Variant report

Variant	esv275463
Chromosome Location	chr19:42688997-42700516
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:127)
CpG islands
(count:61)
Chromatin interactive
region (count:22)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:42696114-42696310	HepG2	liver:	n/a	n/a
2	BCL3	chr19:42688198-42689252	A549	lung:	n/a	n/a
3	BHLHE40	chr19:42695949-42696510	HepG2	liver:	n/a	n/a
4	CBX3	chr19:42697513-42697810	K562	blood:	n/a	n/a
5	CEBPB	chr19:42696167-42696367	HepG2	liver:	n/a	n/a
6	CEBPB	chr19:42699430-42699624	K562	blood:	n/a	n/a
7	CTCF	chr19:42689020-42689170	HVMF	connective:	n/a	n/a
8	CTCF	chr19:42688913-42689001	GM19238	blood:	n/a	n/a
9	CTCF	chr19:42688980-42689130	AG10803	skin:	n/a	n/a
10	CTCF	chr19:42689000-42689150	HFF	foreskin:	n/a	n/a
11	CTCF	chr19:42688114-42689242	SK-N-SH	brain:	n/a	chr19:42688663-42688672 chr19:42688659-42688672 chr19:42688657-42688675 chr19:42688658-42688674 chr19:42688652-42688673 chr19:42688660-42688670
12	CTCF	chr19:42688906-42689019	GM10266	blood:	n/a	n/a
13	CTCF	chr19:42689060-42689210	A549	lung:	n/a	n/a
14	CTCF	chr19:42689410-42689437	GM20000	blood:	n/a	n/a
15	CTCF	chr19:42689020-42689170	A549	lung:	n/a	n/a
16	CTCF	chr19:42689552-42689687	Spleen_OC	spleen:	n/a	n/a
17	CTCF	chr19:42689560-42689710	GM12872	blood:	n/a	n/a
18	CTCF	chr19:42688255-42689027	HCT-116	colon:	n/a	chr19:42688663-42688672 chr19:42688659-42688672 chr19:42688657-42688675 chr19:42688658-42688674 chr19:42688652-42688673 chr19:42688660-42688670
19	CTCF	chr19:42688925-42689035	GM12878	blood:	n/a	n/a
20	CTCF	chr19:42687674-42690231	A549	lung:	n/a	chr19:42688663-42688672 chr19:42688659-42688672 chr19:42688657-42688675 chr19:42688658-42688674 chr19:42688652-42688673 chr19:42688660-42688670
21	CTCF	chr19:42688903-42689014	GM19240	blood:	n/a	n/a
22	CTCF	chr19:42689440-42689590	GM12866	blood:	n/a	n/a
23	CTCF	chr19:42689580-42689730	GM12873	blood:	n/a	n/a
24	E2F4	chr19:42696079-42696336	MCF10A-Er-Src	breast:	n/a	n/a
25	E2F6	chr19:42700409-42701439	H1-hESC	embryonic stem cell:	n/a	chr19:42700947-42700958 chr19:42700902-42700911
26	E2F6	chr19:42699268-42699395	K562	blood:	n/a	n/a
27	EP300	chr19:42696033-42696420	HepG2	liver:	n/a	n/a
28	FOS	chr19:42695989-42696446	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr19:42696005-42696445	MCF10A-Er-Src	breast:	n/a	n/a
30	FOS	chr19:42696032-42696417	MCF10A-Er-Src	breast:	n/a	n/a
31	FOS	chr19:42694158-42694488	MCF10A-Er-Src	breast:	n/a	n/a
32	FOS	chr19:42694158-42694506	MCF10A-Er-Src	breast:	n/a	chr19:42694497-42694506
33	FOS	chr19:42694166-42694454	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chr19:42696046-42696425	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr19:42697836-42698188	MCF10A-Er-Src	breast:	n/a	chr19:42698086-42698097
36	FOS	chr19:42688895-42689075	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr19:42697861-42698277	HUVEC	blood vessel:	n/a	chr19:42698086-42698097
38	FOS	chr19:42697876-42698213	MCF10A-Er-Src	breast:	n/a	chr19:42698086-42698097
39	FOSL1	chr19:42695779-42696533	HCT-116	colon:	n/a	n/a
40	FOSL2	chr19:42696058-42696374	A549	lung:	n/a	n/a
41	FOSL2	chr19:42688473-42689111	A549	lung:	n/a	n/a
42	FOSL2	chr19:42688435-42689041	A549	lung:	n/a	n/a
43	FOSL2	chr19:42695929-42696495	A549	lung:	n/a	n/a
44	FOSL2	chr19:42696066-42696453	HepG2	liver:	n/a	n/a
45	FOSL2	chr19:42700506-42701096	HepG2	liver:	n/a	n/a
46	GATA2	chr19:42697939-42698221	HUVEC	blood vessel:	n/a	chr19:42698098-42698112
47	GATA3	chr19:42688895-42689082	SH-SY5Y	brain:	n/a	n/a
48	GATA3	chr19:42697807-42697968	SH-SY5Y	brain:	n/a	n/a
49	JUN	chr19:42695949-42696600	K562	blood:	n/a	n/a
50	JUND	chr19:42696101-42696360	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:42698077-42698127	GM12892	blood:	n/a
2	chr19:42698077-42698127	BJ	skin:	n/a
3	chr19:42698077-42698127	HCM	heart:	n/a
