Variant report

Variant	nsv896895
Chromosome Location	chr11:3942001-3972236
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	ARID3A	chr11:3963620-3964681	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:3954317-3954983	HepG2	liver:	n/a	n/a
3	ATF1	chr11:3963575-3963897	K562	blood:	n/a	n/a
4	ATF2	chr11:3968153-3968697	GM12878	blood:	n/a	n/a
5	BACH1	chr11:3971505-3971849	K562	blood:	n/a	n/a
6	BACH1	chr11:3971565-3971765	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL11A	chr11:3970401-3970642	GM12878	blood:	n/a	n/a
8	BCLAF1	chr11:3970274-3970766	GM12878	blood:	n/a	n/a
9	BCLAF1	chr11:3968227-3968678	GM12878	blood:	n/a	n/a
10	BHLHE40	chr11:3970329-3970704	GM12878	blood:	n/a	n/a
11	BHLHE40	chr11:3963744-3963892	K562	blood:	n/a	n/a
12	BHLHE40	chr11:3949374-3949457	GM12878	blood:	n/a	n/a
13	BHLHE40	chr11:3950916-3951206	K562	blood:	n/a	chr11:3951092-3951113
14	BHLHE40	chr11:3970486-3970625	K562	blood:	n/a	n/a
15	CEBPB	chr11:3964358-3964930	HepG2	liver:	n/a	chr11:3964784-3964795
16	CEBPB	chr11:3954287-3954951	HepG2	liver:	n/a	chr11:3954478-3954487 chr11:3954477-3954488 chr11:3954409-3954426 chr11:3954476-3954489
17	CEBPB	chr11:3960395-3960770	IMR90	lung:	n/a	chr11:3960532-3960544
18	CEBPB	chr11:3964413-3964934	K562	blood:	n/a	chr11:3964784-3964795
19	CEBPB	chr11:3954448-3954581	A549	lung:	n/a	chr11:3954478-3954487 chr11:3954477-3954488 chr11:3954476-3954489
20	CEBPB	chr11:3954351-3954621	K562	blood:	n/a	chr11:3954478-3954487 chr11:3954477-3954488 chr11:3954409-3954426 chr11:3954476-3954489
21	CEBPB	chr11:3954419-3954547	Hela-S3	cervix:	n/a	chr11:3954478-3954487 chr11:3954477-3954488 chr11:3954476-3954489
22	CEBPB	chr11:3954296-3954870	HepG2	liver:	n/a	chr11:3954478-3954487 chr11:3954477-3954488 chr11:3954409-3954426 chr11:3954476-3954489
23	CEBPB	chr11:3964501-3964952	A549	lung:	n/a	chr11:3964784-3964795
24	CEBPB	chr11:3954325-3954644	K562	blood:	n/a	chr11:3954478-3954487 chr11:3954477-3954488 chr11:3954409-3954426 chr11:3954476-3954489
25	CEBPB	chr11:3954410-3954612	IMR90	lung:	n/a	chr11:3954478-3954487 chr11:3954477-3954488 chr11:3954476-3954489
26	CEBPB	chr11:3964456-3964676	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr11:3954247-3954954	HepG2	liver:	n/a	chr11:3954478-3954487 chr11:3954477-3954488 chr11:3954409-3954426 chr11:3954476-3954489
28	CEBPB	chr11:3954245-3954971	HepG2	liver:	n/a	chr11:3954478-3954487 chr11:3954477-3954488 chr11:3954409-3954426 chr11:3954476-3954489
29	CEBPD	chr11:3954314-3954640	HepG2	liver:	n/a	chr11:3954476-3954487
30	CHD2	chr11:3963662-3963835	HepG2	liver:	n/a	n/a
31	CHD2	chr11:3954365-3954485	HepG2	liver:	n/a	n/a
32	CREB1	chr11:3960458-3960841	GM12878	blood:	n/a	n/a
33	CREB1	chr11:3960363-3960901	GM12878	blood:	n/a	n/a
34	CTCF	chr11:3948474-3948649	HUVEC	blood vessel:	n/a	n/a
35	CTCF	chr11:3963680-3963830	HA-sp	spinal cord:	n/a	chr11:3963810-3963828 chr11:3963811-3963827
36	CTCF	chr11:3948488-3948642	Hela-S3	cervix:	n/a	n/a
37	CTCF	chr11:3948491-3948620	SK-N-SH_RA	brain:	n/a	n/a
38	CTCF	chr11:3948494-3948631	LNCaP	prostate:	n/a	n/a
39	CTCF	chr11:3963745-3963859	Pancreas_OC	pancreas:	n/a	chr11:3963810-3963828 chr11:3963811-3963827
40	CTCF	chr11:3948391-3948711	GM12878	blood:	n/a	n/a
41	CTCF	chr11:3963740-3963890	K562	blood:	n/a	chr11:3963810-3963828 chr11:3963811-3963827
42	CTCF	chr11:3963752-3963872	Lung_OC	lung:	n/a	chr11:3963810-3963828 chr11:3963811-3963827
43	CTCF	chr11:3948513-3948574	GM13977	blood:	n/a	n/a
44	CTCF	chr11:3948511-3948615	HepG2	liver:	n/a	n/a
45	CTCF	chr11:3948529-3948627	Lung_OC	lung:	n/a	n/a
46	CTCF	chr11:3963752-3963857	GM19238	blood:	n/a	chr11:3963810-3963828 chr11:3963811-3963827
47	CTCF	chr11:3948500-3948650	MCF-7	breast:	n/a	n/a
48	CTCF	chr11:3963644-3963999	K562	blood:	n/a	chr11:3963810-3963828 chr11:3963811-3963827
49	CTCF	chr11:3948480-3948630	BE2_C	brain:	n/a	n/a
50	CTCF	chr11:3948507-3948635	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:3950928-3950978	SK-N-SH_RA	brain:	n/a
2	chr11:3950928-3950978	GM12892	blood:	n/a
3	chr11:3961397-3961447	HNPCEpiC	eye:	n/a
