Variant report

Variant	rs1011089
Chromosome Location	chr6:4481750-4481751
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:4481267..4483998-chr6:4490747..4493178,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000260239	Chromatin interaction

Extended variants
information (count: 62 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:57)

rs_ID	r²[population]
rs1009602	0.81[ASN][1000 genomes]
rs1009603	0.88[ASN][1000 genomes]
rs1009604	0.88[ASN][1000 genomes]
rs1011087	1.00[ASN][1000 genomes]
rs1011088	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs12525331	0.91[ASN][1000 genomes]
rs1265250	0.85[ASN][1000 genomes]
rs1265256	0.81[ASN][1000 genomes]
rs1265259	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1265260	0.98[ASN][1000 genomes]
rs13195445	1.00[ASN][1000 genomes]
rs1571630	1.00[ASN][1000 genomes]
rs2021989	0.94[ASN][1000 genomes]
rs2150231	0.84[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs2181015	0.83[CHB][hapmap];0.82[JPT][hapmap]
rs2875945	0.94[ASN][1000 genomes]
rs3929704	0.82[ASN][1000 genomes]
rs4246070	0.93[ASN][1000 genomes]
rs4959295	1.00[ASN][1000 genomes]
rs4959296	1.00[ASN][1000 genomes]
rs4959297	1.00[ASN][1000 genomes]
rs4959298	0.94[ASN][1000 genomes]
rs4959987	0.92[ASN][1000 genomes]
rs4959989	1.00[ASN][1000 genomes]
rs4959990	1.00[ASN][1000 genomes]
rs4959991	1.00[ASN][1000 genomes]
rs4959992	1.00[ASN][1000 genomes]
rs4959993	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs4959994	0.99[ASN][1000 genomes]
rs4959995	0.92[CHB][hapmap];0.81[ASN][1000 genomes]
rs4959997	0.93[CHB][hapmap]
rs4959998	1.00[CHB][hapmap];0.94[JPT][hapmap]
rs60221507	0.94[ASN][1000 genomes]
rs62384876	0.81[ASN][1000 genomes]
rs6914063	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs6930327	0.99[ASN][1000 genomes]
rs7450179	0.93[ASN][1000 genomes]
rs7452972	0.93[ASN][1000 genomes]
rs7453574	0.93[ASN][1000 genomes]
rs911565	0.99[ASN][1000 genomes]
rs911566	0.93[ASN][1000 genomes]
rs911567	0.93[ASN][1000 genomes]
rs9378879	0.93[ASN][1000 genomes]
rs9378880	0.93[ASN][1000 genomes]
rs9378881	0.93[ASN][1000 genomes]
rs9378882	0.94[ASN][1000 genomes]
rs9378883	0.84[ASN][1000 genomes]
rs9392053	1.00[ASN][1000 genomes]
rs9392602	0.95[ASN][1000 genomes]
rs9392603	0.93[ASN][1000 genomes]
rs9405247	0.94[ASN][1000 genomes]
rs9405248	0.94[ASN][1000 genomes]
rs9405748	1.00[ASN][1000 genomes]
rs9502189	1.00[ASN][1000 genomes]
rs9504122	0.98[ASN][1000 genomes]
rs9504123	1.00[ASN][1000 genomes]
rs9504124	1.00[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	nsv1021743	chr6:4382308-4494308	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv538111	chr6:4382308-4494308	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	esv3421990	chr6:4446933-4659639	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv830576	chr6:4447554-4610604	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	esv3366530	chr6:4471528-4865322	ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription 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	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:4480400-4481800	Enhancers	HUES64 Cell Line	embryonic stem cell
2	chr6:4480400-4482400	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr6:4480400-4483000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
4	chr6:4480600-4482800	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
5	chr6:4480600-4483200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr6:4480600-4483400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr6:4481000-4482000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr6:4481000-4482200	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr6:4481000-4482400	Bivalent Enhancer	H9 Cell Line	embryonic stem cell
10	chr6:4481200-4481800	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr6:4481200-4482000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
12	chr6:4481200-4482000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
13	chr6:4481400-4482000	Enhancers	Brain Germinal Matrix	brain
14	chr6:4481400-4482000	Weak transcription	Lung	lung
15	chr6:4481600-4482400	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr6:4481600-4484400	Weak transcription	Right Atrium	heart

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