Variant report

Variant	rs4763813
Chromosome Location	chr12:9862336-9862337
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr12:9798330..9801052-chr12:9860989..9864813,3	K562	blood:
2	chr12:9824506..9827100-chr12:9861527..9863862,2	K562	blood:
3	chr12:9853903..9855741-chr12:9860997..9863949,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000069493	Chromatin interaction
ENSG00000256594	Chromatin interaction
ENSG00000256442	Chromatin interaction

Extended variants
information (count: 28 )
Associated
traits (count: 5 )

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

rs_ID	r²[population]
rs10772060	1.00[CHB][hapmap]
rs10844418	1.00[CHB][hapmap]
rs10844424	1.00[CHB][hapmap];1.00[CHD][hapmap];0.83[GIH][hapmap]
rs10844429	1.00[CHB][hapmap];1.00[CHD][hapmap];0.83[GIH][hapmap]
rs11052430	1.00[CHB][hapmap];1.00[CHD][hapmap];0.83[GIH][hapmap]
rs11052431	1.00[CHB][hapmap]
rs12371981	1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap]
rs12578928	1.00[CHB][hapmap]
rs12810851	1.00[CHB][hapmap]
rs12823653	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs12823699	1.00[CHB][hapmap]
rs12825507	1.00[CHB][hapmap];1.00[CHD][hapmap];0.83[GIH][hapmap]
rs12828602	1.00[CHB][hapmap]
rs1861089	0.87[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.94[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.84[AFR][1000 genomes]
rs2080207	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.87[TSI][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes]
rs2114872	1.00[CHB][hapmap]
rs4763814	1.00[CEU][hapmap];1.00[CHB][hapmap];0.98[AFR][1000 genomes]
rs7310897	1.00[CHB][hapmap]
rs7485402	0.87[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.94[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.82[AFR][1000 genomes]
rs7961812	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap]
rs7975557	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.85[TSI][hapmap]
rs9630265	1.00[CHB][hapmap]
rs982511	1.00[CHD][hapmap]

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	esv2758293	chr12:9371595-9923529	Weak transcription Enhancers Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	40 gene(s)	inside rSNPs	diseases
2	esv2759878	chr12:9371595-9923529	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	40 gene(s)	inside rSNPs	diseases
3	nsv983235	chr12:9852218-9893776	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	esv2757490	chr12:9855958-9888553	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	nsv442255	chr12:9862078-9874924	Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

mRNA abundance (count:5)

SNP	Gene	Cis/trans	Tissue	Source
rs4763813	C12orf59	cis	cerebellum	SCAN
rs4763813	DCAL1	cis	multi-tissue	Pritchard
rs4763813	GSG1	cis	parietal	SCAN
rs4763813	CLEC2D	cis	multi-tissue	Pritchard
rs4763813	LOC171220	cis	cerebellum	SCAN

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:9840600-9864600	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr12:9841800-9863200	Weak transcription	HSMMtube	muscle
3	chr12:9855600-9862800	Weak transcription	Primary hematopoietic stem cells	blood
4	chr12:9858000-9872200	Enhancers	Primary B cells from peripheral blood	blood
5	chr12:9859000-9870200	Enhancers	Primary B cells from cord blood	blood
6	chr12:9860800-9863000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr12:9860800-9863200	Weak transcription	Spleen	Spleen
8	chr12:9860800-9864400	Weak transcription	A549	lung
9	chr12:9861000-9862400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
10	chr12:9861000-9863000	Weak transcription	Placenta	Placenta
11	chr12:9861000-9873200	Weak transcription	Primary monocytes fromperipheralblood	blood
12	chr12:9861000-9874200	Weak transcription	Fetal Thymus	thymus
13	chr12:9861400-9862600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
14	chr12:9861400-9862800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
15	chr12:9861400-9864400	Weak transcription	Rectal Mucosa Donor 29	rectum
16	chr12:9861400-9864600	Weak transcription	Primary T cells from cord blood	blood
17	chr12:9861600-9863000	Weak transcription	Primary T helper cells PMA-I stimulated	--
18	chr12:9861600-9882400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
19	chr12:9861800-9868200	Enhancers	GM12878-XiMat	blood
20	chr12:9861800-9874000	Weak transcription	Primary T helper cells fromperipheralblood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links