Variant report

Variant	rs59764933
Chromosome Location	chr1:45084603-45084604
allele	A/G
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:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:45081603..45085955-chr1:45194609..45197878,5	K562	blood:
2	chr1:45083106..45084761-chr1:45094911..45097627,2	MCF-7	breast:
3	chr1:45083155..45084917-chr1:45193474..45196151,2	MCF-7	breast:
4	chr1:45083755..45085501-chr1:45185803..45188778,2	MCF-7	breast:
5	chr1:45083215..45085000-chr1:45096549..45098340,2	MCF-7	breast:
6	chr1:45075968..45077503-chr1:45081930..45084778,2	MCF-7	breast:
7	chr1:45081887..45084948-chr1:45138825..45141826,3	K562	blood:
8	chr1:45083278..45085001-chr1:45186092..45188777,2	K562	blood:
9	chr1:45083278..45085630-chr1:45186092..45188492,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000126106	Chromatin interaction
ENSG00000200169	Chromatin interaction
ENSG00000198520	Chromatin interaction
ENSG00000199377	Chromatin interaction
ENSG00000187147	Chromatin interaction

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs1051664	0.93[ASN][1000 genomes]
rs1135319	1.00[EUR][1000 genomes]
rs56257701	0.91[ASN][1000 genomes]
rs58019041	0.91[ASN][1000 genomes]
rs58035624	0.87[ASN][1000 genomes]
rs58401148	0.91[ASN][1000 genomes]
rs58678671	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs59370761	0.91[ASN][1000 genomes]
rs59790609	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs60469789	0.91[ASN][1000 genomes]
rs60476008	0.90[ASN][1000 genomes]
rs6429544	0.89[ASN][1000 genomes]
rs6665374	0.87[ASN][1000 genomes]
rs6667593	0.91[ASN][1000 genomes]
rs6698388	0.93[ASN][1000 genomes]
rs72671972	0.91[ASN][1000 genomes]
rs74070566	1.00[ASN][1000 genomes]
rs74070577	0.91[ASN][1000 genomes]
rs7539312	0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533037	chr1:44361728-45333408	Weak transcription Strong transcription Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	469 gene(s)	inside rSNPs	diseases
2	nsv1004861	chr1:44843654-45210176	Flanking Active TSS Genic enhancers Enhancers Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	346 gene(s)	inside rSNPs	diseases
3	nsv534940	chr1:44843654-45210176	Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	346 gene(s)	inside rSNPs	diseases
4	nsv461395	chr1:44898998-45119965	Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	27 gene(s)	inside rSNPs	diseases
5	nsv546144	chr1:44898998-45119965	Genic enhancers Enhancers Strong transcription Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS 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	27 gene(s)	inside rSNPs	diseases
6	nsv998476	chr1:45001278-45311757	Flanking Active TSS Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	426 gene(s)	inside rSNPs	diseases
7	nsv534941	chr1:45001278-45311757	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	426 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	chr1:45074800-45096800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr1:45078000-45084800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
3	chr1:45079600-45096800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr1:45081800-45086000	Enhancers	Brain Inferior Temporal Lobe	brain
5	chr1:45082200-45085800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr1:45082200-45086600	Enhancers	Brain Substantia Nigra	brain
7	chr1:45082800-45087800	Enhancers	Brain Cingulate Gyrus	brain
8	chr1:45083000-45087200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr1:45083000-45087600	Enhancers	Brain Hippocampus Middle	brain
10	chr1:45083000-45097000	Weak transcription	Spleen	Spleen
11	chr1:45083400-45085000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr1:45083400-45085200	Weak transcription	K562	blood
13	chr1:45083400-45089000	Enhancers	NHDF-Ad	bronchial
14	chr1:45083400-45097200	Weak transcription	Gastric	stomach
15	chr1:45083600-45084800	Weak transcription	HSMM	muscle
16	chr1:45083600-45085000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr1:45083600-45085000	Enhancers	Osteobl	bone
18	chr1:45083600-45085200	Weak transcription	Muscle Satellite Cultured Cells	--
19	chr1:45083600-45085600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr1:45083600-45085800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr1:45083600-45085800	Enhancers	Colon Smooth Muscle	Colon
22	chr1:45083600-45086000	Enhancers	Rectal Smooth Muscle	rectum
23	chr1:45083600-45086400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr1:45083600-45086600	Enhancers	NHLF	lung
25	chr1:45083600-45097000	Weak transcription	Right Atrium	heart
26	chr1:45083800-45084800	Weak transcription	Duodenum Smooth Muscle	Duodenum
27	chr1:45083800-45085000	Weak transcription	NHEK	skin
28	chr1:45083800-45091200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
29	chr1:45083800-45096600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
30	chr1:45083800-45096600	Weak transcription	Fetal Heart	heart
31	chr1:45084000-45086000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr1:45084200-45086000	Enhancers	Fetal Lung	lung
33	chr1:45084200-45086400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr1:45084200-45097000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr1:45084400-45085600	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr1:45084400-45085800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr1:45084400-45086000	Enhancers	NH-A	brain
38	chr1:45084400-45087200	Weak transcription	Brain Angular Gyrus	brain
39	chr1:45084600-45084800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
40	chr1:45084600-45084800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr1:45084600-45084800	Bivalent Enhancer	Fetal Stomach	stomach
42	chr1:45084600-45085400	Weak transcription	Brain Anterior Caudate	brain
43	chr1:45084600-45086000	Weak transcription	Primary hematopoietic stem cells	blood
44	chr1:45084600-45086000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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