Variant report

Variant	rs73141002
Chromosome Location	chr3:115979504-115979505
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 68 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:66)

rs_ID	r²[population]
rs10934323	0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10934324	0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10934326	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11719629	0.90[ASN][1000 genomes]
rs12494106	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12496133	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12634800	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12695324	0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13095238	0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1381068	0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1381069	0.81[ASN][1000 genomes]
rs1381070	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1431512	0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1461121	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1461125	0.94[ASN][1000 genomes]
rs1461126	0.94[ASN][1000 genomes]
rs1544994	0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1549831	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1549832	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16824649	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs16824686	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs16824693	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs16824696	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1870707	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1870708	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1870709	0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1993732	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2163505	0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2279109	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2306064	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2867101	0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2867102	0.80[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2903483	0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3195	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs34500521	0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4147304	0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4831090	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4831126	0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4831127	0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4831128	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4831129	0.81[ASN][1000 genomes]
rs61254748	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6438308	0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6438310	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6765043	0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6778040	0.94[ASN][1000 genomes]
rs6805045	0.94[ASN][1000 genomes]
rs73143006	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs73143010	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs73861405	0.82[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7426468	0.82[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7431707	0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7624352	0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7637684	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7642172	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7645796	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7653282	0.94[ASN][1000 genomes]
rs9826213	0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9828943	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9830749	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9835427	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9836892	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9850908	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9866532	0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9866706	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9875017	0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv877360	chr3:115916171-116023990	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
2	esv1808373	chr3:115952799-115984473	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:28 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:115962400-115983200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr3:115965800-115983200	Weak transcription	Fetal Brain Male	brain
3	chr3:115971200-115984800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr3:115973000-115983800	Weak transcription	Brain Hippocampus Middle	brain
5	chr3:115976000-115987000	Weak transcription	Brain Anterior Caudate	brain
6	chr3:115976200-115982800	Weak transcription	Fetal Lung	lung
7	chr3:115976200-115984000	Weak transcription	Brain Cingulate Gyrus	brain
8	chr3:115976200-115987000	Weak transcription	Brain Angular Gyrus	brain
9	chr3:115976800-115982600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr3:115977800-115979600	Enhancers	Colon Smooth Muscle	Colon
11	chr3:115977800-115980400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr3:115977800-115981600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
13	chr3:115977800-115981800	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
14	chr3:115978000-115982600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr3:115978200-115979800	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
16	chr3:115978400-115980400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr3:115978400-115983800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
18	chr3:115978600-115979600	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
19	chr3:115978600-115981400	Weak transcription	Rectal Smooth Muscle	rectum
20	chr3:115978600-115982000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
21	chr3:115979000-115979800	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
22	chr3:115979200-115979600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr3:115979400-115979600	Bivalent Enhancer	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr3:115979400-115979600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr3:115979400-115979600	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
26	chr3:115979400-115979800	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
27	chr3:115979400-115979800	Bivalent Enhancer	H9 Cell Line	embryonic stem cell
28	chr3:115979400-115980400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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