Variant report

Variant	rs11977156
Chromosome Location	chr7:78924696-78924697
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 67 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:62)

rs_ID	r²[population]
rs10085854	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10225318	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10244816	1.00[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs10258290	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10264341	1.00[EUR][1000 genomes]
rs10274797	1.00[EUR][1000 genomes]
rs11972217	0.90[EUR][1000 genomes]
rs11974844	0.90[EUR][1000 genomes]
rs11974872	0.90[EUR][1000 genomes]
rs11979157	0.90[EUR][1000 genomes]
rs11980152	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12666679	0.91[EUR][1000 genomes]
rs12666680	1.00[EUR][1000 genomes]
rs12670442	1.00[EUR][1000 genomes]
rs12670971	0.95[EUR][1000 genomes]
rs12670981	1.00[EUR][1000 genomes]
rs12706106	1.00[EUR][1000 genomes]
rs12706107	1.00[EUR][1000 genomes]
rs1358471	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1406153	1.00[EUR][1000 genomes]
rs1406154	1.00[EUR][1000 genomes]
rs1406155	1.00[EUR][1000 genomes]
rs1406156	1.00[EUR][1000 genomes]
rs1528262	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1534492	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1534493	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1609273	1.00[EUR][1000 genomes]
rs1609274	1.00[EUR][1000 genomes]
rs1609275	1.00[EUR][1000 genomes]
rs1609276	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16886476	0.90[EUR][1000 genomes]
rs17147873	0.90[EUR][1000 genomes]
rs17152224	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17152238	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17152245	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1918932	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1918933	0.85[EUR][1000 genomes]
rs1997277	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2178169	1.00[EUR][1000 genomes]
rs28401690	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28450541	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs28611031	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs28700941	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4727839	1.00[EUR][1000 genomes]
rs4727840	1.00[EUR][1000 genomes]
rs4727842	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4730753	0.87[EUR][1000 genomes]
rs4730757	1.00[EUR][1000 genomes]
rs4730758	1.00[EUR][1000 genomes]
rs56829360	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs59620956	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61075638	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6466602	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6963053	1.00[EUR][1000 genomes]
rs6963068	1.00[EUR][1000 genomes]
rs6975958	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73375128	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73375139	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73375150	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73375151	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73375156	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73375167	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv464598	chr7:78492642-79483480	Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
2	nsv607659	chr7:78492642-79483480	Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
3	nsv1029799	chr7:78608097-79061737	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv831041	chr7:78819499-78973222	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	esv2764028	chr7:78874740-79112630	Bivalent/Poised TSS Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:78922400-78925800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr7:78922400-78929200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr7:78923200-78930000	Weak transcription	Brain Hippocampus Middle	brain
4	chr7:78923800-78924800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr7:78923800-78925000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr7:78923800-78925400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr7:78923800-78925400	Weak transcription	Pancreatic Islets	Pancreatic Islet
8	chr7:78924000-78925000	Weak transcription	HMEC	breast
9	chr7:78924000-78925200	Weak transcription	NHEK	skin
10	chr7:78924000-78926000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr7:78924000-78930600	Weak transcription	A549	lung

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links