Variant report

Variant	nsv890623
Chromosome Location	chr8:19307051-19383697
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:373)
CpG islands
(count:1040)
Chromatin interactive
region (count:13)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:373 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:19315644-19316288	HepG2	liver:	n/a	n/a
2	BHLHE40	chr8:19315585-19316177	HepG2	liver:	n/a	n/a
3	BRCA1	chr8:19340994-19341377	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr8:19359251-19359614	HepG2	liver:	n/a	n/a
5	CEBPB	chr8:19314220-19314355	HepG2	liver:	n/a	n/a
6	CEBPB	chr8:19369943-19370277	HepG2	liver:	n/a	chr8:19370099-19370110
7	CEBPB	chr8:19341066-19341426	IMR90	lung:	n/a	n/a
8	CEBPB	chr8:19382472-19382577	IMR90	lung:	n/a	chr8:19382510-19382523
9	CEBPB	chr8:19357842-19358221	IMR90	lung:	n/a	n/a
10	CEBPB	chr8:19359253-19359610	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr8:19359403-19359451	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr8:19359039-19359621	IMR90	lung:	n/a	chr8:19359166-19359179
13	CEBPB	chr8:19369932-19370292	IMR90	lung:	n/a	chr8:19370099-19370110
14	CEBPB	chr8:19334148-19334165	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr8:19370039-19370238	Hela-S3	cervix:	n/a	chr8:19370099-19370110
16	CEBPB	chr8:19342032-19342249	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr8:19334071-19334621	IMR90	lung:	n/a	n/a
18	CEBPB	chr8:19369979-19370228	H1-hESC	embryonic stem cell:	n/a	chr8:19370099-19370110
19	CEBPB	chr8:19340956-19341667	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr8:19369925-19370259	K562	blood:	n/a	chr8:19370099-19370110
21	CEBPB	chr8:19369972-19370279	A549	lung:	n/a	chr8:19370099-19370110
22	CEBPB	chr8:19359084-19359602	A549	lung:	n/a	chr8:19359166-19359179
23	CHD2	chr8:19340983-19341727	Hela-S3	cervix:	n/a	n/a
24	CREB1	chr8:19315511-19316278	HepG2	liver:	n/a	n/a
25	CTCF	chr8:19325600-19325750	HPAF	blood vessel:	n/a	n/a
26	CTCF	chr8:19325500-19325650	WERI-Rb-1	eye:	n/a	n/a
27	CTCF	chr8:19325560-19325710	AG09319	gingival:	n/a	n/a
28	CTCF	chr8:19369196-19369236	Kidney_OC	kidney:	n/a	n/a
29	CTCF	chr8:19325500-19325650	HPF	lung:	n/a	n/a
30	CTCF	chr8:19325560-19325710	AG04450	lung:	n/a	n/a
31	CTCF	chr8:19346580-19346730	RPTEC	kidney:	n/a	n/a
32	CTCF	chr8:19325540-19325690	HCT-116	colon:	n/a	n/a
33	CTCF	chr8:19325680-19325830	RPTEC	kidney:	n/a	n/a
34	CTCF	chr8:19357360-19357510	AG04450	lung:	n/a	n/a
35	CTCF	chr8:19325600-19325750	HRPEpiC	eye:	n/a	n/a
36	CTCF	chr8:19325627-19325695	GM12878	blood:	n/a	n/a
37	CTCF	chr8:19325520-19325670	HMF	breast:	n/a	n/a
38	CTCF	chr8:19319274-19319328	MCF-7	breast:	n/a	n/a
39	CTCF	chr8:19325483-19325689	A549	lung:	n/a	n/a
40	CTCF	chr8:19325566-19325728	HUVEC	blood vessel:	n/a	n/a
41	CTCF	chr8:19325560-19325710	HCPEpiC	choroid plexus:	n/a	n/a
42	CTCF	chr8:19325522-19325730	HepG2	liver:	n/a	n/a
43	CTCF	chr8:19325435-19325743	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr8:19325560-19325710	Hela-S3	cervix:	n/a	n/a
45	CTCF	chr8:19319235-19319265	GM12891	blood:	n/a	n/a
46	CTCF	chr8:19376140-19376290	HepG2	liver:	n/a	n/a
47	CTCF	chr8:19325540-19325690	MCF-7	breast:	n/a	n/a
48	CTCF	chr8:19325541-19325735	IMR90	lung:	n/a	n/a
49	CTCF	chr8:19325569-19325749	MCF-7	breast:	n/a	n/a
50	CTCF	chr8:19346560-19346710	GM12864	blood:	n/a	n/a

