Variant report

Variant	esv1815453
Chromosome Location	chr19:40360652-40404261
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1009)
CpG islands
(count:1587)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1009 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:40377903-40377918	HepG2	liver:	n/a	n/a
2	ARID3A	chr19:40388564-40388584	HepG2	liver:	n/a	n/a
3	ARID3A	chr19:40372209-40372386	HepG2	liver:	n/a	n/a
4	ATF1	chr19:40372283-40372483	K562	blood:	n/a	n/a
5	ATF2	chr19:40372203-40372491	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr19:40372199-40372449	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL11A	chr19:40372229-40372663	GM12878	blood:	n/a	chr19:40372417-40372430
8	BCL11A	chr19:40404210-40404647	GM12878	blood:	n/a	chr19:40404401-40404414
9	BHLHE40	chr19:40378004-40378342	HepG2	liver:	n/a	n/a
10	BHLHE40	chr19:40372341-40372378	HepG2	liver:	n/a	n/a
11	BHLHE40	chr19:40393689-40394027	HepG2	liver:	n/a	n/a
12	BHLHE40	chr19:40372174-40372382	GM12878	blood:	n/a	n/a
13	BHLHE40	chr19:40404194-40404362	GM12878	blood:	n/a	n/a
14	BHLHE40	chr19:40372310-40372375	K562	blood:	n/a	n/a
15	CBX3	chr19:40372094-40372533	K562	blood:	n/a	n/a
16	CBX3	chr19:40404078-40404473	K562	blood:	n/a	n/a
17	CEBPB	chr19:40369307-40369516	HepG2	liver:	n/a	n/a
18	CEBPB	chr19:40402580-40402849	IMR90	lung:	n/a	chr19:40402707-40402718
19	CEBPB	chr19:40402703-40402726	H1-hESC	embryonic stem cell:	n/a	chr19:40402707-40402718
20	CEBPB	chr19:40402571-40402768	K562	blood:	n/a	chr19:40402707-40402718
21	CEBPB	chr19:40402564-40402888	HepG2	liver:	n/a	chr19:40402707-40402718
22	CEBPB	chr19:40402641-40402841	A549	lung:	n/a	chr19:40402707-40402718
23	CEBPB	chr19:40388532-40388555	Hela-S3	cervix:	n/a	n/a
24	CHD2	chr19:40404120-40404312	GM12878	blood:	n/a	n/a
25	CHD2	chr19:40388541-40388748	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr19:40366072-40366084	Spleen_OC	spleen:	n/a	n/a
27	CTCF	chr19:40404040-40404190	HPAF	blood vessel:	n/a	n/a
28	CTCF	chr19:40372280-40372430	Hela-S3	cervix:	n/a	n/a
29	CTCF	chr19:40404236-40404436	MCF-7	breast:	n/a	n/a
30	CTCF	chr19:40388485-40388708	GM10248	blood:	n/a	n/a
31	CTCF	chr19:40404240-40404390	HBMEC	blood vessel:	n/a	n/a
32	CTCF	chr19:40372280-40372430	MCF-7	breast:	n/a	n/a
33	CTCF	chr19:40404260-40404410	AG04450	lung:	n/a	n/a
34	CTCF	chr19:40404260-40404410	GM12870	blood:	n/a	n/a
35	CTCF	chr19:40388365-40388850	A549	lung:	n/a	n/a
36	CTCF	chr19:40388270-40388904	A549	lung:	n/a	n/a
37	CTCF	chr19:40404099-40404559	A549	lung:	n/a	n/a
38	CTCF	chr19:40404080-40404230	HPAF	blood vessel:	n/a	n/a
39	CTCF	chr19:40404176-40404382	SK-N-SH_RA	brain:	n/a	n/a
40	CTCF	chr19:40372280-40372430	SK-N-SH_RA	brain:	n/a	n/a
41	CTCF	chr19:40372232-40372447	Pancreas_OC	pancreas:	n/a	n/a
42	CTCF	chr19:40388540-40388690	HFF	foreskin:	n/a	n/a
43	CTCF	chr19:40372640-40372790	GM06990	blood:	n/a	n/a
44	CTCF	chr19:40388520-40388670	WI-38	lung:	n/a	n/a
45	CTCF	chr19:40372280-40372430	RPTEC	kidney:	n/a	n/a
46	CTCF	chr19:40404240-40404390	AG09309	skin:	n/a	n/a
47	CTCF	chr19:40404240-40404390	AoAF	blood vessel:	n/a	n/a
48	CTCF	chr19:40372123-40372643	K562	blood:	n/a	chr19:40372450-40372463
49	CTCF	chr19:40388334-40388919	A549	lung:	n/a	n/a
50	CTCF	chr19:40372280-40372430	AoAF	blood vessel:	n/a	n/a

(count:1587 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:40391320-40391370	SK-N-SH	brain:	n/a
2	chr19:40391320-40391370	SK-N-SH	brain:	n/a
3	chr19:40377434-40377484	T-47D	breast:	n/a
4	chr19:40380319-40380369	SAEC	small airway:	n/a
5	chr19:40396538-40396588	ECC-1	luminal epithelium:	n/a
6	chr19:40399454-40399504	Hela-S3	cervix:	n/a
7	chr19:40368830-40368880	SK-N-SH	brain:	n/a
8	chr19:40396032-40396082	U87	brain:	n/a
9	chr19:40399454-40399504	GM19239	blood:	n/a
10	chr19:40397977-40398027	AoSMC	blood vessel:	n/a
11	chr19:40391320-40391370	PANC-1	pancreas:	n/a
12	chr19:40368363-40368413	PANC-1	pancreas:	n/a
13	chr19:40379680-40379730	AG09319	gingival:	n/a
14	chr19:40363285-40363335	PANC-1	pancreas:	n/a
15	chr19:40366394-40366444	NB4	blood:	n/a
16	chr19:40376883-40376933	LNCaP	prostate:	n/a
17	chr19:40379680-40379730	Hela-S3	cervix:	n/a
18	chr19:40398384-40398434	A549	lung:	n/a
