Variant report

Variant	nsv540924
Chromosome Location	chr11:4594628-4685732
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1039)
CpG islands
(count:2325)
Chromatin interactive
region (count:36)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1039 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:4629507-4629808	K562	blood:	n/a	n/a
2	ARID3A	chr11:4679879-4680384	K562	blood:	n/a	n/a
3	ATF1	chr11:4601664-4601807	K562	blood:	n/a	n/a
4	ATF1	chr11:4647476-4647734	K562	blood:	n/a	n/a
5	ATF1	chr11:4640875-4641090	K562	blood:	n/a	n/a
6	ATF1	chr11:4680154-4680354	K562	blood:	n/a	n/a
7	BHLHE40	chr11:4629164-4629819	K562	blood:	n/a	chr11:4629490-4629506
8	BHLHE40	chr11:4679927-4680079	K562	blood:	n/a	n/a
9	BHLHE40	chr11:4658172-4658516	K562	blood:	n/a	n/a
10	BHLHE40	chr11:4658189-4658440	GM12878	blood:	n/a	n/a
11	BHLHE40	chr11:4658886-4659215	GM12878	blood:	n/a	n/a
12	BRCA1	chr11:4629133-4629295	Hela-S3	cervix:	n/a	n/a
13	CBX3	chr11:4628967-4630004	K562	blood:	n/a	n/a
14	CBX3	chr11:4680009-4680493	K562	blood:	n/a	n/a
15	CBX3	chr11:4658108-4658530	K562	blood:	n/a	n/a
16	CCNT2	chr11:4629051-4629981	K562	blood:	n/a	chr11:4629061-4629070
17	CEBPB	chr11:4647442-4647716	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr11:4647421-4647749	K562	blood:	n/a	n/a
19	CEBPB	chr11:4661402-4661517	K562	blood:	n/a	n/a
20	CEBPB	chr11:4680079-4680430	K562	blood:	n/a	n/a
21	CEBPB	chr11:4629219-4629669	Hela-S3	cervix:	n/a	chr11:4629483-4629491 chr11:4629547-4629555
22	CEBPB	chr11:4678840-4679165	K562	blood:	n/a	chr11:4678998-4679009
23	CEBPB	chr11:4680108-4680438	K562	blood:	n/a	n/a
24	CEBPB	chr11:4641031-4641091	K562	blood:	n/a	n/a
25	CEBPB	chr11:4678853-4679138	HepG2	liver:	n/a	chr11:4678998-4679009
26	CEBPB	chr11:4647363-4647690	MCF-7	breast:	n/a	n/a
27	CEBPD	chr11:4680058-4680601	K562	blood:	n/a	n/a
28	CHD2	chr11:4628967-4629798	Hela-S3	cervix:	n/a	n/a
29	CHD2	chr11:4629071-4629849	K562	blood:	n/a	n/a
30	CHD2	chr11:4629007-4629765	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr11:4629022-4629829	GM12878	blood:	n/a	n/a
32	CHD2	chr11:4664571-4664584	K562	blood:	n/a	n/a
33	CHD2	chr11:4665805-4665840	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD2	chr11:4680006-4680343	K562	blood:	n/a	n/a
35	CREB1	chr11:4628953-4629773	A549	lung:	n/a	n/a
36	CREB1	chr11:4658091-4658477	A549	lung:	n/a	n/a
37	CTCF	chr11:4647480-4647630	GM12801	blood:	n/a	n/a
38	CTCF	chr11:4629120-4629270	HMEC	breast:	n/a	n/a
39	CTCF	chr11:4658220-4658370	GM12801	blood:	n/a	chr11:4658301-4658314 chr11:4658299-4658315 chr11:4658300-4658321 chr11:4658298-4658316
40	CTCF	chr11:4647522-4647726	HepG2	liver:	n/a	n/a
41	CTCF	chr11:4647540-4647690	GM12878	blood:	n/a	n/a
42	CTCF	chr11:4647540-4647690	NHDF-neo	bronchial:	n/a	n/a
43	CTCF	chr11:4658157-4658420	GM13976	blood:	n/a	chr11:4658301-4658314 chr11:4658299-4658315 chr11:4658300-4658321 chr11:4658298-4658316
44	CTCF	chr11:4647580-4647730	HFF-Myc	foreskin:	n/a	n/a
45	CTCF	chr11:4647520-4647670	HCM	heart:	n/a	n/a
46	CTCF	chr11:4647540-4647690	HA-sp	spinal cord:	n/a	n/a
47	CTCF	chr11:4658142-4658463	NHEK	skin:	n/a	chr11:4658301-4658314 chr11:4658299-4658315 chr11:4658300-4658321 chr11:4658298-4658316 chr11:4658423-4658431
48	CTCF	chr11:4647540-4647690	AG04450	lung:	n/a	n/a
49	CTCF	chr11:4658104-4658445	T-47D	breast:	n/a	chr11:4658301-4658314 chr11:4658299-4658315 chr11:4658300-4658321 chr11:4658298-4658316 chr11:4658423-4658431
50	CTCF	chr11:4647560-4647710	GM12867	blood:	n/a	n/a