(count:1040 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:19316005-19316055	AG04450	lung:	fetal
2	chr8:19319451-19319501	ECC-1	luminal epithelium:	n/a
3	chr8:19319171-19319221	SAEC	small airway:	n/a
4	chr8:19316005-19316055	AG04450	lung:	fetal
5	chr8:19319451-19319501	ECC-1	luminal epithelium:	n/a
6	chr8:19319171-19319221	SAEC	small airway:	n/a
7	chr8:19321936-19321986	IMR90	lung:	fetal
8	chr8:19347157-19347207	GM12892	blood:	n/a
9	chr8:19317380-19317430	GM06990	blood:	n/a
10	chr8:19319212-19319262	Hepatocyte	liver:	n/a
11	chr8:19319451-19319501	ovcar-3	ovarian:	n/a
12	chr8:19339859-19339909	HAEpiC	amniotic membrane:	n/a
13	chr8:19319171-19319221	T-47D	breast:	n/a
14	chr8:19333253-19333303	AG04449	skin:	fetal
15	chr8:19319451-19319501	HEK293	kidney:	embryo
16	chr8:19318545-19318595	NHDF-neo	bronchial:	n/a
17	chr8:19369752-19369802	IMR90	lung:	fetal
18	chr8:19317380-19317430	NHDF-neo	bronchial:	n/a
19	chr8:19319451-19319501	K562	blood:	n/a
20	chr8:19347157-19347207	GM12878	blood:	n/a
21	chr8:19339859-19339909	MCF10A-Er-Src	breast:	n/a
22	chr8:19369752-19369802	HRCEpiC	kidney:	n/a
23	chr8:19321936-19321986	HUVEC	blood vessel:	n/a
24	chr8:19317380-19317430	HRE	kidney:	n/a
25	chr8:19319031-19319081	MCF-7	breast:	n/a
26	chr8:19347157-19347207	HEK293	kidney:	embryo
27	chr8:19339859-19339909	HEK293	kidney:	embryo
28	chr8:19319451-19319501	HRE	kidney:	n/a
29	chr8:19333253-19333303	HIPEpiC	eye:	n/a
30	chr8:19339859-19339909	GM12892	blood:	n/a
31	chr8:19363452-19363502	NH-A	brain:	n/a
32	chr8:19347157-19347207	AG09319	gingival:	n/a
33	chr8:19319031-19319081	PANC-1	pancreas:	n/a
34	chr8:19319031-19319081	Hepatocyte	liver:	n/a
35	chr8:19347157-19347207	ECC-1	luminal epithelium:	n/a
36	chr8:19347157-19347207	NHDF-neo	bronchial:	n/a
37	chr8:19318545-19318595	AG10803	skin:	n/a
38	chr8:19318545-19318595	HCT-116	colon:	n/a
39	chr8:19339859-19339909	GM06990	blood:	n/a
40	chr8:19318160-19318210	GM12878	blood:	n/a
41	chr8:19347157-19347207	HRPEpiC	eye:	n/a
42	chr8:19354440-19354490	HL-60	blood:	n/a
43	chr8:19347157-19347207	SK-N-SH	brain:	n/a
44	chr8:19310134-19310184	MCF-7	breast:	n/a
45	chr8:19333253-19333303	SAEC	small airway:	n/a
46	chr8:19317380-19317430	NHBE	bronchial:	n/a
47	chr8:19310134-19310184	HRCEpiC	kidney:	n/a
48	chr8:19319171-19319221	Hela-S3	cervix:	n/a
49	chr8:19319031-19319081	HPAEpiC	pulmonary alveolar:	n/a
50	chr8:19318160-19318210	GM19239	blood:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:19335994..19338112-chr8:19352169..19353852,2	K562	blood:
2	chr8:19328304..19330762-chr8:19331773..19333660,2	MCF-7	breast:
3	chr8:19316428..19318779-chr8:19615686..19617194,2	MCF-7	breast:
4	chr2:72613280..72613780-chr8:19325545..19326087,2	MCF-7	breast:
5	chr8:19371116..19373771-chr8:19377059..19378982,3	K562	blood:
6	chr8:19328304..19330762-chr8:19331773..19333660,2	MCF-7	breast:
7	chr8:19329451..19331430-chr8:19331849..19333988,2	K562	blood:
8	chr8:19329451..19331430-chr8:19331849..19333988,2	K562	blood:
9	chr8:19352728..19355401-chr8:19358201..19360523,2	K562	blood:
10	chr8:19371116..19373771-chr8:19377059..19378982,3	K562	blood:
11	chr8:19265734..19267679-chr8:19315325..19317057,2	MCF-7	breast:
12	chr8:19352728..19355401-chr8:19358201..19360523,2	K562	blood:
13	chr8:19265643..19266634-chr8:19325530..19326091,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PSD3-3	chr8:19363627-19363641	NONHSAT125379
2	lnc-PSD3-3	chr8:19363548-19363641	NONHSAT125378
3	lnc-PSD3-3	chr8:19363391-19363641	NONHSAT125376
4	lnc-PSD3-3	chr8:19363417-19363641	NONHSAT125377

