Variant report

Variant	rs62117198
Chromosome Location	chr19:53038777-53038778
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr19:53038658-53038909	H1-hESC	embryonic stem cell:	n/a	n/a
2	POU2F2	chr19:53038580-53039041	GM12878	blood:	n/a	chr19:53038977-53038990
3	ELF1	chr19:53038439-53038911	GM12878	blood:	n/a	n/a
4	JUND	chr19:53038617-53039410	H1-hESC	embryonic stem cell:	n/a	n/a
5	POLR2A	chr19:53038420-53040018	H1-hESC	embryonic stem cell:	n/a	n/a
6	SPI1	chr19:53038732-53038924	K562	blood:	n/a	n/a
7	JUND	chr19:53038713-53038825	H1-hESC	embryonic stem cell:	n/a	n/a
8	POLR2A	chr19:53038521-53040036	GM12892	blood:	n/a	n/a
9	TCF12	chr19:53038639-53038887	GM12878	blood:	n/a	n/a
10	PAX5	chr19:53038720-53038939	GM12878	blood:	n/a	n/a
11	POLR2A	chr19:53038626-53040058	GM12892	blood:	n/a	n/a
12	PAX5	chr19:53038469-53038981	GM12878	blood:	n/a	n/a
13	SIN3AK20	chr19:53038728-53038891	HepG2	liver:	n/a	n/a
14	TAF1	chr19:53038571-53039616	H1-hESC	embryonic stem cell:	n/a	n/a
15	MXI1	chr19:53038730-53039938	IMR90	lung:	n/a	n/a
16	POLR2A	chr19:53038625-53038897	GM12878	blood:	n/a	n/a
17	POLR2A	chr19:53038595-53040407	GM12878	blood:	n/a	n/a
18	MXI1	chr19:53038426-53040206	SK-N-SH	brain:	n/a	n/a
19	POLR2A	chr19:53038629-53038947	H1-hESC	embryonic stem cell:	n/a	n/a
20	POLR2A	chr19:53038602-53038950	H1-hESC	embryonic stem cell:	n/a	n/a
21	SIN3A	chr19:53038741-53039955	H1-hESC	embryonic stem cell:	n/a	chr19:53039875-53039888 chr19:53039670-53039684
22	POLR2A	chr19:53038657-53038795	MCF-7	breast:	n/a	n/a
23	SP1	chr19:53038752-53039389	H1-hESC	embryonic stem cell:	n/a	chr19:53039119-53039131 chr19:53039219-53039231 chr19:53039189-53039198 chr19:53039176-53039188 chr19:53039221-53039230 chr19:53039220-53039229 chr19:53039188-53039197 chr19:53039120-53039129 chr19:53039132-53039141 chr19:53039130-53039142 chr19:53039119-53039131 chr19:53039131-53039141 chr19:53039188-53039197 chr19:53039130-53039142 chr19:53039131-53039145 chr19:53039219-53039231 chr19:53039177-53039191 chr19:53039131-53039140 chr19:53039177-53039186
24	TEAD4	chr19:53038655-53038940	H1-hESC	embryonic stem cell:	n/a	n/a
25	SP1	chr19:53038622-53038890	GM12878	blood:	n/a	n/a
26	POLR2A	chr19:53038558-53040049	GM12892	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr19:53029459..53032258-chr19:53036873..53039549,6	MCF-7	breast:
2	chr19:53031656..53034156-chr19:53037494..53039065,2	MCF-7	breast:

Variant related genes	Relation type
ZNF808	TF binding region
ENSG00000198482	Chromatin interaction

Extended variants
information (count: 81 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:70)

