Variant report

Variant	nsv877700
Chromosome Location	chr3:160223172-160248363
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:116)
CpG islands
(count:122)
Chromatin interactive
region (count:19)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:116 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:160224665-160225118	HepG2	liver:	n/a	n/a
2	BHLHE40	chr3:160224885-160225144	HepG2	liver:	n/a	n/a
3	BHLHE40	chr3:160224835-160225211	HepG2	liver:	n/a	n/a
4	BHLHE40	chr3:160224849-160225136	HepG2	liver:	n/a	n/a
5	CEBPB	chr3:160238089-160238114	K562	blood:	n/a	n/a
6	CEBPB	chr3:160226549-160226835	K562	blood:	n/a	chr3:160226699-160226710 chr3:160226699-160226712
7	CEBPB	chr3:160224786-160225205	HepG2	liver:	n/a	n/a
8	CEBPB	chr3:160224803-160225096	IMR90	lung:	n/a	n/a
9	CEBPB	chr3:160243718-160243984	HepG2	liver:	n/a	chr3:160243843-160243854
10	CEBPB	chr3:160224843-160225101	MCF-7	breast:	n/a	n/a
11	CEBPB	chr3:160226540-160226885	A549	lung:	n/a	chr3:160226699-160226710 chr3:160226699-160226712
12	CEBPB	chr3:160224772-160225172	HepG2	liver:	n/a	n/a
13	CEBPB	chr3:160226526-160226871	HepG2	liver:	n/a	chr3:160226699-160226710 chr3:160226699-160226712
14	CEBPB	chr3:160224769-160225125	HepG2	liver:	n/a	n/a
15	CEBPB	chr3:160224807-160225078	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr3:160224810-160225059	HepG2	liver:	n/a	n/a
17	CEBPB	chr3:160224684-160225085	A549	lung:	n/a	n/a
18	CEBPB	chr3:160226570-160226847	IMR90	lung:	n/a	chr3:160226699-160226710 chr3:160226699-160226712
19	CTCF	chr3:160236650-160236695	Kidney_OC	kidney:	n/a	n/a
20	CTCF	chr3:160231084-160231157	Kidney_OC	kidney:	n/a	n/a
21	CTCF	chr3:160227060-160227210	NB4	blood:	n/a	n/a
22	CUX1	chr3:160237895-160237951	K562	blood:	n/a	n/a
23	E2F4	chr3:160230096-160230102	MCF10A-Er-Src	breast:	n/a	n/a
24	EP300	chr3:160224702-160225119	HepG2	liver:	n/a	chr3:160224902-160224912
25	EP300	chr3:160224681-160225173	HepG2	liver:	n/a	chr3:160224902-160224912
26	FAM48A	chr3:160244863-160244947	GM12878	blood:	n/a	n/a
27	FOS	chr3:160224320-160224413	MCF10A-Er-Src	breast:	n/a	n/a
28	FOS	chr3:160235224-160235418	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr3:160224251-160224520	MCF10A-Er-Src	breast:	n/a	n/a
30	FOS	chr3:160224273-160224466	MCF10A-Er-Src	breast:	n/a	n/a
31	FOS	chr3:160224635-160224783	MCF10A-Er-Src	breast:	n/a	chr3:160224641-160224650 chr3:160224640-160224650 chr3:160224640-160224650
32	FOXA1	chr3:160224794-160225140	HepG2	liver:	n/a	n/a
33	FOXA1	chr3:160224697-160225175	HepG2	liver:	n/a	n/a
34	FOXA1	chr3:160224631-160225130	HepG2	liver:	n/a	n/a
35	FOXA1	chr3:160224609-160225139	HepG2	liver:	n/a	n/a
36	FOXA2	chr3:160224707-160225146	HepG2	liver:	n/a	n/a
37	HDAC2	chr3:160224748-160225134	HepG2	liver:	n/a	n/a
38	HDAC2	chr3:160224798-160225155	HepG2	liver:	n/a	n/a
39	HNF4G	chr3:160224911-160225150	HepG2	liver:	n/a	n/a
40	JUN	chr3:160223213-160223388	H1-hESC	embryonic stem cell:	n/a	n/a
41	JUN	chr3:160224447-160224538	K562	blood:	n/a	n/a
42	MAFF	chr3:160245842-160245941	K562	blood:	n/a	chr3:160245891-160245909
43	MAFF	chr3:160245846-160245970	HepG2	liver:	n/a	chr3:160245891-160245909
44	MAFK	chr3:160245838-160245935	HepG2	liver:	n/a	chr3:160245893-160245904 chr3:160245893-160245908
45	MAFK	chr3:160245770-160246055	HepG2	liver:	n/a	chr3:160245893-160245904 chr3:160245893-160245908
46	MAFK	chr3:160241675-160241858	HepG2	liver:	n/a	chr3:160241754-160241770
47	MAFK	chr3:160245741-160246055	IMR90	lung:	n/a	chr3:160245893-160245904 chr3:160245893-160245908
48	MAFK	chr3:160228174-160228407	HepG2	liver:	n/a	n/a
49	MAFK	chr3:160245802-160245928	Hela-S3	cervix:	n/a	chr3:160245893-160245904 chr3:160245893-160245908
50	MAFK	chr3:160243890-160244033	HepG2	liver:	n/a	chr3:160243939-160243950 chr3:160243938-160243952 chr3:160243939-160243950

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:160233563-160233613	HNPCEpiC	eye:	n/a
2	chr3:160233797-160233847	AG04449	skin:	fetal
3	chr3:160233797-160233847	Hepatocyte	liver:	n/a
4	chr3:160233563-160233613	PANC-1	pancreas:	n/a
5	chr3:160233797-160233847	T-47D	breast:	n/a
6	chr3:160233563-160233613	HCT-116	colon:	n/a
7	chr3:160233563-160233613	AG04450	lung:	fetal
8	chr3:160233797-160233847	HEK293	kidney:	embryo
9	chr3:160233797-160233847	HCM	heart:	n/a
10	chr3:160233797-160233847	U87	brain:	n/a