No data

Variant related genes	Relation type
CSGALNACT1	TF binding region
CSGALNACT1	CpG island
ENSG00000147408	chromatin interactions

Extended variants
information (count: 4623 )
Associated
traits (count: 117 )

Variant overlapped rSNPs/rCNVs (count:4623 , 50 per page) page: 1 2 3 4 5 6 7 ... 93

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7835461	chr8:19307051-19307052	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs537615932	chr8:19307066-19307067	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs79595525	chr8:19307091-19307092	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs199705620	chr8:19307122-19307123	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs532131882	chr8:19307144-19307145	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs551965973	chr8:19307208-19307209	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs201343133	chr8:19307291-19307292	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs180875859	chr8:19307308-19307309	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs576158309	chr8:19307321-19307322	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs544063197	chr8:19307345-19307346	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs567954026	chr8:19307387-19307388	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs370680214	chr8:19307394-19307395	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs562716738	chr8:19307448-19307449	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs529917104	chr8:19307498-19307499	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs542107172	chr8:19307529-19307530	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs534692551	chr8:19307562-19307563	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs139516386	chr8:19307591-19307592	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs552360494	chr8:19307633-19307634	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs186062528	chr8:19307645-19307646	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs202031704	chr8:19307660-19307661	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs138949881	chr8:19307671-19307672	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs187267716	chr8:19307677-19307678	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs548012805	chr8:19307734-19307735	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs568037879	chr8:19307762-19307763	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs572331836	chr8:19307819-19307820	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs565983903	chr8:19307820-19307821	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs534588020	chr8:19307822-19307823	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs144339481	chr8:19307876-19307877	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs146573326	chr8:19307921-19307922	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs190502022	chr8:19307928-19307929	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs117898893	chr8:19307946-19307947	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs559130972	chr8:19307957-19307958	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs572583137	chr8:19307959-19307960	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs73585528	chr8:19307966-19307967	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs561267685	chr8:19307971-19307972	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs574443541	chr8:19307989-19307990	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs543419782	chr8:19308002-19308003	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs189028370	chr8:19308020-19308021	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs532293602	chr8:19308021-19308022	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs552216099	chr8:19308027-19308028	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs111914141	chr8:19308093-19308094	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs528313876	chr8:19308095-19308096	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs548263146	chr8:19308112-19308113	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs568166053	chr8:19308121-19308122	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs35029660	chr8:19308126-19308127	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs193151128	chr8:19308146-19308147	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs570338481	chr8:19308176-19308177	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs539320945	chr8:19308177-19308178	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs149937191	chr8:19308198-19308199	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs144982955	chr8:19308212-19308213	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:117)

