Variant report

Variant	nsv1033297
Chromosome Location	chr8:19108472-19150023
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:797)
CpG islands
(count:61)
Chromatin interactive
region (count:16)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:797 , 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	ARID3A	chr8:19149146-19149417	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:19137599-19138311	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:19128678-19129043	HepG2	liver:	n/a	n/a
4	ARID3A	chr8:19125250-19125277	K562	blood:	n/a	n/a
5	ARID3A	chr8:19124872-19125433	HepG2	liver:	n/a	n/a
6	BCL3	chr8:19148800-19149410	A549	lung:	n/a	n/a
7	BRCA1	chr8:19148949-19149382	Hela-S3	cervix:	n/a	n/a
8	BRCA1	chr8:19125027-19125674	Hela-S3	cervix:	n/a	n/a
9	CBX3	chr8:19148884-19149453	HCT-116	colon:	n/a	n/a
10	CEBPB	chr8:19128684-19129051	HepG2	liver:	n/a	n/a
11	CEBPB	chr8:19128736-19129078	ECC-1	luminal epithelium:	n/a	n/a
12	CEBPB	chr8:19148777-19149483	Hela-S3	cervix:	n/a	chr8:19148933-19148946
13	CEBPB	chr8:19132662-19132800	K562	blood:	n/a	n/a
14	CEBPB	chr8:19148943-19149484	A549	lung:	n/a	n/a
15	CEBPB	chr8:19132686-19132921	A549	lung:	n/a	n/a
16	CEBPB	chr8:19124929-19125474	Hela-S3	cervix:	n/a	chr8:19125053-19125064
17	CEBPB	chr8:19128690-19129046	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr8:19137227-19137431	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr8:19149055-19149255	K562	blood:	n/a	n/a
20	CEBPB	chr8:19128695-19129021	HepG2	liver:	n/a	n/a
21	CEBPB	chr8:19128734-19129031	A549	lung:	n/a	n/a
22	CEBPB	chr8:19149138-19149329	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr8:19148764-19149466	IMR90	lung:	n/a	chr8:19148933-19148946
24	CEBPB	chr8:19128654-19129089	A549	lung:	n/a	n/a
25	CEBPB	chr8:19132687-19132958	HepG2	liver:	n/a	n/a
26	CEBPB	chr8:19128745-19129090	HCT-116	colon:	n/a	n/a
27	CEBPB	chr8:19148893-19149493	MCF-7	breast:	n/a	chr8:19148933-19148946
28	CEBPB	chr8:19148697-19149552	A549	lung:	n/a	chr8:19148933-19148946
29	CEBPB	chr8:19122576-19122892	HepG2	liver:	n/a	chr8:19122725-19122742
30	CEBPB	chr8:19148817-19149547	MCF-7	breast:	n/a	chr8:19148933-19148946
31	CEBPB	chr8:19148959-19149407	HepG2	liver:	n/a	n/a
32	CEBPB	chr8:19148873-19149418	A549	lung:	n/a	chr8:19148933-19148946
33	CEBPB	chr8:19148819-19149581	HCT-116	colon:	n/a	chr8:19148933-19148946
34	CEBPB	chr8:19128702-19129031	HCT-116	colon:	n/a	n/a
35	CEBPB	chr8:19128736-19129013	MCF-7	breast:	n/a	n/a
36	CEBPB	chr8:19128709-19129034	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr8:19128767-19129064	ECC-1	luminal epithelium:	n/a	n/a
38	CEBPB	chr8:19148824-19149440	ECC-1	luminal epithelium:	n/a	chr8:19148933-19148946
39	CEBPB	chr8:19137796-19138239	HepG2	liver:	n/a	n/a
40	CEBPB	chr8:19148912-19149467	HCT-116	colon:	n/a	chr8:19148933-19148946
41	CEBPB	chr8:19128747-19129011	K562	blood:	n/a	n/a
42	CEBPB	chr8:19121978-19122340	HepG2	liver:	n/a	n/a
43	CEBPB	chr8:19128787-19129003	HepG2	liver:	n/a	n/a
44	CEBPB	chr8:19128773-19129043	MCF-7	breast:	n/a	n/a
45	CEBPB	chr8:19122611-19122869	A549	lung:	n/a	chr8:19122725-19122742
46	CEBPB	chr8:19129441-19129898	ECC-1	luminal epithelium:	n/a	n/a
47	CEBPB	chr8:19128679-19129059	HepG2	liver:	n/a	n/a
48	CEBPB	chr8:19128797-19128948	IMR90	lung:	n/a	n/a
49	CEBPB	chr8:19129554-19129721	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr8:19128692-19129039	A549	lung:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:19125368-19125418	SK-N-SH_RA	brain:	n/a
2	chr8:19125368-19125418	HL-60	blood:	n/a
3	chr8:19125368-19125418	HCF	heart:	n/a
