Variant report

Variant	rs6983915
Chromosome Location	chr8:120696556-120696557
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs16892902	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16892921	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16892932	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16892952	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7830283	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv868916	chr8:119911943-120762250	Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Enhancers Genic enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
2	nsv534028	chr8:120348940-120906079	Flanking Active TSS Strong transcription Weak transcription Active TSS Enhancers ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
3	nsv949368	chr8:120568034-121019872	Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
4	nsv1021071	chr8:120589963-120968317	Strong transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
5	nsv891418	chr8:120600965-121301474	Active TSS Flanking Active TSS Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
6	nsv465789	chr8:120636850-120994394	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS 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
7	nsv612111	chr8:120636850-120994394	Flanking Active TSS Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
8	nsv427826	chr8:120642181-120953395	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:120686000-120696800	Weak transcription	Aorta	Aorta
2	chr8:120687000-120697200	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr8:120688800-120697400	Weak transcription	Brain Substantia Nigra	brain
4	chr8:120690800-120696800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr8:120690800-120697400	Weak transcription	Brain Hippocampus Middle	brain
6	chr8:120690800-120700400	Weak transcription	Monocytes-CD14+_RO01746	blood
7	chr8:120693400-120697000	Enhancers	HMEC	breast
8	chr8:120693600-120697200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr8:120693600-120697400	Weak transcription	Right Atrium	heart
10	chr8:120694000-120697000	Enhancers	Breast Myoepithelial Primary Cells	Breast
11	chr8:120694600-120696800	Enhancers	NHEK	skin
12	chr8:120694600-120697200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr8:120695400-120697600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr8:120695400-120697600	Enhancers	NHDF-Ad	bronchial
15	chr8:120695800-120696600	Enhancers	Osteobl	bone
16	chr8:120695800-120697200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr8:120695800-120697800	Enhancers	Adipose Nuclei	Adipose
18	chr8:120695800-120699200	Enhancers	Fetal Lung	lung
19	chr8:120696000-120696600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr8:120696200-120700400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
21	chr8:120696400-120697600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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