Variant report

Variant	nsv1015448
Chromosome Location	chr8:19474715-19520367
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:468)
CpG islands
(count:122)
Chromatin interactive
region (count:7)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:468 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:19518754-19519207	HepG2	liver:	n/a	n/a
2	ATF2	chr8:19495148-19495898	GM12878	blood:	n/a	n/a
3	ATF3	chr8:19518727-19518888	HepG2	liver:	n/a	n/a
4	ATF3	chr8:19499332-19499995	A549	lung:	n/a	n/a
5	BATF	chr8:19486695-19486912	GM12878	blood:	n/a	n/a
6	BATF	chr8:19487422-19487771	GM12878	blood:	n/a	n/a
7	BATF	chr8:19495256-19495900	GM12878	blood:	n/a	n/a
8	BATF	chr8:19481956-19482198	GM12878	blood:	n/a	n/a
9	BATF	chr8:19486678-19486983	GM12878	blood:	n/a	n/a
10	BCL11A	chr8:19495302-19495833	GM12878	blood:	n/a	n/a
11	BCL11A	chr8:19497461-19497603	H1-hESC	embryonic stem cell:	n/a	n/a
12	BCL3	chr8:19478241-19478961	A549	lung:	n/a	chr8:19478549-19478558
13	BCL3	chr8:19499144-19500243	A549	lung:	n/a	n/a
14	BCLAF1	chr8:19495214-19495717	GM12878	blood:	n/a	n/a
15	BCLAF1	chr8:19495178-19495930	GM12878	blood:	n/a	n/a
16	BHLHE40	chr8:19494956-19495854	GM12878	blood:	n/a	n/a
17	BHLHE40	chr8:19519719-19519894	GM12878	blood:	n/a	n/a
18	BHLHE40	chr8:19481892-19482193	GM12878	blood:	n/a	n/a
19	BHLHE40	chr8:19518717-19519016	HepG2	liver:	n/a	n/a
20	BHLHE40	chr8:19486779-19487792	GM12878	blood:	n/a	chr8:19487391-19487412
21	BRCA1	chr8:19518717-19519045	Hela-S3	cervix:	n/a	n/a
22	CBX3	chr8:19518617-19519104	HCT-116	colon:	n/a	n/a
23	CEBPB	chr8:19517100-19517405	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr8:19478287-19479000	A549	lung:	n/a	n/a
25	CEBPB	chr8:19492442-19492675	IMR90	lung:	n/a	chr8:19492573-19492584 chr8:19492575-19492584
26	CEBPB	chr8:19499000-19499931	A549	lung:	n/a	chr8:19499652-19499663
27	CEBPB	chr8:19499477-19499971	Hela-S3	cervix:	n/a	chr8:19499652-19499663
28	CEBPB	chr8:19484772-19485092	A549	lung:	n/a	n/a
29	CEBPB	chr8:19484696-19485174	A549	lung:	n/a	n/a
30	CEBPB	chr8:19484367-19485113	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr8:19483244-19483512	A549	lung:	n/a	n/a
32	CEBPB	chr8:19508784-19508971	A549	lung:	n/a	n/a
33	CEBPB	chr8:19517164-19517396	A549	lung:	n/a	n/a
34	CEBPB	chr8:19518722-19519162	A549	lung:	n/a	n/a
35	CEBPB	chr8:19499472-19499960	IMR90	lung:	n/a	chr8:19499652-19499663
36	CEBPB	chr8:19520279-19521867	A549	lung:	n/a	n/a
37	CEBPB	chr8:19499617-19499817	HepG2	liver:	n/a	chr8:19499652-19499663
38	CEBPB	chr8:19499265-19500222	A549	lung:	n/a	chr8:19499652-19499663
39	CEBPB	chr8:19520331-19520728	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr8:19502631-19502953	IMR90	lung:	n/a	n/a
41	CEBPB	chr8:19492234-19492599	A549	lung:	n/a	chr8:19492573-19492584 chr8:19492575-19492584
42	CEBPB	chr8:19478669-19478768	A549	lung:	n/a	n/a
43	CEBPB	chr8:19502647-19502941	A549	lung:	n/a	n/a
44	CEBPB	chr8:19511469-19511875	IMR90	lung:	n/a	n/a
45	CEBPB	chr8:19498610-19498620	A549	lung:	n/a	n/a
46	CEBPB	chr8:19508797-19508947	HepG2	liver:	n/a	n/a
47	CEBPB	chr8:19499531-19499979	HCT-116	colon:	n/a	chr8:19499652-19499663
48	CEBPB	chr8:19499557-19499830	MCF-7	breast:	n/a	chr8:19499652-19499663
49	CEBPB	chr8:19483269-19483843	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr8:19499483-19499943	MCF-7	breast:	n/a	chr8:19499652-19499663

