Variant report

Variant	rs4792637
Chromosome Location	chr17:15533509-15533510
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs1060903	0.92[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs1476728	0.91[CHB][hapmap]
rs16964250	0.81[CEU][hapmap]
rs3785634	1.00[CHB][hapmap]
rs3785642	0.94[CEU][hapmap]
rs4791634	0.89[AMR][1000 genomes]
rs4792636	0.94[ASN][1000 genomes]
rs4792644	0.91[CHB][hapmap]
rs62070411	0.84[AMR][1000 genomes]
rs8066692	1.00[CHB][hapmap]
rs9909900	0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv492304	chr17:15043353-15611753	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
2	nsv916652	chr17:15093600-15856310	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
3	nsv1055677	chr17:15294011-15561130	Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
4	nsv1059056	chr17:15294011-15856861	Strong transcription Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
5	nsv1058286	chr17:15315763-15561130	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
6	nsv543213	chr17:15315763-15561130	Weak transcription Enhancers Genic enhancers Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
7	nsv457695	chr17:15447364-15611495	Active TSS Enhancers Strong transcription Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
8	nsv574462	chr17:15447364-15611495	Active TSS Flanking Active TSS Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
9	nsv1067123	chr17:15482503-15557728	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	16 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	chr17:15515400-15536000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr17:15519600-15538400	Weak transcription	Skeletal Muscle Male	skeletal muscle
3	chr17:15523000-15533600	Weak transcription	Fetal Brain Female	brain
4	chr17:15523000-15544000	Weak transcription	Brain Angular Gyrus	brain
5	chr17:15523000-15544200	Weak transcription	NHDF-Ad	bronchial
6	chr17:15523000-15548600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr17:15523000-15548600	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr17:15523000-15548600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr17:15523000-15548800	Weak transcription	Brain Hippocampus Middle	brain
10	chr17:15523000-15548800	Weak transcription	Brain Substantia Nigra	brain
11	chr17:15523000-15548800	Weak transcription	Fetal Lung	lung
12	chr17:15523000-15551800	Weak transcription	Brain Inferior Temporal Lobe	brain
13	chr17:15524200-15548600	Weak transcription	Esophagus	oesophagus
14	chr17:15524400-15535400	Weak transcription	Aorta	Aorta
15	chr17:15525800-15534800	Weak transcription	NH-A	brain
16	chr17:15527200-15538600	Weak transcription	Cortex derived primary cultured neurospheres	brain
17	chr17:15528200-15544400	Weak transcription	Psoas Muscle	Psoas
18	chr17:15528400-15534400	Weak transcription	HUVEC	blood vessel
19	chr17:15528800-15534400	Strong transcription	A549	lung
20	chr17:15529000-15549200	Weak transcription	H9 Cell Line	embryonic stem cell
21	chr17:15529600-15553600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
22	chr17:15530000-15551800	Weak transcription	Right Ventricle	heart
23	chr17:15530000-15551800	Weak transcription	Small Intestine	intestine
24	chr17:15530200-15547400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr17:15530200-15548800	Weak transcription	Colon Smooth Muscle	Colon
26	chr17:15530200-15549000	Weak transcription	Brain Germinal Matrix	brain
27	chr17:15530200-15552000	Weak transcription	Rectal Mucosa Donor 31	rectum
28	chr17:15530200-15553800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
29	chr17:15530400-15548600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
30	chr17:15530400-15553200	Weak transcription	Spleen	Spleen
31	chr17:15530600-15535600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr17:15530600-15548800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
33	chr17:15531000-15535400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr17:15531400-15533600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr17:15531400-15533800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr17:15531400-15533800	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr17:15531400-15533800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr17:15531400-15535200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
39	chr17:15531400-15535400	Strong transcription	Adipose Nuclei	Adipose
40	chr17:15531400-15549200	Weak transcription	Brain Cingulate Gyrus	brain
41	chr17:15531600-15533800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr17:15531600-15533800	Strong transcription	Fetal Stomach	stomach
43	chr17:15531600-15534200	Weak transcription	Primary T cells fromperipheralblood	blood
44	chr17:15531600-15534200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
45	chr17:15531600-15534200	Weak transcription	Primary T helper cells fromperipheralblood	blood
46	chr17:15531600-15536400	Strong transcription	Fetal Muscle Trunk	muscle
47	chr17:15531600-15545400	Weak transcription	NHEK	skin
48	chr17:15531800-15536600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr17:15531800-15548600	Weak transcription	HUES6 Cell Line	embryonic stem cell
50	chr17:15531800-15553600	Weak transcription	Fetal Kidney	kidney

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