(count:2325 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:4665165-4665215	GM12892	blood:	n/a
2	chr11:4629912-4629962	RPTEC	kidney:	n/a
3	chr11:4629749-4629799	HIPEpiC	eye:	n/a
4	chr11:4631906-4631956	GM12878	blood:	n/a
5	chr11:4629749-4629799	Hela-S3	cervix:	n/a
6	chr11:4629597-4629647	HEK293	kidney:	embryo
7	chr11:4658391-4658441	HRE	kidney:	n/a
8	chr11:4665165-4665215	GM12892	blood:	n/a
9	chr11:4629912-4629962	RPTEC	kidney:	n/a
10	chr11:4629749-4629799	HIPEpiC	eye:	n/a
11	chr11:4631906-4631956	GM12878	blood:	n/a
12	chr11:4629749-4629799	Hela-S3	cervix:	n/a
13	chr11:4629597-4629647	HEK293	kidney:	embryo
14	chr11:4658391-4658441	HRE	kidney:	n/a
15	chr11:4600034-4600084	AG09309	skin:	n/a
16	chr11:4606701-4606751	CMK	blood:	n/a
17	chr11:4629912-4629962	NT2-D1	testis:	n/a
18	chr11:4659811-4659861	HCPEpiC	choroid plexus:	n/a
19	chr11:4629597-4629647	GM06990	blood:	n/a
20	chr11:4599637-4599687	HL-60	blood:	n/a
21	chr11:4615063-4615113	U87	brain:	n/a
22	chr11:4659811-4659861	PFSK-1	brain:	n/a
23	chr11:4629597-4629647	SK-N-SH_RA	brain:	n/a
24	chr11:4664117-4664167	T-47D	breast:	n/a
25	chr11:4629667-4629717	HCPEpiC	choroid plexus:	n/a
26	chr11:4621713-4621763	MCF-7	breast:	n/a
27	chr11:4664117-4664167	GM12878	blood:	n/a
28	chr11:4608359-4608409	SK-N-MC	brain:	n/a
29	chr11:4597246-4597296	Jurkat	blood:	n/a
30	chr11:4621713-4621763	SK-N-MC	brain:	n/a
31	chr11:4621713-4621763	T-47D	breast:	n/a
32	chr11:4608359-4608409	HEK293	kidney:	embryo
33	chr11:4629609-4629659	HL-60	blood:	n/a
34	chr11:4629034-4629084	GM06990	blood:	n/a
35	chr11:4665165-4665215	HAEpiC	amniotic membrane:	n/a
36	chr11:4606632-4606682	SKMC	muscle:	n/a
37	chr11:4615540-4615590	Jurkat	blood:	n/a
38	chr11:4629667-4629717	SAEC	small airway:	n/a
39	chr11:4597246-4597296	GM12892	blood:	n/a
40	chr11:4626526-4626576	ECC-1	luminal epithelium:	n/a
41	chr11:4608359-4608409	AG09319	gingival:	n/a
42	chr11:4628823-4628873	NT2-D1	testis:	n/a
43	chr11:4615063-4615113	SK-N-SH_RA	brain:	n/a
44	chr11:4665165-4665215	NB4	blood:	n/a
45	chr11:4664220-4664270	ovcar-3	ovarian:	n/a
46	chr11:4661335-4661385	HEEpiC	esophagus:	n/a
47	chr11:4597246-4597296	GM12891	blood:	n/a
48	chr11:4629606-4629656	LNCaP	prostate:	n/a
49	chr11:4608359-4608409	HepG2	liver:	n/a
50	chr11:4658391-4658441	MCF10A-Er-Src	breast:	n/a

