Variant report

Variant	rs152606
Chromosome Location	chr5:106771847-106771848
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs115779	0.91[ASN][1000 genomes]
rs149444	0.95[CHB][hapmap];0.88[ASN][1000 genomes]
rs149498	0.96[CHB][hapmap];0.94[ASN][1000 genomes]
rs151956	0.89[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap];0.80[AMR][1000 genomes];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs151958	0.92[ASN][1000 genomes]
rs152582	0.87[ASN][1000 genomes]
rs152584	0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs152585	0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs152587	1.00[CEU][hapmap];0.95[CHB][hapmap];0.81[JPT][hapmap];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs152589	0.87[ASN][1000 genomes]
rs152590	0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs152591	1.00[CHB][hapmap];0.91[JPT][hapmap];0.94[ASN][1000 genomes]
rs152592	1.00[CHB][hapmap];0.91[JPT][hapmap];0.94[ASN][1000 genomes]
rs152593	0.96[CHB][hapmap];0.89[ASN][1000 genomes]
rs152595	0.95[CHB][hapmap];0.81[JPT][hapmap];0.89[ASN][1000 genomes]
rs152596	1.00[CHB][hapmap];0.90[JPT][hapmap];0.94[ASN][1000 genomes]
rs152597	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs152598	0.94[ASN][1000 genomes]
rs152599	1.00[CHB][hapmap];0.95[JPT][hapmap];0.95[ASN][1000 genomes]
rs152601	1.00[CHB][hapmap];0.95[JPT][hapmap];0.97[ASN][1000 genomes]
rs152602	0.88[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs152603	1.00[CEU][hapmap];0.96[CHB][hapmap];0.80[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs152605	1.00[ASN][1000 genomes]
rs152607	0.96[CHB][hapmap];0.86[JPT][hapmap];0.95[ASN][1000 genomes]
rs152608	1.00[CHB][hapmap];0.95[JPT][hapmap];1.00[ASN][1000 genomes]
rs152609	1.00[CHB][hapmap];0.95[JPT][hapmap];0.99[ASN][1000 genomes]
rs152611	1.00[CHB][hapmap];0.95[JPT][hapmap];0.99[ASN][1000 genomes]
rs152612	0.84[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs152613	1.00[CEU][hapmap];0.96[CHB][hapmap];0.86[JPT][hapmap];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs153686	0.95[ASN][1000 genomes]
rs154645	1.00[CEU][hapmap];0.92[CHB][hapmap];0.80[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs154646	1.00[CHB][hapmap];0.95[JPT][hapmap];0.98[ASN][1000 genomes]
rs154647	1.00[CEU][hapmap];0.96[CHB][hapmap];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs154648	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2283	0.88[CEU][hapmap];0.95[CHB][hapmap];0.85[JPT][hapmap];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs252991	1.00[CEU][hapmap];0.81[JPT][hapmap];0.82[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs27661	0.86[CEU][hapmap];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs3843490	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[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	nsv1030118	chr5:106006097-106847949	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription 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 target site	6 gene(s)	inside rSNPs	diseases
2	nsv1034276	chr5:106461538-106944163	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
3	nsv537851	chr5:106461538-106944163	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
4	esv34018	chr5:106720912-107110506	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:33 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:106756600-106772000	Weak transcription	Esophagus	oesophagus
2	chr5:106758600-106772000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr5:106758600-106785000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr5:106762200-106772200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr5:106763000-106772000	Weak transcription	Right Atrium	heart
6	chr5:106763200-106773600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr5:106763200-106773600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr5:106766200-106772000	Weak transcription	Brain Germinal Matrix	brain
9	chr5:106766400-106775200	Weak transcription	Aorta	Aorta
10	chr5:106768000-106772600	Enhancers	A549	lung
11	chr5:106768200-106772000	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr5:106768400-106772000	Weak transcription	Fetal Stomach	stomach
13	chr5:106768600-106772200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr5:106768600-106773600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr5:106768600-106774200	Weak transcription	NHEK	skin
16	chr5:106768600-106775000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr5:106768600-106778800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr5:106768600-106779000	Weak transcription	HSMM	muscle
19	chr5:106770800-106772600	Enhancers	Colon Smooth Muscle	Colon
20	chr5:106771000-106773200	Enhancers	Pancreatic Islets	Pancreatic Islet
21	chr5:106771000-106774200	Enhancers	Fetal Brain Female	brain
22	chr5:106771200-106772400	Enhancers	Right Ventricle	heart
23	chr5:106771200-106772600	Enhancers	Fetal Kidney	kidney
24	chr5:106771400-106773200	Enhancers	Fetal Lung	lung
25	chr5:106771400-106773600	Enhancers	Cortex derived primary cultured neurospheres	brain
26	chr5:106771600-106772000	Enhancers	Rectal Smooth Muscle	rectum
27	chr5:106771600-106774600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr5:106771800-106772000	Flanking Active TSS	Fetal Heart	heart
29	chr5:106771800-106772000	Flanking Active TSS	Sigmoid Colon	Sigmoid Colon
30	chr5:106771800-106772400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr5:106771800-106772600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr5:106771800-106772600	Enhancers	Left Ventricle	heart
33	chr5:106771800-106773200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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