19	chr19:40399454-40399504	HL-60	blood:	n/a
20	chr19:40366394-40366444	RPTEC	kidney:	n/a
21	chr19:40380853-40380903	SK-N-MC	brain:	n/a
22	chr19:40360856-40360906	BJ	skin:	n/a
23	chr19:40376883-40376933	NT2-D1	testis:	n/a
24	chr19:40368363-40368413	AG10803	skin:	n/a
25	chr19:40399454-40399504	HCF	heart:	n/a
26	chr19:40391320-40391370	Hepatocyte	liver:	n/a
27	chr19:40363285-40363335	HRCEpiC	kidney:	n/a
28	chr19:40396032-40396082	AoSMC	blood vessel:	n/a
29	chr19:40398384-40398434	LNCaP	prostate:	n/a
30	chr19:40397977-40398027	SK-N-MC	brain:	n/a
31	chr19:40362928-40362978	HMEC	breast:	n/a
32	chr19:40364151-40364201	HCF	heart:	n/a
33	chr19:40392568-40392618	RPTEC	kidney:	n/a
34	chr19:40360856-40360906	MCF-7	breast:	n/a
35	chr19:40376883-40376933	GM06990	blood:	n/a
36	chr19:40379680-40379730	AoSMC	blood vessel:	n/a
37	chr19:40368363-40368413	ProgFib	skin:	n/a
38	chr19:40388677-40388727	K562	blood:	n/a
39	chr19:40372977-40373027	BJ	skin:	n/a
40	chr19:40392568-40392618	BJ	skin:	n/a
41	chr19:40368363-40368413	HAEpiC	amniotic membrane:	n/a
42	chr19:40398384-40398434	Hepatocyte	liver:	n/a
43	chr19:40396032-40396082	HPAEpiC	pulmonary alveolar:	n/a
44	chr19:40391320-40391370	PrEC	prostate:	n/a
45	chr19:40391320-40391370	HEEpiC	esophagus:	n/a
46	chr19:40396032-40396082	Caco-2	colon:	n/a
47	chr19:40366088-40366138	H1-hESC	embryonic stem cell:	embryo
48	chr19:40368363-40368413	MCF-7	breast:	n/a
49	chr19:40362773-40362823	HIPEpiC	eye:	n/a
50	chr19:40368830-40368880	GM06990	blood:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:40403844..40404724-chr19:40476336..40477181,3	MCF-7	breast:
2	chr19:40371890..40372866-chr19:40388384..40389142,3	MCF-7	breast:
3	chr19:40357371..40360227-chr19:40360263..40362766,2	MCF-7	breast:
4	chr19:40371890..40372866-chr19:40388384..40389142,3	MCF-7	breast:
5	chr19:40371880..40372846-chr19:40476486..40477439,2	MCF-7	breast:

No data

Variant related genes	Relation type
FCGBP	TF binding region
FCGBP	CpG island
ENSG00000013275	chromatin interactions

Extended variants
information (count: 1735 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:1735 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs550855990	chr19:40360678-40360679	Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs558440659	chr19:40360686-40360687	Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs570108429	chr19:40360706-40360707	Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs530809818	chr19:40360723-40360724	Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs552665045	chr19:40360764-40360765	Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs115899699	chr19:40360776-40360777	Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs535080628	chr19:40360806-40360807	Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs112158994	chr19:40360828-40360829	Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs3760929	chr19:40360845-40360846	Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs374569267	chr19:40360867-40360868	Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs568268028	chr19:40360870-40360871	Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs368974681	chr19:40360875-40360876	Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs1053686	chr19:40360928-40360929	Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs199570976	chr19:40360934-40360935	Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs139526217	chr19:40360936-40360937	Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs200125442	chr19:40360937-40360938	Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs371263426	chr19:40360959-40360960	Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs575240993	chr19:40360960-40360961	Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs201020566	chr19:40360969-40360970	Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs145067279	chr19:40360973-40360974	Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs184463001	chr19:40360974-40360975	Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs374766909	chr19:40360981-40360982	Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs73930662	chr19:40361012-40361013	Enhancers Weak transcription