Variant report

Variant	esv3334703
Chromosome Location	chr19:23235234-23310623
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:776)
CpG islands
(count:1099)
Chromatin interactive
region (count:14)
LncRNA
region (count:43)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:776 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr19:23281757-23282018	K562	blood:	n/a	n/a
2	BACH1	chr19:23254012-23254386	K562	blood:	n/a	n/a
3	BACH1	chr19:23299870-23300328	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr19:23258207-23258737	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr19:23241803-23242011	GM12878	blood:	n/a	chr19:23241923-23241934
6	BHLHE40	chr19:23258049-23258086	HepG2	liver:	n/a	n/a
7	BHLHE40	chr19:23257962-23258012	K562	blood:	n/a	n/a
8	BHLHE40	chr19:23254011-23254389	K562	blood:	n/a	chr19:23254215-23254231
9	BRCA1	chr19:23254011-23254388	HepG2	liver:	n/a	n/a
10	BRCA1	chr19:23254014-23254389	Hela-S3	cervix:	n/a	n/a
11	BRCA1	chr19:23234916-23235282	H1-hESC	embryonic stem cell:	n/a	n/a
12	BRCA1	chr19:23300598-23300786	H1-hESC	embryonic stem cell:	n/a	n/a
13	CCNT2	chr19:23254011-23254389	K562	blood:	n/a	n/a
14	CCNT2	chr19:23281868-23282215	K562	blood:	n/a	n/a
15	CEBPB	chr19:23235188-23235496	MCF-7	breast:	n/a	n/a
16	CEBPB	chr19:23280099-23280412	K562	blood:	n/a	n/a
17	CEBPB	chr19:23240034-23240201	HepG2	liver:	n/a	n/a
18	CEBPB	chr19:23239294-23239733	HepG2	liver:	n/a	chr19:23239547-23239558
19	CEBPB	chr19:23280936-23281468	A549	lung:	n/a	n/a
20	CEBPB	chr19:23242586-23242857	HepG2	liver:	n/a	n/a
21	CEBPB	chr19:23277843-23279226	A549	lung:	n/a	chr19:23278069-23278080
22	CEBPB	chr19:23239223-23239759	A549	lung:	n/a	chr19:23239547-23239558
23	CEBPB	chr19:23282653-23283184	MCF-7	breast:	n/a	n/a
24	CEBPB	chr19:23239318-23239698	Hela-S3	cervix:	n/a	chr19:23239547-23239558
25	CEBPB	chr19:23280995-23281455	IMR90	lung:	n/a	n/a
26	CEBPB	chr19:23251316-23251448	HepG2	liver:	n/a	n/a
27	CEBPB	chr19:23235099-23235500	K562	blood:	n/a	n/a
28	CEBPB	chr19:23249983-23250335	IMR90	lung:	n/a	n/a
29	CEBPB	chr19:23257994-23258097	K562	blood:	n/a	n/a
30	CEBPB	chr19:23278916-23279218	HepG2	liver:	n/a	n/a
31	CEBPB	chr19:23249986-23250323	HepG2	liver:	n/a	n/a
32	CEBPB	chr19:23281078-23281462	HepG2	liver:	n/a	n/a
33	CEBPB	chr19:23246651-23246813	IMR90	lung:	n/a	n/a
34	CEBPB	chr19:23243871-23244604	A549	lung:	n/a	n/a
35	CEBPB	chr19:23243902-23244512	HepG2	liver:	n/a	n/a
36	CEBPB	chr19:23245824-23246792	HepG2	liver:	n/a	n/a
37	CEBPB	chr19:23234819-23235804	IMR90	lung:	n/a	chr19:23235596-23235607
38	CEBPB	chr19:23239330-23239725	IMR90	lung:	n/a	chr19:23239547-23239558
39	CEBPB	chr19:23278509-23278519	K562	blood:	n/a	n/a
40	CEBPB	chr19:23284339-23284539	A549	lung:	n/a	chr19:23284427-23284438
41	CEBPB	chr19:23279926-23280490	HepG2	liver:	n/a	n/a
42	CEBPB	chr19:23239380-23239693	MCF-7	breast:	n/a	chr19:23239547-23239558
43	CEBPB	chr19:23284380-23284452	IMR90	lung:	n/a	chr19:23284427-23284438
44	CEBPB	chr19:23282696-23283194	IMR90	lung:	n/a	n/a
45	CEBPB	chr19:23307308-23307376	HepG2	liver:	n/a	chr19:23307325-23307336
46	CEBPB	chr19:23300598-23300666	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr19:23243128-23243227	HepG2	liver:	n/a	n/a
48	CEBPB	chr19:23248322-23248486	A549	lung:	n/a	n/a
49	CEBPB	chr19:23245848-23246757	A549	lung:	n/a	n/a
50	CEBPB	chr19:23249008-23249222	A549	lung:	n/a	n/a