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:19496206-19496256	Jurkat	blood:	n/a
2	chr8:19496206-19496256	Hepatocyte	liver:	n/a
3	chr8:19504047-19504097	AoSMC	blood vessel:	n/a
4	chr8:19496206-19496256	GM12878	blood:	n/a
5	chr8:19504047-19504097	AG09309	skin:	n/a
6	chr8:19504047-19504097	NT2-D1	testis:	n/a
7	chr8:19496206-19496256	AG09319	gingival:	n/a
8	chr8:19496206-19496256	HNPCEpiC	eye:	n/a
9	chr8:19496206-19496256	U87	brain:	n/a
10	chr8:19496206-19496256	HCT-116	colon:	n/a
11	chr8:19504047-19504097	GM19239	blood:	n/a
12	chr8:19496206-19496256	HCF	heart:	n/a
13	chr8:19496206-19496256	HMEC	breast:	n/a
14	chr8:19496206-19496256	HEEpiC	esophagus:	n/a
15	chr8:19496206-19496256	IMR90	lung:	fetal
16	chr8:19496206-19496256	NB4	blood:	n/a
17	chr8:19496206-19496256	MCF-7	breast:	n/a
18	chr8:19504047-19504097	HCPEpiC	choroid plexus:	n/a
19	chr8:19496206-19496256	PFSK-1	brain:	n/a
20	chr8:19496206-19496256	HPAEpiC	pulmonary alveolar:	n/a
21	chr8:19504047-19504097	HAEpiC	amniotic membrane:	n/a
22	chr8:19504047-19504097	NH-A	brain:	n/a
23	chr8:19496206-19496256	HAEpiC	amniotic membrane:	n/a
24	chr8:19504047-19504097	GM12892	blood:	n/a
25	chr8:19496206-19496256	HCM	heart:	n/a
26	chr8:19504047-19504097	RPTEC	kidney:	n/a
27	chr8:19504047-19504097	MCF10A-Er-Src	breast:	n/a
28	chr8:19504047-19504097	GM12891	blood:	n/a
29	chr8:19504047-19504097	HIPEpiC	eye:	n/a
30	chr8:19496206-19496256	SK-N-SH_RA	brain:	n/a
31	chr8:19496206-19496256	LNCaP	prostate:	n/a
32	chr8:19496206-19496256	MCF10A-Er-Src	breast:	n/a
33	chr8:19504047-19504097	ProgFib	skin:	n/a
34	chr8:19496206-19496256	HepG2	liver:	n/a
35	chr8:19496206-19496256	AG09309	skin:	n/a
36	chr8:19504047-19504097	HNPCEpiC	eye:	n/a
37	chr8:19504047-19504097	Jurkat	blood:	n/a
38	chr8:19504047-19504097	HRPEpiC	eye:	n/a
39	chr8:19504047-19504097	HL-60	blood:	n/a
40	chr8:19504047-19504097	PANC-1	pancreas:	n/a
41	chr8:19496206-19496256	PANC-1	pancreas:	n/a
42	chr8:19504047-19504097	HRE	kidney:	n/a
43	chr8:19496206-19496256	BE2_C	brain:	n/a
44	chr8:19496206-19496256	GM12891	blood:	n/a
45	chr8:19496206-19496256	AoSMC	blood vessel:	n/a
46	chr8:19496206-19496256	SAEC	small airway:	n/a
47	chr8:19496206-19496256	NH-A	brain:	n/a
48	chr8:19496206-19496256	AG10803	skin:	n/a
49	chr8:19504047-19504097	ECC-1	luminal epithelium:	n/a
50	chr8:19504047-19504097	K562	blood:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:19517559..19519398-chr8:19521074..19523001,2	MCF-7	breast:
2	chr8:19482760..19485283-chr8:19485806..19488434,2	K562	blood:
3	chr8:19481550..19484260-chr8:19486287..19488434,2	K562	blood:
4	chr8:19497421..19499586-chr8:19613571..19616001,2	MCF-7	breast:
5	chr8:19481550..19484260-chr8:19486287..19488434,2	K562	blood:
6	chr8:19490728..19492543-chr8:19497647..19500468,2	K562	blood:
7	chr8:19482760..19485283-chr8:19485806..19488434,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PSD3-3	chr8:19499298-19499533	NONHSAT125376

No data

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

Extended variants
information (count: 2480 )
Associated
traits (count: 117 )

