Variant report

Variant	nsv876966
Chromosome Location	chr3:75350891-75489636
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1878)
CpG islands
(count:1893)
Chromatin interactive
region (count:9)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1878 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:75482025-75482381	HepG2	liver:	n/a	n/a
2	ATF1	chr3:75442553-75442767	K562	blood:	n/a	n/a
3	ATF1	chr3:75482136-75482245	K562	blood:	n/a	n/a
4	ATF1	chr3:75484451-75484710	K562	blood:	n/a	n/a
5	ATF3	chr3:75482035-75482349	A549	lung:	n/a	n/a
6	ATF3	chr3:75482021-75482341	K562	blood:	n/a	n/a
7	BACH1	chr3:75390901-75391145	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr3:75484448-75484647	GM12878	blood:	n/a	n/a
9	BATF	chr3:75466554-75466845	GM12878	blood:	n/a	chr3:75466774-75466785
10	BATF	chr3:75478786-75479063	GM12878	blood:	n/a	n/a
11	BATF	chr3:75411520-75411813	GM12878	blood:	n/a	n/a
12	BATF	chr3:75471237-75471503	GM12878	blood:	n/a	n/a
13	BATF	chr3:75386395-75386620	GM12878	blood:	n/a	n/a
14	BATF	chr3:75467667-75467909	GM12878	blood:	n/a	n/a
15	BATF	chr3:75483970-75484356	GM12878	blood:	n/a	n/a
16	BATF	chr3:75483065-75483278	GM12878	blood:	n/a	n/a
17	BATF	chr3:75411604-75411874	GM12878	blood:	n/a	n/a
18	BATF	chr3:75468128-75468306	GM12878	blood:	n/a	n/a
19	BATF	chr3:75483500-75483898	GM12878	blood:	n/a	chr3:75483518-75483528 chr3:75483514-75483524
20	BATF	chr3:75483026-75483267	GM12878	blood:	n/a	n/a
21	BATF	chr3:75471192-75471564	GM12878	blood:	n/a	n/a
22	BATF	chr3:75466555-75466915	GM12878	blood:	n/a	chr3:75466774-75466785
23	BCL11A	chr3:75467554-75467709	GM12878	blood:	n/a	n/a
24	BCL11A	chr3:75483449-75483810	GM12878	blood:	n/a	chr3:75483516-75483525
25	BCL11A	chr3:75471159-75471563	GM12878	blood:	n/a	n/a
26	BCL11A	chr3:75466632-75466905	GM12878	blood:	n/a	chr3:75466778-75466787
27	BCL11A	chr3:75483447-75484322	GM12878	blood:	n/a	chr3:75483516-75483525
28	BCL11A	chr3:75484021-75484296	GM12878	blood:	n/a	n/a
29	BCL11A	chr3:75483008-75483267	GM12878	blood:	n/a	n/a
30	BCL11A	chr3:75482472-75482657	GM12878	blood:	n/a	n/a
31	BCL11A	chr3:75471268-75471550	GM12878	blood:	n/a	n/a
32	BCL11A	chr3:75466653-75466911	GM12878	blood:	n/a	chr3:75466778-75466787
33	BCL3	chr3:75395680-75395995	GM12878	blood:	n/a	n/a
34	BCL3	chr3:75416737-75417040	GM12878	blood:	n/a	n/a
35	BCL3	chr3:75429024-75429912	GM12878	blood:	n/a	n/a
36	BCL3	chr3:75417319-75417660	GM12878	blood:	n/a	n/a
37	BCL3	chr3:75417298-75417641	GM12878	blood:	n/a	n/a
38	BCL3	chr3:75407756-75407999	GM12878	blood:	n/a	n/a
39	BCL3	chr3:75428941-75429895	GM12878	blood:	n/a	n/a
40	BHLHE40	chr3:75484999-75485288	GM12878	blood:	n/a	chr3:75485139-75485155
41	BHLHE40	chr3:75482189-75482389	K562	blood:	n/a	n/a
42	BHLHE40	chr3:75483691-75484340	GM12878	blood:	n/a	n/a
43	BHLHE40	chr3:75442538-75442564	K562	blood:	n/a	n/a
44	BHLHE40	chr3:75485018-75485031	K562	blood:	n/a	n/a
45	BHLHE40	chr3:75483642-75484400	HepG2	liver:	n/a	n/a
46	BHLHE40	chr3:75484050-75484096	K562	blood:	n/a	n/a
47	BHLHE40	chr3:75429659-75429896	K562	blood:	n/a	n/a
48	BRCA1	chr3:75482245-75482385	Hela-S3	cervix:	n/a	n/a
49	CBX3	chr3:75483939-75484360	K562	blood:	n/a	n/a
50	CBX3	chr3:75484372-75484891	K562	blood:	n/a	n/a