11	chr3:160233563-160233613	U87	brain:	n/a
12	chr3:160233797-160233847	BE2_C	brain:	n/a
13	chr3:160233797-160233847	RPTEC	kidney:	n/a
14	chr3:160233563-160233613	HCPEpiC	choroid plexus:	n/a
15	chr3:160233563-160233613	GM06990	blood:	n/a
16	chr3:160233797-160233847	NB4	blood:	n/a
17	chr3:160233563-160233613	HCF	heart:	n/a
18	chr3:160233563-160233613	LNCaP	prostate:	n/a
19	chr3:160233797-160233847	K562	blood:	n/a
20	chr3:160233797-160233847	HCF	heart:	n/a
21	chr3:160233797-160233847	HepG2	liver:	n/a
22	chr3:160233797-160233847	NHBE	bronchial:	n/a
23	chr3:160233563-160233613	AoSMC	blood vessel:	n/a
24	chr3:160233797-160233847	SK-N-SH	brain:	n/a
25	chr3:160233563-160233613	GM12891	blood:	n/a
26	chr3:160233563-160233613	HEEpiC	esophagus:	n/a
27	chr3:160233797-160233847	ovcar-3	ovarian:	n/a
28	chr3:160233797-160233847	SAEC	small airway:	n/a
29	chr3:160233797-160233847	MCF-7	breast:	n/a
30	chr3:160233797-160233847	GM12892	blood:	n/a
31	chr3:160233563-160233613	SK-N-SH	brain:	n/a
32	chr3:160233563-160233613	RPTEC	kidney:	n/a
33	chr3:160233797-160233847	AG09309	skin:	n/a
34	chr3:160233797-160233847	BJ	skin:	n/a
35	chr3:160233797-160233847	NT2-D1	testis:	n/a
36	chr3:160233797-160233847	ECC-1	luminal epithelium:	n/a
37	chr3:160233797-160233847	GM06990	blood:	n/a
38	chr3:160233563-160233613	NT2-D1	testis:	n/a
39	chr3:160233563-160233613	SK-N-SH_RA	brain:	n/a
40	chr3:160233797-160233847	HRPEpiC	eye:	n/a
41	chr3:160233797-160233847	Caco-2	colon:	n/a
42	chr3:160233797-160233847	PANC-1	pancreas:	n/a
43	chr3:160233563-160233613	ProgFib	skin:	n/a
44	chr3:160233563-160233613	HPAEpiC	pulmonary alveolar:	n/a
45	chr3:160233797-160233847	SK-N-SH_RA	brain:	n/a
46	chr3:160233563-160233613	HCM	heart:	n/a
47	chr3:160233563-160233613	NB4	blood:	n/a
48	chr3:160233563-160233613	AG04449	skin:	fetal
49	chr3:160233797-160233847	H1-hESC	embryonic stem cell:	embryo
50	chr3:160233563-160233613	A549	lung:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:160210254..160212371-chr3:160246508..160248687,2	K562	blood:
2	chr3:160243874..160245789-chr3:160246088..160248768,2	K562	blood:
3	chr3:160220685..160224773-chr3:160234023..160237053,3	MCF-7	breast:
4	chr3:160223761..160225418-chr3:160235399..160237999,2	K562	blood:
5	chr3:160220685..160224773-chr3:160234023..160237053,3	MCF-7	breast:
6	chr3:160247630..160249536-chr3:160251457..160253058,2	K562	blood:
7	chr3:160167035..160169821-chr3:160232708..160234646,2	K562	blood:
8	chr3:160242999..160245781-chr3:160282351..160283886,2	MCF-7	breast:
9	chr3:160245830..160248208-chr3:160254358..160256155,2	K562	blood:
10	chr3:160243874..160245789-chr3:160246088..160248768,2	K562	blood:
11	chr3:160221864..160223670-chr3:160224243..160226921,2	MCF-7	breast:
12	chr3:160230934..160232886-chr3:160280729..160283145,2	K562	blood:
13	chr3:160243184..160245065-chr3:160260331..160263083,2	K562	blood:
14	chr3:160119557..160121442-chr3:160246035..160249000,2	K562	blood:
15	chr3:160221864..160223670-chr3:160224243..160226921,2	MCF-7	breast:
16	chr3:160223761..160225418-chr3:160235399..160237999,2	K562	blood:
17	chr3:160247380..160250170-chr3:160281727..160283723,2	K562	blood:
18	chr3:160167490..160169764-chr3:160223909..160225875,2	K562	blood:
19	chr3:160229725..160231499-chr3:160231673..160233379,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TRIM59-2	chr3:160232695-160233024	NONHSAT092997

No data

Variant related genes	Relation type
KPNA4	TF binding region
SCARNA7	TF binding region
KPNA4	CpG island
SCARNA7	CpG island
ENSG00000113810	chromatin interactions
ENSG00000186432	chromatin interactions
ENSG00000238741	chromatin interactions
ENSG00000229320	chromatin interactions
ENSG00000213186	chromatin interactions

Extended variants