4	chr11:3961397-3961447	GM19239	blood:	n/a
5	chr11:3950928-3950978	HRE	kidney:	n/a
6	chr11:3961397-3961447	HepG2	liver:	n/a
7	chr11:3950928-3950978	HNPCEpiC	eye:	n/a
8	chr11:3950928-3950978	NHBE	bronchial:	n/a
9	chr11:3961397-3961447	GM12891	blood:	n/a
10	chr11:3950928-3950978	SAEC	small airway:	n/a
11	chr11:3961397-3961447	Jurkat	blood:	n/a
12	chr11:3961397-3961447	AG04450	lung:	fetal
13	chr11:3961397-3961447	LNCaP	prostate:	n/a
14	chr11:3950928-3950978	GM19239	blood:	n/a
15	chr11:3950928-3950978	HL-60	blood:	n/a
16	chr11:3950928-3950978	LNCaP	prostate:	n/a
17	chr11:3961397-3961447	SK-N-MC	brain:	n/a
18	chr11:3950928-3950978	HCF	heart:	n/a
19	chr11:3950928-3950978	HRPEpiC	eye:	n/a
20	chr11:3961397-3961447	HRE	kidney:	n/a
21	chr11:3950928-3950978	HepG2	liver:	n/a
22	chr11:3950928-3950978	Jurkat	blood:	n/a
23	chr11:3950928-3950978	PrEC	prostate:	n/a
24	chr11:3961397-3961447	GM12892	blood:	n/a
25	chr11:3961397-3961447	HPAEpiC	pulmonary alveolar:	n/a
26	chr11:3950928-3950978	HPAEpiC	pulmonary alveolar:	n/a
27	chr11:3950928-3950978	SK-N-MC	brain:	n/a
28	chr11:3950928-3950978	GM12891	blood:	n/a
29	chr11:3961397-3961447	NHBE	bronchial:	n/a
30	chr11:3950928-3950978	AG10803	skin:	n/a
31	chr11:3961397-3961447	GM06990	blood:	n/a
32	chr11:3961397-3961447	U87	brain:	n/a
33	chr11:3950928-3950978	AG09309	skin:	n/a
34	chr11:3950928-3950978	NT2-D1	testis:	n/a
35	chr11:3961397-3961447	HUVEC	blood vessel:	n/a
36	chr11:3961397-3961447	MCF-7	breast:	n/a
37	chr11:3961397-3961447	HCM	heart:	n/a
38	chr11:3950928-3950978	HAEpiC	amniotic membrane:	n/a
39	chr11:3950928-3950978	NHDF-neo	bronchial:	n/a
40	chr11:3950928-3950978	NB4	blood:	n/a
41	chr11:3961397-3961447	AG10803	skin:	n/a
42	chr11:3950928-3950978	ovcar-3	ovarian:	n/a
43	chr11:3961397-3961447	Caco-2	colon:	n/a
44	chr11:3961397-3961447	SK-N-SH	brain:	n/a
45	chr11:3961397-3961447	Hela-S3	cervix:	n/a
46	chr11:3950928-3950978	A549	lung:	n/a
47	chr11:3961397-3961447	SK-N-SH_RA	brain:	n/a
48	chr11:3961397-3961447	NH-A	brain:	n/a
49	chr11:3961397-3961447	GM12878	blood:	n/a
50	chr11:3961397-3961447	BE2_C	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:3941075..3943493-chr11:3946471..3948853,2	K562	blood:
2	chr11:3966514..3968687-chr11:3969725..3973118,3	K562	blood:
3	chr11:3946137..3948260-chr11:3950901..3953972,3	MCF-7	breast:
4	chr11:3941075..3946343-chr11:3946471..3949436,5	K562	blood:
5	chr11:3959785..3962625-chr11:3963394..3965455,2	K562	blood:
6	chr11:3953433..3955295-chr11:3966912..3968910,2	K562	blood:
7	chr11:3963150..3965730-chr11:3971154..3972718,2	K562	blood:
8	chr11:3952025..3954655-chr11:3956750..3959173,2	MCF-7	breast:
9	chr11:3844015..3846583-chr11:3941327..3942924,2	K562	blood:
10	chr11:3945769..3947956-chr11:3954532..3958241,3	K562	blood:
11	chr11:3952025..3954655-chr11:3956750..3959173,2	MCF-7	breast:
12	chr11:3952774..3955430-chr11:3970846..3973149,2	K562	blood:
13	chr11:3945769..3947956-chr11:3954532..3958241,3	K562	blood:
14	chr11:3860417..3863176-chr11:3955299..3957072,2	MCF-7	breast:
15	chr11:3952774..3955430-chr11:3970846..3973149,2	K562	blood:
16	chr11:3860976..3863338-chr11:3950724..3953405,2	K562	blood:
17	chr11:3963150..3965730-chr11:3971154..3972718,2	K562	blood:
18	chr11:3941075..3943493-chr11:3946471..3948853,2	K562	blood:
19	chr11:3959785..3962625-chr11:3963394..3965455,2	K562	blood:
20	chr11:3945861..3948795-chr11:3974406..3976438,2	K562	blood:
21	chr11:3948392..3949376-chr11:4093449..4094397,2	MCF-7	breast:
22	chr11:3946137..3948260-chr11:3950901..3953972,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000206976	TF binding region
STIM1	TF binding region
ENSG00000206976	CpG island
STIM1	CpG island
ENSG00000148985	chromatin interactions
ENSG00000206976	chromatin interactions
ENSG00000177105	chromatin interactions
ENSG00000167323	chromatin interactions

Extended variants