(count:1893 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:75445738-75445788	HIPEpiC	eye:	n/a
2	chr3:75414693-75414743	SK-N-MC	brain:	n/a
3	chr3:75445738-75445788	HIPEpiC	eye:	n/a
4	chr3:75414693-75414743	SK-N-MC	brain:	n/a
5	chr3:75412866-75412916	GM12892	blood:	n/a
6	chr3:75411217-75411267	HCM	heart:	n/a
7	chr3:75411421-75411471	PANC-1	pancreas:	n/a
8	chr3:75411217-75411267	SAEC	small airway:	n/a
9	chr3:75410789-75410839	NH-A	brain:	n/a
10	chr3:75483803-75483853	SAEC	small airway:	n/a
11	chr3:75441804-75441854	SAEC	small airway:	n/a
12	chr3:75411038-75411088	Caco-2	colon:	n/a
13	chr3:75414486-75414536	NB4	blood:	n/a
14	chr3:75484440-75484490	IMR90	lung:	fetal
15	chr3:75448983-75449033	HRPEpiC	eye:	n/a
16	chr3:75445610-75445660	AG09319	gingival:	n/a
17	chr3:75485448-75485498	Hepatocyte	liver:	n/a
18	chr3:75410747-75410797	MCF-7	breast:	n/a
19	chr3:75415591-75415641	MCF-7	breast:	n/a
20	chr3:75485448-75485498	HMEC	breast:	n/a
21	chr3:75484516-75484566	HRE	kidney:	n/a
22	chr3:75482182-75482232	U87	brain:	n/a
23	chr3:75445502-75445552	AG10803	skin:	n/a
24	chr3:75443047-75443097	SK-N-SH	brain:	n/a
25	chr3:75445738-75445788	SK-N-SH	brain:	n/a
26	chr3:75443047-75443097	ECC-1	luminal epithelium:	n/a
27	chr3:75411038-75411088	SK-N-SH_RA	brain:	n/a
28	chr3:75410789-75410839	AG10803	skin:	n/a
29	chr3:75416171-75416221	HRCEpiC	kidney:	n/a
30	chr3:75481281-75481331	AoSMC	blood vessel:	n/a
31	chr3:75410789-75410839	HCPEpiC	choroid plexus:	n/a
32	chr3:75413083-75413133	Hepatocyte	liver:	n/a
33	chr3:75411421-75411471	CMK	blood:	n/a
34	chr3:75410789-75410839	H1-hESC	embryonic stem cell:	embryo
35	chr3:75414693-75414743	GM06990	blood:	n/a
36	chr3:75415561-75415611	HCPEpiC	choroid plexus:	n/a
37	chr3:75416171-75416221	A549	lung:	n/a
38	chr3:75410747-75410797	Jurkat	blood:	n/a
39	chr3:75483803-75483853	AG09309	skin:	n/a
40	chr3:75448983-75449033	AoSMC	blood vessel:	n/a
41	chr3:75445502-75445552	SK-N-SH	brain:	n/a
42	chr3:75416171-75416221	GM12892	blood:	n/a
43	chr3:75416171-75416221	HCPEpiC	choroid plexus:	n/a
44	chr3:75415526-75415576	BJ	skin:	n/a
45	chr3:75484209-75484259	HL-60	blood:	n/a
46	chr3:75483803-75483853	NHDF-neo	bronchial:	n/a
47	chr3:75411038-75411088	GM06990	blood:	n/a
48	chr3:75415561-75415611	AG09319	gingival:	n/a
49	chr3:75410747-75410797	HCPEpiC	choroid plexus:	n/a
50	chr3:75414486-75414536	ECC-1	luminal epithelium:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:75466672..75467412-chr3:129812592..129813394,2	NB4	blood:
2	chr3:75484863..75485638-chr6:26156199..26156944,2	HCT-116	colon:
3	chr3:75343035..75343810-chr3:75470999..75471871,7	MCF-7	breast:
4	chr3:75343239..75343917-chr3:75478470..75479360,2	MCF-7	breast:
5	chr11:71498107..71498639-chr3:75483883..75484386,2	Hela-S3	cervix:
6	chr3:75343052..75344300-chr3:75470848..75471840,6	MCF-7	breast:
7	chr3:75390707..75391392-chr3:75471007..75471537,3	MCF-7	breast:
8	chr3:75343455..75344253-chr3:75389889..75390567,2	MCF-7	breast:
9	chr3:75390707..75391392-chr3:75471007..75471537,3	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FRG2C-3	chr3:75488905-75488997	XLOC_002710
2	lnc-FRG2C-3	chr3:75488905-75488988	XLOC_002710
3	lnc-FRG2C-3	chr3:75484499-75484564	ENSG00000272690.1
4	lnc-FRG2C-3	chr3:75486207-75486426	XLOC_002710
5	lnc-FRG2C-3	chr3:75485367-75485503	XLOC_002710
6	lnc-FRG2C-3	chr3:75485928-75486426	XLOC_002710

