Variant report

Variant	rs9366788
Chromosome Location	chr6:11414705-11414706
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:8)
CpG islands
(count:0)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:8 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CBX3	chr6:11414677-11415325	HCT-116	colon:	n/a	n/a
2	SRF	chr6:11414697-11415338	MCF-7	breast:	n/a	n/a
3	POLR2A	chr6:11413990-11415487	MCF10A-Er-Src	breast:	n/a	n/a
4	FOXM1	chr6:11414611-11415460	ECC-1	luminal epithelium:	n/a	n/a
5	SP1	chr6:11414700-11415391	A549	lung:	n/a	n/a
6	MYC	chr6:11414675-11415198	MCF10A-Er-Src	breast:	n/a	n/a
7	MYBL2	chr6:11414635-11415360	HepG2	liver:	n/a	n/a
8	POLR2A	chr6:11414693-11415292	MCF10A-Er-Src	breast:	n/a	n/a

No data

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:11228618..11230806-chr6:11414420..11416664,2	MCF-7	breast:
2	chr6:11229922..11234167-chr6:11411662..11415515,7	MCF-7	breast:
3	chr6:11387321..11394874-chr6:11409302..11416244,8	MCF-7	breast:
4	chr6:11216036..11217997-chr6:11412401..11415164,2	MCF-7	breast:
5	chr6:11413490..11417171-chr6:11433636..11437714,3	MCF-7	breast:
6	chr6:11394123..11395903-chr6:11413687..11415867,2	MCF-7	breast:
7	chr6:11388874..11392122-chr6:11413409..11415866,5	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000233656	TF binding region
ENSG00000111859	Chromatin interaction

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs12210644	0.86[AMR][1000 genomes]
rs13198555	0.82[AMR][1000 genomes]
rs4276494	0.86[AMR][1000 genomes]
rs4330532	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4368806	0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4370358	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4632886	0.84[AMR][1000 genomes]
rs4713491	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4713493	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4713494	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6457458	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6901388	0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6904848	0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6908442	0.84[AFR][1000 genomes];0.99[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6916534	0.86[AMR][1000 genomes]
rs6919269	0.81[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6931599	0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7740314	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7751151	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7752735	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7762454	0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7766220	0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs8180674	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9368701	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs9380270	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1021078	chr6:10819083-11558560	Enhancers Strong transcription Active TSS Flanking Active TSS Weak transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
2	nsv538135	chr6:10819083-11558560	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS 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 target site	47 gene(s)	inside rSNPs	diseases
3	nsv432848	chr6:11371614-11560114	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:37 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:11405400-11419400	Weak transcription	Aorta	Aorta
2	chr6:11411000-11415200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr6:11411200-11415000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
4	chr6:11411200-11415000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
5	chr6:11411200-11415600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
6	chr6:11411600-11417000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr6:11412200-11415400	Enhancers	Primary T helper cells PMA-I stimulated	--
8	chr6:11412400-11415200	Enhancers	Primary monocytes fromperipheralblood	blood
9	chr6:11412400-11415200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
10	chr6:11412400-11415400	Enhancers	Primary T helper cells fromperipheralblood	blood
11	chr6:11412400-11416400	Weak transcription	Fetal Kidney	kidney
12	chr6:11412600-11414800	Weak transcription	HUES6 Cell Line	embryonic stem cell
13	chr6:11412600-11416000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr6:11412600-11416200	Weak transcription	Placenta Amnion	Placenta Amnion
15	chr6:11412600-11416400	Weak transcription	NH-A	brain
16	chr6:11412600-11425600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr6:11412600-11425600	Weak transcription	NHLF	lung
18	chr6:11412800-11414800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr6:11412800-11414800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr6:11412800-11415000	Weak transcription	NHDF-Ad	bronchial
21	chr6:11412800-11415200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr6:11412800-11416400	Weak transcription	HSMM	muscle
23	chr6:11413400-11415600	Enhancers	Hela-S3	cervix
24	chr6:11413600-11415600	Enhancers	Monocytes-CD14+_RO01746	blood
25	chr6:11413600-11416800	Enhancers	NHEK	skin
26	chr6:11413800-11414800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
27	chr6:11413800-11414800	Weak transcription	Primary B cells from peripheral blood	blood
28	chr6:11413800-11414800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
29	chr6:11413800-11415800	Enhancers	Primary neutrophils fromperipheralblood	blood
30	chr6:11413800-11416600	Enhancers	HepG2	liver
31	chr6:11414200-11414800	Enhancers	GM12878-XiMat	blood
32	chr6:11414200-11415000	Enhancers	Pancreatic Islets	Pancreatic Islet
33	chr6:11414200-11415200	Enhancers	HUVEC	blood vessel
34	chr6:11414600-11415000	Enhancers	Liver	Liver
35	chr6:11414600-11415200	Enhancers	Primary B cells from cord blood	blood
36	chr6:11414600-11415400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr6:11414600-11415400	Flanking Active TSS	A549	lung

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