Variant report

Variant	nsv589285
Chromosome Location	chr3:253573-297321
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:141)
CpG islands
(count:122)
Chromatin interactive
region (count:2)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:141 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:291259-291870	HepG2	liver:	n/a	n/a
2	ATF2	chr3:254098-254530	GM12878	blood:	n/a	n/a
3	ATF2	chr3:254017-254518	GM12878	blood:	n/a	n/a
4	BACH1	chr3:271174-271333	K562	blood:	n/a	n/a
5	BATF	chr3:259675-259847	GM12878	blood:	n/a	n/a
6	BATF	chr3:254085-254416	GM12878	blood:	n/a	n/a
7	BHLHE40	chr3:260263-260618	GM12878	blood:	n/a	n/a
8	BHLHE40	chr3:260829-261058	GM12878	blood:	n/a	n/a
9	CEBPB	chr3:271018-271333	H1-hESC	embryonic stem cell:	n/a	chr3:271305-271317
10	CEBPB	chr3:284758-286178	IMR90	lung:	n/a	chr3:284916-284933 chr3:285984-286001 chr3:284887-284900
11	CEBPB	chr3:291583-291816	HepG2	liver:	n/a	chr3:291705-291716
12	CEBPB	chr3:279120-279410	A549	lung:	n/a	chr3:279226-279239 chr3:279227-279238
13	CEBPB	chr3:291542-291836	HepG2	liver:	n/a	chr3:291705-291716
14	CEBPB	chr3:279116-279413	HepG2	liver:	n/a	chr3:279226-279239 chr3:279227-279238
15	CEBPB	chr3:291612-291803	H1-hESC	embryonic stem cell:	n/a	chr3:291705-291716
16	CREB1	chr3:254049-254528	GM12878	blood:	n/a	n/a
17	CTCF	chr3:278947-279007	MCF-7	breast:	n/a	n/a
18	CTCF	chr3:266691-266735	GM20000	blood:	n/a	n/a
19	CTCF	chr3:287360-287510	MCF-7	breast:	n/a	n/a
20	CTCF	chr3:278940-279009	GM19238	blood:	n/a	n/a
21	CTCF	chr3:287440-287590	GM12869	blood:	n/a	n/a
22	E2F4	chr3:284901-285229	MCF10A-Er-Src	breast:	n/a	n/a
23	E2F4	chr3:285810-286234	MCF10A-Er-Src	breast:	n/a	n/a
24	EBF1	chr3:278951-279133	GM12878	blood:	n/a	n/a
25	EBF1	chr3:280766-280963	GM12878	blood:	n/a	n/a
26	EBF1	chr3:254125-254530	GM12878	blood:	n/a	n/a
27	EBF1	chr3:260927-261165	GM12878	blood:	n/a	chr3:261010-261021
28	EGR1	chr3:260837-260993	GM12878	blood:	n/a	chr3:260903-260917
29	EP300	chr3:260882-260922	GM12878	blood:	n/a	n/a
30	FAM48A	chr3:269401-269442	GM12878	blood:	n/a	n/a
31	FOS	chr3:284903-285477	MCF10A-Er-Src	breast:	n/a	n/a
32	FOS	chr3:284921-285373	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr3:284855-285381	MCF10A-Er-Src	breast:	n/a	chr3:284862-284874
34	FOS	chr3:284929-285522	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr3:285827-286162	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr3:285774-286081	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr3:283085-283384	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr3:285829-286080	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr3:285762-286097	MCF10A-Er-Src	breast:	n/a	n/a
40	FOXA1	chr3:270033-270288	T-47D	breast:	n/a	chr3:270233-270245
41	FOXA1	chr3:291289-291627	HepG2	liver:	n/a	n/a
42	FOXA1	chr3:291207-291600	HepG2	liver:	n/a	n/a
43	GATA2	chr3:290698-291090	SH-SY5Y	brain:	n/a	n/a
44	GATA3	chr3:292892-293251	SH-SY5Y	brain:	n/a	chr3:293158-293167
