Variant report

Variant	nsv1024012
Chromosome Location	chr8:19377703-19409791
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:136)
CpG islands
(count:122)
Chromatin interactive
region (count:2)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:136 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr8:19397005-19397325	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr8:19397098-19397291	K562	blood:	n/a	n/a
3	BHLHE40	chr8:19404897-19405037	GM12878	blood:	n/a	n/a
4	BRCA1	chr8:19402552-19402726	H1-hESC	embryonic stem cell:	n/a	n/a
5	CBX3	chr8:19394499-19395151	HCT-116	colon:	n/a	n/a
6	CEBPB	chr8:19382472-19382577	IMR90	lung:	n/a	chr8:19382510-19382523
7	CEBPB	chr8:19405290-19405812	A549	lung:	n/a	chr8:19405792-19405805 chr8:19405792-19405805
8	CEBPB	chr8:19398095-19398487	Hela-S3	cervix:	n/a	n/a
9	CHD2	chr8:19398211-19398539	Hela-S3	cervix:	n/a	n/a
10	CHD2	chr8:19394530-19394963	Hela-S3	cervix:	n/a	n/a
11	CHD2	chr8:19404901-19405060	GM12878	blood:	n/a	n/a
12	CTCF	chr8:19397759-19397779	Kidney_OC	kidney:	n/a	n/a
13	CTCF	chr8:19389280-19389430	A549	lung:	n/a	chr8:19389393-19389406
14	CTCF	chr8:19389351-19389384	Hela-S3	cervix:	n/a	n/a
15	CTCF	chr8:19408780-19408930	WERI-Rb-1	eye:	n/a	n/a
16	CTCF	chr8:19389320-19389470	HBMEC	blood vessel:	n/a	chr8:19389393-19389406
17	E2F4	chr8:19405378-19405578	MCF10A-Er-Src	breast:	n/a	n/a
18	EBF1	chr8:19405332-19405567	GM12878	blood:	n/a	n/a
19	EBF1	chr8:19391999-19392430	GM12878	blood:	n/a	n/a
20	EP300	chr8:19398209-19398526	Hela-S3	cervix:	n/a	n/a
21	EP300	chr8:19405140-19405752	A549	lung:	n/a	n/a
22	EP300	chr8:19405309-19405808	A549	lung:	n/a	n/a
23	FOS	chr8:19405326-19405686	MCF10A-Er-Src	breast:	n/a	n/a
24	FOS	chr8:19394491-19395005	MCF10A-Er-Src	breast:	n/a	n/a
25	FOS	chr8:19398194-19398587	Hela-S3	cervix:	n/a	n/a
26	FOS	chr8:19394484-19395020	MCF10A-Er-Src	breast:	n/a	n/a
27	FOS	chr8:19405420-19405664	MCF10A-Er-Src	breast:	n/a	n/a
28	FOS	chr8:19394476-19395008	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr8:19394486-19395010	MCF10A-Er-Src	breast:	n/a	n/a
30	FOS	chr8:19405301-19405703	MCF10A-Er-Src	breast:	n/a	chr8:19405324-19405336 chr8:19405307-19405316
31	FOS	chr8:19398204-19398569	MCF10A-Er-Src	breast:	n/a	n/a
32	FOS	chr8:19398194-19398561	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr8:19398189-19398563	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chr8:19398796-19398826	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr8:19394527-19394952	Hela-S3	cervix:	n/a	n/a
36	FOS	chr8:19398775-19398809	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr8:19398192-19398567	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr8:19405456-19405564	MCF10A-Er-Src	breast:	n/a	n/a
39	FOSL1	chr8:19394354-19395117	HCT-116	colon:	n/a	n/a
40	FOSL2	chr8:19398136-19398630	MCF-7	breast:	n/a	n/a
41	FOSL2	chr8:19394385-19395099	A549	lung:	n/a	n/a
42	FOSL2	chr8:19398251-19398476	A549	lung:	n/a	n/a
43	FOSL2	chr8:19405257-19405773	A549	lung:	n/a	chr8:19405324-19405336 chr8:19405307-19405316
44	FOSL2	chr8:19405344-19405649	A549	lung:	n/a	n/a
45	FOSL2	chr8:19394475-19394927	A549	lung:	n/a	n/a
46	FOSL2	chr8:19398040-19398674	A549	lung:	n/a	n/a
47	GATA3	chr8:19402294-19402387	SH-SY5Y	brain:	n/a	n/a
48	GATA3	chr8:19398109-19398610	MCF-7	breast:	n/a	n/a
49	JUN	chr8:19394299-19394966	Hela-S3	cervix:	n/a	n/a
50	JUND	chr8:19394363-19395092	HCT-116	colon:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:19401411-19401461	Hepatocyte	liver:	n/a
2	chr8:19401411-19401461	AoSMC	blood vessel:	n/a
3	chr8:19401411-19401461	GM12892	blood:	n/a
4	chr8:19409023-19409073	BJ	skin:	n/a
5	chr8:19401411-19401461	NT2-D1	testis:	n/a
6	chr8:19401411-19401461	HRE	kidney:	n/a
7	chr8:19401411-19401461	PrEC	prostate:	n/a
8	chr8:19409023-19409073	NB4	blood:	n/a
9	chr8:19409023-19409073	K562	blood:	n/a
10	chr8:19409023-19409073	H1-hESC	embryonic stem cell:	embryo
11	chr8:19409023-19409073	GM12878	blood:	n/a
12	chr8:19409023-19409073	PFSK-1	brain:	n/a
13	chr8:19401411-19401461	AG04449	skin:	fetal
14	chr8:19401411-19401461	T-47D	breast:	n/a
15	chr8:19401411-19401461	NB4	blood:	n/a
16	chr8:19401411-19401461	MCF-7	breast:	n/a
17	chr8:19401411-19401461	AG10803	skin:	n/a
18	chr8:19409023-19409073	NT2-D1	testis:	n/a
19	chr8:19409023-19409073	HUVEC	blood vessel:	n/a
20	chr8:19401411-19401461	ovcar-3	ovarian:	n/a
21	chr8:19409023-19409073	SKMC	muscle:	n/a
22	chr8:19401411-19401461	ProgFib	skin:	n/a
23	chr8:19401411-19401461	Jurkat	blood:	n/a
24	chr8:19401411-19401461	GM19239	blood:	n/a
25	chr8:19409023-19409073	HRE	kidney:	n/a
26	chr8:19409023-19409073	HRPEpiC	eye:	n/a
27	chr8:19409023-19409073	HCT-116	colon:	n/a
28	chr8:19409023-19409073	T-47D	breast:	n/a
29	chr8:19401411-19401461	HEEpiC	esophagus:	n/a
30	chr8:19409023-19409073	A549	lung:	n/a
31	chr8:19409023-19409073	HAEpiC	amniotic membrane:	n/a
32	chr8:19401411-19401461	H1-hESC	embryonic stem cell:	embryo
33	chr8:19409023-19409073	GM06990	blood:	n/a
34	chr8:19401411-19401461	HRPEpiC	eye:	n/a
35	chr8:19401411-19401461	SK-N-MC	brain:	n/a
36	chr8:19409023-19409073	Hela-S3	cervix:	n/a
37	chr8:19401411-19401461	PFSK-1	brain:	n/a
38	chr8:19409023-19409073	SAEC	small airway:	n/a
39	chr8:19409023-19409073	MCF10A-Er-Src	breast:	n/a
40	chr8:19401411-19401461	HCM	heart:	n/a
41	chr8:19401411-19401461	SK-N-SH	brain:	n/a
42	chr8:19401411-19401461	HepG2	liver:	n/a
43	chr8:19409023-19409073	AG04449	skin:	fetal
44	chr8:19401411-19401461	HIPEpiC	eye:	n/a
45	chr8:19401411-19401461	SAEC	small airway:	n/a
46	chr8:19409023-19409073	IMR90	lung:	fetal
47	chr8:19409023-19409073	NHBE	bronchial:	n/a
48	chr8:19409023-19409073	PrEC	prostate:	n/a
49	chr8:19409023-19409073	BE2_C	brain:	n/a
50	chr8:19409023-19409073	AG09309	skin:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:19371116..19373771-chr8:19377059..19378982,3	K562	blood:
2	chr8:19391042..19393600-chr8:19578654..19580566,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PSD3-3	chr8:19389330-19389531	NONHSAT125378

