Variant report

Variant	rs9855011
Chromosome Location	chr3:112971606-112971607
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:112970765..112972828-chr3:112974570..112977015,2	MCF-7	breast:

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs1499898	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16845106	0.81[JPT][hapmap];0.82[ASN][1000 genomes]
rs16860709	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs16860720	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16860770	0.82[ASN][1000 genomes]
rs17320040	1.00[ASN][1000 genomes]
rs17320242	1.00[ASN][1000 genomes]
rs2399476	0.82[ASN][1000 genomes]
rs34600669	0.82[ASN][1000 genomes]
rs3814399	0.88[CHB][hapmap];0.82[JPT][hapmap]
rs41271353	0.82[ASN][1000 genomes]
rs57104308	0.93[ASN][1000 genomes]
rs59590258	0.82[ASN][1000 genomes]
rs60070011	1.00[ASN][1000 genomes]
rs61035513	1.00[ASN][1000 genomes]
rs9820139	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9832953	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9849714	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9872998	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9878424	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs998647	0.95[ASN][1000 genomes]
rs999365	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[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	esv3431441	chr3:112453467-113213252	Active TSS Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Enhancers Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
2	nsv829677	chr3:112857075-113038987	Flanking Active TSS Enhancers Bivalent/Poised TSS Genic enhancers Weak transcription Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
3	nsv1003511	chr3:112858775-112989045	Weak transcription Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv1013506	chr3:112890608-113680951	Weak transcription Bivalent/Poised TSS Enhancers Strong transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
5	nsv877348	chr3:112914756-113012509	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:82 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:112932000-112972800	Weak transcription	Aorta	Aorta
2	chr3:112961600-112983000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr3:112962800-112972400	Weak transcription	Brain Germinal Matrix	brain
4	chr3:112963000-112972800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
5	chr3:112966200-112972400	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr3:112966800-112972600	Weak transcription	Duodenum Mucosa	Duodenum
7	chr3:112966800-112973600	Weak transcription	Rectal Mucosa Donor 29	rectum
8	chr3:112967000-112972400	Weak transcription	HUES6 Cell Line	embryonic stem cell
9	chr3:112967200-112972200	Weak transcription	Fetal Thymus	thymus
10	chr3:112967200-112973200	Weak transcription	Colonic Mucosa	Colon
11	chr3:112967200-112973200	Weak transcription	Right Atrium	heart
12	chr3:112967400-112972600	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr3:112967400-112972600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
14	chr3:112967400-112972600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
15	chr3:112968000-112973200	Weak transcription	Left Ventricle	heart
16	chr3:112968200-112972400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr3:112968200-112972400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr3:112968200-112972400	Weak transcription	Skeletal Muscle Female	skeletal muscle
19	chr3:112968400-112972400	Weak transcription	Fetal Brain Male	brain
20	chr3:112968400-112973000	Weak transcription	Skeletal Muscle Male	skeletal muscle
21	chr3:112968600-112972000	Genic enhancers	Cortex derived primary cultured neurospheres	brain
22	chr3:112968600-112972400	Strong transcription	Fetal Intestine Small	intestine
23	chr3:112968600-112972600	Weak transcription	Brain Angular Gyrus	brain
24	chr3:112968600-112980000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr3:112968800-112971800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr3:112968800-112972400	Weak transcription	Brain Inferior Temporal Lobe	brain
27	chr3:112968800-112972600	Weak transcription	Brain Hippocampus Middle	brain
28	chr3:112968800-112973200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr3:112968800-112973400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr3:112969000-112971800	Strong transcription	Placenta Amnion	Placenta Amnion
31	chr3:112969000-112995200	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
32	chr3:112969200-112971800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr3:112969200-112972000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr3:112969200-112972600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr3:112969400-112972800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr3:112969400-112973200	Weak transcription	Muscle Satellite Cultured Cells	--
37	chr3:112969600-112972200	Weak transcription	Brain Substantia Nigra	brain
38	chr3:112969600-112973600	Weak transcription	Osteobl	bone
39	chr3:112969600-112981000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr3:112969800-112972800	Weak transcription	HMEC	breast
41	chr3:112969800-112991800	Weak transcription	Right Ventricle	heart
42	chr3:112969800-112994200	Weak transcription	Spleen	Spleen
43	chr3:112970000-112971800	Genic enhancers	Colon Smooth Muscle	Colon
44	chr3:112970000-112972000	Weak transcription	Fetal Intestine Large	intestine
45	chr3:112970000-112972600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
46	chr3:112970000-112972600	Weak transcription	HSMM	muscle
47	chr3:112970000-112972800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr3:112970000-112973600	Genic enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr3:112970000-112973600	Weak transcription	Sigmoid Colon	Sigmoid Colon
50	chr3:112970200-112971800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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