Bivalent/Poised TSS Strong transcription Bivalent Enhancer Active TSS ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs367934901	chr19:40361013-40361014	Enhancers Weak transcription Bivalent/Poised TSS Strong transcription Bivalent Enhancer Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs140648438	chr19:40361031-40361032	Enhancers Weak transcription Bivalent/Poised TSS Strong transcription Bivalent Enhancer Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs370106966	chr19:40361038-40361039	Enhancers Weak transcription Bivalent/Poised TSS Strong transcription Bivalent Enhancer Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs540284772	chr19:40361042-40361043	Enhancers Weak transcription Bivalent/Poised TSS Strong transcription Bivalent Enhancer Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs200378087	chr19:40361055-40361056	Enhancers Weak transcription Bivalent/Poised TSS Strong transcription Bivalent Enhancer Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs373880753	chr19:40361101-40361102	Enhancers Weak transcription Bivalent/Poised TSS Strong transcription Bivalent Enhancer Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs3760931	chr19:40361112-40361113	Enhancers Weak transcription Bivalent/Poised TSS Strong transcription Bivalent Enhancer Active TSS ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs544566860	chr19:40361145-40361146	Enhancers Weak transcription Bivalent/Poised TSS Strong transcription Bivalent Enhancer Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs562621506	chr19:40361146-40361147	Enhancers Weak transcription Bivalent/Poised TSS Strong transcription Bivalent Enhancer Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs148526142	chr19:40361150-40361151	Enhancers Weak transcription Bivalent/Poised TSS Strong transcription Bivalent Enhancer Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs552303848	chr19:40361228-40361229	Enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs188932726	chr19:40361234-40361235	Enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs34811614	chr19:40361248-40361249	Enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs369065225	chr19:40361295-40361296	Enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs181666139	chr19:40361343-40361344	Enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs568355361	chr19:40361349-40361350	Enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs535648601	chr19:40361444-40361445	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs557258797	chr19:40361509-40361510	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs569466678	chr19:40361519-40361520	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs12972702	chr19:40361576-40361577	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs186164715	chr19:40361614-40361615	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs553433862	chr19:40361632-40361633	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs372514677	chr19:40361650-40361651	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs12972915	chr19:40361665-40361666	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs572009248	chr19:40361679-40361680	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs572758006	chr19:40361705-40361706	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs545902437	chr19:40361724-40361725	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Ovarian cancer	21720365	CNVD
Cancer	20164919	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Ductal carcinoma	22052326	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Breast cancer	21858162	CNVD
Breast cancer	17603634	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
renal disease	20603712	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21364760	CNVD
Invasive pancreatic ductal carcinoma	18765526	CNVD
Rhabdomyosarcoma	16790082	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Ovarian neoplasms	16753589	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Lung cancer	21569311	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	19029149	CNVD
