Variant report

Variant	rs691830
Chromosome Location	chr15:41387312-41387313
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	chr15:41384971..41389195-chr15:41407627..41410447,4	MCF-7	breast:

Variant related genes	Relation type
ENSG00000128908	Chromatin interaction

Extended variants
information (count: 47 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs1009913	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11853192	0.83[ASN][1000 genomes]
rs11854472	0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11856572	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11856577	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11856848	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12101934	0.97[ASN][1000 genomes]
rs1678750	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1717200	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1962410	0.88[EUR][1000 genomes]
rs1983400	0.83[ASN][1000 genomes]
rs2176998	0.91[EUR][1000 genomes]
rs2306083	0.90[EUR][1000 genomes]
rs2412601	0.88[EUR][1000 genomes]
rs28455998	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs28510775	0.84[ASN][1000 genomes]
rs28581803	0.90[EUR][1000 genomes]
rs28613002	0.84[ASN][1000 genomes]
rs28688742	0.84[ASN][1000 genomes]
rs28729675	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs28866311	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2925345	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2925346	0.81[EUR][1000 genomes]
rs2928148	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2947493	0.83[ASN][1000 genomes]
rs2947494	0.83[ASN][1000 genomes]
rs3101442	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs3214068	0.80[EUR][1000 genomes]
rs4592624	0.86[ASN][1000 genomes]
rs476633	0.86[ASN][1000 genomes]
rs516156	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs544744	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs57393155	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs61203391	0.97[ASN][1000 genomes]
rs66818965	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs692155	0.92[EUR][1000 genomes]
rs7179681	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7181816	0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs72737704	0.83[EUR][1000 genomes]
rs8023345	0.83[EUR][1000 genomes]
rs8037837	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs8042088	0.90[EUR][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	nsv1053462	chr15:41270067-41396094	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
2	nsv569229	chr15:41361138-41483682	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
3	nsv904107	chr15:41361138-41493013	Weak transcription Strong transcription Flanking Active TSS Active TSS Enhancers Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
4	nsv569230	chr15:41384649-41483682	Flanking Active TSS Strong transcription Weak transcription Enhancers Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
5	nsv904108	chr15:41384649-41486990	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs691830	NDUFAF1	cis	Muscle Skeletal	GTEx
rs691830	NDUFAF1	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:41328800-41388600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr15:41334600-41389000	Strong transcription	Primary T helper cells PMA-I stimulated	--
3	chr15:41341600-41389000	Strong transcription	Liver	Liver
4	chr15:41354200-41389200	Strong transcription	HUES6 Cell Line	embryonic stem cell
5	chr15:41354600-41388800	Strong transcription	Fetal Intestine Large	intestine
6	chr15:41354600-41389000	Strong transcription	Duodenum Mucosa	Duodenum
7	chr15:41354800-41388600	Strong transcription	Primary T cells fromperipheralblood	blood
8	chr15:41354800-41389200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr15:41355000-41388400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
10	chr15:41355000-41389400	Strong transcription	Placenta	Placenta
11	chr15:41355000-41392000	Strong transcription	Fetal Thymus	thymus
12	chr15:41355000-41392400	Strong transcription	Monocytes-CD14+_RO01746	blood
13	chr15:41355000-41393800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr15:41355200-41388600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
15	chr15:41355200-41388800	Strong transcription	Primary T cells from cord blood	blood
16	chr15:41355400-41388800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
17	chr15:41355400-41389200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
18	chr15:41355400-41390200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
19	chr15:41355400-41393200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr15:41355600-41390800	Strong transcription	Primary monocytes fromperipheralblood	blood
21	chr15:41355800-41389200	Strong transcription	Dnd41	blood
22	chr15:41355800-41391000	Strong transcription	HUES48 Cell Line	embryonic stem cell
23	chr15:41356400-41388600	Strong transcription	Duodenum Smooth Muscle	Duodenum
24	chr15:41356600-41387600	Strong transcription	Fetal Stomach	stomach
25	chr15:41356600-41388600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr15:41356600-41388600	Strong transcription	Fetal Muscle Trunk	muscle
27	chr15:41356600-41389000	Strong transcription	Rectal Mucosa Donor 29	rectum
28	chr15:41356800-41391000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr15:41356800-41392200	Strong transcription	HUES64 Cell Line	embryonic stem cell
30	chr15:41358000-41393600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr15:41358200-41392000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr15:41359600-41388800	Strong transcription	Skeletal Muscle Female	skeletal muscle
33	chr15:41359800-41388600	Strong transcription	Fetal Brain Female	brain
34	chr15:41360400-41389200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr15:41361200-41407200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr15:41363800-41388600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr15:41365200-41388600	Strong transcription	Brain Anterior Caudate	brain
38	chr15:41365200-41391000	Strong transcription	Primary T helper cells fromperipheralblood	blood
39	chr15:41365400-41388600	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
40	chr15:41365400-41389800	Strong transcription	Stomach Smooth Muscle	stomach
41	chr15:41368000-41388800	Strong transcription	HepG2	liver
42	chr15:41369000-41391800	Weak transcription	Right Atrium	heart
43	chr15:41369400-41388600	Strong transcription	H1 Cell Line	embryonic stem cell
44	chr15:41369600-41388600	Strong transcription	NHEK	skin
45	chr15:41369600-41389000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
46	chr15:41370600-41388600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr15:41370600-41388600	Strong transcription	Colon Smooth Muscle	Colon
48	chr15:41370800-41390800	Strong transcription	Muscle Satellite Cultured Cells	--
49	chr15:41371200-41388200	Strong transcription	Adipose Nuclei	Adipose
50	chr15:41371800-41390800	Weak transcription	Stomach Mucosa	stomach

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