Variant report

Variant	rs1200097
Chromosome Location	chr1:169047462-169047463
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:169041515..169047951-chr1:169073926..169082165,10	MCF-7	breast:
2	chr1:169041497..169044026-chr1:169046311..169049297,2	MCF-7	breast:
3	chr1:169041292..169045198-chr1:169046298..169050573,7	MCF-7	breast:
4	chr1:169045647..169050705-chr1:169071889..169078389,7	MCF-7	breast:

Variant related genes	Relation type
ENSG00000237707	Chromatin interaction
ENSG00000143153	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs1040506	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1200089	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1200092	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1200099	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1200103	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1200105	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1200106	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1200108	0.90[EUR][1000 genomes]
rs1200114	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1200115	0.83[AMR][1000 genomes]
rs1200122	0.82[AMR][1000 genomes]
rs1200125	0.83[AMR][1000 genomes]
rs1200128	0.83[AMR][1000 genomes]
rs1320974	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1575041	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1575042	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2982459	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2982461	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3007364	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3007369	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3007370	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4656175	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs932393	0.82[AMR][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	nsv869415	chr1:168467284-169153863	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	44 gene(s)	inside rSNPs	diseases
2	esv3522071	chr1:168978325-169339044	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
3	esv3522072	chr1:168978325-169339044	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3' Weak transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
4	nsv831858	chr1:169022383-169179068	Weak transcription Flanking Active TSS Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
5	esv2181463	chr1:169047461-169047463	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:169043000-169047600	Weak transcription	Brain Hippocampus Middle	brain
2	chr1:169043000-169050800	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr1:169043200-169047600	Weak transcription	Brain Angular Gyrus	brain
4	chr1:169043200-169056000	Weak transcription	Stomach Mucosa	stomach
5	chr1:169045200-169050600	Weak transcription	Fetal Heart	heart
6	chr1:169047000-169047800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr1:169047000-169048400	Enhancers	Liver	Liver
8	chr1:169047000-169050000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr1:169047200-169048000	Enhancers	Pancreas	Pancrea
10	chr1:169047400-169048000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr1:169047400-169048600	Weak transcription	Gastric	stomach

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