Variant report

Variant	rs1078001
Chromosome Location	chr15:59167865-59167866
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr15:59167284..59169096-chr15:59170311..59173301,2	K562	blood:
2	chr15:59162668..59165557-chr15:59167625..59170277,3	K562	blood:
3	chr15:59166234..59168603-chr15:59169493..59172522,3	MCF-7	breast:
4	chr15:59167194..59169096-chr15:59170311..59172735,2	K562	blood:

Extended variants
information (count: 59 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs10162821	0.92[ASN][1000 genomes]
rs10518991	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];1.00[MEX][hapmap];0.92[TSI][hapmap];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10518992	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];0.98[GIH][hapmap];0.95[JPT][hapmap];0.96[TSI][hapmap];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1092172	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11071400	0.82[CEU][hapmap];0.86[CHB][hapmap];0.90[CHD][hapmap];0.87[GIH][hapmap];0.95[JPT][hapmap];0.92[ASN][1000 genomes]
rs11071401	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11630160	1.00[CEU][hapmap];0.82[CHB][hapmap];0.95[CHD][hapmap];0.95[GIH][hapmap];0.95[JPT][hapmap];1.00[MEX][hapmap];0.96[TSI][hapmap];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11631540	0.90[CEU][hapmap]
rs11636723	1.00[CEU][hapmap];0.91[CHB][hapmap];0.95[JPT][hapmap];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11637077	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];0.98[GIH][hapmap];0.95[JPT][hapmap];0.96[TSI][hapmap];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11856640	1.00[CEU][hapmap];0.91[CHB][hapmap];0.91[JPT][hapmap]
rs11858989	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];1.00[MEX][hapmap];0.96[TSI][hapmap];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12148858	0.92[ASN][1000 genomes]
rs12438918	0.81[EUR][1000 genomes]
rs12438961	0.84[EUR][1000 genomes]
rs12440904	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12443436	0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12595482	0.95[CEU][hapmap];0.91[CHB][hapmap];1.00[CHD][hapmap];0.98[GIH][hapmap];0.95[JPT][hapmap];0.96[TSI][hapmap];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12708456	0.91[ASN][1000 genomes]
rs12910580	0.90[CEU][hapmap];0.84[GIH][hapmap];0.80[TSI][hapmap]
rs12914723	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12916751	0.87[ASN][1000 genomes]
rs1446240	0.85[CEU][hapmap]
rs17302038	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17302045	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];0.98[GIH][hapmap];0.95[JPT][hapmap];0.81[MKK][hapmap];0.96[TSI][hapmap];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs173214	1.00[CEU][hapmap];0.91[CHB][hapmap];0.85[CHD][hapmap];0.98[GIH][hapmap];0.91[JPT][hapmap];0.94[MEX][hapmap];0.96[TSI][hapmap];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2013117	0.94[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2270664	0.82[CEU][hapmap];0.86[CHB][hapmap];0.95[JPT][hapmap];0.93[ASN][1000 genomes]
rs2279719	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs28473013	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28529423	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28538484	0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs28641638	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];0.95[JPT][hapmap];1.00[MEX][hapmap];0.96[TSI][hapmap];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs28709922	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3145	0.82[CEU][hapmap];0.86[CHB][hapmap];0.92[CHD][hapmap];0.82[GIH][hapmap];0.95[JPT][hapmap];0.94[MEX][hapmap];0.93[ASN][1000 genomes]
rs35477914	0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs431414	0.94[CEU][hapmap];0.84[TSI][hapmap];0.88[EUR][1000 genomes]
rs4328375	0.90[CEU][hapmap]
rs4774315	0.90[CHD][hapmap];0.82[GIH][hapmap];0.95[JPT][hapmap];0.92[ASN][1000 genomes]
rs4775101	0.82[CEU][hapmap];0.86[CHB][hapmap];0.90[CHD][hapmap];0.81[GIH][hapmap];0.95[JPT][hapmap];0.94[MEX][hapmap];0.88[ASN][1000 genomes]
rs592407	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs604057	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs637918	0.85[EUR][1000 genomes]
rs677933	0.95[CEU][hapmap];0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs67851431	0.93[ASN][1000 genomes]
rs694918	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs71407077	0.93[ASN][1000 genomes]
rs7173317	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs8029301	0.85[CEU][hapmap]
rs8035628	0.90[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];1.00[MEX][hapmap];0.83[MKK][hapmap];0.96[TSI][hapmap];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs813219	0.88[EUR][1000 genomes]
rs813220	0.81[EUR][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	esv34110	chr15:58949991-59381634	Weak transcription Bivalent Enhancer Strong transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