information (count: 1095 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:1095 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7945639	chr11:3942001-3942002	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs79312669	chr11:3942011-3942012	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs78111369	chr11:3942012-3942013	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs529164811	chr11:3942015-3942016	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs550887220	chr11:3942020-3942021	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs539182387	chr11:3942022-3942023	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs559103662	chr11:3942023-3942024	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs573992305	chr11:3942031-3942032	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs552169559	chr11:3942032-3942033	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs543004050	chr11:3942033-3942034	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs570574313	chr11:3942044-3942045	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs534798330	chr11:3942050-3942051	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs143584559	chr11:3942107-3942108	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs371713712	chr11:3942108-3942109	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs535749838	chr11:3942118-3942119	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs561860445	chr11:3942146-3942147	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs557602918	chr11:3942173-3942174	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs377751065	chr11:3942185-3942186	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs148055798	chr11:3942214-3942215	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs58677531	chr11:3942227-3942228	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs564074312	chr11:3942232-3942233	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs192520072	chr11:3942241-3942242	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs540369479	chr11:3942261-3942262	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs561719566	chr11:3942306-3942307	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs544481360	chr11:3942321-3942322	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs116773994	chr11:3942324-3942325	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs564292838	chr11:3942342-3942343	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs533110410	chr11:3942355-3942356	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs73425485	chr11:3942400-3942401	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs562768653	chr11:3942460-3942461	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs11030266	chr11:3942508-3942509	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs533069670	chr11:3942509-3942510	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs79919409	chr11:3942534-3942535	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs115582999	chr11:3942535-3942536	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs114524936	chr11:3942564-3942565	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs371839914	chr11:3942575-3942576	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs554166146	chr11:3942597-3942598	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs574172274	chr11:3942607-3942608	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs184025898	chr11:3942627-3942628	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs568481654	chr11:3942646-3942647	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs188029949	chr11:3942666-3942667	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs557278313	chr11:3942703-3942704	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs569487457	chr11:3942708-3942709	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs192074697	chr11:3942738-3942739	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs546384993	chr11:3942746-3942747	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs557775609	chr11:3942760-3942761	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs145937776	chr11:3942781-3942782	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs138621120	chr11:3942793-3942794	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs141591838	chr11:3942813-3942814	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs573670917	chr11:3942856-3942857	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Ovarian cancer	21720365	CNVD
