Variant report

Variant	rs7636826
Chromosome Location	chr3:23638308-23638309
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 82 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:78)

rs_ID	r²[population]
rs11129119	0.81[ASN][1000 genomes]
rs11708160	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11715841	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11718082	0.91[ASN][1000 genomes]
rs11916411	0.84[ASN][1000 genomes]
rs11918529	0.91[ASN][1000 genomes]
rs13064035	0.82[ASN][1000 genomes]
rs1498809	0.82[ASN][1000 genomes]
rs1498811	0.82[ASN][1000 genomes]
rs1692612	0.82[ASN][1000 genomes]
rs1692620	0.82[ASN][1000 genomes]
rs1692650	0.85[ASN][1000 genomes]
rs1695200	0.88[ASN][1000 genomes]
rs17194786	0.84[ASN][1000 genomes]
rs2036226	0.86[ASN][1000 genomes]
rs2055310	0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2133331	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2173460	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3104244	0.89[ASN][1000 genomes]
rs3111311	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs34080387	0.82[ASN][1000 genomes]
rs3817002	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4383458	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4456808	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4484143	0.81[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4513393	0.91[ASN][1000 genomes]
rs4635650	0.93[ASN][1000 genomes]
rs4858518	0.80[ASN][1000 genomes]
rs57137870	0.99[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs58748418	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs60430884	0.82[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs62256993	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs62256994	0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6550766	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6550767	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6763329	0.86[ASN][1000 genomes]
rs6763535	0.86[ASN][1000 genomes]
rs6767599	0.81[ASN][1000 genomes]
rs6770079	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6775232	0.82[ASN][1000 genomes]
rs6776424	0.84[ASN][1000 genomes]
rs6780723	0.82[ASN][1000 genomes]
rs6780787	0.82[ASN][1000 genomes]
rs6788167	0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6795470	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6797907	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6798153	0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6798328	0.80[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6808513	0.87[ASN][1000 genomes]
rs6810100	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs704533	0.86[ASN][1000 genomes]
rs73043614	0.86[ASN][1000 genomes]
rs7612666	0.82[ASN][1000 genomes]
rs7613091	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7614146	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7634117	0.89[ASN][1000 genomes]
rs7640308	0.91[ASN][1000 genomes]
rs7644666	0.91[ASN][1000 genomes]
rs7645209	0.81[ASN][1000 genomes]
rs7648443	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7651893	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs778475	0.82[ASN][1000 genomes]
rs778480	0.84[ASN][1000 genomes]
rs778482	0.80[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs778496	0.81[ASN][1000 genomes]
rs778499	0.87[ASN][1000 genomes]
rs778500	0.88[ASN][1000 genomes]
rs778501	0.82[ASN][1000 genomes]
rs778503	0.80[ASN][1000 genomes]
rs778510	0.82[ASN][1000 genomes]
rs778514	0.82[ASN][1000 genomes]
rs778523	0.83[ASN][1000 genomes]
rs778526	0.82[ASN][1000 genomes]
rs9815921	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9824359	0.89[ASN][1000 genomes]
rs9830388	0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9830742	0.82[ASN][1000 genomes]
rs9856169	0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1007373	chr3:23367952-23710331	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Genic enhancers Strong transcription Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
2	nsv533980	chr3:23445901-24311972	ZNF genes & repeats Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
3	nsv460479	chr3:23626919-23807550	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	nsv589949	chr3:23626919-23807550	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:51 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:23606000-23643000	Weak transcription	Primary T cells from cord blood	blood
2	chr3:23607000-23640400	Weak transcription	Brain Substantia Nigra	brain
3	chr3:23621000-23642800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr3:23624400-23641600	Weak transcription	Stomach Smooth Muscle	stomach
5	chr3:23628800-23647200	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr3:23629800-23640800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr3:23630600-23641000	Weak transcription	Skeletal Muscle Male	skeletal muscle
8	chr3:23631400-23643200	Weak transcription	Left Ventricle	heart
9	chr3:23632600-23640600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr3:23632600-23642400	Weak transcription	Brain Angular Gyrus	brain
11	chr3:23632800-23643200	Weak transcription	Right Ventricle	heart
12	chr3:23632800-23647200	Weak transcription	Brain Cingulate Gyrus	brain
13	chr3:23634600-23641600	Weak transcription	Fetal Muscle Trunk	muscle
14	chr3:23635000-23640600	Weak transcription	Primary hematopoietic stem cells	blood
15	chr3:23635400-23642000	Weak transcription	Monocytes-CD14+_RO01746	blood
16	chr3:23635600-23638800	Strong transcription	Primary B cells from cord blood	blood
17	chr3:23635800-23641400	Weak transcription	Psoas Muscle	Psoas
18	chr3:23636600-23641400	Weak transcription	HUES48 Cell Line	embryonic stem cell
19	chr3:23636800-23641600	Weak transcription	NHLF	lung
20	chr3:23637000-23641000	Weak transcription	Muscle Satellite Cultured Cells	--
21	chr3:23637000-23641600	Weak transcription	NHDF-Ad	bronchial
22	chr3:23637800-23638400	Strong transcription	H9 Cell Line	embryonic stem cell
23	chr3:23637800-23638400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr3:23637800-23638400	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr3:23637800-23638400	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr3:23637800-23638400	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr3:23637800-23638400	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr3:23637800-23638400	ZNF genes & repeats	Adipose Nuclei	Adipose
29	chr3:23637800-23638400	Strong transcription	Aorta	Aorta
30	chr3:23637800-23638400	ZNF genes & repeats	Esophagus	oesophagus
31	chr3:23637800-23638400	ZNF genes & repeats	Ovary	ovary
32	chr3:23637800-23638400	ZNF genes & repeats	HSMM	muscle
33	chr3:23637800-23638600	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
34	chr3:23637800-23638600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr3:23637800-23638600	ZNF genes & repeats	Liver	Liver
36	chr3:23637800-23638600	ZNF genes & repeats	Fetal Stomach	stomach
37	chr3:23637800-23638600	ZNF genes & repeats	HSMMtube	muscle
38	chr3:23637800-23642400	Weak transcription	Fetal Kidney	kidney
39	chr3:23637800-23642600	Weak transcription	Fetal Heart	heart
40	chr3:23638000-23638400	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
41	chr3:23638000-23638400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
42	chr3:23638000-23638400	ZNF genes & repeats	Fetal Lung	lung
43	chr3:23638000-23638600	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr3:23638200-23638400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr3:23638200-23638400	ZNF genes & repeats	A549	lung
46	chr3:23638200-23638600	Weak transcription	Primary B cells from peripheral blood	blood
47	chr3:23638200-23638800	Weak transcription	Duodenum Smooth Muscle	Duodenum
48	chr3:23638200-23640000	Weak transcription	GM12878-XiMat	blood
49	chr3:23638200-23640800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
50	chr3:23638200-23642200	Weak transcription	HUES6 Cell Line	embryonic stem cell

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