(count:36 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:4626393..4630553-chr11:4632444..4636618,6	K562	blood:
2	chr11:4620058..4622735-chr11:4626222..4629091,3	K562	blood:
3	chr11:4208515..4209433-chr11:4658248..4659042,2	K562	blood:
4	chr11:4622993..4626979-chr11:4627107..4631153,5	K562	blood:
5	chr11:4208255..4208841-chr11:4647118..4648091,2	K562	blood:
6	chr11:4598261..4600650-chr11:4609395..4611487,2	K562	blood:
7	chr11:4619771..4622013-chr11:4626774..4630457,4	MCF-7	breast:
8	chr11:4604767..4606458-chr11:4610235..4612075,2	K562	blood:
9	chr11:4657872..4658731-chr11:5025387..5026540,3	K562	blood:
10	chr11:4619365..4621558-chr11:4626252..4629277,3	K562	blood:
11	chr11:4625479..4627156-chr11:4627233..4629279,2	K562	blood:
12	chr11:4647199..4648030-chr11:5025327..5026179,2	K562	blood:
13	chr11:4625479..4627156-chr11:4627233..4629279,2	K562	blood:
14	chr11:4647527..4648151-chr11:5025801..5026495,2	MCF-7	breast:
15	chr11:4676620..4679350-chr11:4683230..4685666,3	K562	blood:
16	chr11:4614691..4617476-chr11:4618507..4620828,3	K562	blood:
17	chr11:4657777..4658387-chr11:5025582..5026377,4	MCF-7	breast:
18	chr11:4618307..4620413-chr11:4621041..4623976,4	K562	blood:
19	chr11:4620058..4622735-chr11:4626222..4629091,3	K562	blood:
20	chr11:4604767..4606458-chr11:4610235..4612075,2	K562	blood:
21	chr11:4667581..4670496-chr11:4674502..4676349,2	K562	blood:
22	chr11:4658042..4658694-chr11:4667228..4668066,2	K562	blood:
23	chr11:4658184..4658763-chr11:5145307..5145823,2	MCF-7	breast:
24	chr11:4619365..4621558-chr11:4626252..4629277,3	K562	blood:
25	chr11:4667581..4670496-chr11:4674502..4676349,2	K562	blood:
26	chr11:4677690..4682058-chr11:4682699..4685666,4	K562	blood:
27	chr11:4658272..4658813-chr11:5025400..5026262,2	MCF-7	breast:
28	chr11:4657777..4658777-chr11:5012019..5012933,4	K562	blood:
29	chr11:4657833..4658473-chr11:4847439..4848013,2	MCF-7	breast:
30	chr11:4623027..4625969-chr11:4627672..4630327,2	MCF-7	breast:
31	chr1:45195876..45196736-chr11:4594433..4595433,5	Hela-S3	cervix:
32	chr11:4595698..4599305-chr11:4600956..4604069,3	K562	blood:
33	chr11:4657985..4658755-chr11:5391194..5391750,2	MCF-7	breast:
34	chr11:4676620..4679350-chr11:4683230..4685666,3	K562	blood:
35	chr11:4623447..4627456-chr11:4629484..4632827,3	K562	blood:
36	chr11:4658042..4658694-chr11:4667228..4668066,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OR51D1-1	chr11:4647477-4647663	l_424_chr11:4644432-4650062_testes
2	lnc-OR51D1-1	chr11:4644433-4644768	l_424_chr11:4644432-4650062_testes
3	lnc-OR51D1-1	chr11:4649827-4650062	l_424_chr11:4644432-4650062_testes

