Variant report

Variant	rs13437156
Chromosome Location	chr6:142735870-142735871
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	CEBPB	chr6:142735600-142735951	MCF-7	breast:	n/a	n/a
2	CEBPB	chr6:142735549-142735973	MCF-7	breast:	n/a	n/a
3	ZNF217	chr6:142735691-142735964	MCF-7	breast:	n/a	n/a
4	POLR2A	chr6:142735252-142736340	HepG2	liver:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:142734245..142735957-chr6:142740878..142742479,2	MCF-7	breast:
2	chr6:142733339..142736237-chr6:142747446..142749492,2	MCF-7	breast:
3	chr6:142733840..142736279-chr6:142738480..142740069,2	MCF-7	breast:

Variant related genes	Relation type
GPR126	TF binding region

Extended variants
information (count: 33 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1411147	1.00[AMR][1000 genomes]
rs6921559	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7760219	0.90[AFR][1000 genomes]
rs9484627	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9484628	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9484629	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9484634	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9484635	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9484636	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9484638	1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9484640	1.00[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9484641	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9484644	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9496336	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9496350	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9496351	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9496359	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9496362	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9496363	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9496375	1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9496376	1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9496381	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9496383	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9496384	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9496385	1.00[AMR][1000 genomes]
rs9496386	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9496387	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9496393	1.00[AMR][1000 genomes]
rs9496407	1.00[AMR][1000 genomes]
rs9496408	1.00[AMR][1000 genomes]
rs9496410	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949088	chr6:142561402-143128849	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv830825	chr6:142585242-142752575	Enhancers Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:56 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:142718000-142763200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr6:142720600-142736800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr6:142721600-142749200	Weak transcription	Duodenum Smooth Muscle	Duodenum
4	chr6:142722000-142743400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr6:142726200-142736000	Weak transcription	Duodenum Mucosa	Duodenum
6	chr6:142726600-142737400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr6:142726800-142738000	Weak transcription	Stomach Mucosa	stomach
8	chr6:142727000-142743400	Strong transcription	HepG2	liver
9	chr6:142728400-142736800	Weak transcription	Fetal Intestine Large	intestine
10	chr6:142729200-142743200	Strong transcription	Liver	Liver
11	chr6:142730200-142747600	Weak transcription	Fetal Intestine Small	intestine
12	chr6:142730400-142738200	Weak transcription	Primary hematopoietic stem cells	blood
13	chr6:142731200-142737000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
14	chr6:142731600-142737600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr6:142732600-142737000	Weak transcription	Primary T cells from cord blood	blood
16	chr6:142733000-142738600	Enhancers	NHDF-Ad	bronchial
17	chr6:142733200-142736000	Enhancers	NHLF	lung
18	chr6:142733400-142737600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr6:142733400-142739200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr6:142733400-142739200	Enhancers	Osteobl	bone
21	chr6:142733600-142736800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
22	chr6:142733600-142737800	Enhancers	HSMMtube	muscle
23	chr6:142733800-142736800	Weak transcription	HUES48 Cell Line	embryonic stem cell
24	chr6:142733800-142736800	Weak transcription	HUES6 Cell Line	embryonic stem cell
25	chr6:142733800-142736800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
26	chr6:142733800-142736800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr6:142733800-142738600	Weak transcription	H1 Cell Line	embryonic stem cell
28	chr6:142733800-142758000	Weak transcription	Stomach Smooth Muscle	stomach
29	chr6:142734200-142737000	Weak transcription	HUES64 Cell Line	embryonic stem cell
30	chr6:142734200-142739200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr6:142734600-142738200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr6:142734800-142736800	Strong transcription	Fetal Lung	lung
33	chr6:142734800-142738800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr6:142734800-142743200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr6:142735000-142736000	Enhancers	Muscle Satellite Cultured Cells	--
36	chr6:142735000-142736200	Genic enhancers	HSMM	muscle
37	chr6:142735000-142736600	Genic enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr6:142735000-142737000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr6:142735200-142736800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr6:142735200-142736800	Weak transcription	Placenta	Placenta
41	chr6:142735200-142738400	Genic enhancers	A549	lung
42	chr6:142735200-142760200	Weak transcription	Esophagus	oesophagus
43	chr6:142735200-142765400	Weak transcription	Hela-S3	cervix
44	chr6:142735600-142736800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr6:142735600-142738600	Genic enhancers	HUVEC	blood vessel
46	chr6:142735600-142743600	Weak transcription	Sigmoid Colon	Sigmoid Colon
47	chr6:142735800-142736800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
48	chr6:142735800-142736800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr6:142735800-142736800	Weak transcription	Fetal Brain Male	brain
50	chr6:142735800-142736800	Weak transcription	HMEC	breast

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