Variant report

Variant	rs9394515
Chromosome Location	chr6:38520259-38520260
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 67 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:64)

rs_ID	r²[population]
rs10947742	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs10947743	0.82[ASN][1000 genomes]
rs10947753	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs16890743	0.83[EUR][1000 genomes]
rs2748156	0.90[JPT][hapmap];0.83[ASN][1000 genomes]
rs4141854	1.00[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4631264	1.00[ASW][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.96[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.96[YRI][hapmap];0.96[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4711552	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4711553	0.84[GIH][hapmap];1.00[MEX][hapmap];0.93[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4711554	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4711555	1.00[EUR][1000 genomes]
rs4714166	0.83[EUR][1000 genomes]
rs4714171	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4714173	0.90[GIH][hapmap];1.00[MEX][hapmap];0.93[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4714174	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs58362455	0.83[EUR][1000 genomes]
rs58648636	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs59793635	0.83[EUR][1000 genomes]
rs6900106	0.86[ASN][1000 genomes]
rs6905545	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs6910904	0.86[CHB][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes]
rs6924443	0.90[JPT][hapmap]
rs6925790	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs6931745	0.83[EUR][1000 genomes]
rs6938737	1.00[CHB][hapmap];0.90[JPT][hapmap];0.86[ASN][1000 genomes]
rs724242	1.00[ASW][hapmap];0.93[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs7750482	0.90[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7750997	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7752972	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7753374	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7761154	0.89[JPT][hapmap]
rs7767791	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7775968	0.84[GIH][hapmap];0.93[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9296252	0.90[ASW][hapmap];0.93[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.89[LWK][hapmap];0.91[MKK][hapmap];0.84[YRI][hapmap];0.94[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs9296254	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9296255	0.84[GIH][hapmap];1.00[MEX][hapmap];0.90[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9349092	0.87[AMR][1000 genomes]
rs9349093	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9349094	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9357277	0.93[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs9366965	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9366969	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9369065	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9369069	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9369073	0.84[GIH][hapmap];1.00[MEX][hapmap];0.93[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9380757	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9380759	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9380760	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9380762	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9380763	0.83[EUR][1000 genomes]
rs9394513	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9394514	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9394516	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9394519	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9462439	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9462441	1.00[CHB][hapmap];0.90[JPT][hapmap];0.83[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9462442	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9462446	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9470901	0.88[CHD][hapmap];0.81[GIH][hapmap];0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9470902	0.85[CHB][hapmap];0.93[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9470906	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9470908	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9470913	0.83[EUR][1000 genomes]
rs9470916	0.83[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1021991	chr6:37893949-38738720	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	nsv885817	chr6:38036420-39019503	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
3	nsv534620	chr6:38049585-38602064	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:31 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:38494400-38524200	Weak transcription	Aorta	Aorta
2	chr6:38494800-38522600	Weak transcription	Ovary	ovary
3	chr6:38495000-38521800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
4	chr6:38496600-38539600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
5	chr6:38496800-38521600	Weak transcription	Lung	lung
6	chr6:38497000-38538800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
7	chr6:38497000-38539400	Weak transcription	Primary T cells fromperipheralblood	blood
8	chr6:38500800-38520800	Weak transcription	Fetal Intestine Small	intestine
9	chr6:38508200-38522200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr6:38510200-38522200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr6:38510400-38522600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr6:38510600-38546800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr6:38511600-38522800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr6:38513000-38522400	Weak transcription	Skeletal Muscle Male	skeletal muscle
15	chr6:38513000-38539200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
16	chr6:38514200-38539400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
17	chr6:38515600-38535800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
18	chr6:38516000-38538800	Weak transcription	Primary T helper cells PMA-I stimulated	--
19	chr6:38517800-38535000	Weak transcription	Brain Substantia Nigra	brain
20	chr6:38518000-38522200	Weak transcription	HSMMtube	muscle
21	chr6:38518400-38520600	Enhancers	Primary B cells from cord blood	blood
22	chr6:38518600-38521200	Enhancers	Primary B cells from peripheral blood	blood
23	chr6:38518800-38521200	Weak transcription	Right Atrium	heart
24	chr6:38519000-38520800	Enhancers	Primary monocytes fromperipheralblood	blood
25	chr6:38519200-38538800	Weak transcription	Primary T cells from cord blood	blood
26	chr6:38519200-38539400	Weak transcription	Left Ventricle	heart
27	chr6:38519400-38520600	Enhancers	Monocytes-CD14+_RO01746	blood
28	chr6:38519600-38520400	Enhancers	Primary neutrophils fromperipheralblood	blood
29	chr6:38519600-38554800	Weak transcription	Sigmoid Colon	Sigmoid Colon
30	chr6:38520200-38520400	Enhancers	GM12878-XiMat	blood
31	chr6:38520200-38521800	Weak transcription	Fetal Heart	heart

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