Variant report

Variant	nsv877310
Chromosome Location	chr3:105409321-105495841
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr3:105493244-105493687	GM12878	blood:	n/a	n/a
2	ATF2	chr3:105493136-105493706	GM12878	blood:	n/a	n/a
3	ATF2	chr3:105471808-105472363	GM12878	blood:	n/a	n/a
4	ATF2	chr3:105441559-105442445	GM12878	blood:	n/a	n/a
5	ATF2	chr3:105441592-105442539	GM12878	blood:	n/a	n/a
6	ATF2	chr3:105483224-105483608	GM12878	blood:	n/a	n/a
7	ATF2	chr3:105483253-105483868	GM12878	blood:	n/a	n/a
8	BACH1	chr3:105438790-105438901	H1-hESC	embryonic stem cell:	n/a	chr3:105438804-105438818
9	BATF	chr3:105442092-105442360	GM12878	blood:	n/a	chr3:105442227-105442238 chr3:105442228-105442238
10	BATF	chr3:105441735-105442039	GM12878	blood:	n/a	n/a
11	BATF	chr3:105482183-105482519	GM12878	blood:	n/a	n/a
12	BATF	chr3:105442084-105442403	GM12878	blood:	n/a	chr3:105442227-105442238 chr3:105442228-105442238
13	BATF	chr3:105492176-105492536	GM12878	blood:	n/a	chr3:105492369-105492379 chr3:105492406-105492415 chr3:105492368-105492379
14	BATF	chr3:105493258-105493654	GM12878	blood:	n/a	n/a
15	BATF	chr3:105493281-105493650	GM12878	blood:	n/a	n/a
16	BATF	chr3:105449914-105450106	GM12878	blood:	n/a	n/a
17	BCL11A	chr3:105441762-105442353	GM12878	blood:	n/a	chr3:105442230-105442239 chr3:105442244-105442253 chr3:105442231-105442240
18	BCL11A	chr3:105493269-105493642	GM12878	blood:	n/a	n/a
19	BCL3	chr3:105493306-105493673	GM12878	blood:	n/a	n/a
20	BCL3	chr3:105442069-105442429	GM12878	blood:	n/a	chr3:105442230-105442239 chr3:105442244-105442253 chr3:105442231-105442240
21	BCLAF1	chr3:105441666-105442424	GM12878	blood:	n/a	chr3:105442230-105442239 chr3:105442244-105442253 chr3:105442231-105442240
22	BCLAF1	chr3:105491471-105491958	GM12878	blood:	n/a	n/a
23	BCLAF1	chr3:105483867-105484184	GM12878	blood:	n/a	n/a
24	BHLHE40	chr3:105441702-105442406	GM12878	blood:	n/a	n/a
25	BHLHE40	chr3:105472150-105472218	GM12878	blood:	n/a	n/a
26	BRCA1	chr3:105417156-105417285	GM12878	blood:	n/a	n/a
27	BRCA1	chr3:105459233-105459283	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr3:105472774-105473077	A549	lung:	n/a	n/a
29	CEBPB	chr3:105426427-105426731	K562	blood:	n/a	chr3:105426584-105426597 chr3:105426586-105426595 chr3:105426586-105426597
30	CEBPB	chr3:105423663-105423882	A549	lung:	n/a	chr3:105423741-105423752 chr3:105423743-105423754 chr3:105423741-105423754 chr3:105423741-105423754
31	CEBPB	chr3:105434341-105434547	A549	lung:	n/a	chr3:105434439-105434452
32	CEBPB	chr3:105472751-105473087	K562	blood:	n/a	n/a
33	CEBPB	chr3:105426417-105426701	IMR90	lung:	n/a	chr3:105426584-105426597 chr3:105426586-105426595 chr3:105426586-105426597
34	CEBPB	chr3:105472761-105473043	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr3:105423688-105423827	HepG2	liver:	n/a	chr3:105423741-105423752 chr3:105423743-105423754 chr3:105423741-105423754 chr3:105423741-105423754
36	CEBPB	chr3:105472775-105473017	A549	lung:	n/a	n/a
37	CEBPB	chr3:105477311-105477351	HepG2	liver:	n/a	chr3:105477332-105477343
38	CEBPB	chr3:105472737-105473017	MCF-7	breast:	n/a	n/a
39	CEBPB	chr3:105434263-105434621	IMR90	lung:	n/a	chr3:105434439-105434452
40	CEBPB	chr3:105472768-105473078	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr3:105426429-105426670	A549	lung:	n/a	chr3:105426584-105426597 chr3:105426586-105426595 chr3:105426586-105426597
42	CEBPB	chr3:105472741-105473094	IMR90	lung:	n/a	n/a
43	CEBPB	chr3:105472743-105473085	HepG2	liver:	n/a	n/a
44	CEBPB	chr3:105426446-105426711	A549	lung:	n/a	chr3:105426584-105426597 chr3:105426586-105426595 chr3:105426586-105426597
45	CHD1	chr3:105472931-105473056	GM12878	blood:	n/a	n/a
46	CHD2	chr3:105471807-105472285	GM12878	blood:	n/a	n/a
47	CHD2	chr3:105486693-105486862	GM12878	blood:	n/a	n/a
48	CHD2	chr3:105441736-105442375	GM12878	blood:	n/a	n/a
49	CHD2	chr3:105417799-105417842	GM12878	blood:	n/a	n/a
50	CTCF	chr3:105477018-105477064	GM13976	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:105466016-105466066	HCF	heart:	n/a
2	chr3:105466016-105466066	HCT-116	colon:	n/a
3	chr3:105466016-105466066	MCF-7	breast:	n/a
4	chr3:105466016-105466066	HNPCEpiC	eye:	n/a
5	chr3:105466016-105466066	NH-A	brain:	n/a