4	chr19:42698077-42698127	AG09319	gingival:	n/a
5	chr19:42698077-42698127	SK-N-SH	brain:	n/a
6	chr19:42698077-42698127	Caco-2	colon:	n/a
7	chr19:42698077-42698127	PrEC	prostate:	n/a
8	chr19:42698077-42698127	NB4	blood:	n/a
9	chr19:42698077-42698127	AG04450	lung:	fetal
10	chr19:42698077-42698127	Hepatocyte	liver:	n/a
11	chr19:42698077-42698127	A549	lung:	n/a
12	chr19:42698077-42698127	PFSK-1	brain:	n/a
13	chr19:42698077-42698127	GM12878	blood:	n/a
14	chr19:42698077-42698127	GM06990	blood:	n/a
15	chr19:42698077-42698127	HCT-116	colon:	n/a
16	chr19:42698077-42698127	SAEC	small airway:	n/a
17	chr19:42698077-42698127	T-47D	breast:	n/a
18	chr19:42698077-42698127	GM19239	blood:	n/a
19	chr19:42698077-42698127	HIPEpiC	eye:	n/a
20	chr19:42698077-42698127	GM12891	blood:	n/a
21	chr19:42698077-42698127	AoSMC	blood vessel:	n/a
22	chr19:42698077-42698127	HL-60	blood:	n/a
23	chr19:42698077-42698127	MCF10A-Er-Src	breast:	n/a
24	chr19:42698077-42698127	NH-A	brain:	n/a
25	chr19:42698077-42698127	NT2-D1	testis:	n/a
26	chr19:42698077-42698127	HRPEpiC	eye:	n/a
27	chr19:42698077-42698127	HRCEpiC	kidney:	n/a
28	chr19:42698077-42698127	HMEC	breast:	n/a
29	chr19:42698077-42698127	Jurkat	blood:	n/a
30	chr19:42698077-42698127	AG09309	skin:	n/a
31	chr19:42698077-42698127	HPAEpiC	pulmonary alveolar:	n/a
32	chr19:42698077-42698127	HUVEC	blood vessel:	n/a
33	chr19:42698077-42698127	SK-N-SH_RA	brain:	n/a
34	chr19:42698077-42698127	BE2_C	brain:	n/a
35	chr19:42698077-42698127	H1-hESC	embryonic stem cell:	embryo
36	chr19:42698077-42698127	ovcar-3	ovarian:	n/a
37	chr19:42698077-42698127	HRE	kidney:	n/a
38	chr19:42698077-42698127	PANC-1	pancreas:	n/a
39	chr19:42698077-42698127	AG10803	skin:	n/a
40	chr19:42698077-42698127	HCPEpiC	choroid plexus:	n/a
41	chr19:42698077-42698127	LNCaP	prostate:	n/a
42	chr19:42698077-42698127	AG04449	skin:	fetal
43	chr19:42698077-42698127	U87	brain:	n/a
44	chr19:42698077-42698127	HepG2	liver:	n/a
45	chr19:42698077-42698127	SK-N-MC	brain:	n/a
46	chr19:42698077-42698127	RPTEC	kidney:	n/a
47	chr19:42698077-42698127	K562	blood:	n/a
48	chr19:42698077-42698127	HCF	heart:	n/a
49	chr19:42698077-42698127	Hela-S3	cervix:	n/a
50	chr19:42698077-42698127	HEEpiC	esophagus:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:42612392..42613330-chr19:42688089..42689604,8	MCF-7	breast:
2	chr19:42635897..42638300-chr19:42689525..42691049,2	MCF-7	breast:
3	chr19:42687399..42690060-chr19:42770420..42772705,2	K562	blood:
4	chr19:42689537..42691602-chr19:42692357..42693858,2	K562	blood:
5	chr19:42689537..42691602-chr19:42692357..42693858,2	K562	blood:
6	chr19:42695805..42698002-chr19:42744697..42747110,2	MCF-7	breast:
7	chr19:42612768..42613292-chr19:42688394..42689113,3	MCF-7	breast:
8	chr19:42692989..42696202-chr19:42701763..42704726,3	K562	blood:
9	chr19:42636977..42638186-chr19:42688284..42689046,3	MCF-7	breast:
10	chr19:42695492..42697523-chr19:42700242..42702425,2	MCF-7	breast:
11	chr16:1920642..1922271-chr19:42698953..42700453,2	K562	blood:
12	chr19:42637295..42639499-chr19:42687538..42690053,2	K562	blood:
13	chr19:42696224..42699166-chr19:42699583..42702405,3	K562	blood:
14	chr19:42695492..42697523-chr19:42700242..42702425,2	MCF-7	breast:
15	chr19:42696224..42699166-chr19:42699583..42702405,3	K562	blood:
16	chr19:42612418..42613472-chr19:42688181..42689150,6	K562	blood:
17	chr19:42699372..42701986-chr19:42805446..42807216,2	K562	blood:
18	chr19:42686573..42689269-chr19:42737459..42739419,2	MCF-7	breast:
19	chr19:42687243..42689479-chr19:42729926..42732337,2	MCF-7	breast:
20	chr19:42636571..42637932-chr19:42687904..42689192,14	MCF-7	breast:
21	chr19:42636828..42638293-chr19:42687653..42689156,13	K562	blood:
22	chr19:42687341..42690027-chr19:42800548..42802977,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DEDD2-3	chr19:42689379-42689519	l_1694_chr19:42679914-42689519_brain