2	esv1826703	chr15:59005922-59213678	Flanking Active TSS Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats 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	44 gene(s)	inside rSNPs	diseases
3	esv1798487	chr15:59027139-59213678	Strong transcription Weak transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
4	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
5	nsv1035640	chr15:59105360-59190930	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
6	nsv904270	chr15:59140329-59238415	Genic enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Enhancers ZNF genes & repeats Bivalent Enhancer 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	48 gene(s)	inside rSNPs	diseases
7	nsv94675	chr15:59164881-59174380	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region miRNA target site	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:112 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:59120000-59169000	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr15:59147200-59169000	Weak transcription	K562	blood
3	chr15:59147600-59174600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
4	chr15:59148000-59168600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr15:59148000-59169000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr15:59154600-59170200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
7	chr15:59157200-59168600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr15:59157400-59168800	Weak transcription	Brain Angular Gyrus	brain
9	chr15:59157400-59170400	Weak transcription	Aorta	Aorta
10	chr15:59157600-59169000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
11	chr15:59157600-59169400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
12	chr15:59157600-59169400	Weak transcription	Brain Germinal Matrix	brain
13	chr15:59157600-59170200	Weak transcription	Primary T helper cells PMA-I stimulated	--
14	chr15:59157600-59170200	Weak transcription	Primary T helper cells fromperipheralblood	blood
15	chr15:59157600-59170200	Weak transcription	Brain Cingulate Gyrus	brain
16	chr15:59157600-59170200	Weak transcription	Fetal Brain Female	brain
17	chr15:59157800-59169000	Weak transcription	HUES64 Cell Line	embryonic stem cell
18	chr15:59157800-59169400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr15:59157800-59169400	Weak transcription	Rectal Mucosa Donor 29	rectum
20	chr15:59157800-59170000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr15:59157800-59170200	Weak transcription	Primary B cells from peripheral blood	blood
22	chr15:59157800-59170200	Weak transcription	Primary T cells from cord blood	blood
23	chr15:59157800-59170400	Weak transcription	Primary B cells from cord blood	blood
24	chr15:59157800-59170400	Weak transcription	Primary hematopoietic stem cells	blood
25	chr15:59157800-59172600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
26	chr15:59158000-59168400	Weak transcription	Gastric	stomach
27	chr15:59158000-59168400	Weak transcription	Stomach Smooth Muscle	stomach
28	chr15:59158000-59168800	Weak transcription	Adipose Nuclei	Adipose
29	chr15:59158000-59169000	Weak transcription	HUES48 Cell Line	embryonic stem cell
30	chr15:59158000-59169000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
31	chr15:59158000-59169400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
32	chr15:59158000-59170000	Weak transcription	H9 Cell Line	embryonic stem cell
33	chr15:59158000-59170000	Weak transcription	Liver	Liver
34	chr15:59158000-59170000	Weak transcription	Skeletal Muscle Female	skeletal muscle
35	chr15:59158000-59170200	Weak transcription	Left Ventricle	heart
36	chr15:59158000-59170400	Weak transcription	Fetal Lung	lung
37	chr15:59158000-59170400	Weak transcription	Rectal Mucosa Donor 31	rectum
38	chr15:59158000-59170600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
39	chr15:59158000-59171800	Weak transcription	Right Ventricle	heart
40	chr15:59158200-59168200	Weak transcription	Fetal Muscle Trunk	muscle
41	chr15:59158200-59168200	Weak transcription	Fetal Thymus	thymus
42	chr15:59158200-59168400	Weak transcription	Duodenum Smooth Muscle	Duodenum
43	chr15:59158200-59168600	Weak transcription	Stomach Mucosa	stomach
44	chr15:59158200-59174600	Weak transcription	Pancreatic Islets	Pancreatic Islet
45	chr15:59158400-59169200	Weak transcription	H1 Cell Line	embryonic stem cell
46	chr15:59158600-59170000	Weak transcription	Ovary	ovary
47	chr15:59158800-59168600	Weak transcription	Primary neutrophils fromperipheralblood	blood
48	chr15:59159800-59168600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
49	chr15:59160000-59168200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr15:59160000-59169800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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