Variant report

Variant	rs1329177
Chromosome Location	chr10:91940137-91940138
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:91938353..91941143-chr10:91951885..91953423,2	MCF-7	breast:

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs10732771	0.82[EUR][1000 genomes]
rs10732772	0.83[EUR][1000 genomes]
rs10736057	0.82[EUR][1000 genomes]
rs10736058	0.82[EUR][1000 genomes]
rs10748541	0.84[EUR][1000 genomes]
rs10748542	0.85[EUR][1000 genomes]
rs10748543	0.82[EUR][1000 genomes]
rs10785945	0.85[EUR][1000 genomes]
rs10785947	0.86[EUR][1000 genomes]
rs10881766	0.84[EUR][1000 genomes]
rs11510151	0.81[AFR][1000 genomes]
rs1326842	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1329171	0.83[EUR][1000 genomes]
rs1329172	0.85[EUR][1000 genomes]
rs1329173	0.80[EUR][1000 genomes]
rs1329174	0.86[EUR][1000 genomes]
rs1329176	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2148554	1.00[ASN][1000 genomes]
rs2323	0.86[EUR][1000 genomes]
rs2419647	0.83[EUR][1000 genomes]
rs4933176	1.00[ASN][1000 genomes]
rs4933177	0.80[EUR][1000 genomes]
rs4933178	0.83[EUR][1000 genomes]
rs4933566	0.86[EUR][1000 genomes]
rs4933568	0.87[EUR][1000 genomes]
rs4933569	0.88[EUR][1000 genomes]
rs4933570	0.88[EUR][1000 genomes]
rs4933571	0.87[EUR][1000 genomes]
rs4933573	0.85[EUR][1000 genomes]
rs4933574	0.85[EUR][1000 genomes]
rs7069482	0.83[EUR][1000 genomes]
rs7474551	0.85[EUR][1000 genomes]
rs750312	1.00[ASN][1000 genomes]
rs7902781	0.85[EUR][1000 genomes]
rs7903912	0.84[EUR][1000 genomes]
rs7908376	1.00[ASN][1000 genomes]
rs7908608	1.00[ASN][1000 genomes]
rs913626	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1043571	chr10:91568555-92036154	Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
2	nsv551874	chr10:91570211-92036154	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
3	nsv949678	chr10:91589048-92016474	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	nsv895883	chr10:91610601-92195828	Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Active TSS Bivalent/Poised TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
5	nsv1039731	chr10:91645718-92198264	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
6	nsv540743	chr10:91645718-92198264	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
7	nsv467430	chr10:91681344-92297943	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
8	nsv551875	chr10:91681344-92297943	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
9	nsv895884	chr10:91861413-91959144	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
10	esv3375393	chr10:91880933-92243227	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
11	nsv895885	chr10:91912493-91988922	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
12	nsv467431	chr10:91922383-91942219	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	n/a
13	nsv551878	chr10:91922383-91942219	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:91938800-91940800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr10:91939000-91940200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr10:91939000-91940200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr10:91939000-91940200	Enhancers	NH-A	brain
5	chr10:91939000-91940200	Enhancers	NHDF-Ad	bronchial
6	chr10:91939000-91940400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr10:91939000-91940400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr10:91939000-91940400	Enhancers	HMEC	breast
9	chr10:91939000-91941200	Enhancers	NHLF	lung
10	chr10:91939000-91941400	Enhancers	NHEK	skin
11	chr10:91939000-91941600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr10:91939200-91940200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr10:91939200-91940200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr10:91939200-91940200	Enhancers	Muscle Satellite Cultured Cells	--
15	chr10:91939200-91940200	Enhancers	HSMM	muscle
16	chr10:91939200-91940200	Enhancers	Osteobl	bone
17	chr10:91939200-91940400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr10:91939200-91940400	Enhancers	Primary hematopoietic stem cells short term culture	blood
19	chr10:91939400-91940200	Enhancers	Placenta Amnion	Placenta Amnion
20	chr10:91939800-91940400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin

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