No data

Variant related genes	Relation type
ENSG00000265122	TF binding region
ENSG00000265122	CpG island
ENSG00000266226	chromatin interactions
ENSG00000079462	chromatin interactions
ENSG00000162039	chromatin interactions
ENSG00000204957	chromatin interactions
ENSG00000105723	chromatin interactions
ENSG00000028277	chromatin interactions
ENSG00000265122	chromatin interactions
ENSG00000254887	chromatin interactions
ENSG00000079432	chromatin interactions
ENSG00000188368	chromatin interactions

Extended variants
information (count: 368 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:368 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs190934103	chr19:42688999-42689000	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs570563960	chr19:42689105-42689106	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs113494984	chr19:42689192-42689193	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs546234738	chr19:42689232-42689233	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs144217158	chr19:42689254-42689255	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs182758656	chr19:42689295-42689296	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs558275974	chr19:42689324-42689325	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs559668211	chr19:42689330-42689331	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs570175448	chr19:42689341-42689342	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs537679527	chr19:42689352-42689353	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs112606622	chr19:42689357-42689358	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs113328316	chr19:42689371-42689372	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs558876552	chr19:42689465-42689466	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
14	rs187878015	chr19:42689469-42689470	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
15	rs541491710	chr19:42689538-42689539	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs79589916	chr19:42689567-42689568	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs35088672	chr19:42689581-42689582	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs35366645	chr19:42689585-42689586	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs574854831	chr19:42689599-42689600	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs541783018	chr19:42689633-42689634	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs368180013	chr19:42689690-42689691	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs141804516	chr19:42689702-42689703	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs114204850	chr19:42689712-42689713	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs546018210	chr19:42689750-42689751	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs34611415	chr19:42689754-42689755	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs192602309	chr19:42689802-42689803	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs528173207	chr19:42689821-42689822	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs546245311	chr19:42689846-42689847	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs112181536	chr19:42689909-42689910	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs528852674	chr19:42689913-42689914	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs74730154	chr19:42689926-42689927	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs570054465	chr19:42689987-42689988	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs542603129	chr19:42690000-42690001	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs75694591	chr19:42690067-42690068	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs184582292	chr19:42690068-42690069	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs370891383	chr19:42690090-42690091	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs537343367	chr19:42690127-42690128	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs552742838	chr19:42690159-42690160	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs187417968	chr19:42690163-42690164	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs555954805	chr19:42690177-42690178	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs139352465	chr19:42690188-42690189	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs79971819	chr19:42690194-42690195	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs144083997	chr19:42690196-42690197	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs535879977	chr19:42690198-42690199	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs557071477	chr19:42690203-42690204	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs114861879	chr19:42690239-42690240	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs368890040	chr19:42690290-42690291	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs191899609	chr19:42690325-42690326	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs563946601	chr19:42690326-42690327	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs75662791	chr19:42690327-42690328	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:62)

