Variant report

Variant	rs977795
Chromosome Location	chr8:98996027-98996028
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr8:98994950..98998234-chr8:99001793..99004607,3	K562	blood:
2	chr8:98983972..98985766-chr8:98995097..98997700,2	MCF-7	breast:
3	chr8:98994617..98996981-chr8:99019389..99021453,2	MCF-7	breast:
4	chr8:98992573..98995424-chr8:98996000..98998679,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000132561	Chromatin interaction

Extended variants
information (count: 10 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs12546715	0.80[EUR][1000 genomes]
rs13268771	0.80[EUR][1000 genomes]
rs4735517	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[CHD][hapmap];0.90[GIH][hapmap];1.00[JPT][hapmap];0.88[MEX][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57279022	0.80[EUR][1000 genomes]
rs6987225	0.85[CEU][hapmap]
rs7835120	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.89[MEX][hapmap];0.92[MKK][hapmap];1.00[TSI][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7835897	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1032904	chr8:98756076-99476925	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
2	nsv539687	chr8:98756076-99476925	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
3	nsv528695	chr8:98960813-99022009	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:44 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:98976200-98996200	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr8:98986000-98997400	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr8:98987400-98998400	Weak transcription	Pancreas	Pancrea
4	chr8:98988000-99011800	Weak transcription	Aorta	Aorta
5	chr8:98989200-98997200	Weak transcription	Liver	Liver
6	chr8:98990600-98997200	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr8:98990800-98997000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
8	chr8:98991000-98997800	Enhancers	Osteobl	bone
9	chr8:98992200-98996400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr8:98992200-98998200	Enhancers	NHLF	lung
11	chr8:98992600-99019400	Weak transcription	Rectal Mucosa Donor 31	rectum
12	chr8:98992800-98996400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr8:98992800-98996600	Weak transcription	NHEK	skin
14	chr8:98994200-98996200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr8:98994200-99014800	Weak transcription	Duodenum Mucosa	Duodenum
16	chr8:98994400-98997200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr8:98994400-99003200	Weak transcription	Brain Substantia Nigra	brain
18	chr8:98994600-98996400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr8:98994600-98997400	Weak transcription	Cortex derived primary cultured neurospheres	brain
20	chr8:98994600-98997400	Weak transcription	Brain Hippocampus Middle	brain
21	chr8:98994600-98998000	Weak transcription	Brain Inferior Temporal Lobe	brain
22	chr8:98994600-99008200	Weak transcription	Fetal Muscle Trunk	muscle
23	chr8:98994600-99008400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
24	chr8:98994600-99014200	Weak transcription	Ovary	ovary
25	chr8:98995200-98996200	Weak transcription	HUES64 Cell Line	embryonic stem cell
26	chr8:98995200-98998200	Enhancers	NHDF-Ad	bronchial
27	chr8:98995200-99008000	Weak transcription	Fetal Stomach	stomach
28	chr8:98995400-98996400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
29	chr8:98995600-98996200	Enhancers	NH-A	brain
30	chr8:98995600-98997200	Enhancers	HSMMtube	muscle
31	chr8:98995600-98997600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr8:98995600-98997600	Enhancers	HSMM	muscle
33	chr8:98995800-98996400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr8:98995800-98996800	Enhancers	Skeletal Muscle Female	skeletal muscle
35	chr8:98995800-98997000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
36	chr8:98995800-98997400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr8:98995800-98997800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr8:98995800-98997800	Enhancers	A549	lung
39	chr8:98995800-99003400	Weak transcription	Fetal Muscle Leg	muscle
40	chr8:98996000-98996400	Enhancers	Psoas Muscle	Psoas
41	chr8:98996000-98996600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr8:98996000-98997000	Enhancers	HMEC	breast
43	chr8:98996000-98997600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr8:98996000-98998200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

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