Variant overlapped rSNPs/rCNVs (count:2480 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4922069	chr8:19474715-19474716	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs114094516	chr8:19474723-19474724	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs565204496	chr8:19474741-19474742	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs373579010	chr8:19474747-19474748	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs374409867	chr8:19474758-19474759	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs375266511	chr8:19474775-19474776	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs537339401	chr8:19474796-19474797	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs557570615	chr8:19474802-19474803	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs577353286	chr8:19474810-19474811	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs56393158	chr8:19474823-19474824	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs553479256	chr8:19474824-19474825	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs377445587	chr8:19474832-19474833	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs370295669	chr8:19474833-19474834	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs542205597	chr8:19474849-19474850	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs190758415	chr8:19474902-19474903	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs530882892	chr8:19474922-19474923	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs544161418	chr8:19474956-19474957	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs564332604	chr8:19474960-19474961	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs532954470	chr8:19474969-19474970	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs562172415	chr8:19474999-19475000	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs183875845	chr8:19475015-19475016	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs566186165	chr8:19475017-19475018	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs375420699	chr8:19475018-19475019	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs77474575	chr8:19475023-19475024	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs78508683	chr8:19475025-19475026	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs373465665	chr8:19475065-19475066	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs375576097	chr8:19475074-19475075	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs568502112	chr8:19475135-19475136	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs189227204	chr8:19475137-19475138	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs192179540	chr8:19475200-19475201	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs368366915	chr8:19475346-19475347	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs4452801	chr8:19475347-19475348	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs370466319	chr8:19475348-19475349	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs571048778	chr8:19475375-19475376	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs539614078	chr8:19475419-19475420	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs553514038	chr8:19475440-19475441	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs372759758	chr8:19475461-19475462	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs573328648	chr8:19475516-19475517	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs149748940	chr8:19475517-19475518	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs555840515	chr8:19475551-19475552	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs564292814	chr8:19475557-19475558	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs575527389	chr8:19475567-19475568	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs531806598	chr8:19475592-19475593	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs544515629	chr8:19475594-19475595	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs564191238	chr8:19475635-19475636	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs540780258	chr8:19475642-19475643	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs377148121	chr8:19475648-19475649	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs370358342	chr8:19475649-19475650	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs118043416	chr8:19475656-19475657	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs559910743	chr8:19475701-19475702	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
Melanoma	20688739	CNVD

Chromatin state (count:898 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:19445600-19481400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
2	chr8:19456200-19479600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
3	chr8:19464200-19476400	Weak transcription	Primary neutrophils fromperipheralblood	blood
4	chr8:19466600-19477000	Weak transcription	Aorta	Aorta
5	chr8:19466600-19477000	Weak transcription	Fetal Lung	lung
6	chr8:19467000-19476600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr8:19468000-19483400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
8	chr8:19468400-19475400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
9	chr8:19472200-19481200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr8:19472600-19475600	Weak transcription	Osteobl	bone
11	chr8:19472600-19480000	Weak transcription	Primary T cells from cord blood	blood
12	chr8:19472800-19476400	Weak transcription	Right Ventricle	heart
13	chr8:19472800-19482400	Weak transcription	Spleen	Spleen
14	chr8:19473000-19475800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
15	chr8:19473000-19476600	Weak transcription	Ovary	ovary
16	chr8:19473000-19481200	Weak transcription	Hela-S3	cervix
17	chr8:19473000-19481400	Weak transcription	Primary monocytes fromperipheralblood	blood
18	chr8:19473000-19481800	Weak transcription	HUVEC	blood vessel
19	chr8:19473200-19483600	Enhancers	A549	lung
20	chr8:19474400-19475400	Weak transcription	Primary B cells from peripheral blood	blood
21	chr8:19474400-19476400	Weak transcription	Left Ventricle	heart
22	chr8:19474400-19478000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr8:19474400-19482400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr8:19474600-19474800	Enhancers	Pancreas	Pancrea
25	chr8:19474600-19475000	Enhancers	Fetal Stomach	stomach
26	chr8:19474600-19475000	Enhancers	Right Atrium	heart
27	chr8:19474600-19475800	Enhancers	Primary B cells from cord blood	blood
28	chr8:19474800-19476400	Weak transcription	Pancreas	Pancrea
29	chr8:19475000-19476200	Weak transcription	Right Atrium	heart
30	chr8:19475400-19475800	Enhancers	Primary B cells from peripheral blood	blood
31	chr8:19475400-19475800	Enhancers	Primary hematopoietic stem cells short term culture	blood
32	chr8:19475600-19476000	Enhancers	Osteobl	bone
33	chr8:19475800-19476000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
34	chr8:19475800-19476400	Weak transcription	Primary B cells from cord blood	blood
35	chr8:19475800-19481400	Weak transcription	Primary B cells from peripheral blood	blood
36	chr8:19476000-19476400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
37	chr8:19476200-19477400	Enhancers	Right Atrium	heart
38	chr8:19476400-19476600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr8:19476400-19476600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
40	chr8:19476400-19476800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr8:19476400-19477000	Enhancers	Primary B cells from cord blood	blood
42	chr8:19476400-19477200	Strong transcription	Primary neutrophils fromperipheralblood	blood
43	chr8:19476400-19477200	Enhancers	Right Ventricle	heart
44	chr8:19476400-19478200	Enhancers	Left Ventricle	heart
45	chr8:19476400-19478200	Enhancers	Pancreas	Pancrea
46	chr8:19476600-19477000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr8:19476600-19477200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr8:19476600-19477400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr8:19476600-19479200	Enhancers	Ovary	ovary
50	chr8:19476600-19479800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood

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