No data

Variant related genes	Relation type
CSGALNACT1	TF binding region
CSGALNACT1	CpG island

Extended variants
information (count: 1808 )
Associated
traits (count: 118 )

Variant overlapped rSNPs/rCNVs (count:1808 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2975467	chr8:19377703-19377704	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs192061242	chr8:19377739-19377740	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs2958588	chr8:19377749-19377750	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs2975468	chr8:19377781-19377782	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs77782727	chr8:19377794-19377795	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs563926791	chr8:19377853-19377854	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs532433296	chr8:19377880-19377881	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs114464466	chr8:19377885-19377886	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs2975469	chr8:19377911-19377912	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs76423287	chr8:19377921-19377922	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs548576104	chr8:19377944-19377945	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs112547126	chr8:19377975-19377976	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs184659514	chr8:19377985-19377986	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs144593660	chr8:19377986-19377987	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs2958587	chr8:19377987-19377988	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs2958586	chr8:19377997-19377998	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs542425108	chr8:19378000-19378001	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs28460428	chr8:19378009-19378010	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs572866742	chr8:19378068-19378069	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs367855350	chr8:19378091-19378092	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs562113593	chr8:19378112-19378113	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs535065227	chr8:19378125-19378126	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs555344482	chr8:19378137-19378138	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs575002330	chr8:19378176-19378177	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs2975470	chr8:19378190-19378191	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs544108289	chr8:19378192-19378193	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs12682614	chr8:19378211-19378212	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs17408078	chr8:19378213-19378214	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs140478443	chr8:19378250-19378251	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs10110641	chr8:19378274-19378275	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs150141752	chr8:19378317-19378318	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs564133149	chr8:19378356-19378357	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs189327267	chr8:19378362-19378363	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs562131391	chr8:19378365-19378366	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs10096490	chr8:19378409-19378410	Strong transcription Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs550880882	chr8:19378410-19378411	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs376252532	chr8:19378421-19378422	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs539685031	chr8:19378457-19378458	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs546825701	chr8:19378468-19378469	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs138586869	chr8:19378469-19378470	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs535557592	chr8:19378475-19378476	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs181983882	chr8:19378484-19378485	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs10096638	chr8:19378518-19378519	Strong transcription Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs148913784	chr8:19378525-19378526	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs537319210	chr8:19378548-19378549	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs143595128	chr8:19378558-19378559	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs577131953	chr8:19378580-19378581	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs2975471	chr8:19378581-19378582	Strong transcription Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs559545321	chr8:19378585-19378586	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs573223480	chr8:19378596-19378597	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:118)

