Variant report

Variant	rs72937653
Chromosome Location	chr3:101522059-101522060
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr3:101520497..101522468-chr3:101943285..101944945,2	MCF-7	breast:
2	chr3:101520405..101523122-chr3:101567761..101569731,2	MCF-7	breast:
3	chr3:101521699..101522654-chr3:101944004..101944935,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000144802	Chromatin interaction

Extended variants
information (count: 56 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs16844264	1.00[AMR][1000 genomes]
rs56871732	1.00[AMR][1000 genomes]
rs57768297	1.00[AMR][1000 genomes]
rs58060577	1.00[AMR][1000 genomes]
rs59212280	1.00[AMR][1000 genomes]
rs59610252	1.00[AMR][1000 genomes]
rs59761426	1.00[AMR][1000 genomes]
rs59790563	1.00[AMR][1000 genomes]
rs60491518	1.00[AMR][1000 genomes]
rs61302621	1.00[AMR][1000 genomes]
rs61468230	1.00[AMR][1000 genomes]
rs72931705	1.00[AMR][1000 genomes]
rs72931709	1.00[AMR][1000 genomes]
rs72931710	1.00[AMR][1000 genomes]
rs72931711	1.00[AMR][1000 genomes]
rs72931715	1.00[AMR][1000 genomes]
rs72931719	1.00[AMR][1000 genomes]
rs72931774	1.00[AMR][1000 genomes]
rs72931789	1.00[AMR][1000 genomes]
rs72933808	1.00[AMR][1000 genomes]
rs72933810	1.00[AMR][1000 genomes]
rs72933821	1.00[AMR][1000 genomes]
rs72933838	1.00[AMR][1000 genomes]
rs72935816	1.00[AMR][1000 genomes]
rs72935835	1.00[AMR][1000 genomes]
rs72935839	1.00[AMR][1000 genomes]
rs72935846	1.00[AMR][1000 genomes]
rs72935852	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72935865	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72935871	1.00[AMR][1000 genomes]
rs72935875	1.00[AMR][1000 genomes]
rs72935894	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72937635	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72937638	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72937639	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72937642	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72937646	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72937664	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72937667	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72937684	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72937701	1.00[AMR][1000 genomes]
rs72937810	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72937817	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72939605	1.00[AMR][1000 genomes]
rs72939606	1.00[AMR][1000 genomes]
rs72947370	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72947385	1.00[AMR][1000 genomes]
rs72948050	1.00[AMR][1000 genomes]
rs72948052	1.00[AMR][1000 genomes]
rs72948055	1.00[AMR][1000 genomes]
rs72948056	1.00[AMR][1000 genomes]
rs72948070	1.00[AMR][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	nsv497784	chr3:101315009-102092989	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
2	nsv997407	chr3:101384031-101611391	Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	76 gene(s)	inside rSNPs	diseases
3	nsv536675	chr3:101384031-101611391	Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	76 gene(s)	inside rSNPs	diseases
4	esv3351469	chr3:101511702-101866448	Weak transcription Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:118 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:101498800-101533800	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr3:101498800-101546200	Weak transcription	Esophagus	oesophagus
3	chr3:101499000-101523000	Weak transcription	Stomach Mucosa	stomach
4	chr3:101499000-101533000	Weak transcription	Fetal Intestine Large	intestine
5	chr3:101499200-101529600	Weak transcription	Small Intestine	intestine
6	chr3:101499800-101524800	Weak transcription	HepG2	liver
7	chr3:101502600-101540200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr3:101502600-101540200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr3:101502800-101528200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr3:101503200-101522400	Weak transcription	Rectal Mucosa Donor 31	rectum
11	chr3:101504600-101524400	Weak transcription	Gastric	stomach
12	chr3:101504800-101533600	Weak transcription	Pancreas	Pancrea
13	chr3:101504800-101546000	Weak transcription	Colonic Mucosa	Colon
14	chr3:101505400-101533600	Weak transcription	Right Atrium	heart
15	chr3:101509800-101528200	Weak transcription	Fetal Intestine Small	intestine
16	chr3:101510000-101522400	Weak transcription	Sigmoid Colon	Sigmoid Colon
17	chr3:101510200-101522400	Weak transcription	Fetal Brain Male	brain
18	chr3:101510200-101525600	Weak transcription	Placenta	Placenta
19	chr3:101511000-101527200	Weak transcription	Skeletal Muscle Female	skeletal muscle
20	chr3:101511000-101536000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr3:101513000-101528000	Weak transcription	Pancreatic Islets	Pancreatic Islet
22	chr3:101515200-101522200	Weak transcription	Primary hematopoietic stem cells	blood
23	chr3:101515200-101522800	Weak transcription	NHDF-Ad	bronchial
24	chr3:101515200-101528200	Weak transcription	NH-A	brain
25	chr3:101515200-101540200	Weak transcription	NHLF	lung
26	chr3:101515400-101522800	Weak transcription	HUVEC	blood vessel
27	chr3:101515400-101523000	Weak transcription	Rectal Mucosa Donor 29	rectum
28	chr3:101515400-101527800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr3:101515400-101528600	Weak transcription	HMEC	breast
30	chr3:101515400-101535800	Weak transcription	NHEK	skin
31	chr3:101515400-101546000	Weak transcription	H9 Cell Line	embryonic stem cell
32	chr3:101515600-101522200	Weak transcription	Colon Smooth Muscle	Colon
33	chr3:101515600-101525800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr3:101516000-101546000	Weak transcription	Cortex derived primary cultured neurospheres	brain
35	chr3:101516200-101522400	Weak transcription	Muscle Satellite Cultured Cells	--
36	chr3:101516200-101527800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
37	chr3:101519000-101522200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
38	chr3:101519400-101522400	Strong transcription	Primary monocytes fromperipheralblood	blood
39	chr3:101519400-101523400	Strong transcription	Primary B cells from peripheral blood	blood
40	chr3:101519600-101522400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
41	chr3:101519600-101523200	Strong transcription	Fetal Thymus	thymus
42	chr3:101519800-101522800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
43	chr3:101519800-101522800	Strong transcription	Fetal Muscle Trunk	muscle
44	chr3:101519800-101522800	Strong transcription	Left Ventricle	heart
45	chr3:101519800-101523400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr3:101519800-101524200	Strong transcription	Dnd41	blood
47	chr3:101520000-101522800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr3:101520000-101523800	Strong transcription	Brain Substantia Nigra	brain
49	chr3:101520200-101522200	Strong transcription	HSMMtube	muscle
50	chr3:101520200-101523000	Strong transcription	HUES48 Cell Line	embryonic stem cell

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