Variant report

Variant	rs10867367
Chromosome Location	chr9:71949333-71949334
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr9:71937291..71938805-chr9:71947853..71950647,2	MCF-7	breast:
2	chr9:71938980..71942989-chr9:71948719..71952041,5	MCF-7	breast:
3	chr9:71939962..71941547-chr9:71947725..71950010,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000135063	Chromatin interaction

Extended variants
information (count: 34 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10735538	0.83[AMR][1000 genomes]
rs10780308	0.82[CHD][hapmap];0.80[MEX][hapmap];0.83[TSI][hapmap];0.83[AMR][1000 genomes]
rs10867357	0.95[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];0.94[TSI][hapmap];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10867360	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11791211	0.86[ASN][1000 genomes]
rs13287458	0.84[AMR][1000 genomes]
rs13292207	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1339544	0.95[CHB][hapmap];0.97[CHD][hapmap];0.87[ASN][1000 genomes]
rs3750552	0.85[CEU][hapmap];0.95[CHB][hapmap];0.90[GIH][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];0.89[TSI][hapmap];0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4382537	0.82[CHD][hapmap];0.80[MEX][hapmap];0.80[TSI][hapmap];0.83[AMR][1000 genomes]
rs4515616	0.80[CHD][hapmap]
rs4537363	0.83[AMR][1000 genomes]
rs4744566	0.82[CHD][hapmap];0.80[MEX][hapmap];0.83[TSI][hapmap];0.83[AMR][1000 genomes]
rs4744879	0.83[AMR][1000 genomes]
rs4744880	0.83[AMR][1000 genomes]
rs4744881	0.82[CHD][hapmap];0.80[MEX][hapmap];0.83[TSI][hapmap];0.83[AMR][1000 genomes]
rs4744882	0.83[AMR][1000 genomes]
rs4744883	0.83[AMR][1000 genomes]
rs6559468	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6559472	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6559478	0.83[AMR][1000 genomes]
rs7021089	0.83[AMR][1000 genomes]
rs7027671	1.00[CHB][hapmap];0.97[CHD][hapmap];0.89[ASN][1000 genomes]
rs7028837	0.83[AMR][1000 genomes]
rs7045431	0.83[AMR][1000 genomes]
rs7852930	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7875734	0.83[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1051723	chr9:71398713-71971285	Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
2	nsv931684	chr9:71417110-71957723	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
3	nsv1049175	chr9:71418242-71986910	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
4	nsv1035477	chr9:71511927-71959487	Enhancers Strong transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
5	nsv817406	chr9:71675454-72179318	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
6	nsv831610	chr9:71846941-72016835	Flanking Bivalent TSS/Enh Weak transcription Enhancers Bivalent/Poised TSS Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
7	nsv893428	chr9:71926658-72027641	Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs10867367	FAM189A2	cis	parietal	SCAN
rs10867367	TJP2	cis	parietal	SCAN
rs10867367	C9orf57	cis	cerebellum	SCAN

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:71941400-71954400	Weak transcription	Brain Anterior Caudate	brain
2	chr9:71941600-71950400	Weak transcription	Gastric	stomach
3	chr9:71942200-71950400	Weak transcription	Lung	lung
4	chr9:71942400-71950200	Weak transcription	Ovary	ovary
5	chr9:71942800-71954400	Weak transcription	Stomach Smooth Muscle	stomach
6	chr9:71943200-71954400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr9:71944600-71954400	Weak transcription	Brain Substantia Nigra	brain
8	chr9:71947000-71950400	Weak transcription	Psoas Muscle	Psoas
9	chr9:71947000-71958000	Weak transcription	H1 Cell Line	embryonic stem cell
10	chr9:71947200-71949800	Weak transcription	Left Ventricle	heart
11	chr9:71947200-71950200	Weak transcription	Esophagus	oesophagus
12	chr9:71947200-71954400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr9:71947200-71962000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr9:71947400-71949400	Weak transcription	HUES64 Cell Line	embryonic stem cell
15	chr9:71947400-71954600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr9:71947600-71954400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr9:71948600-71949400	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
18	chr9:71948600-71949400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr9:71948600-71949400	Enhancers	NHEK	skin
20	chr9:71948600-71949600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr9:71948600-71951000	Enhancers	Skeletal Muscle Female	skeletal muscle
22	chr9:71948800-71949400	Enhancers	HMEC	breast
23	chr9:71948800-71950400	Enhancers	Fetal Heart	heart
24	chr9:71948800-71962000	Weak transcription	Pancreas	Pancrea
25	chr9:71949200-71949400	Enhancers	Skeletal Muscle Male	skeletal muscle
26	chr9:71949200-71950200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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