Variant report

Variant	rs7250351
Chromosome Location	chr19:56603034-56603035
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr19:56601536..56604040-chr19:56606734..56609466,2	MCF-7	breast:
2	chr19:56600333..56603154-chr19:56649687..56651196,2	K562	blood:
3	chr19:56602725..56603273-chr6:28891014..28891894,2	Hela-S3	cervix:
4	chr19:56601293..56604131-chr19:56623089..56625582,2	MCF-7	breast:
5	chr19:56592253..56593839-chr19:56602016..56603722,2	K562	blood:
6	chr19:56601141..56604014-chr19:56651251..56654882,5	MCF-7	breast:

Variant related genes	Relation type
ENSG00000167685	Chromatin interaction
ENSG00000204713	Chromatin interaction

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs1007851	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11673628	0.84[ASN][1000 genomes]
rs12459102	0.82[ASN][1000 genomes]
rs35766803	0.92[ASN][1000 genomes]
rs4077285	0.83[ASN][1000 genomes]
rs4801676	0.80[ASN][1000 genomes]
rs481936	0.85[ASN][1000 genomes]
rs492078	0.83[ASN][1000 genomes]
rs501798	0.85[ASN][1000 genomes]
rs504350	0.82[ASN][1000 genomes]
rs517582	0.83[ASN][1000 genomes]
rs521092	0.87[ASN][1000 genomes]
rs533640	0.85[ASN][1000 genomes]
rs533734	0.85[ASN][1000 genomes]
rs535393	0.82[ASN][1000 genomes]
rs536342	0.85[ASN][1000 genomes]
rs536414	0.83[ASN][1000 genomes]
rs537425	0.82[ASN][1000 genomes]
rs540900	0.85[ASN][1000 genomes]
rs564050	0.85[ASN][1000 genomes]
rs570210	0.82[ASN][1000 genomes]
rs582271	0.86[ASN][1000 genomes]
rs588574	0.85[ASN][1000 genomes]
rs609736	0.87[ASN][1000 genomes]
rs609755	0.87[ASN][1000 genomes]
rs619934	0.85[ASN][1000 genomes]
rs630704	0.83[ASN][1000 genomes]
rs642776	0.85[ASN][1000 genomes]
rs6509982	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs665846	0.83[ASN][1000 genomes]
rs677142	0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1056598	chr19:56331762-56703428	Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	50 gene(s)	inside rSNPs	diseases
2	nsv1058988	chr19:56382492-56609032	Flanking Active TSS Strong transcription ZNF genes & repeats Enhancers Weak transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
3	nsv1064371	chr19:56418215-56842450	ZNF genes & repeats Strong transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	65 gene(s)	inside rSNPs	diseases
4	nsv1057316	chr19:56418215-56849458	Strong transcription Enhancers ZNF genes & repeats Weak transcription Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	65 gene(s)	inside rSNPs	diseases
5	nsv580354	chr19:56505685-56723492	Weak transcription Genic enhancers Enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	48 gene(s)	inside rSNPs	diseases
6	nsv833883	chr19:56512601-56640089	Strong transcription Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
7	nsv523651	chr19:56537528-56707048	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	47 gene(s)	inside rSNPs	diseases
8	nsv1057820	chr19:56555942-56720262	Weak transcription Genic enhancers Flanking Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	47 gene(s)	inside rSNPs	diseases
9	nsv528998	chr19:56578238-56707048	Active TSS Genic enhancers Weak transcription Strong transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	47 gene(s)	inside rSNPs	diseases
10	nsv912512	chr19:56592286-56636759	Enhancers Genic enhancers Weak transcription Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
11	nsv517365	chr19:56592286-56674548	Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
12	nsv912513	chr19:56592286-56685463	Flanking Active TSS Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
13	nsv521744	chr19:56592286-56686953	Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
14	nsv912514	chr19:56596815-56636759	Flanking Active TSS Genic enhancers Enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
15	nsv912515	chr19:56598829-56623710	Weak transcription Genic enhancers Strong transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases
16	nsv912516	chr19:56601298-56981382	Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	93 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:56592600-56620000	Weak transcription	HSMMtube	muscle
2	chr19:56592800-56622600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
3	chr19:56593000-56606400	Weak transcription	Duodenum Smooth Muscle	Duodenum
4	chr19:56593000-56616200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
5	chr19:56593000-56616600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
6	chr19:56593000-56616800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
7	chr19:56593000-56631200	Weak transcription	Pancreatic Islets	Pancreatic Islet
8	chr19:56593600-56616000	Weak transcription	Stomach Mucosa	stomach
9	chr19:56594800-56616800	Weak transcription	HUVEC	blood vessel
10	chr19:56596200-56603400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr19:56596400-56605400	Strong transcription	Primary neutrophils fromperipheralblood	blood
12	chr19:56596600-56603600	Strong transcription	Fetal Intestine Small	intestine
13	chr19:56596600-56604000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr19:56596600-56604200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
15	chr19:56596600-56604400	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr19:56596600-56604600	Weak transcription	HUES64 Cell Line	embryonic stem cell
17	chr19:56596600-56614800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
18	chr19:56597000-56603600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr19:56597000-56604000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr19:56597200-56619400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
21	chr19:56597800-56604000	Strong transcription	Primary monocytes fromperipheralblood	blood
22	chr19:56598000-56604000	Weak transcription	GM12878-XiMat	blood
23	chr19:56598000-56605400	Strong transcription	Sigmoid Colon	Sigmoid Colon
24	chr19:56598200-56604800	Strong transcription	Gastric	stomach
25	chr19:56598600-56603200	Strong transcription	Primary T helper cells fromperipheralblood	blood
26	chr19:56598800-56603200	Strong transcription	Fetal Intestine Large	intestine
27	chr19:56598800-56604600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr19:56599800-56605400	Strong transcription	Primary B cells from peripheral blood	blood
29	chr19:56599800-56615200	Strong transcription	Liver	Liver
30	chr19:56600000-56603200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
31	chr19:56600000-56603600	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr19:56600000-56604000	Strong transcription	Fetal Muscle Leg	muscle
33	chr19:56600000-56604200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr19:56600000-56604600	Strong transcription	Primary T cells from cord blood	blood
35	chr19:56600000-56619000	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr19:56600400-56603600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr19:56600400-56604800	Weak transcription	Aorta	Aorta
38	chr19:56600400-56614400	Strong transcription	HepG2	liver
39	chr19:56600600-56604200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr19:56600600-56609000	Weak transcription	Placenta Amnion	Placenta Amnion
41	chr19:56600800-56603200	Genic enhancers	Skeletal Muscle Male	skeletal muscle
42	chr19:56600800-56604800	Weak transcription	H9 Cell Line	embryonic stem cell
43	chr19:56600800-56616800	Weak transcription	Small Intestine	intestine
44	chr19:56601000-56603600	Strong transcription	K562	blood
45	chr19:56601000-56604800	Weak transcription	Ovary	ovary
46	chr19:56601000-56607000	Weak transcription	Colon Smooth Muscle	Colon
47	chr19:56601200-56604200	Enhancers	Brain Hippocampus Middle	brain
48	chr19:56601400-56603200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr19:56601400-56603600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr19:56601400-56604400	Weak transcription	Primary B cells from cord blood	blood

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