45	GATA3	chr3:290744-290940	SH-SY5Y	brain:	n/a	n/a
46	IKZF1	chr3:254051-254650	GM12878	blood:	n/a	n/a
47	JUN	chr3:275041-275218	H1-hESC	embryonic stem cell:	n/a	n/a
48	JUN	chr3:273795-273935	HepG2	liver:	n/a	chr3:273866-273879 chr3:273837-273850
49	JUN	chr3:253163-253648	K562	blood:	n/a	n/a
50	JUND	chr3:274916-275140	H1-hESC	embryonic stem cell:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:285234-285284	HCPEpiC	choroid plexus:	n/a
2	chr3:271185-271235	HPAEpiC	pulmonary alveolar:	n/a
3	chr3:271185-271235	HL-60	blood:	n/a
4	chr3:271185-271235	HepG2	liver:	n/a
5	chr3:271185-271235	HMEC	breast:	n/a
6	chr3:285234-285284	SK-N-MC	brain:	n/a
7	chr3:271185-271235	AG09319	gingival:	n/a
8	chr3:271185-271235	AG10803	skin:	n/a
9	chr3:285234-285284	NT2-D1	testis:	n/a
10	chr3:285234-285284	HCF	heart:	n/a
11	chr3:285234-285284	MCF-7	breast:	n/a
12	chr3:285234-285284	HCM	heart:	n/a
13	chr3:285234-285284	HAEpiC	amniotic membrane:	n/a
14	chr3:285234-285284	SK-N-SH	brain:	n/a
15	chr3:285234-285284	Hela-S3	cervix:	n/a
16	chr3:285234-285284	U87	brain:	n/a
17	chr3:285234-285284	HRE	kidney:	n/a
18	chr3:285234-285284	PANC-1	pancreas:	n/a
19	chr3:271185-271235	NHBE	bronchial:	n/a
20	chr3:271185-271235	LNCaP	prostate:	n/a
21	chr3:271185-271235	HCPEpiC	choroid plexus:	n/a
22	chr3:285234-285284	ovcar-3	ovarian:	n/a
23	chr3:285234-285284	HEEpiC	esophagus:	n/a
24	chr3:285234-285284	AG10803	skin:	n/a
25	chr3:285234-285284	AG09309	skin:	n/a
26	chr3:285234-285284	SAEC	small airway:	n/a
27	chr3:285234-285284	NB4	blood:	n/a
28	chr3:271185-271235	ProgFib	skin:	n/a
29	chr3:271185-271235	NB4	blood:	n/a
30	chr3:271185-271235	SAEC	small airway:	n/a
31	chr3:271185-271235	K562	blood:	n/a
32	chr3:285234-285284	SK-N-SH_RA	brain:	n/a
33	chr3:285234-285284	ProgFib	skin:	n/a
34	chr3:285234-285284	NH-A	brain:	n/a
35	chr3:271185-271235	HUVEC	blood vessel:	n/a
36	chr3:285234-285284	PrEC	prostate:	n/a
37	chr3:271185-271235	Hela-S3	cervix:	n/a
38	chr3:271185-271235	AoSMC	blood vessel:	n/a
39	chr3:285234-285284	HRCEpiC	kidney:	n/a
40	chr3:285234-285284	HepG2	liver:	n/a
41	chr3:271185-271235	BJ	skin:	n/a
42	chr3:271185-271235	Hepatocyte	liver:	n/a
43	chr3:271185-271235	MCF-7	breast:	n/a
44	chr3:271185-271235	Caco-2	colon:	n/a
45	chr3:285234-285284	HRPEpiC	eye:	n/a
46	chr3:285234-285284	BE2_C	brain:	n/a
47	chr3:285234-285284	GM19239	blood:	n/a
48	chr3:271185-271235	HIPEpiC	eye:	n/a
49	chr3:285234-285284	A549	lung:	n/a
50	chr3:271185-271235	NH-A	brain:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:291331..293955-chr3:294697..297452,2	MCF-7	breast:
2	chr3:291331..293955-chr3:294697..297452,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CNTN6-7	chr3:286296-286375	NONHSAT087560
2	lnc-CNTN6-7	chr3:254887-255362	NONHSAT087562
3	lnc-CNTN6-7	chr3:286296-286375	NONHSAT087561
4	lnc-CNTN6-7	chr3:288251-290282	NONHSAT087561
5	lnc-CNTN6-7	chr3:288251-288539	NONHSAT087560