No data

Variant related genes	Relation type
OR51E1	TF binding region
OR51A9P	TF binding region
TRIM68	TF binding region
OR52I2	TF binding region
OR52I1	TF binding region
OR51D1	TF binding region
C11orf40	TF binding region
OR51E1	CpG island
OR51A9P	CpG island
TRIM68	CpG island
OR52I2	CpG island
OR52I1	CpG island
OR51D1	CpG island
C11orf40	CpG island
ENSG00000171987	chromatin interactions
ENSG00000254480	chromatin interactions
ENSG00000232268	chromatin interactions
ENSG00000180723	chromatin interactions
ENSG00000167333	chromatin interactions
ENSG00000205494	chromatin interactions

Extended variants
information (count: 3773 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:3773 , 50 per page) page: 1 2 3 4 5 6 7 ... 76

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs142914019	chr11:4594629-4594630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs146123854	chr11:4594638-4594639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs565080030	chr11:4594640-4594641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs112134330	chr11:4594647-4594648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs370731730	chr11:4594653-4594654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs532423858	chr11:4594663-4594664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs139000281	chr11:4594665-4594666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs559356940	chr11:4594685-4594686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs144108344	chr11:4594697-4594698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs73395847	chr11:4594703-4594704	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs201148464	chr11:4594704-4594705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs369996262	chr11:4594705-4594706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs199641398	chr11:4594708-4594709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs530603688	chr11:4594711-4594712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs374574636	chr11:4594713-4594714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs368592772	chr11:4594714-4594715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs77038820	chr11:4594722-4594723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs376481565	chr11:4594729-4594730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs201276258	chr11:4594734-4594735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs5789333	chr11:4594737-4594738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs371753414	chr11:4594739-4594740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs550336820	chr11:4594745-4594746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs368195548	chr11:4594751-4594752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs369039073	chr11:4594813-4594814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs145985260	chr11:4594849-4594850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs113470635	chr11:4594853-4594854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs191944972	chr11:4594873-4594874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs2657148	chr11:4594885-4594886	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs7122433	chr11:4594891-4594892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs537223510	chr11:4594910-4594911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs919518	chr11:4594924-4594925	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs528644374	chr11:4594936-4594937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs577528598	chr11:4594975-4594976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs66754161	chr11:4594980-4594981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs3064137	chr11:4594987-4594988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs534663307	chr11:4594988-4594989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs553105893	chr11:4594990-4594991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs183003934	chr11:4595010-4595011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs139975580	chr11:4595035-4595036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs186927007	chr11:4595041-4595042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs575469019	chr11:4595043-4595044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs562321749	chr11:4595053-4595054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs545710946	chr11:4595059-4595060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs7106078	chr11:4595065-4595066	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs191876095	chr11:4595095-4595096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs532684317	chr11:4595106-4595107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs375047727	chr11:4595107-4595108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs531081968	chr11:4595108-4595109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs2657149	chr11:4595124-4595125	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs559459453	chr11:4595125-4595126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
Neuroblastoma	18923191	CNVD
Breast cancer	19432969	CNVD
Alzheimer''s disease	17576883	CNVD
Long-qt syndrome	17576883	CNVD
Emphysema	19352772	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chordoma	18071362	CNVD
Breast cancer	16608533	CNVD
Cancer	21183584	CNVD
Gastric adenocarcinoma	19115996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Myelofibrosis	22110671	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Neuroblastoma	21124317	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Schizophrenia	21399695	CNVD
Gastric cancer	16891809	CNVD
Cancer	17160897	CNVD
Multiple myeloma	16616336	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD