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
Autism	22495311	CNVD
Lung cancer	18438408	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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Neuroblastoma	18923524	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1199 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:3916600-3943800	Weak transcription	Fetal Stomach	stomach
2	chr11:3916600-3948800	Weak transcription	Aorta	Aorta
3	chr11:3924000-3950600	Weak transcription	Rectal Smooth Muscle	rectum
4	chr11:3927200-3942600	Weak transcription	Spleen	Spleen
5	chr11:3927600-3943600	Weak transcription	Duodenum Smooth Muscle	Duodenum
6	chr11:3929400-3950600	Weak transcription	Ovary	ovary
7	chr11:3931600-3942600	Enhancers	Primary T helper cells fromperipheralblood	blood
8	chr11:3932200-3942800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
9	chr11:3932400-3944000	Enhancers	Primary monocytes fromperipheralblood	blood
10	chr11:3934800-3951000	Weak transcription	Gastric	stomach
11	chr11:3935400-3942400	Enhancers	Primary T helper cells PMA-I stimulated	--
12	chr11:3935400-3943000	Weak transcription	Fetal Lung	lung
13	chr11:3935400-3944000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
14	chr11:3935600-3942600	Enhancers	Primary B cells from peripheral blood	blood
15	chr11:3935600-3943200	Enhancers	Primary T cells fromperipheralblood	blood
16	chr11:3935600-3943400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
17	chr11:3936000-3943200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
18	chr11:3936000-3943600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
19	chr11:3937800-3950600	Weak transcription	Lung	lung
20	chr11:3938400-3956400	Weak transcription	Dnd41	blood
21	chr11:3938600-3949800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr11:3939000-3950200	Weak transcription	Left Ventricle	heart
23	chr11:3939000-3950200	Weak transcription	Pancreas	Pancrea
24	chr11:3939000-3956000	Weak transcription	Esophagus	oesophagus
25	chr11:3939200-3942200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
26	chr11:3939400-3947200	Weak transcription	Liver	Liver
27	chr11:3939600-3947800	Weak transcription	Skeletal Muscle Male	skeletal muscle
28	chr11:3939600-3948800	Weak transcription	Thymus	Thymus
29	chr11:3939600-3950000	Weak transcription	Colon Smooth Muscle	Colon
30	chr11:3939600-3950200	Weak transcription	Fetal Thymus	thymus
31	chr11:3940000-3947400	Weak transcription	Psoas Muscle	Psoas
32	chr11:3940200-3942200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr11:3940200-3947800	Weak transcription	HepG2	liver
34	chr11:3940800-3942200	Enhancers	HMEC	breast
35	chr11:3940800-3942600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr11:3940800-3943400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
37	chr11:3941200-3944000	Weak transcription	HUVEC	blood vessel
38	chr11:3941200-3948600	Weak transcription	Right Ventricle	heart
39	chr11:3941600-3942400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
40	chr11:3941600-3942600	Weak transcription	Primary hematopoietic stem cells	blood
41	chr11:3941600-3942600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr11:3941600-3942600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr11:3941600-3943800	Enhancers	Primary neutrophils fromperipheralblood	blood
44	chr11:3941600-3947800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
45	chr11:3941600-3948000	Weak transcription	Skeletal Muscle Female	skeletal muscle
46	chr11:3941600-3950600	Weak transcription	Stomach Mucosa	stomach
47	chr11:3941600-3951000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr11:3941800-3942200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr11:3942000-3942600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr11:3942000-3942600	Weak transcription	Primary B cells from cord blood	blood

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