6	chr3:105466016-105466066	BJ	skin:	n/a
7	chr3:105466016-105466066	A549	lung:	n/a
8	chr3:105466016-105466066	MCF10A-Er-Src	breast:	n/a
9	chr3:105466016-105466066	GM12891	blood:	n/a
10	chr3:105466016-105466066	NT2-D1	testis:	n/a
11	chr3:105466016-105466066	Jurkat	blood:	n/a
12	chr3:105466016-105466066	AG09309	skin:	n/a
13	chr3:105466016-105466066	GM19239	blood:	n/a
14	chr3:105466016-105466066	HRPEpiC	eye:	n/a
15	chr3:105466016-105466066	AoSMC	blood vessel:	n/a
16	chr3:105466016-105466066	ProgFib	skin:	n/a
17	chr3:105466016-105466066	HPAEpiC	pulmonary alveolar:	n/a
18	chr3:105466016-105466066	HMEC	breast:	n/a
19	chr3:105466016-105466066	SAEC	small airway:	n/a
20	chr3:105466016-105466066	GM12892	blood:	n/a
21	chr3:105466016-105466066	SKMC	muscle:	n/a
22	chr3:105466016-105466066	HUVEC	blood vessel:	n/a
23	chr3:105466016-105466066	AG04449	skin:	fetal
24	chr3:105466016-105466066	PFSK-1	brain:	n/a
25	chr3:105466016-105466066	SK-N-SH	brain:	n/a
26	chr3:105466016-105466066	HEK293	kidney:	embryo
27	chr3:105466016-105466066	GM06990	blood:	n/a
28	chr3:105466016-105466066	PrEC	prostate:	n/a
29	chr3:105466016-105466066	ECC-1	luminal epithelium:	n/a
30	chr3:105466016-105466066	HL-60	blood:	n/a
31	chr3:105466016-105466066	T-47D	breast:	n/a
32	chr3:105466016-105466066	CMK	blood:	n/a
33	chr3:105466016-105466066	Hepatocyte	liver:	n/a
34	chr3:105466016-105466066	HIPEpiC	eye:	n/a
35	chr3:105466016-105466066	NB4	blood:	n/a
36	chr3:105466016-105466066	HCPEpiC	choroid plexus:	n/a
37	chr3:105466016-105466066	H1-hESC	embryonic stem cell:	embryo
38	chr3:105466016-105466066	NHDF-neo	bronchial:	n/a
39	chr3:105466016-105466066	SK-N-MC	brain:	n/a
40	chr3:105466016-105466066	BE2_C	brain:	n/a
41	chr3:105466016-105466066	HRE	kidney:	n/a
42	chr3:105466016-105466066	AG09319	gingival:	n/a
43	chr3:105466016-105466066	Hela-S3	cervix:	n/a
44	chr3:105466016-105466066	AG10803	skin:	n/a
45	chr3:105466016-105466066	LNCaP	prostate:	n/a
46	chr3:105466016-105466066	HRCEpiC	kidney:	n/a
47	chr3:105466016-105466066	K562	blood:	n/a
48	chr3:105466016-105466066	AG04450	lung:	fetal
49	chr3:105466016-105466066	GM12878	blood:	n/a
50	chr3:105466016-105466066	HepG2	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:105452868..105454661-chr3:105463117..105465166,2	K562	blood:
2	chr3:105409741..105412023-chr3:105415903..105417976,2	K562	blood:
3	chr3:105431222..105434203-chr3:105434765..105437080,2	MCF-7	breast:
4	chr3:105481713..105484437-chr7:147483253..147485905,2	MCF-7	breast:
5	chr3:105429146..105430827-chr3:105431044..105433948,2	K562	blood:
6	chr3:105435086..105438281-chr3:105439598..105442695,3	MCF-7	breast:
7	chr3:105438428..105441312-chr3:105441392..105443154,2	K562	blood:
8	chr3:105429146..105430827-chr3:105431044..105433948,2	K562	blood:
9	chr3:105409741..105412023-chr3:105415903..105417976,2	K562	blood:
10	chr3:105435161..105438047-chr3:105586543..105588230,2	MCF-7	breast:
11	chr3:105452868..105454661-chr3:105463117..105465166,2	K562	blood:
12	chr3:105435086..105438281-chr3:105439598..105442695,3	MCF-7	breast:
13	chr3:105438428..105441312-chr3:105441392..105443154,2	K562	blood:
14	chr3:105431222..105434203-chr3:105434765..105437080,2	MCF-7	breast:
15	chr3:105388584..105391376-chr3:105413040..105414567,2	MCF-7	breast:

Variant related genes	Relation type
CBLB	TF binding region
CBLB	CpG island
ENSG00000114423	chromatin interactions

Extended variants
information (count: 3266 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:3266 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1546733	chr3:105409321-105409322	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs72993723	chr3:105409352-105409353	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs111946960	chr3:105409366-105409367	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs559794772	chr3:105409376-105409377	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs561333200	chr3:105409387-105409388	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs186373696	chr3:105409422-105409423	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs146417331	chr3:105409522-105409523	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs548420202	chr3:105409529-105409530	