472	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
6	nsv932229	chr7:38248340-38727527	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
7	nsv1020990	chr7:38257707-38503472	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
8	nsv1031936	chr7:38319437-38503472	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
9	nsv830965	chr7:38350614-38521047	Strong transcription Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
10	nsv830966	chr7:38393663-38602553	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
11	nsv887964	chr7:38457144-38501065	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
12	esv1825425	chr7:38457144-38507180	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	1 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	chr7:38431600-38489000	Weak transcription	Brain Angular Gyrus	brain
2	chr7:38439000-38483000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr7:38456200-38481400	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr7:38457400-38479600	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr7:38467800-38495600	Weak transcription	Aorta	Aorta
6	chr7:38468400-38480800	Weak transcription	Fetal Brain Female	brain
7	chr7:38468400-38492000	Weak transcription	Fetal Heart	heart
8	chr7:38469000-38477000	Weak transcription	Fetal Brain Male	brain
9	chr7:38469200-38491600	Weak transcription	Fetal Stomach	stomach
10	chr7:38469600-38476800	Weak transcription	Brain Anterior Caudate	brain
11	chr7:38471200-38492200	Weak transcription	Fetal Lung	lung
12	chr7:38471800-38498200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr7:38473000-38477600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
14	chr7:38473400-38476000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr7:38473400-38476000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr7:38475400-38478000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr7:38475600-38488600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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