Breast cancer	20409316	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Renal cell carcinoma	18765545	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Genital abnormality	22378287	CNVD
Hypospadia	22378287	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Astrocytoma	22246337	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:263 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:40349800-40369000	Weak transcription	Brain Anterior Caudate	brain
2	chr19:40350400-40372200	Weak transcription	Dnd41	blood
3	chr19:40350600-40365200	Weak transcription	Placenta	Placenta
4	chr19:40351000-40361000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chr19:40352000-40363200	Weak transcription	Duodenum Mucosa	Duodenum
6	chr19:40352000-40364200	Weak transcription	Fetal Muscle Trunk	muscle
7	chr19:40352000-40372600	Weak transcription	Primary T helper cells fromperipheralblood	blood
8	chr19:40352400-40372400	Weak transcription	Fetal Intestine Large	intestine
9	chr19:40352600-40364000	Weak transcription	Rectal Smooth Muscle	rectum
10	chr19:40353400-40366000	Strong transcription	Rectal Mucosa Donor 29	rectum
11	chr19:40354200-40370800	Weak transcription	Fetal Brain Female	brain
12	chr19:40354400-40362600	Weak transcription	Gastric	stomach
13	chr19:40354600-40362800	Weak transcription	Stomach Mucosa	stomach
14	chr19:40354600-40372200	Weak transcription	HepG2	liver
15	chr19:40355200-40372200	Weak transcription	Primary T helper cells PMA-I stimulated	--
16	chr19:40355800-40367200	Strong transcription	Primary T cells from cord blood	blood
17	chr19:40356200-40364400	Strong transcription	Fetal Intestine Small	intestine
18	chr19:40356200-40364600	Strong transcription	Colonic Mucosa	Colon
19	chr19:40356200-40365800	Strong transcription	Fetal Stomach	stomach
20	chr19:40357000-40362600	Strong transcription	Primary T killer naive cells fromperipheralblood	blood
21	chr19:40358000-40364000	Weak transcription	Primary B cells from cord blood	blood
22	chr19:40358400-40372200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
23	chr19:40358600-40363800	Weak transcription	Right Atrium	heart
24	chr19:40359800-40369600	Weak transcription	Fetal Muscle Leg	muscle
25	chr19:40360000-40361600	Weak transcription	Rectal Mucosa Donor 31	rectum
26	chr19:40360400-40363200	Strong transcription	Primary T cells fromperipheralblood	blood
27	chr19:40360400-40367000	Strong transcription	Sigmoid Colon	Sigmoid Colon
28	chr19:40360600-40360800	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr19:40360600-40360800	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr19:40360600-40360800	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
31	chr19:40360600-40360800	Active TSS	iPS-20b Cell Line	embryonic stem cell
32	chr19:40360600-40361000	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
33	chr19:40360600-40361200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr19:40360600-40361200	ZNF genes & repeats	Spleen	Spleen
35	chr19:40360600-40361400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
36	chr19:40360600-40361400	Enhancers	H1 Cell Line	embryonic stem cell
37	chr19:40360600-40361400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr19:40360600-40361400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
39	chr19:40360600-40366200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
40	chr19:40360800-40361000	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr19:40360800-40361000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
42	chr19:40360800-40361000	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
43	chr19:40360800-40361000	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
44	chr19:40360800-40361000	Enhancers	iPS-18 Cell Line	embryonic stem cell
45	chr19:40360800-40361000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
46	chr19:40360800-40361000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr19:40360800-40361200	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr19:40360800-40361400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr19:40360800-40361400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
50	chr19:40361000-40361200	Enhancers	HUES64 Cell Line	embryonic stem cell

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