Variant report

Variant	rs4367140
Chromosome Location	chr4:90044292-90044293
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr4:90031396..90034227-chr4:90041663..90045608,5	MCF-7	breast:
2	chr4:90036870..90039187-chr4:90043124..90046686,3	MCF-7	breast:
3	chr4:90036910..90039747-chr4:90043122..90045290,2	MCF-7	breast:
4	chr4:90043352..90045261-chr4:90054968..90057885,2	MCF-7	breast:
5	chr4:90043393..90046238-chr4:90047056..90051826,4	K562	blood:

Variant related genes	Relation type
ENSG00000138640	Chromatin interaction
ENSG00000271359	Chromatin interaction
ENSG00000180346	Chromatin interaction

Extended variants
information (count: 39 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10004795	0.86[ASN][1000 genomes]
rs10015415	0.81[CHB][hapmap]
rs10433948	0.84[ASN][1000 genomes]
rs10433949	0.89[CHD][hapmap];0.88[JPT][hapmap];0.84[ASN][1000 genomes]
rs10470936	0.82[JPT][hapmap]
rs11097216	0.88[JPT][hapmap];0.85[YRI][hapmap];0.98[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs11726708	0.88[JPT][hapmap]
rs12502070	0.94[ASN][1000 genomes]
rs12505696	0.86[CHD][hapmap];0.88[JPT][hapmap]
rs12507131	0.88[JPT][hapmap];0.85[ASN][1000 genomes]
rs12508524	0.86[CHD][hapmap];0.88[JPT][hapmap]
rs12509305	0.81[CHB][hapmap];0.88[JPT][hapmap]
rs1398942	0.86[CHD][hapmap];0.88[JPT][hapmap]
rs1533292	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.97[MKK][hapmap];1.00[TSI][hapmap];0.93[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1533293	0.88[JPT][hapmap];0.85[ASN][1000 genomes]
rs1795739	0.81[CHB][hapmap];0.81[JPT][hapmap]
rs3733448	0.84[ASN][1000 genomes]
rs4627822	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs59799062	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs62304448	0.89[ASN][1000 genomes]
rs66475381	0.85[ASN][1000 genomes]
rs66500341	0.84[ASN][1000 genomes]
rs67412466	0.84[ASN][1000 genomes]
rs67706608	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6817766	1.00[ASW][hapmap];0.89[CHD][hapmap];0.88[JPT][hapmap];1.00[LWK][hapmap];0.87[MKK][hapmap];0.86[YRI][hapmap];0.98[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs6825998	0.89[ASN][1000 genomes]
rs6828137	0.86[CHD][hapmap]
rs6838424	0.82[JPT][hapmap]
rs6849143	0.87[CHD][hapmap]
rs6849540	0.89[ASN][1000 genomes]
rs6852928	0.87[CHD][hapmap]
rs72613157	0.84[ASN][1000 genomes]
rs72877639	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9994655	0.88[JPT][hapmap];0.84[YRI][hapmap];0.98[AFR][1000 genomes];0.85[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	nsv470051	chr4:89644931-90643144	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
2	nsv1007025	chr4:89837734-90098046	Enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv537176	chr4:89837734-90098046	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	nsv1002448	chr4:89933385-90128133	Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Genic enhancers Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
5	esv3349403	chr4:90044204-90044398	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs4367140	DSPP	cis	cerebellum	SCAN
rs4367140	ANKMY1	trans	parietal	SCAN

Chromatin state (count:40 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:90033400-90048200	Weak transcription	Ovary	ovary
2	chr4:90033400-90049200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr4:90033600-90045600	Weak transcription	Esophagus	oesophagus
4	chr4:90033600-90045600	Weak transcription	Pancreas	Pancrea
5	chr4:90033600-90049200	Weak transcription	Gastric	stomach
6	chr4:90033600-90052200	Weak transcription	Aorta	Aorta
7	chr4:90034800-90049200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr4:90035400-90044600	Weak transcription	Fetal Muscle Leg	muscle
9	chr4:90036600-90044800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr4:90037000-90046200	Weak transcription	Primary T cells from cord blood	blood
11	chr4:90039200-90044600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr4:90041600-90045200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr4:90042200-90047600	Enhancers	Fetal Intestine Large	intestine
14	chr4:90042400-90044800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr4:90042600-90049600	Enhancers	Fetal Intestine Small	intestine
16	chr4:90043000-90045200	Enhancers	Stomach Mucosa	stomach
17	chr4:90043200-90044400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
18	chr4:90043200-90045000	Enhancers	NHEK	skin
19	chr4:90043200-90045800	Enhancers	HMEC	breast
20	chr4:90043400-90050200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr4:90043600-90044800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr4:90043600-90044800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr4:90043600-90045200	Flanking Active TSS	HepG2	liver
24	chr4:90043600-90046000	Enhancers	Breast Myoepithelial Primary Cells	Breast
25	chr4:90043600-90046000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr4:90043800-90045200	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr4:90043800-90045200	Flanking Active TSS	A549	lung
28	chr4:90043800-90045800	Enhancers	Liver	Liver
29	chr4:90043800-90046000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr4:90044000-90044400	Weak transcription	Placenta	Placenta
31	chr4:90044000-90044600	Enhancers	Rectal Mucosa Donor 31	rectum
32	chr4:90044000-90044800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr4:90044000-90044800	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr4:90044000-90045000	Enhancers	Brain Substantia Nigra	brain
35	chr4:90044000-90045000	Enhancers	NH-A	brain
36	chr4:90044000-90045400	Weak transcription	Sigmoid Colon	Sigmoid Colon
37	chr4:90044000-90045800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
38	chr4:90044000-90046000	Enhancers	Duodenum Mucosa	Duodenum
39	chr4:90044200-90044600	Weak transcription	HUES6 Cell Line	embryonic stem cell
40	chr4:90044200-90045400	Weak transcription	Small Intestine	intestine

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