No data

Variant related genes	Relation type
OR7E66P	TF binding region
MYLKP1	TF binding region
ENSG00000272690	TF binding region
FAM86DP	TF binding region
ENSG00000266685	TF binding region
ENSG00000242953	TF binding region
OR7E55P	TF binding region
OR7E22P	TF binding region
LSP1P2	TF binding region
ENSG00000263782	TF binding region
ALG1L6P	TF binding region
ENSG00000244699	TF binding region
OR7E66P	CpG island
MYLKP1	CpG island
ENSG00000272690	CpG island
FAM86DP	CpG island
ENSG00000266685	CpG island
ENSG00000242953	CpG island
OR7E55P	CpG island
OR7E22P	CpG island
LSP1P2	CpG island
ENSG00000263782	CpG island
ALG1L6P	CpG island
ENSG00000244699	CpG island
ENSG00000168298	chromatin interactions
ENSG00000248243	chromatin interactions
ENSG00000158483	chromatin interactions
ENSG00000251287	chromatin interactions
ITGB1	miRNA target sites

Extended variants
information (count: 6208 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:6208 , 50 per page) page: 1 2 3 4 5 6 7 ... 125

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12490207	chr3:75350891-75350892	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs544102976	chr3:75350922-75350923	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs536267837	chr3:75350941-75350942	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs548525327	chr3:75350942-75350943	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs570259075	chr3:75350965-75350966	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs537749685	chr3:75351062-75351063	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs558766890	chr3:75351105-75351106	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs375243821	chr3:75351114-75351115	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs577008754	chr3:75351199-75351200	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs557290307	chr3:75351242-75351243	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs534441026	chr3:75351317-75351318	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs552673575	chr3:75351323-75351324	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs115093930	chr3:75351333-75351334	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs188700836	chr3:75351359-75351360	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs556913577	chr3:75351538-75351539	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs575489748	chr3:75351553-75351554	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs546059400	chr3:75351563-75351564	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs369273958	chr3:75351564-75351565	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs199671907	chr3:75351678-75351679	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs181127533	chr3:75351706-75351707	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs117207452	chr3:75351731-75351732	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs540393984	chr3:75351732-75351733	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs559897591	chr3:75351762-75351763	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs530165331	chr3:75351771-75351772	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs149705986	chr3:75351772-75351773	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs570023537	chr3:75351812-75351813	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs184094783	chr3:75351813-75351814	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs189173009	chr3:75351827-75351828	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs147769645	chr3:75351842-75351843	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs181708374	chr3:75351849-75351850	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs560985070	chr3:75351894-75351895	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs553102850	chr3:75351928-75351929	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs187634436	chr3:75351945-75351946	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs141164405	chr3:75351967-75351968	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs147108997	chr3:75352036-75352037	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs138517567	chr3:75352037-75352038	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs575152866	chr3:75352084-75352085	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs545785359	chr3:75352090-75352091	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs142646211	chr3:75352156-75352157	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs573136431	chr3:75352163-75352164	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs540432754	chr3:75352180-75352181	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs561863522	chr3:75352191-75352192	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs530178354	chr3:75352225-75352226	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs543797863	chr3:75352258-75352259	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs528498670	chr3:75352291-75352292	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs59748764	chr3:75352299-75352300	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs143316149	chr3:75352301-75352302	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs530958078	chr3:75352306-75352307	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs564906726	chr3:75352327-75352328	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs570811575	chr3:75352329-75352330	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Acute myeloid leukemia	20729466	CNVD
