Variant report

Variant	rs7162228
Chromosome Location	chr15:59645075-59645076
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 65 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:59)

rs_ID	r²[population]
rs10851653	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs11071430	0.98[AMR][1000 genomes]
rs11071432	0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11071433	0.87[ASN][1000 genomes]
rs11630796	0.92[ASN][1000 genomes]
rs11631146	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs11631451	0.88[ASN][1000 genomes]
rs11632346	0.93[ASN][1000 genomes]
rs11635849	0.88[ASN][1000 genomes]
rs11637840	0.88[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11639217	0.92[ASN][1000 genomes]
rs11854356	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11854697	0.87[CEU][hapmap];0.84[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.98[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11855765	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11858264	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs11858313	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12050546	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12441388	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12442217	0.96[ASN][1000 genomes]
rs12593355	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12595769	0.98[AMR][1000 genomes]
rs12899138	0.88[ASN][1000 genomes]
rs12905793	0.90[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs12911676	0.97[ASN][1000 genomes]
rs1580426	0.96[ASN][1000 genomes]
rs16941369	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17236578	0.95[AMR][1000 genomes]
rs17236585	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17302351	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.80[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2170895	0.97[ASN][1000 genomes]
rs28363891	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs28380572	0.97[ASN][1000 genomes]
rs28572451	0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4774327	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4775158	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs59107240	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs61692274	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62012550	0.80[ASN][1000 genomes]
rs6494101	0.95[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs6494102	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6494105	1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs66595425	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs66991143	0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs67017396	0.98[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs67498027	0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs67552459	0.90[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs7168074	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7171696	1.00[CEU][hapmap];0.93[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs7173362	0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7178041	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs8024396	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8024879	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8024906	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8025242	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8025360	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8031423	0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs8039327	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs8041804	0.90[CHB][hapmap];0.94[JPT][hapmap];0.97[ASN][1000 genomes]
rs965929	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv527307	chr15:59103328-60018487	Enhancers Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	145 gene(s)	inside rSNPs	diseases
2	nsv934082	chr15:59608605-59733211	Flanking Active TSS Enhancers Active TSS Weak transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
3	nsv457175	chr15:59609753-59681214	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
4	nsv569603	chr15:59609753-59681214	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
5	nsv471246	chr15:59610743-59681214	Enhancers Flanking Active TSS Active TSS Weak transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
6	nsv904274	chr15:59623576-59689378	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:88 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:59623200-59662800	Weak transcription	Stomach Smooth Muscle	stomach
2	chr15:59624600-59650000	Weak transcription	Rectal Mucosa Donor 29	rectum
3	chr15:59634800-59662600	Weak transcription	Colonic Mucosa	Colon
4	chr15:59636400-59652800	Weak transcription	HepG2	liver
5	chr15:59637800-59645200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr15:59637800-59662000	Weak transcription	Right Ventricle	heart
7	chr15:59638600-59653000	Weak transcription	Esophagus	oesophagus
8	chr15:59638600-59654600	Weak transcription	Liver	Liver
9	chr15:59640200-59648000	Enhancers	Primary hematopoietic stem cells short term culture	blood
10	chr15:59641400-59645600	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr15:59641400-59646000	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr15:59641400-59646400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr15:59641400-59649000	Enhancers	Primary B cells from peripheral blood	blood
14	chr15:59641600-59645400	Enhancers	Adipose Nuclei	Adipose
15	chr15:59641600-59645600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr15:59641600-59646000	Enhancers	H1 Cell Line	embryonic stem cell
17	chr15:59641800-59645200	Enhancers	Brain Hippocampus Middle	brain
18	chr15:59641800-59645200	Enhancers	Brain Substantia Nigra	brain
19	chr15:59641800-59645200	Enhancers	Monocytes-CD14+_RO01746	blood
20	chr15:59641800-59645400	Enhancers	Skeletal Muscle Male	skeletal muscle
21	chr15:59641800-59645800	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr15:59641800-59646000	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr15:59641800-59646000	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr15:59641800-59646000	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr15:59642200-59645400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr15:59642600-59659400	Weak transcription	Ovary	ovary
27	chr15:59642800-59646400	Weak transcription	Aorta	Aorta
28	chr15:59642800-59646600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr15:59642800-59651600	Weak transcription	Pancreas	Pancrea
30	chr15:59642800-59653200	Weak transcription	Rectal Smooth Muscle	rectum
31	chr15:59642800-59658600	Weak transcription	Rectal Mucosa Donor 31	rectum
32	chr15:59643000-59645200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr15:59643000-59645200	Enhancers	Muscle Satellite Cultured Cells	--
34	chr15:59643000-59646200	Weak transcription	Duodenum Smooth Muscle	Duodenum
35	chr15:59643000-59653000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr15:59643000-59653000	Weak transcription	HSMMtube	muscle
37	chr15:59643000-59653200	Weak transcription	NHLF	lung
38	chr15:59643000-59656200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr15:59643000-59659400	Weak transcription	Fetal Intestine Small	intestine
40	chr15:59643200-59645400	Genic enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr15:59643200-59646200	Weak transcription	NH-A	brain
42	chr15:59643200-59648000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr15:59643200-59650000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr15:59643200-59650000	Weak transcription	HSMM	muscle
45	chr15:59643400-59645400	Enhancers	H9 Cell Line	embryonic stem cell
46	chr15:59643400-59646400	Weak transcription	Fetal Muscle Trunk	muscle
47	chr15:59643600-59645200	Enhancers	Fetal Heart	heart
48	chr15:59643600-59645200	Enhancers	Psoas Muscle	Psoas
49	chr15:59643600-59645400	Genic enhancers	A549	lung
50	chr15:59643600-59648000	Enhancers	Primary B cells from cord blood	blood

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