information (count: 946 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:946 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs721023	chr3:160223172-160223173	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs368628410	chr3:160223281-160223282	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs565328042	chr3:160223297-160223298	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs9821659	chr3:160223299-160223300	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs544984297	chr3:160223382-160223383	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs138470425	chr3:160223402-160223403	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs559701155	chr3:160223469-160223470	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs75277608	chr3:160223594-160223595	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs548434349	chr3:160223636-160223637	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs575512278	chr3:160223641-160223642	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs142987416	chr3:160223649-160223650	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs537195131	chr3:160223663-160223664	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs551987320	chr3:160223721-160223722	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs554926417	chr3:160223746-160223747	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs570484753	chr3:160223747-160223748	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs534335632	chr3:160223762-160223763	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs544416828	chr3:160223767-160223768	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs572433452	chr3:160223823-160223824	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs189932441	chr3:160223880-160223881	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs115464858	chr3:160223896-160223897	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs200226140	chr3:160223961-160223962	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs201292039	chr3:160223966-160223967	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs368228537	chr3:160224045-160224046	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs543951050	chr3:160224067-160224068	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs565244948	chr3:160224075-160224076	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs146130005	chr3:160224097-160224098	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs10212236	chr3:160224114-160224115	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs564440269	chr3:160224115-160224116	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs183273400	chr3:160224130-160224131	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs533056264	chr3:160224146-160224147	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs140112788	chr3:160224160-160224161	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs552311725	chr3:160224193-160224194	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs570473546	chr3:160224205-160224206	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs528152077	chr3:160224255-160224256	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs373102557	chr3:160224265-160224266	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs542474400	chr3:160224357-160224358	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs188144947	chr3:160224414-160224415	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs567707304	chr3:160224439-160224440	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs536594109	chr3:160224584-160224585	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs193080823	chr3:160224589-160224590	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs554846480	chr3:160224595-160224596	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs185285672	chr3:160224652-160224653	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs537264201	chr3:160224683-160224684	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs73023851	chr3:160224703-160224704	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs376804924	chr3:160224814-160224815	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs541524761	chr3:160224856-160224857	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs188943977	chr3:160224865-160224866	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs144296141	chr3:160224868-160224869	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs534208930	chr3:160224901-160224902	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs367793590	chr3:160224942-160224943	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	21115979	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Hepatocellular carcinoma	16750200	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Basal cell lymphoma	17170743	CNVD
Breast cancer	16608533	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-small cell lung cancer	19010865	CNVD
