Variant report

Variant	rs3845775
Chromosome Location	chr2:33602571-33602572
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:33591629..33594068-chr2:33601379..33603892,2	MCF-7	breast:

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs10167082	1.00[CEU][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10185344	0.92[CEU][hapmap];1.00[GIH][hapmap];0.87[TSI][hapmap];0.90[EUR][1000 genomes]
rs10190501	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12328065	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13386072	0.92[EUR][1000 genomes]
rs13404913	0.82[MEX][hapmap]
rs13428115	0.92[CEU][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6706620	0.84[CEU][hapmap];1.00[GIH][hapmap];0.87[TSI][hapmap];0.90[EUR][1000 genomes]
rs6709900	0.81[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6736026	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72861454	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs72861492	0.91[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1005435	chr2:33136117-33747159	Weak transcription Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' 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	22 gene(s)	inside rSNPs	diseases
2	nsv535624	chr2:33136117-33747159	Weak transcription Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats 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	22 gene(s)	inside rSNPs	diseases
3	nsv1012967	chr2:33533340-33638312	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
4	nsv535627	chr2:33533340-33638312	Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:48 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:33529800-33609400	Weak transcription	Right Ventricle	heart
2	chr2:33578800-33612200	Weak transcription	Fetal Kidney	kidney
3	chr2:33581600-33611400	Weak transcription	Fetal Stomach	stomach
4	chr2:33586200-33603600	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr2:33588400-33624400	Weak transcription	Gastric	stomach
6	chr2:33589200-33623000	Weak transcription	Duodenum Smooth Muscle	Duodenum
7	chr2:33590600-33615800	Weak transcription	Fetal Muscle Trunk	muscle
8	chr2:33590600-33624800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
9	chr2:33590800-33612600	Weak transcription	Ovary	ovary
10	chr2:33591400-33616000	Weak transcription	Colon Smooth Muscle	Colon
11	chr2:33592000-33624800	Weak transcription	Skeletal Muscle Male	skeletal muscle
12	chr2:33595200-33609200	Weak transcription	Left Ventricle	heart
13	chr2:33596200-33614400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr2:33596400-33613800	Weak transcription	Liver	Liver
15	chr2:33596600-33603800	Weak transcription	NH-A	brain
16	chr2:33597000-33609000	Weak transcription	Fetal Heart	heart
17	chr2:33597200-33622200	Weak transcription	Fetal Muscle Leg	muscle
18	chr2:33597400-33603600	Weak transcription	Brain Anterior Caudate	brain
19	chr2:33597400-33610200	Weak transcription	Stomach Smooth Muscle	stomach
20	chr2:33598000-33603800	Weak transcription	Brain Cingulate Gyrus	brain
21	chr2:33598200-33605000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr2:33600600-33603400	Weak transcription	Muscle Satellite Cultured Cells	--
23	chr2:33600600-33603600	Weak transcription	Brain Hippocampus Middle	brain
24	chr2:33600600-33603600	Weak transcription	Brain Substantia Nigra	brain
25	chr2:33600600-33603800	Weak transcription	Brain Inferior Temporal Lobe	brain
26	chr2:33600600-33604000	Weak transcription	Adipose Nuclei	Adipose
27	chr2:33601200-33602600	Enhancers	NHDF-Ad	bronchial
28	chr2:33601400-33602600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr2:33601400-33602800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr2:33601400-33603000	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr2:33601400-33603000	Enhancers	Aorta	Aorta
32	chr2:33601400-33603200	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr2:33601600-33602600	Enhancers	HSMM	muscle
34	chr2:33601600-33602800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr2:33601600-33603200	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr2:33601600-33604800	Enhancers	Cortex derived primary cultured neurospheres	brain
37	chr2:33601800-33602600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr2:33602000-33602600	Enhancers	HSMMtube	muscle
39	chr2:33602200-33603000	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr2:33602200-33603800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr2:33602200-33613600	Weak transcription	NHLF	lung
42	chr2:33602400-33602600	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr2:33602400-33602600	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chr2:33602400-33602600	Genic enhancers	Osteobl	bone
45	chr2:33602400-33603800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr2:33602400-33603800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
47	chr2:33602400-33604600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
48	chr2:33602400-33604600	Weak transcription	HUVEC	blood vessel

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