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
Non-syndromic sensorineural hearing loss	21293372	CNVD
Melanoma	20688739	CNVD

Chromatin state (count:334 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:19367000-19385000	Weak transcription	Ovary	ovary
2	chr8:19370800-19381200	Weak transcription	Fetal Stomach	stomach
3	chr8:19370800-19385000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
4	chr8:19371200-19380000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr8:19371800-19378400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr8:19373000-19380600	Weak transcription	Lung	lung
7	chr8:19373400-19381600	Weak transcription	Spleen	Spleen
8	chr8:19373400-19382000	Weak transcription	Pancreas	Pancrea
9	chr8:19373600-19378400	Weak transcription	Placenta	Placenta
10	chr8:19373600-19382000	Weak transcription	Fetal Muscle Leg	muscle
11	chr8:19373600-19382200	Weak transcription	Gastric	stomach
12	chr8:19373800-19380000	Strong transcription	Primary neutrophils fromperipheralblood	blood
13	chr8:19374000-19379800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr8:19374000-19382200	Weak transcription	Primary hematopoietic stem cells	blood
15	chr8:19374400-19380200	Strong transcription	A549	lung
16	chr8:19374400-19385400	Weak transcription	Thymus	Thymus
17	chr8:19374600-19382400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
18	chr8:19375600-19390000	Weak transcription	Right Atrium	heart
19	chr8:19376200-19388000	Weak transcription	Primary T helper cells fromperipheralblood	blood
20	chr8:19376400-19379000	Weak transcription	Primary B cells from peripheral blood	blood
21	chr8:19376400-19380600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
22	chr8:19376400-19388400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
23	chr8:19376600-19378200	Weak transcription	Primary T cells from cord blood	blood
24	chr8:19377000-19380600	Strong transcription	Primary B cells from cord blood	blood
25	chr8:19377000-19388400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
26	chr8:19377200-19379200	Weak transcription	Hela-S3	cervix
27	chr8:19377200-19388400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
28	chr8:19377600-19378000	Weak transcription	Esophagus	oesophagus
29	chr8:19377600-19378400	Weak transcription	Right Ventricle	heart
30	chr8:19377600-19379000	Weak transcription	Left Ventricle	heart
31	chr8:19377600-19388200	Weak transcription	Primary T helper cells PMA-I stimulated	--
32	chr8:19377800-19378800	Enhancers	Fetal Heart	heart
33	chr8:19378200-19379400	Strong transcription	Primary T cells from cord blood	blood
34	chr8:19378400-19378600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr8:19378400-19379000	Enhancers	Right Ventricle	heart
36	chr8:19378400-19379400	Strong transcription	Placenta	Placenta
37	chr8:19379000-19379600	Strong transcription	Primary B cells from peripheral blood	blood
38	chr8:19379000-19379600	Genic enhancers	Left Ventricle	heart
39	chr8:19379000-19380000	Weak transcription	Right Ventricle	heart
40	chr8:19379200-19379800	Strong transcription	Hela-S3	cervix
41	chr8:19379400-19385800	Weak transcription	Primary T cells from cord blood	blood
42	chr8:19379400-19434200	Weak transcription	Placenta	Placenta
43	chr8:19379600-19385000	Weak transcription	Primary B cells from peripheral blood	blood
44	chr8:19379600-19385000	Weak transcription	Left Ventricle	heart
45	chr8:19379800-19380600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr8:19379800-19386200	Weak transcription	Hela-S3	cervix
47	chr8:19380000-19380200	Enhancers	Right Ventricle	heart
48	chr8:19380000-19380600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr8:19380000-19380800	Genic enhancers	Primary neutrophils fromperipheralblood	blood
50	chr8:19380200-19380600	Weak transcription	Right Ventricle	heart

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links