4	chr8:19125368-19125418	IMR90	lung:	fetal
5	chr8:19125368-19125418	MCF10A-Er-Src	breast:	n/a
6	chr8:19125368-19125418	NB4	blood:	n/a
7	chr8:19125368-19125418	A549	lung:	n/a
8	chr8:19125368-19125418	HCT-116	colon:	n/a
9	chr8:19125368-19125418	HEEpiC	esophagus:	n/a
10	chr8:19125368-19125418	HRPEpiC	eye:	n/a
11	chr8:19125368-19125418	GM19239	blood:	n/a
12	chr8:19125368-19125418	PFSK-1	brain:	n/a
13	chr8:19125368-19125418	HepG2	liver:	n/a
14	chr8:19125368-19125418	Hepatocyte	liver:	n/a
15	chr8:19125368-19125418	K562	blood:	n/a
16	chr8:19125368-19125418	Caco-2	colon:	n/a
17	chr8:19125368-19125418	GM12891	blood:	n/a
18	chr8:19125368-19125418	AG04449	skin:	fetal
19	chr8:19125368-19125418	GM06990	blood:	n/a
20	chr8:19125368-19125418	HUVEC	blood vessel:	n/a
21	chr8:19125368-19125418	PANC-1	pancreas:	n/a
22	chr8:19125368-19125418	H1-hESC	embryonic stem cell:	embryo
23	chr8:19125368-19125418	GM12892	blood:	n/a
24	chr8:19125368-19125418	RPTEC	kidney:	n/a
25	chr8:19125368-19125418	ProgFib	skin:	n/a
26	chr8:19125368-19125418	HEK293	kidney:	embryo
27	chr8:19125368-19125418	CMK	blood:	n/a
28	chr8:19125368-19125418	NHDF-neo	bronchial:	n/a
29	chr8:19125368-19125418	AG10803	skin:	n/a
30	chr8:19125368-19125418	Jurkat	blood:	n/a
31	chr8:19125368-19125418	BJ	skin:	n/a
32	chr8:19125368-19125418	AoSMC	blood vessel:	n/a
33	chr8:19125368-19125418	HCM	heart:	n/a
34	chr8:19125368-19125418	NHBE	bronchial:	n/a
35	chr8:19125368-19125418	SKMC	muscle:	n/a
36	chr8:19125368-19125418	HRCEpiC	kidney:	n/a
37	chr8:19125368-19125418	LNCaP	prostate:	n/a
38	chr8:19125368-19125418	AG04450	lung:	fetal
39	chr8:19125368-19125418	HRE	kidney:	n/a
40	chr8:19125368-19125418	T-47D	breast:	n/a
41	chr8:19125368-19125418	AG09309	skin:	n/a
42	chr8:19125368-19125418	MCF-7	breast:	n/a
43	chr8:19125368-19125418	HCPEpiC	choroid plexus:	n/a
44	chr8:19125368-19125418	ovcar-3	ovarian:	n/a
45	chr8:19125368-19125418	HAEpiC	amniotic membrane:	n/a
46	chr8:19125368-19125418	Hela-S3	cervix:	n/a
47	chr8:19125368-19125418	ECC-1	luminal epithelium:	n/a
48	chr8:19125368-19125418	AG09319	gingival:	n/a
49	chr8:19125368-19125418	PrEC	prostate:	n/a
50	chr8:19125368-19125418	BE2_C	brain:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:19147926..19150795-chr8:19170285..19172249,2	MCF-7	breast:
2	chr8:19125143..19125678-chr8:19171239..19172025,2	MCF-7	breast:
3	chr8:19148156..19152459-chr8:19169128..19172088,7	MCF-7	breast:
4	chr8:18769464..18770410-chr8:19124856..19125711,4	K562	blood:
5	chr8:19126347..19128223-chr8:19186550..19188769,2	K562	blood:
6	chr8:19120168..19121747-chr8:19134338..19135929,2	K562	blood:
7	chr8:19123737..19126710-chr8:19170516..19173345,2	MCF-7	breast:
8	chr8:19142668..19144947-chr8:19171540..19174164,2	MCF-7	breast:
9	chr8:19034788..19035554-chr8:19124800..19125342,2	MCF-7	breast:
10	chr8:19128887..19134305-chr8:19169094..19173373,6	MCF-7	breast:
11	chr8:19144461..19147739-chr8:19170304..19172981,3	MCF-7	breast:
12	chr8:19148177..19150555-chr8:19150746..19153628,2	K562	blood:
13	chr8:19146966..19149051-chr8:19185409..19187470,2	MCF-7	breast:
14	chr8:19120168..19121747-chr8:19134338..19135929,2	K562	blood:
15	chr8:19149962..19152072-chr8:19173164..19175700,2	MCF-7	breast:
16	chr8:19147589..19149540-chr8:19523160..19524664,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CSGALNACT1-1	chr8:19111751-19111827	ENSG00000253280
2	lnc-CSGALNACT1-1	chr8:19114707-19114844	ENSG00000253280
3	lnc-CSGALNACT1-1	chr8:19113688-19113737	ENSG00000253280
4	lnc-CSGALNACT1-1	chr8:19113263-19113359	ENSG00000253280

