Variant report

Variant	rs1360741
Chromosome Location	chr7:80247030-80247031
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 50 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs10428893	0.95[ASN][1000 genomes]
rs10429164	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs10499857	0.95[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs10499858	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs1133344	0.80[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11768747	0.94[ASN][1000 genomes]
rs11768817	0.95[ASN][1000 genomes]
rs11771839	0.95[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs11772036	0.95[ASN][1000 genomes]
rs1194181	0.85[CEU][hapmap];0.89[EUR][1000 genomes]
rs11971740	0.84[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs11971793	1.00[ASN][1000 genomes]
rs11972894	0.99[ASN][1000 genomes]
rs11974227	0.95[ASN][1000 genomes]
rs1334511	0.84[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs1537593	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs17154130	0.95[ASN][1000 genomes]
rs17154181	0.84[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs3173798	0.84[CEU][hapmap]
rs3173799	0.94[JPT][hapmap];0.85[ASN][1000 genomes]
rs3211817	0.84[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs3211828	0.84[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs3211830	0.90[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs3211838	0.90[ASN][1000 genomes]
rs3211851	0.84[CHB][hapmap];0.93[JPT][hapmap];0.92[ASN][1000 genomes]
rs3211867	0.84[CHB][hapmap];0.94[JPT][hapmap];0.88[ASN][1000 genomes]
rs3211869	0.84[CEU][hapmap]
rs3211883	1.00[CEU][hapmap];0.97[EUR][1000 genomes]
rs3212162	0.91[ASN][1000 genomes]
rs3212163	0.97[ASN][1000 genomes]
rs35179913	0.93[ASN][1000 genomes]
rs41364549	0.84[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs58408258	0.97[ASN][1000 genomes]
rs60133848	0.98[ASN][1000 genomes]
rs60854150	0.97[ASN][1000 genomes]
rs6960369	0.96[ASN][1000 genomes]
rs9641866	0.84[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs9784998	0.84[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs9918530	0.96[ASN][1000 genomes]
rs9918586	0.84[CEU][hapmap]

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	nsv888524	chr7:80107798-80723062	Active TSS Strong transcription Enhancers Genic enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	nsv831043	chr7:80119414-80322092	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
3	nsv948605	chr7:80119690-80298887	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv1020682	chr7:80120651-80297697	Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv464606	chr7:80177084-80311794	Active TSS Flanking Active TSS Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
6	nsv607682	chr7:80177084-80311794	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
7	nsv1025144	chr7:80197286-80271841	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv1026688	chr7:80231657-80307236	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
9	nsv1020745	chr7:80231657-80309495	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
10	nsv888526	chr7:80240943-80354229	Enhancers Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:80241000-80251200	Weak transcription	Psoas Muscle	Psoas
2	chr7:80242200-80252800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr7:80243000-80247200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr7:80244400-80248000	Weak transcription	Left Ventricle	heart
5	chr7:80244400-80252000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr7:80244400-80253000	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr7:80244600-80251600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr7:80244600-80251600	Weak transcription	Osteobl	bone
9	chr7:80244800-80249400	Weak transcription	Right Atrium	heart
10	chr7:80244800-80253000	Weak transcription	Duodenum Mucosa	Duodenum
11	chr7:80245600-80247600	Enhancers	Fetal Heart	heart
12	chr7:80246400-80247600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr7:80246400-80247800	Weak transcription	Adipose Nuclei	Adipose
14	chr7:80246400-80251600	Weak transcription	Skeletal Muscle Female	skeletal muscle
15	chr7:80246600-80247800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
16	chr7:80246800-80247400	Enhancers	Primary neutrophils fromperipheralblood	blood
17	chr7:80246800-80254000	Enhancers	Primary monocytes fromperipheralblood	blood
18	chr7:80247000-80247600	Enhancers	Skeletal Muscle Male	skeletal muscle
19	chr7:80247000-80248600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood

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