Variant report

Variant	rs61840137
Chromosome Location	chr1:223276028-223276029
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:223271779..223273735-chr1:223275202..223277036,2	MCF-7	breast:
2	chr1:223268458..223270530-chr1:223275710..223277683,2	MCF-7	breast:
3	chr1:223275284..223278279-chr1:223280567..223284100,3	MCF-7	breast:

Extended variants
information (count: 84 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:78)

rs_ID	r²[population]
rs10443637	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10443638	0.92[AFR][1000 genomes];0.94[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10443639	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10443640	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1100886	0.85[AFR][1000 genomes];0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1100887	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12729658	0.94[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12748315	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1640840	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1773714	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1773718	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1773726	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1773727	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1773729	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1861172	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2110582	0.81[AMR][1000 genomes]
rs2353480	0.85[AMR][1000 genomes]
rs2430402	0.91[EUR][1000 genomes]
rs2430403	0.91[EUR][1000 genomes]
rs2487831	0.91[EUR][1000 genomes]
rs2487833	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs28368761	0.81[AMR][1000 genomes]
rs28411712	0.82[AMR][1000 genomes]
rs28460738	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs28470412	0.81[AMR][1000 genomes]
rs28499047	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs28516626	0.80[AMR][1000 genomes]
rs28522106	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs28594689	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs28691199	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs28880136	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs34253986	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs34270714	0.81[AMR][1000 genomes]
rs35251562	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs3795742	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs3795743	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4661281	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4661282	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs5744174	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs61840074	0.82[EUR][1000 genomes]
rs61840078	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs61840135	0.84[AMR][1000 genomes]
rs61840136	0.85[AMR][1000 genomes]
rs61840138	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs61840140	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs61840141	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs61840142	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs67762955	0.81[AMR][1000 genomes]
rs712866	0.91[EUR][1000 genomes]
rs7365624	0.81[AMR][1000 genomes]
rs7366469	0.81[AMR][1000 genomes]
rs7413993	0.82[AMR][1000 genomes]
rs7414121	0.84[AMR][1000 genomes]
rs7415320	0.81[AMR][1000 genomes]
rs7547359	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs851134	0.92[EUR][1000 genomes]
rs851135	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs851136	0.82[EUR][1000 genomes]
rs851137	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs851138	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs851139	0.81[EUR][1000 genomes]
rs851178	0.92[EUR][1000 genomes]
rs851179	0.92[EUR][1000 genomes]
rs851180	0.91[EUR][1000 genomes]
rs851181	0.92[EUR][1000 genomes]
rs851183	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs851184	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs851185	0.82[EUR][1000 genomes]
rs851186	0.90[EUR][1000 genomes]
rs851187	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs851188	0.91[EUR][1000 genomes]
rs851189	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs851190	0.84[EUR][1000 genomes]
rs851192	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs851193	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs864834	0.91[EUR][1000 genomes]
rs877327	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs887947	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv999185	chr1:222500725-223278032	Strong transcription Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
2	nsv535304	chr1:222500725-223278032	Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
3	nsv1012537	chr1:222755091-223512243	Weak transcription Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
4	nsv1014896	chr1:223070446-223327185	Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv873207	chr1:223078802-223292632	Genic enhancers Enhancers Weak transcription Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	esv1004280	chr1:223273275-223277103	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:223274400-223276400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr1:223275600-223276400	Enhancers	HUVEC	blood vessel
3	chr1:223276000-223276400	Enhancers	Skeletal Muscle Male	skeletal muscle
4	chr1:223276000-223277000	Enhancers	Fetal Intestine Small	intestine
5	chr1:223276000-223283800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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