No data

Variant related genes	Relation type
ENSG00000253557	TF binding region
ENSG00000253280	TF binding region
ENSG00000253557	CpG island
ENSG00000253280	CpG island
ENSG00000104611	chromatin interactions

Extended variants
information (count: 2110 )
Associated
traits (count: 114 )

Variant overlapped rSNPs/rCNVs (count:2110 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs545081543	chr8:19109813-19109814	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs386723216	chr8:19109892-19109893	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs564727002	chr8:19109894-19109895	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs533330649	chr8:19109907-19109908	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs547305996	chr8:19109918-19109919	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs376431811	chr8:19109940-19109941	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs529335894	chr8:19110009-19110010	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs145243089	chr8:19110021-19110022	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs568864438	chr8:19110050-19110051	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs550360336	chr8:19110071-19110072	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs537971352	chr8:19110126-19110127	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs557794502	chr8:19110127-19110128	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs571451688	chr8:19110174-19110175	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs148008523	chr8:19110179-19110180	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs554080403	chr8:19110211-19110212	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs573842244	chr8:19110222-19110223	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs537480950	chr8:19110224-19110225	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs542904802	chr8:19110236-19110237	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs568611233	chr8:19110257-19110258	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs141661209	chr8:19110280-19110281	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs188079903	chr8:19110290-19110291	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs193053057	chr8:19110292-19110293	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs533603559	chr8:19110307-19110308	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs34340292	chr8:19110332-19110333	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs11986943	chr8:19110345-19110346	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs548305334	chr8:19110381-19110382	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs529544650	chr8:19110396-19110397	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs566726397	chr8:19110403-19110404	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs549236762	chr8:19110409-19110410	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs534215194	chr8:19110416-19110417	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs562558152	chr8:19110474-19110475	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs78482807	chr8:19110491-19110492	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs551485743	chr8:19110548-19110549	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs571645795	chr8:19110583-19110584	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs534030879	chr8:19110607-19110608	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs9325852	chr8:19110649-19110650	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs567409698	chr8:19110652-19110653	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs536575320	chr8:19110720-19110721	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs184591888	chr8:19110751-19110752	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs373689568	chr8:19110785-19110786	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs576142120	chr8:19110801-19110802	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs35713916	chr8:19110814-19110815	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs558667894	chr8:19110860-19110861	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs577468207	chr8:19110870-19110871	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs370657346	chr8:19110876-19110877	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs2683311	chr8:19110919-19110920	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs541074133	chr8:19110945-19110946	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs560541680	chr8:19111011-19111012	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs368214471	chr8:19111016-19111017	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs573861202	chr8:19111048-19111049	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:114)