rs_ID	r²[population]
rs11668903	0.82[EUR][1000 genomes]
rs12610240	0.81[EUR][1000 genomes]
rs1676153	0.89[ASN][1000 genomes]
rs2045754	0.86[ASN][1000 genomes]
rs2608513	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2608522	0.95[ASN][1000 genomes]
rs2608527	0.88[ASN][1000 genomes]
rs2615586	0.87[ASN][1000 genomes]
rs2615587	0.93[ASN][1000 genomes]
rs2615588	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2617795	0.88[ASN][1000 genomes]
rs2633502	0.90[ASN][1000 genomes]
rs2633513	0.93[ASN][1000 genomes]
rs2633514	0.86[ASN][1000 genomes]
rs2633517	0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2925976	0.92[ASN][1000 genomes]
rs326439	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs326440	0.84[ASN][1000 genomes]
rs326441	0.84[ASN][1000 genomes]
rs326443	0.86[ASN][1000 genomes]
rs326444	0.89[ASN][1000 genomes]
rs326446	0.87[ASN][1000 genomes]
rs326447	0.86[ASN][1000 genomes]
rs326448	0.86[ASN][1000 genomes]
rs326449	0.86[ASN][1000 genomes]
rs368922	0.93[ASN][1000 genomes]
rs375267	0.89[ASN][1000 genomes]
rs376595	0.95[ASN][1000 genomes]
rs396663	0.95[ASN][1000 genomes]
rs400709	0.95[ASN][1000 genomes]
rs402737	0.91[ASN][1000 genomes]
rs410046	0.93[ASN][1000 genomes]
rs413751	0.91[ASN][1000 genomes]
rs413814	0.87[ASN][1000 genomes]
rs417599	0.95[ASN][1000 genomes]
rs422195	0.95[ASN][1000 genomes]
rs429367	0.93[ASN][1000 genomes]
rs434709	0.95[ASN][1000 genomes]
rs434788	0.91[ASN][1000 genomes]
rs439618	0.95[ASN][1000 genomes]
rs440545	0.93[ASN][1000 genomes]
rs441549	0.89[ASN][1000 genomes]
rs441850	0.84[ASN][1000 genomes]
rs445500	0.94[ASN][1000 genomes]
rs449671	0.86[ASN][1000 genomes]
rs4802971	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4802972	0.95[ASN][1000 genomes]
rs520958	0.85[ASN][1000 genomes]
rs521703	0.89[ASN][1000 genomes]
rs529698	0.92[ASN][1000 genomes]
rs532449	0.92[ASN][1000 genomes]
rs606521	0.88[ASN][1000 genomes]
rs606538	0.88[ASN][1000 genomes]
rs606914	0.91[ASN][1000 genomes]
rs607477	0.90[ASN][1000 genomes]
rs62117197	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62117199	0.90[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs62119356	0.83[EUR][1000 genomes]
rs62119359	0.93[ASN][1000 genomes]
rs642493	0.89[ASN][1000 genomes]
rs653483	0.85[ASN][1000 genomes]
rs655580	0.81[ASN][1000 genomes]
rs656541	0.93[ASN][1000 genomes]
rs666356	0.82[ASN][1000 genomes]
rs668882	0.92[ASN][1000 genomes]
rs685200	0.92[ASN][1000 genomes]
rs688646	0.94[ASN][1000 genomes]
rs781129	0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs92520	0.87[ASN][1000 genomes]
rs9676916	0.83[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1066537	chr19:52794424-53044977	Active TSS ZNF genes & repeats Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
2	nsv544060	chr19:52794424-53044977	ZNF genes & repeats Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
3	nsv580026	chr19:52937100-53059872	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv1063648	chr19:52938131-53041119	ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv1057296	chr19:52950339-53396986	Weak transcription Active TSS ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
6	nsv978841	chr19:52983057-53088237	ZNF genes & repeats Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
7	nsv1066717	chr19:52993620-53041995	Active TSS ZNF genes & repeats Flanking Active TSS Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	nsv1064342	chr19:52996710-53041119	ZNF genes & repeats Active TSS Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
9	nsv1055859	chr19:53001299-53041119	Enhancers Active TSS Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
10	nsv1060656	chr19:53001299-53041995	Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
11	nsv510772	chr19:53037211-53103470	ZNF genes & repeats Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:53031800-53038800	Weak transcription	Ovary	ovary
2	chr19:53032000-53038800	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr19:53032000-53038800	Weak transcription	Small Intestine	intestine
4	chr19:53032000-53039000	Weak transcription	HSMMtube	muscle
5	chr19:53032200-53039400	Weak transcription	Stomach Mucosa	stomach
6	chr19:53032200-53057000	Weak transcription	Hela-S3	cervix
7	chr19:53032400-53038800	Weak transcription	Fetal Kidney	kidney
8	chr19:53032400-53038800	Weak transcription	Placenta Amnion	Placenta Amnion
9	chr19:53032600-53038800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
10	chr19:53032600-53039200	Weak transcription	Spleen	Spleen
11	chr19:53032600-53049800	Weak transcription	HepG2	liver
12	chr19:53033800-53040200	ZNF genes & repeats	Liver	Liver
13	chr19:53036400-53040000	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr19:53036400-53040400	ZNF genes & repeats	Fetal Adrenal Gland	Adrenal Gland
15	chr19:53037000-53039200	Enhancers	Fetal Heart	heart
16	chr19:53037200-53038800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr19:53037400-53040400	ZNF genes & repeats	Sigmoid Colon	Sigmoid Colon
18	chr19:53037600-53051800	Weak transcription	K562	blood
19	chr19:53038000-53038800	Weak transcription	Fetal Intestine Large	intestine
20	chr19:53038000-53038800	Weak transcription	Gastric	stomach
21	chr19:53038000-53039000	Enhancers	Fetal Brain Male	brain
22	chr19:53038000-53039200	Flanking Active TSS	Dnd41	blood
23	chr19:53038000-53040800	Active TSS	HUES6 Cell Line	embryonic stem cell
24	chr19:53038200-53038800	Enhancers	Colon Smooth Muscle	Colon
25	chr19:53038200-53039400	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr19:53038200-53039800	Active TSS	iPS-20b Cell Line	embryonic stem cell
27	chr19:53038200-53040000	Active TSS	Fetal Brain Female	brain
28	chr19:53038200-53040200	Active TSS	iPS-15b Cell Line	embryonic stem cell
29	chr19:53038200-53040200	Active TSS	GM12878-XiMat	blood
30	chr19:53038200-53040400	Active TSS	HUES64 Cell Line	embryonic stem cell
31	chr19:53038400-53038800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr19:53038400-53038800	Weak transcription	Fetal Lung	lung
33	chr19:53038400-53039000	Flanking Active TSS	Fetal Muscle Leg	muscle
34	chr19:53038400-53039200	Active TSS	Brain Germinal Matrix	brain
35	chr19:53038400-53039600	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr19:53038400-53039600	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr19:53038400-53039600	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr19:53038400-53040000	Active TSS	H1 Cell Line	embryonic stem cell
39	chr19:53038400-53040000	Active TSS	iPS-18 Cell Line	embryonic stem cell
40	chr19:53038400-53040000	Active TSS	Brain Inferior Temporal Lobe	brain
41	chr19:53038400-53040200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
42	chr19:53038400-53040200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr19:53038400-53040400	Active TSS	H9 Cell Line	embryonic stem cell
44	chr19:53038400-53040400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr19:53038400-53040400	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr19:53038400-53040400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr19:53038600-53038800	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr19:53038600-53038800	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
49	chr19:53038600-53038800	Active TSS	Primary hematopoietic stem cells short term culture	blood
50	chr19:53038600-53038800	Active TSS	Primary T helper memory cells from peripheral blood 1	blood

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