Disease	PMID	Source
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Colorectal cancer	16272173	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Epilepsy	22083797	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	17603634	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Bladder cancer	21909424	CNVD
Multiple myeloma	17550852	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21364760	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cancer	18840272	CNVD
Breast cancer	19602461	CNVD
Osteosarcoma	19286668	CNVD
Prostate cancer	19242612	CNVD
Prostate cancer	19258508	CNVD
small cell lung cancer	20016488	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Gastric adenocarcinoma	19115996	CNVD
Colorectal cancer	19455253	CNVD
Prostate cancer	22341455	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	22522925	CNVD
Renal cell carcinoma	21215367	CNVD

Chromatin state (count:1760 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:19277600-19307800	Weak transcription	Fetal Stomach	stomach
2	chr8:19283800-19307800	Weak transcription	Ovary	ovary
3	chr8:19291600-19308000	Weak transcription	Right Ventricle	heart
4	chr8:19295000-19318800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr8:19296600-19309400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr8:19296600-19317400	Weak transcription	Hela-S3	cervix
7	chr8:19297200-19309200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr8:19297400-19313400	Weak transcription	Brain Cingulate Gyrus	brain
9	chr8:19297600-19307800	Weak transcription	Left Ventricle	heart
10	chr8:19297600-19308000	Weak transcription	Monocytes-CD14+_RO01746	blood
11	chr8:19297600-19319000	Weak transcription	Spleen	Spleen
12	chr8:19300000-19313800	Weak transcription	Fetal Heart	heart
13	chr8:19300600-19319200	Weak transcription	Gastric	stomach
14	chr8:19301600-19317200	Weak transcription	Skeletal Muscle Male	skeletal muscle
15	chr8:19301800-19307800	Weak transcription	Right Atrium	heart
16	chr8:19302800-19317800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr8:19303000-19307800	Weak transcription	Primary monocytes fromperipheralblood	blood
18	chr8:19303200-19307800	Weak transcription	Adipose Nuclei	Adipose
19	chr8:19303200-19307800	Weak transcription	Thymus	Thymus
20	chr8:19303200-19307800	Weak transcription	Dnd41	blood
21	chr8:19303200-19308000	Weak transcription	Primary B cells from cord blood	blood
22	chr8:19303200-19308000	Weak transcription	HepG2	liver
23	chr8:19303200-19309200	Weak transcription	Brain Angular Gyrus	brain
24	chr8:19303200-19309800	Weak transcription	Primary hematopoietic stem cells	blood
25	chr8:19303200-19313800	Weak transcription	HUVEC	blood vessel
26	chr8:19303400-19307800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
27	chr8:19303400-19315200	Enhancers	Primary T helper cells PMA-I stimulated	--
28	chr8:19303800-19307400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
29	chr8:19304200-19310200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
30	chr8:19304400-19308800	Weak transcription	Pancreatic Islets	Pancreatic Islet
31	chr8:19304800-19307800	Weak transcription	Primary T cells fromperipheralblood	blood
32	chr8:19305200-19307800	Weak transcription	Fetal Thymus	thymus
33	chr8:19305600-19313200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr8:19305600-19317600	Weak transcription	Placenta Amnion	Placenta Amnion
35	chr8:19305600-19318400	Weak transcription	Pancreas	Pancrea
36	chr8:19305800-19307200	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr8:19305800-19307200	Weak transcription	A549	lung
38	chr8:19305800-19313000	Weak transcription	Placenta	Placenta
39	chr8:19306000-19307400	Enhancers	HUES64 Cell Line	embryonic stem cell
40	chr8:19306000-19307800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
41	chr8:19306200-19307200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
42	chr8:19306200-19307800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr8:19306200-19309600	Weak transcription	HUES48 Cell Line	embryonic stem cell
44	chr8:19306400-19307800	Weak transcription	Primary neutrophils fromperipheralblood	blood
45	chr8:19306400-19312000	Enhancers	Primary T cells from cord blood	blood
46	chr8:19306600-19307400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr8:19306600-19312000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
48	chr8:19306800-19307200	Enhancers	iPS-20b Cell Line	embryonic stem cell
49	chr8:19306800-19307600	Enhancers	Primary T killer memory cells from peripheral blood	blood
50	chr8:19306800-19308000	Enhancers	Fetal Brain Male	brain

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