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
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
Melanoma	20877625	CNVD

Chromatin state (count:462 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:42681800-42703600	Weak transcription	Right Atrium	heart
2	chr19:42686000-42690200	Enhancers	Primary B cells from cord blood	blood
3	chr19:42686000-42691200	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr19:42686600-42690800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
5	chr19:42687200-42689400	Enhancers	Primary T helper cells PMA-I stimulated	--
6	chr19:42687200-42690600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
7	chr19:42687400-42690200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
8	chr19:42687800-42690000	Enhancers	Primary B cells from peripheral blood	blood
9	chr19:42687800-42690400	Enhancers	Primary neutrophils fromperipheralblood	blood
10	chr19:42688000-42690800	Enhancers	Primary T cells fromperipheralblood	blood
11	chr19:42688000-42691000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
12	chr19:42688200-42689000	Enhancers	H1 Cell Line	embryonic stem cell
13	chr19:42688200-42689000	Enhancers	H9 Cell Line	embryonic stem cell
14	chr19:42688200-42689000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
15	chr19:42688200-42689200	Enhancers	HSMMtube	muscle
16	chr19:42688200-42689800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr19:42688200-42689800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr19:42688200-42689800	Enhancers	Duodenum Mucosa	Duodenum
19	chr19:42688200-42689800	Enhancers	HSMM	muscle
20	chr19:42688200-42690000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
21	chr19:42688200-42690200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr19:42688200-42690200	Enhancers	Primary T cells from cord blood	blood
23	chr19:42688200-42690200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
24	chr19:42688200-42690200	Enhancers	Primary T killer memory cells from peripheral blood	blood
25	chr19:42688200-42690200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr19:42688200-42690200	Enhancers	Dnd41	blood
27	chr19:42688200-42691000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
28	chr19:42688200-42691000	Enhancers	Primary T helper cells fromperipheralblood	blood
29	chr19:42688400-42689000	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr19:42688400-42689000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
31	chr19:42688400-42689000	Enhancers	Fetal Intestine Small	intestine
32	chr19:42688400-42689000	Enhancers	Rectal Mucosa Donor 29	rectum
33	chr19:42688400-42689200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
34	chr19:42688400-42689600	Enhancers	NH-A	brain
35	chr19:42688400-42689800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr19:42688400-42689800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr19:42688400-42689800	Enhancers	Rectal Mucosa Donor 31	rectum
38	chr19:42688400-42689800	Enhancers	Stomach Mucosa	stomach
39	chr19:42688400-42689800	Enhancers	HMEC	breast
40	chr19:42688400-42689800	Enhancers	NHEK	skin
41	chr19:42688400-42689800	Enhancers	Osteobl	bone
42	chr19:42688400-42690000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr19:42688400-42690200	Enhancers	Primary hematopoietic stem cells	blood
44	chr19:42688400-42690200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr19:42688400-42690200	Enhancers	Thymus	Thymus
46	chr19:42688400-42690200	Enhancers	Spleen	Spleen
47	chr19:42688400-42690800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr19:42688400-42690800	Enhancers	Fetal Thymus	thymus
49	chr19:42688600-42689000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr19:42688600-42689200	Enhancers	Muscle Satellite Cultured Cells	--

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