Variant report

Variant	rs13160021
Chromosome Location	chr5:112935515-112935516
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 78 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:71)

rs_ID	r²[population]
rs10037429	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10072577	0.91[ASN][1000 genomes]
rs1035409	0.82[ASN][1000 genomes]
rs11739848	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11744710	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11744737	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11745445	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11746529	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11746565	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11747062	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11953034	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs13153791	1.00[AFR][1000 genomes];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs13161610	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs13161969	0.91[CEU][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs13166822	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs13167659	0.91[ASN][1000 genomes]
rs13170908	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13171273	1.00[AFR][1000 genomes];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs13171389	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs13172774	1.00[CHB][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13180262	0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs13187776	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs164252	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17332053	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17333442	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs182988	0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs255857	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs26965	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs26980	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs26982	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs26984	0.85[CEU][hapmap];1.00[JPT][hapmap]
rs26989	0.84[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs26990	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2860483	0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs2910017	0.87[AFR][1000 genomes];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2914151	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2914152	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs34158516	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs34554590	0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs34870059	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs348919	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs348921	0.87[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs348922	0.87[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs348923	0.87[AFR][1000 genomes]
rs348934	1.00[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs348935	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs348939	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs35077609	1.00[AFR][1000 genomes];0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs35274088	0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs35364742	1.00[AFR][1000 genomes];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs36611	0.86[CEU][hapmap];1.00[JPT][hapmap]
rs36613	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs3763141	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs414475	0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes]
rs419483	0.87[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs421515	1.00[AFR][1000 genomes]
rs4410636	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs446272	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs458055	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes]
rs4705554	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4705829	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs58479323	0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6594727	1.00[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs66838021	0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs67382821	0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs67881502	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs68131815	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs71577453	0.87[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs7703186	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7705255	0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7736165	0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv882721	chr5:112859994-112963488	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA target site	1 gene(s)	inside rSNPs	diseases
2	nsv1033202	chr5:112891857-112945992	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region miRNA target site	1 gene(s)	inside rSNPs	diseases
3	nsv520674	chr5:112911165-112942820	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region miRNA target site	1 gene(s)	inside rSNPs	diseases
4	esv2752057	chr5:112916398-112945992	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region miRNA target site	1 gene(s)	inside rSNPs	diseases
5	nsv1029507	chr5:112916398-112945992	Strong transcription Weak transcription Genic enhancers Enhancers Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region miRNA target site	1 gene(s)	inside rSNPs	diseases
6	esv2763910	chr5:112916398-112951827	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region miRNA target site	1 gene(s)	inside rSNPs	diseases
7	nsv1031336	chr5:112916398-112956588	Weak transcription Strong transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:49 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:112910600-112936600	Weak transcription	Colonic Mucosa	Colon
2	chr5:112910600-112942000	Weak transcription	Brain Substantia Nigra	brain
3	chr5:112910800-112937400	Weak transcription	Fetal Intestine Small	intestine
4	chr5:112910800-112938200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr5:112910800-112942200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr5:112916800-112936000	Weak transcription	Fetal Heart	heart
7	chr5:112917200-112942000	Weak transcription	K562	blood
8	chr5:112917400-112937600	Weak transcription	HSMMtube	muscle
9	chr5:112918000-112939000	Weak transcription	NHEK	skin
10	chr5:112920400-112939000	Weak transcription	HMEC	breast
11	chr5:112920600-112936000	Weak transcription	Brain Anterior Caudate	brain
12	chr5:112920800-112938600	Weak transcription	Sigmoid Colon	Sigmoid Colon
13	chr5:112920800-112942000	Weak transcription	Ovary	ovary
14	chr5:112927000-112936600	Weak transcription	Fetal Muscle Leg	muscle
15	chr5:112927200-112941800	Weak transcription	HUVEC	blood vessel
16	chr5:112927800-112939200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
17	chr5:112928200-112936600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
18	chr5:112928800-112937800	Weak transcription	Osteobl	bone
19	chr5:112929200-112941400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
20	chr5:112929800-112936000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
21	chr5:112929800-112942000	Weak transcription	NH-A	brain
22	chr5:112929800-112943800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr5:112930000-112937600	Weak transcription	Primary B cells from cord blood	blood
24	chr5:112930000-112941800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
25	chr5:112930000-112941800	Weak transcription	HUES64 Cell Line	embryonic stem cell
26	chr5:112930000-112942000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr5:112930000-112942200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
28	chr5:112930000-112943800	Weak transcription	Muscle Satellite Cultured Cells	--
29	chr5:112930000-112944000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr5:112930200-112942000	Weak transcription	Left Ventricle	heart
31	chr5:112930200-112944000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr5:112930400-112942000	Weak transcription	A549	lung
33	chr5:112930800-112937200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
34	chr5:112930800-112942200	Weak transcription	Brain Hippocampus Middle	brain
35	chr5:112931400-112943600	Weak transcription	NHDF-Ad	bronchial
36	chr5:112931800-112936600	Weak transcription	Liver	Liver
37	chr5:112931800-112941800	Weak transcription	Placenta	Placenta
38	chr5:112931800-112943600	Weak transcription	Dnd41	blood
39	chr5:112932000-112939800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
40	chr5:112932400-112937200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr5:112932600-112936200	Weak transcription	Fetal Lung	lung
42	chr5:112932600-112942200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr5:112933000-112937600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
44	chr5:112933600-112941800	Weak transcription	HUES6 Cell Line	embryonic stem cell
45	chr5:112933600-112942000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr5:112933800-112936600	Weak transcription	Rectal Mucosa Donor 31	rectum
47	chr5:112933800-112940000	Weak transcription	HSMM	muscle
48	chr5:112933800-112943800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr5:112934000-112938600	Weak transcription	Brain Angular Gyrus	brain

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