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs372257695	chr3:105409534-105409535	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs113049998	chr3:105409535-105409536	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs551872020	chr3:105409538-105409539	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs548525419	chr3:105409548-105409549	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs374726594	chr3:105409549-105409550	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs2301047	chr3:105409581-105409582	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs554000219	chr3:105409620-105409621	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs572418481	chr3:105409623-105409624	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs536417704	chr3:105409644-105409645	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs531755500	chr3:105409651-105409652	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs576441897	chr3:105409695-105409696	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs201638137	chr3:105409701-105409702	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs565131256	chr3:105409807-105409808	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs574495227	chr3:105409850-105409851	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs577122711	chr3:105409904-105409905	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs541446799	chr3:105409936-105409937	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs370063701	chr3:105410017-105410018	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs17202257	chr3:105410023-105410024	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs530039816	chr3:105410114-105410115	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs150112335	chr3:105410131-105410132	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs563534856	chr3:105410140-105410141	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs138614774	chr3:105410144-105410145	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs552299353	chr3:105410171-105410172	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs570459590	chr3:105410178-105410179	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs528052465	chr3:105410309-105410310	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs12489983	chr3:105410342-105410343	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs547973926	chr3:105410366-105410367	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs566008195	chr3:105410376-105410377	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs372010123	chr3:105410393-105410394	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs554731899	chr3:105410410-105410411	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs372774520	chr3:105410464-105410465	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs3821490	chr3:105410477-105410478	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs558968245	chr3:105410482-105410483	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs577282412	chr3:105410509-105410510	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs541409981	chr3:105410529-105410530	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs368321139	chr3:105410536-105410537	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs545663503	chr3:105410602-105410603	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs574770262	chr3:105410605-105410606	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs542187348	chr3:105410610-105410611	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs182780453	chr3:105410635-105410636	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs536902453	chr3:105410642-105410643	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs13090541	chr3:105410650-105410651	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	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
Renal cell carcinoma	21668985	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	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
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Neurodevelopmental disorder	22521361	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
