Variant report

Variant	rs13344210
Chromosome Location	chr19:52704431-52704432
allele	A/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	chr19:52703908-52705233	GM12891	blood:	n/a	n/a
2	POLR2A	chr19:52703434-52705471	GM12878	blood:	n/a	n/a
3	POLR2A	chr19:52703896-52704528	GM12891	blood:	n/a	n/a
4	POLR2A	chr19:52704190-52704454	GM12878	blood:	n/a	n/a
5	POLR2A	chr19:52703878-52704514	GM12892	blood:	n/a	n/a
6	POLR2A	chr19:52704036-52704499	H1-hESC	embryonic stem cell:	n/a	n/a
7	POLR2A	chr19:52703914-52704500	H1-hESC	embryonic stem cell:	n/a	n/a
8	POLR2A	chr19:52703869-52704532	GM12892	blood:	n/a	n/a
9	POLR2A	chr19:52703862-52704547	GM12891	blood:	n/a	n/a
10	POLR2A	chr19:52703156-52705303	GM12878	blood:	n/a	n/a
11	POLR2A	chr19:52703334-52705311	GM12892	blood:	n/a	n/a
12	POLR2A	chr19:52704115-52704507	Hela-S3	cervix:	n/a	n/a
13	POLR2A	chr19:52703409-52705333	GM12892	blood:	n/a	n/a
14	POLR2A	chr19:52704306-52704451	Hela-S3	cervix:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr19:52692900..52696088-chr19:52702014..52707428,7	MCF-7	breast:

Variant related genes	Relation type
PPP2R1A	TF binding region
ENSG00000105568	Chromatin interaction

Extended variants
information (count: 35 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10401204	1.00[AMR][1000 genomes]
rs10401416	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10401502	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10402794	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10403938	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10403948	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10405253	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10406072	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10406808	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10409046	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10409432	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10410464	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10410678	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10412757	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10414703	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10415398	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10415475	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10416801	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10418737	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10418798	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10420092	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10421004	0.88[AFR][1000 genomes]
rs10421813	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10423725	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10423756	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10424090	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10425820	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10426412	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13344188	1.00[AMR][1000 genomes]
rs1366243	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1366244	1.00[AFR][1000 genomes];1.00[AMR][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	nsv1065410	chr19:52103914-52889530	Genic enhancers Enhancers ZNF genes & repeats Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	596 gene(s)	inside rSNPs	diseases
2	esv3366000	chr19:52491073-52842946	Strong transcription ZNF genes & repeats Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
3	nsv1066015	chr19:52502213-52890308	Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Genic enhancers Active TSS Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
4	nsv544059	chr19:52502213-52890308	Active TSS Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	49 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:52694400-52710200	ZNF genes & repeats	A549	lung
2	chr19:52694600-52732800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr19:52695200-52708400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr19:52695200-52711200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr19:52695400-52707600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr19:52695400-52732200	Strong transcription	Fetal Lung	lung
7	chr19:52695400-52733200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
8	chr19:52695600-52717400	Strong transcription	Primary hematopoietic stem cells	blood
9	chr19:52696000-52710800	Strong transcription	Thymus	Thymus
10	chr19:52696000-52723000	Strong transcription	Fetal Muscle Trunk	muscle
11	chr19:52696000-52732200	Strong transcription	Monocytes-CD14+_RO01746	blood
12	chr19:52696000-52732400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr19:52696000-52733000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr19:52696200-52704600	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
15	chr19:52696200-52705200	Weak transcription	Small Intestine	intestine
16	chr19:52696200-52729200	Strong transcription	Fetal Intestine Large	intestine
17	chr19:52696200-52732400	Strong transcription	HUES6 Cell Line	embryonic stem cell
18	chr19:52696200-52732400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
19	chr19:52696200-52732400	Strong transcription	Primary B cells from cord blood	blood
20	chr19:52696800-52705600	Weak transcription	Pancreatic Islets	Pancreatic Islet
21	chr19:52697600-52732400	Strong transcription	Sigmoid Colon	Sigmoid Colon
22	chr19:52697600-52733200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
23	chr19:52697800-52732200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr19:52697800-52732400	Strong transcription	HUES64 Cell Line	embryonic stem cell
25	chr19:52697800-52732400	Strong transcription	Rectal Mucosa Donor 29	rectum
26	chr19:52697800-52732600	Strong transcription	Primary T cells from cord blood	blood
27	chr19:52697800-52733000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr19:52698000-52730400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
29	chr19:52698000-52732200	Strong transcription	Rectal Mucosa Donor 31	rectum
30	chr19:52698000-52732200	Strong transcription	Dnd41	blood
31	chr19:52698200-52706400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr19:52698200-52714400	Weak transcription	Stomach Mucosa	stomach
33	chr19:52698200-52732000	Strong transcription	GM12878-XiMat	blood
34	chr19:52698200-52732400	Strong transcription	HUES48 Cell Line	embryonic stem cell
35	chr19:52698200-52732400	Strong transcription	HepG2	liver
36	chr19:52698200-52732600	Strong transcription	Fetal Brain Female	brain
37	chr19:52698400-52732400	Strong transcription	Fetal Thymus	thymus
38	chr19:52698600-52732000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
39	chr19:52698800-52732400	Strong transcription	Liver	Liver
40	chr19:52699400-52704600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
41	chr19:52700200-52712600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr19:52700400-52705000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
43	chr19:52700800-52732200	Strong transcription	Primary T helper cells fromperipheralblood	blood
44	chr19:52701200-52704600	Enhancers	Right Ventricle	heart
45	chr19:52701400-52705000	Genic enhancers	Brain Angular Gyrus	brain
46	chr19:52702200-52704600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr19:52702200-52705000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
48	chr19:52702200-52731800	Strong transcription	Primary B cells from peripheral blood	blood
49	chr19:52702200-52732200	Strong transcription	H1 Cell Line	embryonic stem cell
50	chr19:52702600-52732200	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--

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