Variant report

Variant	rs61500565
Chromosome Location	chr3:23485522-23485523
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:23483538..23485535-chr3:23501695..23503485,2	K562	blood:
2	chr3:23482059..23483566-chr3:23484032..23486053,2	MCF-7	breast:

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs11922562	1.00[AMR][1000 genomes]
rs17013009	1.00[AMR][1000 genomes]
rs17013099	1.00[AMR][1000 genomes]
rs17013329	0.89[AFR][1000 genomes]
rs28548892	1.00[AMR][1000 genomes]
rs28567933	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58047209	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58879825	1.00[AMR][1000 genomes]
rs60014070	1.00[AMR][1000 genomes]
rs61081559	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61636332	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6768277	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6795043	1.00[AMR][1000 genomes]
rs73138415	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73138434	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73138436	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73138449	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73138480	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73138490	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73138492	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73140509	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73140514	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73141810	1.00[AMR][1000 genomes]
rs7611624	1.00[AMR][1000 genomes]
rs7634565	1.00[AMR][1000 genomes]
rs7652287	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9310716	1.00[AMR][1000 genomes]
rs9681506	1.00[AMR][1000 genomes]
rs9809364	1.00[AMR][1000 genomes]
rs9810378	1.00[AMR][1000 genomes]
rs9811442	1.00[AMR][1000 genomes]
rs9819566	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9819788	1.00[AMR][1000 genomes]
rs9821681	1.00[AMR][1000 genomes]
rs9829577	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9834737	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9842159	1.00[AMR][1000 genomes]
rs9845340	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9852053	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9866889	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9869171	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9878638	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9879132	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9879217	0.80[AFR][1000 genomes];1.00[AMR][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	nsv1002823	chr3:23277838-23623083	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1007373	chr3:23367952-23710331	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Genic enhancers Strong transcription Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv876625	chr3:23390301-23509597	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv533980	chr3:23445901-24311972	ZNF genes & repeats Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:25 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:23472800-23488000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr3:23473800-23494000	Weak transcription	Skeletal Muscle Male	skeletal muscle
3	chr3:23477800-23487800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr3:23478600-23485800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr3:23478600-23489400	Weak transcription	Left Ventricle	heart
6	chr3:23479800-23485600	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr3:23479800-23490200	Weak transcription	Brain Substantia Nigra	brain
8	chr3:23482600-23486800	Weak transcription	Fetal Heart	heart
9	chr3:23483200-23491200	Weak transcription	Psoas Muscle	Psoas
10	chr3:23483400-23486200	Enhancers	GM12878-XiMat	blood
11	chr3:23484200-23486200	Enhancers	Skeletal Muscle Female	skeletal muscle
12	chr3:23484200-23487200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr3:23484600-23486200	Enhancers	HSMMtube	muscle
14	chr3:23484800-23487800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr3:23484800-23487800	Weak transcription	HUES6 Cell Line	embryonic stem cell
16	chr3:23484800-23488400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr3:23484800-23496000	Weak transcription	HUES64 Cell Line	embryonic stem cell
18	chr3:23484800-23496000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
19	chr3:23485000-23485600	Enhancers	Dnd41	blood
20	chr3:23485000-23487400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
21	chr3:23485000-23487800	Weak transcription	H1 Cell Line	embryonic stem cell
22	chr3:23485200-23490200	Weak transcription	Primary B cells from peripheral blood	blood
23	chr3:23485200-23490600	Weak transcription	Primary B cells from cord blood	blood
24	chr3:23485200-23496400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr3:23485200-23498600	Weak transcription	Primary T helper cells PMA-I stimulated	--

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