Variant report

Variant	rs240379
Chromosome Location	chr6:75996785-75996786
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	MAFK	chr6:75996722-75996982	IMR90	lung:	n/a	chr6:75996883-75996894 chr6:75996879-75996894 chr6:75996846-75996861
2	MAFK	chr6:75996737-75997016	HepG2	liver:	n/a	chr6:75996883-75996894 chr6:75996879-75996894 chr6:75996846-75996861
3	MAFK	chr6:75996703-75997007	HepG2	liver:	n/a	chr6:75996883-75996894 chr6:75996879-75996894 chr6:75996846-75996861
4	STAT3	chr6:75996250-75996911	MCF10A-Er-Src	breast:	n/a	chr6:75996593-75996604 chr6:75996859-75996867

No.	Distal block	Cell Line	Cell type
1	chr6:75962314..75964868-chr6:75994799..75997539,2	K562	blood:
2	chr6:75995037..75997566-chr6:76015682..76017767,2	K562	blood:
3	chr6:75993518..75995468-chr6:75996205..75998181,2	K562	blood:

Variant related genes	Relation type
TMEM30A	TF binding region
ENSG00000225793	Chromatin interaction
ENSG00000112697	Chromatin interaction

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs1018471	0.84[CEU][hapmap];0.90[JPT][hapmap];0.89[YRI][hapmap];0.88[AFR][1000 genomes];0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10806035	0.84[CEU][hapmap];0.95[JPT][hapmap];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs171263	0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2250989	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs240374	1.00[YRI][hapmap];0.83[AFR][1000 genomes]
rs240375	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs240378	0.99[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs240380	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2748252	0.92[CEU][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2808201	0.80[CEU][hapmap]
rs2808203	0.80[CEU][hapmap]
rs2842445	0.86[EUR][1000 genomes]
rs2842446	0.96[CEU][hapmap];0.96[CHB][hapmap];0.95[JPT][hapmap];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2842458	0.88[AFR][1000 genomes];0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2842459	0.89[CEU][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2842462	0.84[CEU][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2842463	0.84[CEU][hapmap];0.82[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4275021	0.84[CEU][hapmap];0.83[EUR][1000 genomes]
rs4374801	0.82[CEU][hapmap]
rs4412169	0.80[EUR][1000 genomes]
rs4708179	0.84[CEU][hapmap];0.95[JPT][hapmap];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6903526	0.80[CEU][hapmap];0.82[EUR][1000 genomes]
rs6904580	0.80[CEU][hapmap]
rs6929270	0.80[CEU][hapmap]
rs7743227	0.89[CEU][hapmap];0.95[JPT][hapmap];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7771904	0.80[CEU][hapmap]
rs7772989	0.85[JPT][hapmap]
rs9341515	0.81[EUR][1000 genomes]
rs9343283	0.82[EUR][1000 genomes]
rs9352202	0.84[CEU][hapmap];0.95[JPT][hapmap];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9359122	0.80[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1016804	chr6:75775846-76188585	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
2	nsv538310	chr6:75775846-76188585	Flanking Active TSS Active TSS Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
3	nsv1024079	chr6:75848556-76238519	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
4	nsv1027915	chr6:75893542-76510113	Active TSS Enhancers Strong transcription Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	70 gene(s)	inside rSNPs	diseases
5	nsv538311	chr6:75893542-76510113	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	70 gene(s)	inside rSNPs	diseases
6	nsv603763	chr6:75923605-76009426	Genic enhancers Active TSS Strong transcription Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
7	nsv603764	chr6:75963751-76025603	Weak transcription Active TSS Genic enhancers Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
8	nsv830698	chr6:75968810-76115592	Strong transcription Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:86 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:75991600-75997000	Active TSS	A549	lung
2	chr6:75991800-75997600	Active TSS	K562	blood
3	chr6:75995000-75999600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr6:75995200-76010000	Weak transcription	Lung	lung
5	chr6:75995200-76016800	Weak transcription	Left Ventricle	heart
6	chr6:75995400-75996800	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr6:75995400-75997400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
8	chr6:75995400-75999600	Weak transcription	Brain Angular Gyrus	brain
9	chr6:75995400-76021800	Weak transcription	Right Ventricle	heart
10	chr6:75995400-76027600	Weak transcription	Aorta	Aorta
11	chr6:75995600-75997200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
12	chr6:75995600-75999400	Weak transcription	Fetal Brain Female	brain
13	chr6:75995600-75999400	Weak transcription	Fetal Kidney	kidney
14	chr6:75995600-75999600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr6:75995600-75999600	Weak transcription	HUES48 Cell Line	embryonic stem cell
16	chr6:75995600-75999600	Weak transcription	Brain Cingulate Gyrus	brain
17	chr6:75995600-75999800	Weak transcription	Brain Germinal Matrix	brain
18	chr6:75995600-76009600	Weak transcription	Duodenum Smooth Muscle	Duodenum
19	chr6:75995800-75996800	Weak transcription	Primary monocytes fromperipheralblood	blood
20	chr6:75995800-75996800	Weak transcription	Brain Hippocampus Middle	brain
21	chr6:75995800-75996800	Weak transcription	Monocytes-CD14+_RO01746	blood
22	chr6:75995800-75997000	Enhancers	Liver	Liver
23	chr6:75995800-75997200	Weak transcription	Placenta	Placenta
24	chr6:75995800-75997200	Enhancers	HepG2	liver
25	chr6:75995800-75997200	Weak transcription	NHEK	skin
26	chr6:75995800-75997600	Enhancers	Primary hematopoietic stem cells short term culture	blood
27	chr6:75995800-75997600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
28	chr6:75995800-75997600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr6:75995800-75997600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr6:75995800-75997800	Enhancers	Primary neutrophils fromperipheralblood	blood
31	chr6:75995800-75997800	Enhancers	Primary T helper cells fromperipheralblood	blood
32	chr6:75995800-75999600	Weak transcription	H1 Cell Line	embryonic stem cell
33	chr6:75995800-75999600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr6:75995800-75999600	Weak transcription	HUES64 Cell Line	embryonic stem cell
35	chr6:75995800-75999600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
36	chr6:75995800-75999600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
37	chr6:75995800-75999600	Weak transcription	Cortex derived primary cultured neurospheres	brain
38	chr6:75995800-75999600	Weak transcription	Fetal Lung	lung
39	chr6:75995800-75999800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
40	chr6:75995800-75999800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr6:75995800-75999800	Weak transcription	Fetal Brain Male	brain
42	chr6:75995800-75999800	Weak transcription	Stomach Smooth Muscle	stomach
43	chr6:75995800-76000000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr6:75995800-76000000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
45	chr6:75995800-76000200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr6:75995800-76000200	Weak transcription	Primary B cells from peripheral blood	blood
47	chr6:75995800-76000400	Weak transcription	Skeletal Muscle Male	skeletal muscle
48	chr6:75995800-76000600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr6:75995800-76001200	Weak transcription	Skeletal Muscle Female	skeletal muscle
50	chr6:75995800-76002600	Weak transcription	Rectal Mucosa Donor 31	rectum

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links