Variant report

Variant	rs17484810
Chromosome Location	chr8:119212095-119212096
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs11562666	1.00[AMR][1000 genomes]
rs11562691	1.00[AMR][1000 genomes]
rs11562692	1.00[AMR][1000 genomes]
rs11562712	1.00[AMR][1000 genomes]
rs11562713	1.00[AMR][1000 genomes]
rs11562714	1.00[AMR][1000 genomes]
rs11562745	1.00[AMR][1000 genomes]
rs11562746	1.00[AMR][1000 genomes]
rs11562803	1.00[AMR][1000 genomes]
rs11562804	1.00[AMR][1000 genomes]
rs17484670	1.00[AMR][1000 genomes]
rs17484677	1.00[AMR][1000 genomes]
rs17484698	1.00[AMR][1000 genomes]
rs17507089	1.00[AMR][1000 genomes]
rs17507096	1.00[AMR][1000 genomes]
rs17507138	1.00[AMR][1000 genomes]
rs17507180	1.00[AMR][1000 genomes]
rs17507187	1.00[AMR][1000 genomes]
rs17507278	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17507285	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4259442	1.00[AMR][1000 genomes]
rs4265214	1.00[AMR][1000 genomes]
rs6996485	1.00[AMR][1000 genomes]
rs7014868	1.00[AMR][1000 genomes]
rs7014943	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv612047	chr8:118939094-119468609	Flanking Active TSS Enhancers Genic enhancers Weak transcription Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv1015380	chr8:118948652-119418389	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
3	nsv539736	chr8:118948652-119418389	Flanking Active TSS Active TSS Weak transcription Genic enhancers Enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
4	nsv831441	chr8:119055370-119262970	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
5	nsv821660	chr8:119082062-119312183	Flanking Active TSS Enhancers Genic enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
6	nsv1032681	chr8:119153316-119609948	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
7	nsv539737	chr8:119153316-119609948	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
8	nsv1016379	chr8:119164234-119448910	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
9	nsv831442	chr8:119181675-119390122	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
10	esv1822901	chr8:119207029-119214396	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region miRNA target site	n/a	inside rSNPs	diseases

No data

Chromatin state (count:37 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:119200800-119218800	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr8:119203800-119215200	Weak transcription	Liver	Liver
3	chr8:119206200-119212200	Weak transcription	Duodenum Mucosa	Duodenum
4	chr8:119206400-119214400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr8:119206600-119214200	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr8:119208200-119213200	Weak transcription	Right Ventricle	heart
7	chr8:119208400-119213000	Weak transcription	Spleen	Spleen
8	chr8:119208400-119214600	Weak transcription	Lung	lung
9	chr8:119208400-119292400	Weak transcription	Pancreas	Pancrea
10	chr8:119208600-119213000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr8:119208600-119214600	Weak transcription	Left Ventricle	heart
12	chr8:119208600-119214600	Weak transcription	Right Atrium	heart
13	chr8:119208600-119217600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr8:119208800-119213400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr8:119209000-119214000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr8:119209200-119213200	Weak transcription	Primary monocytes fromperipheralblood	blood
17	chr8:119209200-119213200	Weak transcription	Monocytes-CD14+_RO01746	blood
18	chr8:119209200-119214000	Weak transcription	HSMMtube	muscle
19	chr8:119209200-119219000	Weak transcription	NHEK	skin
20	chr8:119209400-119213800	Weak transcription	HUVEC	blood vessel
21	chr8:119209600-119214400	Weak transcription	Ovary	ovary
22	chr8:119209600-119219000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr8:119209800-119214000	Weak transcription	NH-A	brain
24	chr8:119209800-119214600	Weak transcription	NHLF	lung
25	chr8:119210000-119213800	Weak transcription	NHDF-Ad	bronchial
26	chr8:119210000-119214400	Weak transcription	HSMM	muscle
27	chr8:119210200-119214400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr8:119210400-119214000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr8:119210400-119214000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr8:119210400-119214000	Weak transcription	Muscle Satellite Cultured Cells	--
31	chr8:119210400-119214000	Weak transcription	Adipose Nuclei	Adipose
32	chr8:119210400-119214000	Weak transcription	Osteobl	bone
33	chr8:119210400-119214200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr8:119210400-119216400	Weak transcription	Aorta	Aorta
35	chr8:119210600-119213800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr8:119211400-119212400	Weak transcription	Fetal Heart	heart
37	chr8:119211800-119221600	Weak transcription	H9 Cell Line	embryonic stem cell

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