No data

Variant related genes	Relation type
CHL1	TF binding region
CHL1	CpG island

Extended variants
information (count: 2312 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:2312 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17006405	chr3:253573-253574	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs533396375	chr3:253678-253679	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs17329688	chr3:253679-253680	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs187867459	chr3:253690-253691	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs192550127	chr3:253691-253692	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs548973053	chr3:253696-253697	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs566168359	chr3:253700-253701	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs148742698	chr3:253729-253730	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs537944284	chr3:253738-253739	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs556419915	chr3:253750-253751	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs184843999	chr3:253764-253765	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs17006420	chr3:253784-253785	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs554002585	chr3:253785-253786	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs6768035	chr3:253799-253800	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs376591943	chr3:253821-253822	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs542600176	chr3:253836-253837	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs189774670	chr3:253839-253840	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs576148413	chr3:253876-253877	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs543528364	chr3:253879-253880	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs201275626	chr3:253887-253888	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs561370192	chr3:253888-253889	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs181526872	chr3:253889-253890	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs533542509	chr3:253899-253900	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs11917787	chr3:253919-253920	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	disease
25	rs13083041	chr3:253920-253921	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs374103658	chr3:253931-253932	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs144762364	chr3:253945-253946	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs6782582	chr3:253952-253953	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs531627559	chr3:253983-253984	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs550223635	chr3:254032-254033	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs147485781	chr3:254040-254041	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs538787611	chr3:254044-254045	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs115231278	chr3:254069-254070	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs112763125	chr3:254075-254076	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs536543184	chr3:254168-254169	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs17263957	chr3:254202-254203	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs577705382	chr3:254219-254220	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs545073787	chr3:254240-254241	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs543463345	chr3:254278-254279	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs139841446	chr3:254313-254314	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs145362172	chr3:254319-254320	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs536975169	chr3:254332-254333	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs184663971	chr3:254336-254337	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs371033559	chr3:254362-254363	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs527394336	chr3:254367-254368	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs527919126	chr3:254369-254370	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs542822646	chr3:254388-254389	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs151218188	chr3:254391-254392	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs374289736	chr3:254392-254393	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs111967035	chr3:254505-254506	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Cancer	20164920	CNVD
Lung cancer	16618734	CNVD
Autism	18349135	CNVD
Breast cancer	20409316	CNVD
Myelofibrosis	22110671	CNVD
Autism	22241247	CNVD
Intellectual disability	22045946	CNVD
Squamous cell cancer	19607727	CNVD
Gastric adenocarcinoma	19115996	CNVD
sporadic birth defects	19047251	CNVD
Mental retardation	17124404	CNVD
abnormal development	18461090	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Sudden cardiac death	19188705	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian cancer	21720365	CNVD
Neuroblastoma	18923191	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	17327916	CNVD
Glioblastoma multiforme	21080181	CNVD
Colorectal cancer	21297112	CNVD
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	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
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
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	20967226	CNVD
Autism	22543975	CNVD
Attention deficit hyperactivity disorder	19546859	CNVD
lymphocytic leukemia	21291569	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Tetralogy of Fallot	22912587	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	20685689	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:225 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:244400-254200	Weak transcription	Brain Anterior Caudate	brain
2	chr3:244800-254200	Weak transcription	Brain Germinal Matrix	brain
3	chr3:246200-258600	Weak transcription	Fetal Brain Female	brain
4	chr3:251600-255400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr3:251800-255200	Enhancers	Cortex derived primary cultured neurospheres	brain
6	chr3:252800-256400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr3:253000-254000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr3:253200-258200	Weak transcription	Fetal Brain Male	brain
9	chr3:253600-254600	Enhancers	Primary B cells from peripheral blood	blood
10	chr3:253800-254000	Enhancers	GM12878-XiMat	blood
11	chr3:253800-254600	Enhancers	Primary B cells from cord blood	blood
12	chr3:254000-254400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr3:254000-254400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr3:254000-254400	Flanking Active TSS	GM12878-XiMat	blood
15	chr3:254000-254600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr3:254000-255200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr3:254200-254400	Enhancers	Brain Germinal Matrix	brain
18	chr3:254200-254600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr3:254400-254600	Enhancers	Brain Anterior Caudate	brain
20	chr3:254400-255400	Weak transcription	GM12878-XiMat	blood
21	chr3:254400-258400	Weak transcription	Brain Germinal Matrix	brain
22	chr3:254600-258400	Weak transcription	Primary B cells from peripheral blood	blood
23	chr3:255200-258400	Weak transcription	Cortex derived primary cultured neurospheres	brain
24	chr3:255400-265400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr3:257000-257200	Enhancers	Pancreatic Islets	Pancreatic Islet
26	chr3:257200-258200	Weak transcription	Pancreatic Islets	Pancreatic Islet
27	chr3:258200-258600	Enhancers	Pancreatic Islets	Pancreatic Islet
28	chr3:258200-259400	Enhancers	Fetal Brain Male	brain
29	chr3:258400-258600	Enhancers	Brain Cingulate Gyrus	brain
30	chr3:258400-258800	Enhancers	Brain Hippocampus Middle	brain
31	chr3:258400-259400	Enhancers	Cortex derived primary cultured neurospheres	brain
32	chr3:258400-261400	Enhancers	Primary B cells from peripheral blood	blood
33	chr3:258600-258800	Enhancers	Brain Germinal Matrix	brain
34	chr3:258600-259400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr3:258600-259400	Enhancers	Fetal Brain Female	brain
36	chr3:258600-259400	Active TSS	Pancreatic Islets	Pancreatic Islet
37	chr3:259200-259400	Enhancers	Esophagus	oesophagus
38	chr3:259200-260000	Enhancers	Breast Myoepithelial Primary Cells	Breast
39	chr3:259200-260000	Weak transcription	GM12878-XiMat	blood
40	chr3:259600-261400	Enhancers	Primary B cells from cord blood	blood
41	chr3:260000-261000	Enhancers	GM12878-XiMat	blood
42	chr3:265400-265800	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr3:265800-267000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr3:266000-266200	Weak transcription	Cortex derived primary cultured neurospheres	brain
45	chr3:268200-268400	Enhancers	Ovary	ovary
46	chr3:268400-271000	Weak transcription	Ovary	ovary
47	chr3:269000-269200	Enhancers	Pancreatic Islets	Pancreatic Islet
48	chr3:269200-270200	Weak transcription	Pancreatic Islets	Pancreatic Islet
49	chr3:269400-269600	Enhancers	Brain Anterior Caudate	brain
50	chr3:269400-271200	Enhancers	Breast Myoepithelial Primary Cells	Breast

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