(count:1099 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:23300066-23300116	PFSK-1	brain:	n/a
2	chr19:23300066-23300116	PFSK-1	brain:	n/a
3	chr19:23250275-23250325	HIPEpiC	eye:	n/a
4	chr19:23253797-23253847	MCF10A-Er-Src	breast:	n/a
5	chr19:23258096-23258146	HCF	heart:	n/a
6	chr19:23250275-23250325	MCF10A-Er-Src	breast:	n/a
7	chr19:23253797-23253847	GM12891	blood:	n/a
8	chr19:23258148-23258198	GM12891	blood:	n/a
9	chr19:23253834-23253884	NT2-D1	testis:	n/a
10	chr19:23300066-23300116	ovcar-3	ovarian:	n/a
11	chr19:23250275-23250325	BJ	skin:	n/a
12	chr19:23299889-23299939	SKMC	muscle:	n/a
13	chr19:23300243-23300293	HCM	heart:	n/a
14	chr19:23253797-23253847	NHDF-neo	bronchial:	n/a
15	chr19:23299889-23299939	HEEpiC	esophagus:	n/a
16	chr19:23253834-23253884	BJ	skin:	n/a
17	chr19:23258573-23258623	NHDF-neo	bronchial:	n/a
18	chr19:23299728-23299778	AG09309	skin:	n/a
19	chr19:23254131-23254181	HIPEpiC	eye:	n/a
20	chr19:23254381-23254431	GM19239	blood:	n/a
21	chr19:23253834-23253884	SAEC	small airway:	n/a
22	chr19:23258096-23258146	HEK293	kidney:	embryo
23	chr19:23300243-23300293	HCT-116	colon:	n/a
24	chr19:23254131-23254181	HCT-116	colon:	n/a
25	chr19:23258573-23258623	SAEC	small airway:	n/a
26	chr19:23253797-23253847	PrEC	prostate:	n/a
27	chr19:23258484-23258534	PrEC	prostate:	n/a
28	chr19:23258096-23258146	HPAEpiC	pulmonary alveolar:	n/a
29	chr19:23253797-23253847	GM12878	blood:	n/a
30	chr19:23300066-23300116	U87	brain:	n/a
31	chr19:23254381-23254431	ECC-1	luminal epithelium:	n/a
32	chr19:23250275-23250325	SK-N-SH_RA	brain:	n/a
33	chr19:23257319-23257369	HCPEpiC	choroid plexus:	n/a
34	chr19:23299889-23299939	A549	lung:	n/a
35	chr19:23299649-23299699	AoSMC	blood vessel:	n/a
36	chr19:23299649-23299699	GM12892	blood:	n/a
37	chr19:23253834-23253884	ECC-1	luminal epithelium:	n/a
38	chr19:23299889-23299939	LNCaP	prostate:	n/a
39	chr19:23300243-23300293	AG10803	skin:	n/a
40	chr19:23253797-23253847	HRCEpiC	kidney:	n/a
41	chr19:23253455-23253505	AG10803	skin:	n/a
42	chr19:23299889-23299939	HRCEpiC	kidney:	n/a
43	chr19:23299889-23299939	HPAEpiC	pulmonary alveolar:	n/a
44	chr19:23253316-23253366	GM12891	blood:	n/a
45	chr19:23258148-23258198	HCM	heart:	n/a
46	chr19:23253455-23253505	AG04449	skin:	fetal
47	chr19:23253834-23253884	HEEpiC	esophagus:	n/a
48	chr19:23254381-23254431	NHBE	bronchial:	n/a
49	chr19:23258148-23258198	HCPEpiC	choroid plexus:	n/a
50	chr19:23253834-23253884	HRCEpiC	kidney:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:23256417..23259218-chr19:23299816..23301387,2	MCF-7	breast:
2	chr19:23305214..23307140-chr19:23310499..23313073,2	MCF-7	breast:
3	chr19:23252878..23255716-chr19:23257879..23260190,3	MCF-7	breast:
4	chr1:156184731..156186500-chr19:23252697..23254216,3	K562	blood:
5	chr19:23258209..23259774-chr19:23281850..23284587,2	MCF-7	breast:
6	chr19:23257908..23260117-chr19:23261003..23263965,2	MCF-7	breast:
7	chr19:23299713..23300295-chr19:24269911..24270643,3	Hela-S3	cervix:
8	chr19:23305214..23307140-chr19:23310499..23313073,2	MCF-7	breast:
9	chr19:23252878..23255716-chr19:23257879..23260190,3	MCF-7	breast:
10	chr19:23252641..23255002-chr19:23257415..23259086,2	K562	blood:
11	chr19:23258209..23259774-chr19:23281850..23284587,2	MCF-7	breast:
12	chr19:23257421..23258419-chr3:62304521..62305100,2	MCF-7	breast:
13	chr19:23298392..23301079-chr19:23302375..23304174,2	MCF-7	breast:
14	chr19:23252641..23255002-chr19:23257415..23259086,2	K562	blood:

