Variant report

Variant	rs9548929
Chromosome Location	chr13:40341921-40341922
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 56 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs11147769	0.99[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11618960	0.86[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs17591231	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17591266	0.81[AFR][1000 genomes];0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4133063	0.83[AFR][1000 genomes]
rs4245396	0.91[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4288869	0.83[AFR][1000 genomes]
rs4338665	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4403927	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4408422	0.89[AFR][1000 genomes];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4409964	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4943694	0.93[AFR][1000 genomes];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4943695	0.99[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4943696	0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7319128	0.99[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7325068	0.89[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7327824	0.99[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7330211	0.83[AFR][1000 genomes]
rs7334651	0.89[AFR][1000 genomes];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7337585	0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7998641	0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs8000009	0.83[AFR][1000 genomes];0.82[AMR][1000 genomes]
rs9315729	0.99[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9315730	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9532429	0.99[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9532432	0.89[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9532436	0.81[AFR][1000 genomes];0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9532439	0.82[AMR][1000 genomes]
rs9548898	0.83[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs9548900	0.89[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9548901	0.89[AFR][1000 genomes];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9548913	0.83[AFR][1000 genomes]
rs9548916	0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9548917	0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9548918	0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9548919	0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9548920	0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9548922	0.86[AFR][1000 genomes];0.82[AMR][1000 genomes]
rs9548926	0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9548927	0.90[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs9548928	0.99[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9548930	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9566474	0.99[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9576891	0.88[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9576892	0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9576894	0.83[AFR][1000 genomes]
rs9576895	0.85[AFR][1000 genomes]
rs9576896	0.99[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9576897	0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9576898	0.99[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][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:2)

SNP	Gene	Cis/trans	Tissue	Source
rs9548929	COG6	cis	Muscle Skeletal	GTEx
rs9548929	COG6	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:52 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:40311400-40347200	Weak transcription	HSMM	muscle
2	chr13:40312200-40351200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr13:40327400-40344400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr13:40327400-40352200	Weak transcription	Primary T cells from cord blood	blood
5	chr13:40327800-40347400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr13:40330000-40345200	Weak transcription	Aorta	Aorta
7	chr13:40339200-40342600	Enhancers	Fetal Brain Male	brain
8	chr13:40339200-40342800	Enhancers	Breast Myoepithelial Primary Cells	Breast
9	chr13:40339400-40342600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr13:40339400-40342600	Enhancers	Adipose Nuclei	Adipose
11	chr13:40339400-40342800	Enhancers	Fetal Brain Female	brain
12	chr13:40339600-40343200	Enhancers	Brain Germinal Matrix	brain
13	chr13:40339800-40342600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr13:40339800-40342600	Enhancers	Cortex derived primary cultured neurospheres	brain
15	chr13:40339800-40342600	Enhancers	Brain Anterior Caudate	brain
16	chr13:40339800-40343200	Enhancers	Rectal Mucosa Donor 31	rectum
17	chr13:40340000-40342200	Enhancers	Ovary	ovary
18	chr13:40340000-40342600	Enhancers	Fetal Muscle Leg	muscle
19	chr13:40340000-40343000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr13:40340400-40342400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr13:40340400-40342400	Weak transcription	Lung	lung
22	chr13:40340400-40347000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr13:40340400-40347800	Weak transcription	HUVEC	blood vessel
24	chr13:40340400-40353600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr13:40340400-40361200	Weak transcription	Pancreas	Pancrea
26	chr13:40340600-40345800	Weak transcription	Left Ventricle	heart
27	chr13:40340600-40351200	Weak transcription	Gastric	stomach
28	chr13:40340600-40351200	Weak transcription	Right Ventricle	heart
29	chr13:40341000-40344200	Weak transcription	Liver	Liver
30	chr13:40341000-40346800	Weak transcription	Fetal Stomach	stomach
31	chr13:40341200-40342200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr13:40341200-40342800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
33	chr13:40341200-40343000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr13:40341200-40343200	Enhancers	HUES6 Cell Line	embryonic stem cell
35	chr13:40341400-40342400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
36	chr13:40341400-40342400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
37	chr13:40341400-40342400	Weak transcription	Fetal Lung	lung
38	chr13:40341400-40350600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr13:40341600-40342000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr13:40341600-40342200	Enhancers	Colon Smooth Muscle	Colon
41	chr13:40341800-40342200	Enhancers	Colonic Mucosa	Colon
42	chr13:40341800-40342400	Enhancers	HSMMtube	muscle
43	chr13:40341800-40342600	Enhancers	H1 Cell Line	embryonic stem cell
44	chr13:40341800-40342600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
45	chr13:40341800-40342600	Enhancers	Fetal Muscle Trunk	muscle
46	chr13:40341800-40342800	Enhancers	Primary B cells from peripheral blood	blood
47	chr13:40341800-40342800	Enhancers	Primary T helper cells fromperipheralblood	blood
48	chr13:40341800-40342800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
49	chr13:40341800-40342800	Enhancers	Esophagus	oesophagus
50	chr13:40341800-40342800	Enhancers	Psoas Muscle	Psoas

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