Variant report

Variant	rs6650766
Chromosome Location	chr2:149196365-149196366
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 57 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs11884622	1.00[ASN][1000 genomes]
rs11885393	1.00[ASN][1000 genomes]
rs11887387	1.00[ASN][1000 genomes]
rs11891262	1.00[ASN][1000 genomes]
rs11899300	1.00[ASN][1000 genomes]
rs11900654	1.00[ASN][1000 genomes]
rs11901992	1.00[ASN][1000 genomes]
rs11902437	0.93[ASN][1000 genomes]
rs1446552	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1524370	0.98[ASN][1000 genomes]
rs16828606	0.98[ASN][1000 genomes]
rs16828609	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs34415030	0.98[ASN][1000 genomes]
rs35180858	0.98[ASN][1000 genomes]
rs35431687	0.98[ASN][1000 genomes]
rs35975590	0.98[ASN][1000 genomes]
rs56887986	1.00[ASN][1000 genomes]
rs57192354	1.00[ASN][1000 genomes]
rs57905160	1.00[ASN][1000 genomes]
rs60061051	0.93[ASN][1000 genomes]
rs60973488	1.00[ASN][1000 genomes]
rs61319805	1.00[ASN][1000 genomes]
rs61587331	0.81[ASN][1000 genomes]
rs62182802	0.81[ASN][1000 genomes]
rs62182829	0.81[ASN][1000 genomes]
rs66509437	0.81[ASN][1000 genomes]
rs66820471	1.00[ASN][1000 genomes]
rs6706461	1.00[ASN][1000 genomes]
rs67081781	0.98[ASN][1000 genomes]
rs6713264	0.88[JPT][hapmap]
rs67148212	0.93[ASN][1000 genomes]
rs67201811	0.98[ASN][1000 genomes]
rs6759300	1.00[ASN][1000 genomes]
rs67778375	1.00[ASN][1000 genomes]
rs67852977	0.98[ASN][1000 genomes]
rs67918539	0.81[ASN][1000 genomes]
rs67948770	0.98[ASN][1000 genomes]
rs72618898	0.83[ASN][1000 genomes]
rs72618899	0.88[ASN][1000 genomes]
rs72618900	0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs72618901	1.00[ASN][1000 genomes]
rs72618902	1.00[ASN][1000 genomes]
rs72620204	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72620205	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72620209	1.00[ASN][1000 genomes]
rs72620210	0.96[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7561976	1.00[ASN][1000 genomes]
rs7582000	1.00[ASN][1000 genomes]
rs7595203	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2753542	chr2:149004714-149268503	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv1012275	chr2:149031668-149316793	Enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv875278	chr2:149094415-149201775	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	nsv875279	chr2:149111470-149201775	Enhancers ZNF genes & repeats Weak transcription Strong transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv875280	chr2:149115432-149198275	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv875281	chr2:149115432-149206943	ZNF genes & repeats Enhancers Bivalent Enhancer Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
7	esv2751831	chr2:149151358-150105603	Weak transcription Flanking Bivalent TSS/Enh Strong transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
8	nsv1000101	chr2:149165813-149361220	Enhancers Strong transcription Genic enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 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	chr2:149172600-149205000	Weak transcription	Colon Smooth Muscle	Colon
2	chr2:149174200-149221400	Weak transcription	Primary T cells from cord blood	blood
3	chr2:149174400-149221400	Weak transcription	Primary B cells from cord blood	blood
4	chr2:149179400-149198800	Weak transcription	Fetal Stomach	stomach
5	chr2:149193000-149226000	Weak transcription	Primary hematopoietic stem cells	blood
6	chr2:149193400-149221600	Weak transcription	Primary T helper cells fromperipheralblood	blood
7	chr2:149193600-149201600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr2:149194000-149216200	Weak transcription	Fetal Intestine Small	intestine
9	chr2:149194800-149200200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr2:149194800-149216200	Weak transcription	Psoas Muscle	Psoas
11	chr2:149195000-149198400	Weak transcription	HSMM	muscle

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links