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
Non-syndromic sensorineural hearing loss	18451855	CNVD
small cell lung cancer	20016488	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Gastric adenocarcinoma	19115996	CNVD
Colorectal cancer	19455253	CNVD

Chromatin state (count:444 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:19109800-19111400	Enhancers	Monocytes-CD14+_RO01746	blood
2	chr8:19109800-19112200	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr8:19110000-19113400	Enhancers	Primary neutrophils fromperipheralblood	blood
4	chr8:19111400-19111800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr8:19111400-19111800	Enhancers	Lung	lung
6	chr8:19111400-19111800	Enhancers	Ovary	ovary
7	chr8:19111400-19112000	Enhancers	Primary T cells from cord blood	blood
8	chr8:19111400-19113000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
9	chr8:19111400-19113400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
10	chr8:19111600-19112000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr8:19111600-19112400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr8:19111600-19113200	Enhancers	Primary hematopoietic stem cells	blood
13	chr8:19111800-19112600	Enhancers	Primary B cells from cord blood	blood
14	chr8:19111800-19112800	Weak transcription	Ovary	ovary
15	chr8:19112000-19112600	Flanking Active TSS	Primary T cells from cord blood	blood
16	chr8:19112000-19113000	Enhancers	Primary hematopoietic stem cells short term culture	blood
17	chr8:19112200-19112600	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
18	chr8:19112200-19112600	Enhancers	Primary B cells from peripheral blood	blood
19	chr8:19112200-19112600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
20	chr8:19112200-19112600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr8:19112200-19112800	Enhancers	Primary T helper cells PMA-I stimulated	--
22	chr8:19112200-19112800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr8:19112600-19113000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr8:19112600-19113000	Enhancers	Thymus	Thymus
25	chr8:19112600-19113400	Enhancers	Primary monocytes fromperipheralblood	blood
26	chr8:19112600-19113400	Enhancers	Primary T cells from cord blood	blood
27	chr8:19112800-19113400	Enhancers	Ovary	ovary
28	chr8:19113400-19119600	Weak transcription	Ovary	ovary
29	chr8:19118400-19119000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr8:19118600-19118800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr8:19119000-19121800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr8:19119000-19122000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr8:19119600-19119800	Enhancers	HepG2	liver
34	chr8:19119600-19120400	Enhancers	Ovary	ovary
35	chr8:19119600-19120400	Enhancers	A549	lung
36	chr8:19119600-19120400	Enhancers	Osteobl	bone
37	chr8:19119600-19120600	Enhancers	NH-A	brain
38	chr8:19119600-19123800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
39	chr8:19119600-19124600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr8:19119800-19121000	Weak transcription	HepG2	liver
41	chr8:19120400-19121200	Weak transcription	Ovary	ovary
42	chr8:19120400-19124600	Weak transcription	Osteobl	bone
43	chr8:19120400-19124800	Weak transcription	A549	lung
44	chr8:19120600-19124600	Weak transcription	NH-A	brain
45	chr8:19121000-19121600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr8:19121000-19123000	Enhancers	Fetal Heart	heart
47	chr8:19121000-19123600	Enhancers	HepG2	liver
48	chr8:19121200-19121800	Enhancers	Brain Anterior Caudate	brain
49	chr8:19121200-19122200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr8:19121200-19123800	Enhancers	Ovary	ovary

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links