microdeletion syndrome	22180640	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
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	16608533	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Renal cell carcinoma	18765545	CNVD
Developmental delay	22180640	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Myelofibrosis	22110671	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:2445 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:105373000-105419600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr3:105373600-105419600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr3:105375800-105419600	Weak transcription	Colonic Mucosa	Colon
4	chr3:105375800-105464600	Weak transcription	Small Intestine	intestine
5	chr3:105376000-105438200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr3:105376800-105440000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr3:105378000-105420800	Weak transcription	HUVEC	blood vessel
8	chr3:105378000-105455400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr3:105378600-105438600	Weak transcription	Spleen	Spleen
10	chr3:105379000-105437400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr3:105379200-105440400	Weak transcription	Thymus	Thymus
12	chr3:105380600-105411800	Weak transcription	Brain Substantia Nigra	brain
13	chr3:105385400-105411000	Weak transcription	HMEC	breast
14	chr3:105387200-105420800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr3:105388400-105421000	Weak transcription	Gastric	stomach
16	chr3:105388600-105419800	Weak transcription	Brain Germinal Matrix	brain
17	chr3:105389200-105467200	Weak transcription	Stomach Mucosa	stomach
18	chr3:105393600-105420800	Weak transcription	Colon Smooth Muscle	Colon
19	chr3:105394200-105438800	Weak transcription	NHEK	skin
20	chr3:105396000-105411800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr3:105396000-105420200	Weak transcription	Cortex derived primary cultured neurospheres	brain
22	chr3:105396000-105420800	Weak transcription	Brain Angular Gyrus	brain
23	chr3:105396000-105432600	Weak transcription	Pancreas	Pancrea
24	chr3:105396000-105437200	Weak transcription	Psoas Muscle	Psoas
25	chr3:105396000-105437400	Weak transcription	Brain Cingulate Gyrus	brain
26	chr3:105396000-105438200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
27	chr3:105396000-105438400	Weak transcription	Brain Inferior Temporal Lobe	brain
28	chr3:105396200-105430400	Weak transcription	Fetal Brain Male	brain
29	chr3:105397600-105410600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr3:105397600-105411200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
31	chr3:105397800-105410000	Weak transcription	Fetal Heart	heart
32	chr3:105397800-105419600	Weak transcription	Fetal Thymus	thymus
33	chr3:105399600-105419600	Weak transcription	Brain Hippocampus Middle	brain
34	chr3:105399600-105420000	Weak transcription	Right Ventricle	heart
35	chr3:105400000-105437200	Weak transcription	Primary neutrophils fromperipheralblood	blood
36	chr3:105400200-105411000	Weak transcription	Fetal Kidney	kidney
37	chr3:105400200-105420600	Weak transcription	Brain Anterior Caudate	brain
38	chr3:105400400-105410400	Weak transcription	Monocytes-CD14+_RO01746	blood
39	chr3:105400400-105419600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
40	chr3:105400600-105409800	Weak transcription	HUES48 Cell Line	embryonic stem cell
41	chr3:105400600-105410400	Weak transcription	H1 Cell Line	embryonic stem cell
42	chr3:105400600-105410600	Weak transcription	Dnd41	blood
43	chr3:105400600-105410800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
44	chr3:105400600-105411600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
45	chr3:105400600-105411600	Weak transcription	Fetal Brain Female	brain
46	chr3:105400600-105411800	Weak transcription	Ovary	ovary
47	chr3:105400600-105419600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr3:105400600-105419600	Weak transcription	Primary monocytes fromperipheralblood	blood
49	chr3:105400600-105419600	Weak transcription	Skeletal Muscle Male	skeletal muscle
50	chr3:105400600-105420800	Weak transcription	HUES6 Cell Line	embryonic stem cell

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