Chromatin state (count:1325 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:4593200-4596800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr11:4596600-4597800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr11:4596800-4597000	ZNF genes & repeats	ES-WA7 Cell Line	embryonic stem cell
4	chr11:4596800-4597200	Enhancers	Primary hematopoietic stem cells	blood
5	chr11:4596800-4597400	Enhancers	Dnd41	blood
6	chr11:4596800-4597800	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
7	chr11:4596800-4597800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr11:4597200-4597600	Enhancers	GM12878-XiMat	blood
9	chr11:4597400-4597800	Bivalent Enhancer	Dnd41	blood
10	chr11:4597600-4598800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr11:4598200-4599000	Enhancers	Gastric	stomach
12	chr11:4598600-4598800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr11:4600000-4600200	Enhancers	Psoas Muscle	Psoas
14	chr11:4600200-4602600	Weak transcription	Psoas Muscle	Psoas
15	chr11:4609800-4610000	Enhancers	Left Ventricle	heart
16	chr11:4610000-4619600	Weak transcription	Left Ventricle	heart
17	chr11:4611000-4616800	Weak transcription	Primary B cells from peripheral blood	blood
18	chr11:4611400-4611600	Enhancers	Stomach Mucosa	stomach
19	chr11:4611600-4621400	Weak transcription	Stomach Mucosa	stomach
20	chr11:4611800-4612000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr11:4611800-4612000	Enhancers	Sigmoid Colon	Sigmoid Colon
22	chr11:4612000-4618600	Weak transcription	Sigmoid Colon	Sigmoid Colon
23	chr11:4612000-4622400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr11:4612400-4620800	Weak transcription	Brain Substantia Nigra	brain
25	chr11:4612400-4621400	Weak transcription	Small Intestine	intestine
26	chr11:4612600-4616200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
27	chr11:4612600-4616600	Weak transcription	Brain Hippocampus Middle	brain
28	chr11:4612600-4620800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr11:4612800-4615800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
30	chr11:4612800-4616000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr11:4612800-4616400	Weak transcription	Ovary	ovary
32	chr11:4612800-4618000	Weak transcription	Primary B cells from cord blood	blood
33	chr11:4612800-4621000	Weak transcription	A549	lung
34	chr11:4613000-4615200	Weak transcription	Primary T cells from cord blood	blood
35	chr11:4613000-4619600	Weak transcription	Primary monocytes fromperipheralblood	blood
36	chr11:4613400-4619600	Weak transcription	Psoas Muscle	Psoas
37	chr11:4613600-4618600	Weak transcription	Aorta	Aorta
38	chr11:4613600-4619600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr11:4613600-4621000	Weak transcription	Fetal Kidney	kidney
40	chr11:4613800-4616200	Weak transcription	Primary T helper cells fromperipheralblood	blood
41	chr11:4613800-4618000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr11:4613800-4618600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
43	chr11:4613800-4619400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
44	chr11:4614000-4619800	Weak transcription	Fetal Lung	lung
45	chr11:4614200-4618400	Weak transcription	Primary hematopoietic stem cells	blood
46	chr11:4614200-4619800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr11:4614200-4620000	Weak transcription	Muscle Satellite Cultured Cells	--
48	chr11:4614400-4616000	Weak transcription	Adipose Nuclei	Adipose
49	chr11:4614400-4618800	Weak transcription	Gastric	stomach
50	chr11:4614600-4616200	Weak transcription	Brain Inferior Temporal Lobe	brain

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