Variant report

Variant	rs7017817
Chromosome Location	chr8:119062596-119062597
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs10087091	0.85[CHB][hapmap];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11562686	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11562698	0.85[CHB][hapmap];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11562758	0.86[CHB][hapmap];1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11562761	0.85[CHB][hapmap];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17476728	0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17480096	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.85[ASN][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	nsv1030459	chr8:118840179-119155835	Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	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
3	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
4	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
5	nsv1025002	chr8:118970940-119069418	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	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
7	esv2752195	chr8:119058819-119139819	Weak transcription Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:79 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:119048600-119063800	Weak transcription	HSMMtube	muscle
2	chr8:119055200-119065400	Weak transcription	HepG2	liver
3	chr8:119056000-119066200	Weak transcription	Right Ventricle	heart
4	chr8:119057000-119062800	Enhancers	Fetal Lung	lung
5	chr8:119057000-119068400	Weak transcription	Hela-S3	cervix
6	chr8:119057800-119065800	Weak transcription	Fetal Intestine Small	intestine
7	chr8:119057800-119065800	Weak transcription	Rectal Mucosa Donor 31	rectum
8	chr8:119058600-119062800	Enhancers	NH-A	brain
9	chr8:119058600-119062800	Enhancers	NHLF	lung
10	chr8:119058800-119064600	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr8:119058800-119065000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr8:119058800-119065000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr8:119059600-119062800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr8:119059600-119065000	Weak transcription	Spleen	Spleen
15	chr8:119060000-119062800	Enhancers	Liver	Liver
16	chr8:119060000-119062800	Enhancers	NHDF-Ad	bronchial
17	chr8:119060200-119064800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr8:119060400-119062800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr8:119060400-119062800	Enhancers	A549	lung
20	chr8:119060400-119063000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr8:119060600-119062800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr8:119060600-119063800	Weak transcription	HSMM	muscle
23	chr8:119060600-119064800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
24	chr8:119061000-119062600	Enhancers	Brain Angular Gyrus	brain
25	chr8:119061000-119066000	Weak transcription	Duodenum Mucosa	Duodenum
26	chr8:119061200-119066000	Weak transcription	Small Intestine	intestine
27	chr8:119061400-119062800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr8:119061400-119062800	Enhancers	Fetal Stomach	stomach
29	chr8:119061600-119062600	Genic enhancers	NHEK	skin
30	chr8:119061600-119062800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr8:119061600-119062800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr8:119061600-119062800	Enhancers	Aorta	Aorta
33	chr8:119061600-119063200	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr8:119061600-119063400	Enhancers	HUES6 Cell Line	embryonic stem cell
35	chr8:119061600-119065800	Weak transcription	Pancreatic Islets	Pancreatic Islet
36	chr8:119061800-119062600	Enhancers	H1 Cell Line	embryonic stem cell
37	chr8:119061800-119062600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr8:119061800-119062600	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
39	chr8:119061800-119062800	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr8:119061800-119062800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
41	chr8:119061800-119064000	Weak transcription	Muscle Satellite Cultured Cells	--
42	chr8:119061800-119064200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr8:119061800-119065000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr8:119062000-119062600	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr8:119062000-119062800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr8:119062000-119062800	Enhancers	Brain Cingulate Gyrus	brain
47	chr8:119062000-119064400	Genic enhancers	Osteobl	bone
48	chr8:119062000-119066400	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr8:119062000-119067400	Weak transcription	Rectal Mucosa Donor 29	rectum
50	chr8:119062000-119072800	Weak transcription	Duodenum Smooth Muscle	Duodenum

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links