Glioblastoma multiforme	21080181	CNVD
Melanoma	18172304	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	21251322	CNVD
Hirschsprung''s Disease	21712996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Autism	22102821	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Prostate cancer	18632612	CNVD
Metanephric adenoma	20802469	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21509527	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Colorectal cancer	16272173	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Soft tissue tumor	16732325	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1383 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:75349600-75351000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
2	chr3:75349800-75351200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr3:75349800-75351600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr3:75350000-75351000	Enhancers	Fetal Lung	lung
5	chr3:75350600-75351400	Enhancers	Lung	lung
6	chr3:75351000-75352200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
7	chr3:75351000-75352600	Weak transcription	Fetal Lung	lung
8	chr3:75351200-75352000	Enhancers	Fetal Muscle Leg	muscle
9	chr3:75351400-75352400	Enhancers	Breast Myoepithelial Primary Cells	Breast
10	chr3:75352600-75353000	Enhancers	Rectal Mucosa Donor 31	rectum
11	chr3:75352600-75353600	Enhancers	Fetal Lung	lung
12	chr3:75353200-75354200	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr3:75353400-75353600	Enhancers	Aorta	Aorta
14	chr3:75358800-75359000	Enhancers	Pancreas	Pancrea
15	chr3:75359000-75374600	Weak transcription	Pancreas	Pancrea
16	chr3:75361600-75362200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr3:75361600-75362800	Enhancers	Primary hematopoietic stem cells	blood
18	chr3:75362800-75369800	Weak transcription	Primary hematopoietic stem cells	blood
19	chr3:75366000-75369800	Enhancers	Primary neutrophils fromperipheralblood	blood
20	chr3:75368800-75370200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr3:75369000-75370400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
22	chr3:75369200-75370000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr3:75369800-75370000	Enhancers	Primary hematopoietic stem cells	blood
24	chr3:75369800-75370600	Enhancers	H1 Cell Line	embryonic stem cell
25	chr3:75369800-75370600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr3:75369800-75373400	Weak transcription	Primary neutrophils fromperipheralblood	blood
27	chr3:75370000-75370400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr3:75370000-75370600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr3:75370200-75370600	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr3:75370200-75370800	Enhancers	H9 Cell Line	embryonic stem cell
31	chr3:75370200-75371400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr3:75370400-75372000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
33	chr3:75370600-75377200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr3:75370800-75373200	Weak transcription	H9 Cell Line	embryonic stem cell
35	chr3:75371400-75371600	Enhancers	Right Atrium	heart
36	chr3:75371400-75372200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr3:75371400-75372200	Enhancers	Fetal Muscle Leg	muscle
38	chr3:75371600-75374600	Weak transcription	Right Atrium	heart
39	chr3:75372000-75372200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
40	chr3:75372200-75373600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr3:75373200-75373400	Enhancers	H9 Cell Line	embryonic stem cell
42	chr3:75373400-75374400	Enhancers	Primary neutrophils fromperipheralblood	blood
43	chr3:75373600-75373800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr3:75374600-75375000	Enhancers	Pancreas	Pancrea
45	chr3:75374600-75375000	Enhancers	Right Atrium	heart
46	chr3:75374600-75377600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr3:75374800-75375000	Enhancers	Gastric	stomach
48	chr3:75375000-75376000	Weak transcription	Pancreas	Pancrea
49	chr3:75375000-75382400	Weak transcription	Gastric	stomach
50	chr3:75375800-75376400	Enhancers	Fetal Stomach	stomach

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