Variant report

Variant	rs9917755
Chromosome Location	chr3:61143781-61143782
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs10049007	0.88[EUR][1000 genomes]
rs10049287	0.88[EUR][1000 genomes]
rs10049452	0.87[EUR][1000 genomes]
rs10049454	0.88[EUR][1000 genomes]
rs10866045	0.95[AFR][1000 genomes];0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11130820	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11707984	0.88[EUR][1000 genomes]
rs11712122	0.88[EUR][1000 genomes]
rs12635622	0.87[EUR][1000 genomes]
rs13320646	0.87[EUR][1000 genomes]
rs13323296	0.86[EUR][1000 genomes]
rs1371095	0.86[EUR][1000 genomes]
rs1550343	0.87[EUR][1000 genomes]
rs1554601	0.88[EUR][1000 genomes]
rs1866433	0.88[EUR][1000 genomes]
rs1866434	0.88[EUR][1000 genomes]
rs1880213	0.87[EUR][1000 genomes]
rs1969420	0.87[EUR][1000 genomes]
rs2886377	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs4688310	0.86[EUR][1000 genomes]
rs62268809	0.99[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs6445196	0.87[EUR][1000 genomes]
rs6807748	0.88[EUR][1000 genomes]
rs753661	0.87[EUR][1000 genomes]
rs753662	0.86[EUR][1000 genomes]
rs7631101	0.87[EUR][1000 genomes]
rs7631246	0.87[EUR][1000 genomes]
rs7636682	0.88[EUR][1000 genomes]
rs7653719	0.81[EUR][1000 genomes]
rs9311799	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9814044	0.87[EUR][1000 genomes]
rs9816087	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9827045	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9839082	0.87[EUR][1000 genomes]
rs9850125	0.87[EUR][1000 genomes]
rs9851485	0.88[EUR][1000 genomes]
rs9871451	0.88[EUR][1000 genomes]
rs9871598	0.88[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2759152	chr3:60781943-61220809	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv948633	chr3:60993915-61171279	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	nsv834710	chr3:60995631-61148157	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
4	esv2757873	chr3:61019003-61185558	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
5	nsv876866	chr3:61054494-61310328	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv876867	chr3:61054494-61474575	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv432423	chr3:61100255-61606060	Enhancers Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
8	nsv1000378	chr3:61103229-61238089	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
9	nsv590425	chr3:61132698-61186550	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
10	nsv1012435	chr3:61136874-61181318	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
11	nsv1014142	chr3:61136874-61184782	Weak transcription Active TSS ZNF genes & repeats Enhancers Flanking Active TSS Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:61138400-61143800	Weak transcription	Primary T cells from cord blood	blood
2	chr3:61140400-61146000	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr3:61140800-61144400	Weak transcription	Fetal Kidney	kidney
4	chr3:61141800-61150800	Weak transcription	Brain Hippocampus Middle	brain
5	chr3:61141800-61152200	Weak transcription	Psoas Muscle	Psoas
6	chr3:61141800-61158400	Weak transcription	Pancreas	Pancrea
7	chr3:61142000-61145600	Weak transcription	Fetal Lung	lung
8	chr3:61142000-61150400	Weak transcription	Brain Angular Gyrus	brain
9	chr3:61142200-61145800	Weak transcription	Fetal Heart	heart
10	chr3:61143200-61145600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
11	chr3:61143400-61144800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr3:61143400-61145600	Weak transcription	iPS-20b Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links