Variant report

Variant	rs11618960
Chromosome Location	chr13:40332260-40332261
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 55 )
Associated
traits (count: 1 )

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

rs_ID	r²[population]
rs11147769	0.86[AFR][1000 genomes]
rs17591231	0.86[AFR][1000 genomes]
rs4133063	0.97[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4245396	0.90[AFR][1000 genomes]
rs4288869	0.97[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4338665	0.86[AFR][1000 genomes]
rs4403927	0.86[AFR][1000 genomes]
rs4408422	0.89[AFR][1000 genomes];0.82[AMR][1000 genomes]
rs4409964	0.86[AFR][1000 genomes]
rs4943694	0.92[AFR][1000 genomes]
rs4943695	0.87[AFR][1000 genomes]
rs4943696	0.87[AFR][1000 genomes];0.82[AMR][1000 genomes]
rs7319128	0.87[AFR][1000 genomes]
rs7325068	0.89[AFR][1000 genomes]
rs7327824	0.87[AFR][1000 genomes]
rs7330211	0.97[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7334651	0.89[AFR][1000 genomes]
rs7337585	0.86[AFR][1000 genomes]
rs7998641	0.90[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs8000009	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9315729	0.86[AFR][1000 genomes]
rs9315730	0.85[AFR][1000 genomes]
rs9532429	0.87[AFR][1000 genomes]
rs9548898	0.97[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9548900	0.89[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs9548901	0.89[AFR][1000 genomes]
rs9548905	0.92[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9548906	0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9548913	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9548914	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9548916	0.90[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs9548917	0.90[AFR][1000 genomes];0.82[AMR][1000 genomes]
rs9548918	0.90[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs9548919	0.89[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs9548920	0.90[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs9548922	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9548926	0.87[AFR][1000 genomes];0.82[AMR][1000 genomes]
rs9548927	0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9548928	0.87[AFR][1000 genomes]
rs9548929	0.86[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs9548930	0.85[AFR][1000 genomes]
rs9566474	0.87[AFR][1000 genomes]
rs9576891	0.87[AFR][1000 genomes];0.82[AMR][1000 genomes]
rs9576892	0.86[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs9576894	0.97[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9576895	0.98[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9576896	0.87[AFR][1000 genomes]
rs9576897	0.86[AFR][1000 genomes]
rs9576898	0.87[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1054600	chr13:39801283-40545027	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
2	nsv1054797	chr13:40198744-40618428	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	10 gene(s)	inside rSNPs	diseases
3	nsv541755	chr13:40198744-40618428	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats 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	10 gene(s)	inside rSNPs	diseases
4	nsv832586	chr13:40222880-40379063	Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA	6 gene(s)	inside rSNPs	diseases
5	nsv1040458	chr13:40249387-40638129	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
6	nsv471130	chr13:40261945-40350912	Strong transcription Enhancers Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs11618960	COG6	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:34 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:40255800-40340200	Weak transcription	Psoas Muscle	Psoas
2	chr13:40267600-40341200	Weak transcription	Rectal Smooth Muscle	rectum
3	chr13:40293000-40340800	Weak transcription	Colon Smooth Muscle	Colon
4	chr13:40294200-40339200	Weak transcription	Fetal Brain Male	brain
5	chr13:40297600-40339800	Weak transcription	Brain Hippocampus Middle	brain
6	chr13:40304600-40340000	Weak transcription	Osteobl	bone
7	chr13:40309200-40334600	Weak transcription	HepG2	liver
8	chr13:40311400-40347200	Weak transcription	HSMM	muscle
9	chr13:40311600-40339800	Weak transcription	Rectal Mucosa Donor 31	rectum
10	chr13:40311600-40340000	Weak transcription	Skeletal Muscle Female	skeletal muscle
11	chr13:40311800-40339800	Weak transcription	Brain Anterior Caudate	brain
12	chr13:40311800-40340000	Weak transcription	Ovary	ovary
13	chr13:40312000-40340000	Weak transcription	Brain Angular Gyrus	brain
14	chr13:40312200-40333000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr13:40312200-40340000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr13:40312200-40340000	Weak transcription	Pancreas	Pancrea
17	chr13:40312200-40340200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr13:40312200-40351200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr13:40315000-40340200	Weak transcription	Muscle Satellite Cultured Cells	--
20	chr13:40325200-40334400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
21	chr13:40325800-40339800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr13:40326200-40339400	Weak transcription	Adipose Nuclei	Adipose
23	chr13:40326400-40334400	Weak transcription	Liver	Liver
24	chr13:40327400-40344400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr13:40327400-40352200	Weak transcription	Primary T cells from cord blood	blood
26	chr13:40327600-40334800	Weak transcription	Primary T cells fromperipheralblood	blood
27	chr13:40327800-40339400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr13:40327800-40347400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr13:40328600-40335000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr13:40330000-40345200	Weak transcription	Aorta	Aorta
31	chr13:40330200-40340000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr13:40330400-40339800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr13:40332200-40332400	ZNF genes & repeats	Esophagus	oesophagus
34	chr13:40332200-40339200	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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