(count:43 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF724P-1	chr19:23244413-23244554	ENSG00000261615.2
2	lnc-ZNF724P-1	chr19:23242976-23243120	ENSG00000261615.2
3	lnc-ZNF724P-5	chr19:23251245-23251366	NONHSAT063851
4	lnc-ZNF724P-1	chr19:23243449-23243800	ENSG00000251233
5	lnc-ZNF724P-1	chr19:23243975-23244067	ENSG00000261615.1
6	lnc-ZNF724P-1	chr19:23239105-23239211	ENSG00000261615.1
7	lnc-ZNF724P-1	chr19:23239105-23239211	ENSG00000251233
8	lnc-ZNF724P-1	chr19:23239814-23240022	ENSG00000261615.1
9	lnc-ZNF724P-1	chr19:23243449-23243800	ENSG00000261615.1
10	lnc-ZNF724P-1	chr19:23239814-23240022	XLOC_013273
11	lnc-ZNF724P-1	chr19:23237629-23238132	ENSG00000251233
12	lnc-ZNF724P-1	chr19:23239105-23239211	XLOC_013273
13	lnc-ZNF730-6	chr19:23282852-23283163	ENSG00000267886.1
14	lnc-ZNF730-1	chr19:23290627-23290865	XLOC_013018
15	lnc-ZNF724P-1	chr19:23239814-23240022	ENSG00000251233
16	lnc-ZNF724P-1	chr19:23241267-23241381	ENSG00000251233
17	lnc-ZNF730-1	chr19:23294625-23294867	XLOC_013018
18	lnc-ZNF730-6	chr19:23278065-23278503	NONHSAT063857
19	lnc-ZNF724P-1	chr19:23237627-23238132	XLOC_013273
20	lnc-ZNF724P-5	chr19:23251848-23252030	NONHSAT063851
21	lnc-ZNF724P-4	chr19:23305990-23306890	NONHSAT063861
22	lnc-ZNF724P-5	chr19:23250758-23250844	NONHSAT063851
23	lnc-ZNF724P-1	chr19:23238284-23238592	XLOC_013273
24	lnc-ZNF724P-1	chr19:23242976-23243120	ENSG00000251233
25	lnc-ZNF724P-1	chr19:23237625-23238132	ENSG00000261615.1
26	lnc-ZNF724P-5	chr19:23251699-23251747	NONHSAT063851
27	lnc-ZNF724P-1	chr19:23242976-23243120	XLOC_013273
28	lnc-ZNF724P-1	chr19:23243449-23243800	XLOC_013273
29	lnc-ZNF730-6	chr19:23278651-23279073	NONHSAT063857
30	lnc-ZNF724P-1	chr19:23241267-23241381	XLOC_013273
31	lnc-ZNF724P-1	chr19:23238284-23238521	XLOC_013273
32	lnc-ZNF724P-1	chr19:23242976-23243244	NONHSAT063850
33	lnc-ZNF724P-1	chr19:23238284-23238592	ENSG00000261615.1
34	lnc-ZNF724P-1	chr19:23243975-23244067	XLOC_013273
35	lnc-ZNF724P-1	chr19:23243975-23244067	ENSG00000251233
36	lnc-ZNF724P-1	chr19:23239420-23240022	NONHSAT063850
37	lnc-ZNF724P-1	chr19:23242976-23243120	ENSG00000261615.1
38	lnc-ZNF724P-1	chr19:23238284-23238592	ENSG00000251233
39	lnc-ZNF724P-1	chr19:23241267-23241381	ENSG00000261615.1
40	lnc-ZNF730-6	chr19:23281142-23281215	ENSG00000267886.1
41	lnc-ZNF730-5	chr19:23299777-23299978	NONHSAT063860
42	lnc-ZNF730-6	chr19:23258013-23258189	ENSG00000267886.1
43	lnc-ZNF724P-1	chr19:23237399-23237800	NONHSAT063848