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16547154	CNVD
Breast cancer	21364760	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Effusion lymphoma	18079361	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	21785460	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Bladder cancer	21909424	CNVD
Myelofibrosis	22110671	CNVD
Cancer	20164919	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:766 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:160204000-160224000	Weak transcription	Gastric	stomach
2	chr3:160204000-160238200	Weak transcription	Small Intestine	intestine
3	chr3:160204200-160224400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr3:160204200-160224800	Weak transcription	GM12878-XiMat	blood
5	chr3:160204200-160225400	Weak transcription	Fetal Kidney	kidney
6	chr3:160213000-160228600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr3:160213600-160223800	Weak transcription	Psoas Muscle	Psoas
8	chr3:160215000-160225400	Weak transcription	Fetal Heart	heart
9	chr3:160215600-160228200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr3:160215600-160254200	Strong transcription	Monocytes-CD14+_RO01746	blood
11	chr3:160215800-160223400	Strong transcription	Primary neutrophils fromperipheralblood	blood
12	chr3:160215800-160227400	Strong transcription	Primary B cells from cord blood	blood
13	chr3:160215800-160227800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr3:160215800-160227800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr3:160215800-160227800	Strong transcription	NHDF-Ad	bronchial
16	chr3:160215800-160228200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr3:160215800-160254000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr3:160215800-160254200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr3:160215800-160254200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr3:160216000-160227800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
21	chr3:160216000-160227800	Strong transcription	Placenta	Placenta
22	chr3:160216000-160228000	Strong transcription	Duodenum Mucosa	Duodenum
23	chr3:160216000-160254200	Strong transcription	Primary monocytes fromperipheralblood	blood
24	chr3:160216200-160227800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr3:160216200-160227800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
26	chr3:160216200-160227800	Strong transcription	Primary T helper cells fromperipheralblood	blood
27	chr3:160216200-160227800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr3:160216200-160227800	Strong transcription	Adipose Nuclei	Adipose
29	chr3:160216200-160228600	Strong transcription	HUES6 Cell Line	embryonic stem cell
30	chr3:160216200-160249200	Strong transcription	Liver	Liver
31	chr3:160216200-160254200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
32	chr3:160216400-160228200	Strong transcription	Rectal Mucosa Donor 29	rectum
33	chr3:160216400-160228800	Strong transcription	HUES64 Cell Line	embryonic stem cell
34	chr3:160216400-160254400	Strong transcription	HUES48 Cell Line	embryonic stem cell
35	chr3:160216800-160224600	Strong transcription	Rectal Mucosa Donor 31	rectum
36	chr3:160216800-160225400	Strong transcription	Hela-S3	cervix
37	chr3:160216800-160253800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
38	chr3:160217000-160226600	Weak transcription	Brain Angular Gyrus	brain
39	chr3:160217000-160227800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr3:160217200-160225400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
41	chr3:160217200-160254000	Strong transcription	Dnd41	blood
42	chr3:160217400-160225400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
43	chr3:160217400-160227800	Strong transcription	HSMM	muscle
44	chr3:160217400-160228000	Strong transcription	Osteobl	bone
45	chr3:160217400-160259600	Weak transcription	Pancreatic Islets	Pancreatic Islet
46	chr3:160217600-160227800	Strong transcription	NH-A	brain
47	chr3:160217800-160235000	Weak transcription	Fetal Brain Male	brain
48	chr3:160218200-160227800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
49	chr3:160218200-160228400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
50	chr3:160218400-160227800	Strong transcription	Primary B cells from peripheral blood	blood

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