Variant report

Variant	rs10981841
Chromosome Location	chr9:116371250-116371251
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:116371231..116372845-chr9:116374624..116376242,2	MCF-7	breast:
2	chr9:116368474..116370761-chr9:116371001..116373367,2	MCF-7	breast:

Extended variants
information (count: 67 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:57)

rs_ID	r²[population]
rs10217237	1.00[ASN][1000 genomes]
rs10217750	1.00[ASN][1000 genomes]
rs10217756	1.00[ASN][1000 genomes]
rs10481640	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10817496	1.00[ASN][1000 genomes]
rs10981794	1.00[ASN][1000 genomes]
rs10981840	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10981843	1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10981844	1.00[ASN][1000 genomes]
rs10981845	1.00[ASN][1000 genomes]
rs10981846	1.00[ASN][1000 genomes]
rs10981847	1.00[ASN][1000 genomes]
rs10981850	1.00[ASN][1000 genomes]
rs12335991	1.00[ASN][1000 genomes]
rs12336983	1.00[ASN][1000 genomes]
rs12338221	1.00[ASN][1000 genomes]
rs12339851	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12344964	1.00[ASN][1000 genomes]
rs16907354	1.00[ASN][1000 genomes]
rs17766289	1.00[ASN][1000 genomes]
rs2812398	0.81[AFR][1000 genomes]
rs28709996	1.00[ASN][1000 genomes]
rs36062487	1.00[ASN][1000 genomes]
rs41276817	1.00[ASN][1000 genomes]
rs41297197	1.00[ASN][1000 genomes]
rs4348575	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4609260	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs511561	1.00[ASN][1000 genomes]
rs530456	1.00[ASN][1000 genomes]
rs538711	1.00[ASN][1000 genomes]
rs551960	1.00[ASN][1000 genomes]
rs55916010	1.00[ASN][1000 genomes]
rs56038206	1.00[ASN][1000 genomes]
rs57989349	1.00[ASN][1000 genomes]
rs585689	0.81[YRI][hapmap]
rs586265	1.00[ASN][1000 genomes]
rs587614	0.81[YRI][hapmap]
rs60302610	1.00[ASN][1000 genomes]
rs608290	1.00[ASN][1000 genomes]
rs611335	1.00[ASN][1000 genomes]
rs6478012	1.00[ASN][1000 genomes]
rs6478017	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs653971	1.00[ASN][1000 genomes]
rs656311	0.81[AFR][1000 genomes]
rs664850	1.00[ASN][1000 genomes]
rs670719	1.00[ASN][1000 genomes]
rs7021491	1.00[ASN][1000 genomes]
rs7033679	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72761905	1.00[ASN][1000 genomes]
rs72761964	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72761969	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72761971	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72761973	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72761978	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72761995	1.00[ASN][1000 genomes]
rs7867203	1.00[ASN][1000 genomes]
rs7870265	0.80[EUR][1000 genomes];1.00[ASN][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	nsv530949	chr9:115821128-116487796	Flanking Active TSS Enhancers Active TSS Weak transcription Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	71 gene(s)	inside rSNPs	diseases
2	nsv893747	chr9:116214058-116386438	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
3	nsv526579	chr9:116244982-116391162	Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
4	nsv893748	chr9:116308709-116421786	Flanking Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
5	nsv430093	chr9:116330446-117325446	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	165 gene(s)	inside rSNPs	diseases
6	nsv466509	chr9:116356516-116396098	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription 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 target site	8 gene(s)	inside rSNPs	diseases
7	nsv615216	chr9:116356516-116396098	Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
8	nsv466510	chr9:116363877-116397397	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
9	nsv615217	chr9:116363877-116397397	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
10	nsv615218	chr9:116365126-116391069	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:36 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:116358000-116371800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr9:116360400-116371800	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr9:116364800-116371800	Weak transcription	Brain Angular Gyrus	brain
4	chr9:116365200-116371800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr9:116365200-116371800	Weak transcription	Gastric	stomach
6	chr9:116365400-116371800	Weak transcription	Stomach Smooth Muscle	stomach
7	chr9:116365600-116371600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr9:116365600-116371800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr9:116365600-116371800	Weak transcription	Fetal Intestine Small	intestine
10	chr9:116366000-116371400	Weak transcription	Fetal Muscle Trunk	muscle
11	chr9:116366200-116371800	Weak transcription	HUES64 Cell Line	embryonic stem cell
12	chr9:116366200-116375800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr9:116366400-116371800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
14	chr9:116366400-116371800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr9:116366400-116371800	Weak transcription	Placenta	Placenta
16	chr9:116366600-116371600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
17	chr9:116366600-116371800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr9:116366600-116371800	Weak transcription	HUES6 Cell Line	embryonic stem cell
19	chr9:116366600-116371800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr9:116366800-116371800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr9:116367000-116371800	Weak transcription	Adipose Nuclei	Adipose
22	chr9:116369000-116371800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr9:116369200-116371800	Weak transcription	Fetal Lung	lung
24	chr9:116369400-116371600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr9:116370200-116373400	Enhancers	Breast Myoepithelial Primary Cells	Breast
26	chr9:116370200-116374000	Enhancers	HUVEC	blood vessel
27	chr9:116370400-116371800	Enhancers	HepG2	liver
28	chr9:116370600-116373000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr9:116371200-116371800	Enhancers	Skeletal Muscle Male	skeletal muscle
30	chr9:116371200-116371800	Enhancers	Skeletal Muscle Female	skeletal muscle
31	chr9:116371200-116372600	Enhancers	Aorta	Aorta
32	chr9:116371200-116373400	Enhancers	Liver	Liver
33	chr9:116371200-116373400	Enhancers	Right Atrium	heart
34	chr9:116371200-116373400	Enhancers	Spleen	Spleen
35	chr9:116371200-116377800	Weak transcription	Esophagus	oesophagus
36	chr9:116371200-116380200	Enhancers	Fetal Muscle Leg	muscle

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