No data

Variant related genes	Relation type
ENSG00000268105	TF binding region
ENSG00000269543	TF binding region
ENSG00000261615	TF binding region
ENSG00000267886	TF binding region
ZNF730	TF binding region
SNX6P1	TF binding region
ENSG00000270479	TF binding region
ENSG00000268105	CpG island
ENSG00000269543	CpG island
ENSG00000261615	CpG island
ENSG00000267886	CpG island
ZNF730	CpG island
SNX6P1	CpG island
ENSG00000270479	CpG island
ENSG00000241472	chromatin interactions
ENSG00000183850	chromatin interactions
ENSG00000267920	chromatin interactions
ENSG00000213096	chromatin interactions
ENSG00000269543	chromatin interactions
ENSG00000114405	chromatin interactions
ENSG00000270479	chromatin interactions
ENSG00000267886	chromatin interactions
PALLD	miRNA target sites
SYVN1	miRNA target sites
ARHGAP28	miRNA target sites
CPEB3	miRNA target sites
SRP9	miRNA target sites
SMARCAD1	miRNA target sites
C11orf57	miRNA target sites
SUV420H2	miRNA target sites

Extended variants
information (count: 2861 )
Associated
traits (count: 45 )

Variant overlapped rSNPs/rCNVs (count:2861 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535305747	chr19:23235308-23235309	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs140949924	chr19:23235322-23235323	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs113614641	chr19:23235337-23235338	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs181183320	chr19:23235370-23235371	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs557373298	chr19:23235402-23235403	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs184661129	chr19:23235464-23235465	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs2126615	chr19:23235485-23235486	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs555662615	chr19:23235489-23235490	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs574141084	chr19:23235524-23235525	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs556458131	chr19:23235549-23235550	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs560038819	chr19:23235575-23235576	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs578252097	chr19:23235626-23235627	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs545410554	chr19:23235684-23235685	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs532187288	chr19:23235724-23235725	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs189209633	chr19:23235746-23235747	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs111594270	chr19:23235748-23235749	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs58704317	chr19:23235767-23235768	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs538849436	chr19:23235787-23235788	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs143723874	chr19:23235798-23235799	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs558422092	chr19:23235813-23235814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs547284718	chr19:23235823-23235824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs74350750	chr19:23235831-23235832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs181589494	chr19:23235841-23235842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs550943178	chr19:23235888-23235889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs569349412	chr19:23235930-23235931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs80277899	chr19:23235948-23235949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs77073981	chr19:23235972-23235973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs375281596	chr19:23235981-23235982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs142783118	chr19:23235993-23235994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs73555455	chr19:23235994-23235995	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs186448331	chr19:23236021-23236022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs578249014	chr19:23236040-23236041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs200237995	chr19:23236115-23236116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs73027665	chr19:23236120-23236121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs116571563	chr19:23236137-23236138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs563657891	chr19:23236158-23236159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs540775488	chr19:23236161-23236162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs575566840	chr19:23236201-23236202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs542659114	chr19:23236261-23236262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs144503765	chr19:23236301-23236302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs560546935	chr19:23236306-23236307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs547188004	chr19:23236349-23236350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs377661178	chr19:23236361-23236362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs559152057	chr19:23236369-23236370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs533044869	chr19:23236380-23236381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs190867227	chr19:23236440-23236441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs551230117	chr19:23236466-23236467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs569870433	chr19:23236515-23236516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs537002931	chr19:23236520-23236521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs180915570	chr19:23236521-23236522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:45)

