Variant report

Variant	rs7162166
Chromosome Location	chr15:72988040-72988041
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs11072380	0.92[CHB][hapmap];0.85[ASN][1000 genomes]
rs11072383	0.92[CHB][hapmap];0.86[ASN][1000 genomes]
rs11856110	0.87[ASN][1000 genomes]
rs12437473	0.84[EUR][1000 genomes]
rs12439200	0.86[CHB][hapmap]
rs12591690	0.86[EUR][1000 genomes]
rs12591728	1.00[CEU][hapmap];0.93[CHB][hapmap];0.94[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12594320	0.84[CHB][hapmap]
rs12898814	1.00[CEU][hapmap];0.92[CHB][hapmap];0.94[JPT][hapmap];0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12902361	0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12906007	0.93[CHB][hapmap];0.88[ASN][1000 genomes]
rs12916448	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1346165	1.00[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs16957257	0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs16957297	1.00[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2162268	0.91[AMR][1000 genomes]
rs2304598	0.87[CHB][hapmap]
rs28397892	0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs28648660	0.84[EUR][1000 genomes]
rs28737436	0.84[EUR][1000 genomes]
rs28866048	0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs33923961	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs34940604	0.86[AMR][1000 genomes]
rs4777541	0.86[CHB][hapmap]
rs6495017	0.88[ASN][1000 genomes]
rs7170394	0.93[CHB][hapmap];0.86[ASN][1000 genomes]
rs7172397	0.93[CHB][hapmap];0.86[ASN][1000 genomes]
rs7175918	0.86[ASN][1000 genomes]
rs7182854	1.00[CEU][hapmap];0.86[CHB][hapmap];0.82[EUR][1000 genomes]
rs8023358	0.86[CHB][hapmap]
rs8026286	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs8026559	0.92[CHB][hapmap];0.87[ASN][1000 genomes]
rs8031691	1.00[CEU][hapmap];0.86[CHB][hapmap];0.84[EUR][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	esv2758386	chr15:72819785-73120560	Strong transcription ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
2	esv2760039	chr15:72819785-73120560	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
3	nsv428307	chr15:72819785-73120560	Strong transcription Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Enhancers Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
4	esv3430383	chr15:72821093-73035167	Strong transcription Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	35 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:36 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:72979200-73023600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr15:72979200-73023600	Weak transcription	Lung	lung
3	chr15:72979400-73002000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
4	chr15:72979400-73002000	Weak transcription	Primary T helper cells fromperipheralblood	blood
5	chr15:72979400-73004400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
6	chr15:72979400-73006000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
7	chr15:72979400-73027200	Weak transcription	Aorta	Aorta
8	chr15:72979600-72998800	Weak transcription	NH-A	brain
9	chr15:72979600-73002200	Weak transcription	Ovary	ovary
10	chr15:72979600-73004000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr15:72979600-73004200	Weak transcription	Skeletal Muscle Female	skeletal muscle
12	chr15:72979600-73004600	Weak transcription	Primary B cells from cord blood	blood
13	chr15:72979600-73004600	Weak transcription	Sigmoid Colon	Sigmoid Colon
14	chr15:72979600-73023200	Weak transcription	Fetal Kidney	kidney
15	chr15:72979600-73026800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr15:72979800-72989600	Weak transcription	Fetal Brain Female	brain
17	chr15:72979800-72998600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr15:72979800-73002000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
19	chr15:72979800-73004000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr15:72979800-73004400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr15:72979800-73007200	Weak transcription	Left Ventricle	heart
22	chr15:72979800-73027400	Weak transcription	Hela-S3	cervix
23	chr15:72980000-73002200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr15:72980000-73002200	Weak transcription	Fetal Stomach	stomach
25	chr15:72980000-73004000	Weak transcription	Fetal Muscle Leg	muscle
26	chr15:72980200-72988800	Weak transcription	A549	lung
27	chr15:72980200-72996200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr15:72980200-72998600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr15:72980200-73004200	Weak transcription	Liver	Liver
30	chr15:72980200-73008000	Weak transcription	Cortex derived primary cultured neurospheres	brain
31	chr15:72981000-73018600	Weak transcription	Pancreas	Pancrea
32	chr15:72985000-73003800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr15:72985200-73002000	Weak transcription	Fetal Lung	lung
34	chr15:72985200-73021000	Weak transcription	Fetal Intestine Small	intestine
35	chr15:72987400-72989600	Weak transcription	Primary T cells from cord blood	blood
36	chr15:72988000-72988200	Enhancers	Primary T helper naive cells from peripheral blood	blood

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