Variant report

Variant	rs7701101
Chromosome Location	chr5:106635174-106635175
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:106633154..106635540-chr5:106637993..106640180,2	K562	blood:
2	chr5:106634442..106636070-chr5:106639631..106642528,2	MCF-7	breast:

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs10058308	0.83[EUR][1000 genomes]
rs10062445	0.83[EUR][1000 genomes]
rs10077806	0.83[EUR][1000 genomes]
rs10515370	1.00[ASN][1000 genomes]
rs10515372	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11948860	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13163748	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13165897	1.00[ASN][1000 genomes]
rs13167605	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13169680	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13179809	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13179824	0.83[EUR][1000 genomes]
rs13184636	1.00[ASN][1000 genomes]
rs13184643	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13184806	1.00[ASN][1000 genomes]
rs13186418	1.00[ASN][1000 genomes]
rs17159641	1.00[ASN][1000 genomes]
rs17159693	0.81[EUR][1000 genomes]
rs17159727	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17159745	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17159751	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17343335	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17343762	1.00[ASN][1000 genomes]
rs17400404	1.00[ASN][1000 genomes]
rs17402238	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17403350	1.00[ASN][1000 genomes]
rs1895462	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35307227	0.83[EUR][1000 genomes]
rs35709847	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35740714	1.00[ASN][1000 genomes]
rs35748495	1.00[ASN][1000 genomes]
rs35775035	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55849939	1.00[ASN][1000 genomes]
rs56283997	1.00[ASN][1000 genomes]
rs56852743	0.83[EUR][1000 genomes]
rs60635486	1.00[ASN][1000 genomes]
rs6596736	0.83[EUR][1000 genomes]
rs66460437	1.00[ASN][1000 genomes]
rs67504033	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67878207	1.00[EUR][1000 genomes]
rs6897756	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72784111	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72784113	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs765075	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7711216	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7735115	0.84[EUR][1000 genomes]
rs9327996	0.83[EUR][1000 genomes]
rs9327997	0.83[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1030118	chr5:106006097-106847949	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
2	nsv823170	chr5:106326293-106673695	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv1034276	chr5:106461538-106944163	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
4	nsv537851	chr5:106461538-106944163	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:106621800-106636600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr5:106631600-106636400	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr5:106632000-106636400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr5:106632000-106636600	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr5:106632200-106636000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr5:106632200-106636400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr5:106632200-106636600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
8	chr5:106632600-106636600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr5:106635000-106635200	Enhancers	Ovary	ovary

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