Disease	PMID	Source
Medulloblastoma	16783165	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Prostate cancer	16573809	CNVD
Chordoma	18071362	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
ovarian endometriomas	16273235	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Cervical cancer	21063398	CNVD
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	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
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Lung cancer	18438408	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Myelofibrosis	22110671	CNVD
Cancer	21183584	CNVD
Colorectal cancer	20459617	CNVD
small cell lung cancer	20016488	CNVD
Ductal carcinoma	22052326	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1287 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:23235000-23235800	Enhancers	Placenta	Placenta
2	chr19:23235800-23237200	Weak transcription	Placenta	Placenta
3	chr19:23237200-23240400	Enhancers	Placenta	Placenta
4	chr19:23240400-23242200	Weak transcription	Placenta	Placenta
5	chr19:23242200-23243200	Enhancers	Placenta	Placenta
6	chr19:23248200-23248600	Enhancers	Placenta	Placenta
7	chr19:23248600-23252600	Weak transcription	Placenta	Placenta
8	chr19:23249800-23253200	Weak transcription	Brain Substantia Nigra	brain
9	chr19:23252000-23253000	Weak transcription	Fetal Kidney	kidney
10	chr19:23252400-23252600	Weak transcription	Pancreas	Pancrea
11	chr19:23252600-23253000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr19:23252800-23253400	Bivalent Enhancer	Placenta	Placenta
13	chr19:23253000-23253200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr19:23253000-23253200	Active TSS	Ovary	ovary
15	chr19:23253000-23253200	Enhancers	Right Ventricle	heart
16	chr19:23253000-23253400	Flanking Bivalent TSS/Enh	Adipose Nuclei	Adipose
17	chr19:23253000-23253400	Active TSS	Colon Smooth Muscle	Colon
18	chr19:23253000-23253400	Active TSS	Fetal Kidney	kidney
19	chr19:23253000-23253600	Active TSS	HUES6 Cell Line	embryonic stem cell
20	chr19:23253000-23253600	Enhancers	Pancreas	Pancrea
21	chr19:23253000-23254400	Bivalent/Poised TSS	Primary T cells from cord blood	blood
22	chr19:23253000-23254400	Active TSS	Muscle Satellite Cultured Cells	--
23	chr19:23253000-23254600	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr19:23253000-23254600	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr19:23253200-23253400	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
26	chr19:23253200-23253400	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
27	chr19:23253200-23253400	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
28	chr19:23253200-23253400	Flanking Bivalent TSS/Enh	Brain Hippocampus Middle	brain
29	chr19:23253200-23253400	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
30	chr19:23253200-23253400	Active TSS	Brain Substantia Nigra	brain
31	chr19:23253200-23253400	Bivalent Enhancer	Esophagus	oesophagus
32	chr19:23253200-23253400	Enhancers	Spleen	Spleen
33	chr19:23253200-23253400	Bivalent/Poised TSS	Monocytes-CD14+_RO01746	blood
34	chr19:23253200-23253600	Flanking Bivalent TSS/Enh	Breast Myoepithelial Primary Cells	Breast
35	chr19:23253200-23253600	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
36	chr19:23253200-23253600	Bivalent/Poised TSS	Brain Anterior Caudate	brain
37	chr19:23253200-23253800	Flanking Active TSS	Primary hematopoietic stem cells	blood
38	chr19:23253200-23253800	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
39	chr19:23253200-23253800	Flanking Active TSS	Ovary	ovary
40	chr19:23253200-23254000	Active TSS	HUES64 Cell Line	embryonic stem cell
41	chr19:23253200-23254000	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
42	chr19:23253200-23254000	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr19:23253200-23254000	Flanking Bivalent TSS/Enh	Fetal Brain Female	brain
44	chr19:23253200-23254000	Active TSS	Pancreatic Islets	Pancreatic Islet
45	chr19:23253200-23254000	Flanking Bivalent TSS/Enh	Fetal Stomach	stomach
46	chr19:23253200-23254000	Active TSS	Right Atrium	heart
47	chr19:23253200-23254200	Active TSS	Primary B cells from cord blood	blood
48	chr19:23253200-23254400	Bivalent Enhancer	Primary B cells from peripheral blood	blood
49	chr19:23253200-23254400	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr19:23253200-23254400	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle

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