Variant report

Variant	rs7865753
Chromosome Location	chr9:97857113-97857114
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:97687308..97690068-chr9:97855270..97858001,3	MCF-7	breast:
2	chr9:97812899..97815881-chr9:97854427..97857279,2	MCF-7	breast:
3	chr9:97682387..97688736-chr9:97850073..97858737,16	MCF-7	breast:
4	chr9:97855830..97857854-chr9:97891574..97893753,2	MCF-7	breast:
5	chr9:97488631..97490154-chr9:97855041..97857989,2	MCF-7	breast:
6	chr9:97676581..97686973-chr9:97850461..97860722,21	MCF-7	breast:
7	chr9:97765900..97771029-chr9:97855530..97860219,8	MCF-7	breast:
8	chr9:97848613..97851879-chr9:97854740..97857228,3	K562	blood:
9	chr9:97851403..97855354-chr9:97856847..97861126,5	K562	blood:
10	chr9:97389746..97395320-chr9:97854192..97858136,7	MCF-7	breast:
11	chr9:97564303..97567097-chr9:97855435..97857190,2	MCF-7	breast:
12	chr9:97763635..97773461-chr9:97847821..97861280,36	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000148120	Chromatin interaction

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs1045276	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10491560	0.86[AFR][1000 genomes];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10761375	0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10761376	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10821446	0.84[AFR][1000 genomes];0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10821450	0.88[AFR][1000 genomes];0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs356675	0.81[EUR][1000 genomes]
rs437511	0.82[EUR][1000 genomes]
rs526189	0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs540412	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs565293	0.81[EUR][1000 genomes]
rs609324	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs657637	0.82[EUR][1000 genomes]
rs7023722	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7033633	0.85[AFR][1000 genomes];0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7034586	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7863582	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs944934	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv933919	chr9:97619512-97919344	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	293 gene(s)	inside rSNPs	diseases
2	nsv1038106	chr9:97793038-97881416	Weak transcription Strong transcription Bivalent/Poised TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	274 gene(s)	inside rSNPs	diseases
3	nsv1038523	chr9:97797032-97923774	Strong transcription Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	274 gene(s)	inside rSNPs	diseases
4	nsv540175	chr9:97797032-97923774	Weak transcription Flanking Bivalent TSS/Enh Enhancers Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	274 gene(s)	inside rSNPs	diseases
5	nsv831656	chr9:97831551-97989980	Weak transcription Strong transcription Active TSS Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	274 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:104 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:97813000-97873000	Weak transcription	K562	blood
2	chr9:97820600-97875000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
3	chr9:97838000-97871200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
4	chr9:97841200-97864400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr9:97844000-97898400	Weak transcription	Primary T helper cells fromperipheralblood	blood
6	chr9:97846000-97861600	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr9:97846200-97880000	Weak transcription	Primary B cells from cord blood	blood
8	chr9:97847600-97878400	Weak transcription	Dnd41	blood
9	chr9:97849000-97858400	Enhancers	Brain Cingulate Gyrus	brain
10	chr9:97849200-97859200	Weak transcription	Fetal Brain Female	brain
11	chr9:97849200-97863800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
12	chr9:97849800-97864600	Enhancers	Psoas Muscle	Psoas
13	chr9:97850000-97858200	Enhancers	Brain Inferior Temporal Lobe	brain
14	chr9:97850000-97862000	Weak transcription	Hela-S3	cervix
15	chr9:97850800-97857400	Enhancers	Fetal Thymus	thymus
16	chr9:97851000-97857600	Enhancers	Brain Angular Gyrus	brain
17	chr9:97851800-97858000	Enhancers	Brain Substantia Nigra	brain
18	chr9:97851800-97858600	Enhancers	Brain Hippocampus Middle	brain
19	chr9:97852000-97858000	Enhancers	Brain Anterior Caudate	brain
20	chr9:97852000-97858200	Enhancers	Right Atrium	heart
21	chr9:97852200-97857600	Enhancers	Adipose Nuclei	Adipose
22	chr9:97852600-97857600	Enhancers	Fetal Muscle Trunk	muscle
23	chr9:97852800-97858000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr9:97853200-97858000	Enhancers	Skeletal Muscle Female	skeletal muscle
25	chr9:97853800-97860400	Weak transcription	Liver	Liver
26	chr9:97854000-97857200	Enhancers	HSMMtube	muscle
27	chr9:97854200-97862200	Weak transcription	Aorta	Aorta
28	chr9:97854200-97862200	Weak transcription	HepG2	liver
29	chr9:97854200-97862400	Weak transcription	Primary hematopoietic stem cells	blood
30	chr9:97854800-97860200	Genic enhancers	Stomach Smooth Muscle	stomach
31	chr9:97855000-97857800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
32	chr9:97855000-97867800	Weak transcription	Primary T cells fromperipheralblood	blood
33	chr9:97855200-97857200	Weak transcription	Lung	lung
34	chr9:97855200-97859600	Weak transcription	Brain Germinal Matrix	brain
35	chr9:97855200-97876800	Weak transcription	GM12878-XiMat	blood
36	chr9:97855400-97857200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr9:97855400-97857600	Enhancers	Gastric	stomach
38	chr9:97855400-97857600	Genic enhancers	HSMM	muscle
39	chr9:97855400-97859000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr9:97855400-97860800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr9:97855400-97862200	Weak transcription	Duodenum Smooth Muscle	Duodenum
42	chr9:97855400-97865400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
43	chr9:97855400-97884800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
44	chr9:97855600-97857400	Strong transcription	A549	lung
45	chr9:97855600-97859000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr9:97855600-97859600	Weak transcription	Duodenum Mucosa	Duodenum
47	chr9:97855600-97860000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr9:97855600-97862200	Enhancers	Muscle Satellite Cultured Cells	--
49	chr9:97855600-97862400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
50	chr9:97855600-97862800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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