Variant report

Variant	nsv896893
Chromosome Location	chr11:3737398-3781601
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:309)
CpG islands
(count:62)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:309 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr11:3753913-3754440	HepG2	liver:	n/a	chr11:3754346-3754357 chr11:3754115-3754128
2	CEBPB	chr11:3768955-3769348	IMR90	lung:	n/a	n/a
3	CEBPB	chr11:3768870-3769429	MCF-7	breast:	n/a	n/a
4	CEBPB	chr11:3766364-3766801	ECC-1	luminal epithelium:	n/a	n/a
5	CEBPB	chr11:3744204-3744817	A549	lung:	n/a	n/a
6	CEBPB	chr11:3766405-3766711	MCF-7	breast:	n/a	n/a
7	CEBPB	chr11:3769003-3769302	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr11:3753956-3754475	K562	blood:	n/a	chr11:3754346-3754357 chr11:3754115-3754128
9	CEBPB	chr11:3744324-3744648	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr11:3749258-3749357	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr11:3749110-3749455	HepG2	liver:	n/a	n/a
12	CEBPB	chr11:3754089-3754402	A549	lung:	n/a	chr11:3754346-3754357 chr11:3754115-3754128
13	CEBPB	chr11:3766361-3766735	MCF-7	breast:	n/a	n/a
14	CEBPB	chr11:3744281-3744729	A549	lung:	n/a	n/a
15	CEBPB	chr11:3749260-3749298	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr11:3768911-3769351	MCF-7	breast:	n/a	n/a
17	CEBPB	chr11:3755549-3755799	HepG2	liver:	n/a	chr11:3755656-3755667
18	CEBPB	chr11:3769014-3769275	A549	lung:	n/a	n/a
19	CEBPB	chr11:3744196-3744772	IMR90	lung:	n/a	n/a
20	CEBPB	chr11:3749129-3749443	IMR90	lung:	n/a	n/a
21	CEBPB	chr11:3749136-3749449	A549	lung:	n/a	n/a
22	CEBPB	chr11:3744296-3744686	A549	lung:	n/a	n/a
23	CEBPB	chr11:3749198-3749438	K562	blood:	n/a	n/a
24	CTCF	chr11:3744500-3744650	NHDF-neo	bronchial:	n/a	n/a
25	CTCF	chr11:3744580-3744730	AG10803	skin:	n/a	n/a
26	CTCF	chr11:3744520-3744670	AG10803	skin:	n/a	n/a
27	CTCF	chr11:3743958-3743977	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr11:3748780-3748930	SK-N-SH_RA	brain:	n/a	n/a
29	CTCF	chr11:3743980-3744130	AG10803	skin:	n/a	n/a
30	CTCF	chr11:3773980-3774130	NHEK	skin:	n/a	n/a
31	CTCF	chr11:3755420-3755570	HepG2	liver:	n/a	n/a
32	CTCF	chr11:3752860-3753010	HRE	kidney:	n/a	n/a
33	E2F4	chr11:3744420-3744800	MCF10A-Er-Src	breast:	n/a	n/a
34	E2F4	chr11:3768949-3769244	MCF10A-Er-Src	breast:	n/a	n/a
35	EBF1	chr11:3779893-3780106	GM12878	blood:	n/a	n/a
36	EGR1	chr11:3768782-3769288	MCF-7	breast:	n/a	n/a
37	EGR1	chr11:3768705-3769320	MCF-7	breast:	n/a	n/a
38	EP300	chr11:3744185-3744604	SK-N-SH_RA	brain:	n/a	n/a
39	EP300	chr11:3744039-3744808	SK-N-SH	brain:	n/a	n/a
40	EP300	chr11:3766237-3766952	ECC-1	luminal epithelium:	n/a	n/a
41	EP300	chr11:3766430-3766736	MCF-7	breast:	n/a	n/a
42	EP300	chr11:3744228-3744640	SK-N-SH_RA	brain:	n/a	n/a
43	ESR1	chr11:3761340-3761807	ECC-1	luminal epithelium:	n/a	n/a
44	ESR1	chr11:3761373-3761785	ECC-1	luminal epithelium:	n/a	n/a
45	ESR1	chr11:3761370-3761766	ECC-1	luminal epithelium:	n/a	n/a
46	ESR1	chr11:3761411-3761799	ECC-1	luminal epithelium:	n/a	n/a
47	FOS	chr11:3757162-3757361	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr11:3744199-3744740	MCF10A-Er-Src	breast:	n/a	chr11:3744439-3744450
49	FOS	chr11:3744299-3744641	HUVEC	blood vessel:	n/a	chr11:3744439-3744450
50	FOS	chr11:3768795-3769362	MCF10A-Er-Src	breast:	n/a	chr11:3769172-3769182 chr11:3769171-3769183 chr11:3769173-3769181

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:3744085-3744135	GM19239	blood:	n/a
2	chr11:3744085-3744135	GM19239	blood:	n/a
3	chr11:3744085-3744135	H1-hESC	embryonic stem cell:	embryo
4	chr11:3744085-3744135	RPTEC	kidney:	n/a
5	chr11:3744085-3744135	SKMC	muscle:	n/a
6	chr11:3744085-3744135	LNCaP	prostate:	n/a
7	chr11:3744085-3744135	IMR90	lung:	fetal
8	chr11:3744085-3744135	HepG2	liver:	n/a
9	chr11:3744085-3744135	U87	brain:	n/a
10	chr11:3744085-3744135	MCF-7	breast:	n/a
11	chr11:3744085-3744135	HEK293	kidney:	embryo
12	chr11:3744085-3744135	AG10803	skin:	n/a
13	chr11:3744085-3744135	Caco-2	colon:	n/a
14	chr11:3744085-3744135	SAEC	small airway:	n/a
15	chr11:3744085-3744135	AG04449	skin:	fetal
16	chr11:3744085-3744135	Hela-S3	cervix:	n/a
17	chr11:3744085-3744135	Hepatocyte	liver:	n/a
18	chr11:3744085-3744135	NHBE	bronchial:	n/a
19	chr11:3744085-3744135	HAEpiC	amniotic membrane:	n/a
20	chr11:3744085-3744135	SK-N-SH_RA	brain:	n/a
21	chr11:3744085-3744135	HRCEpiC	kidney:	n/a
22	chr11:3744085-3744135	PrEC	prostate:	n/a
23	chr11:3744085-3744135	BJ	skin:	n/a
24	chr11:3744085-3744135	HMEC	breast:	n/a
25	chr11:3744085-3744135	AG09309	skin:	n/a
26	chr11:3744085-3744135	PFSK-1	brain:	n/a
27	chr11:3744085-3744135	GM06990	blood:	n/a
28	chr11:3744085-3744135	NB4	blood:	n/a
29	chr11:3744085-3744135	BE2_C	brain:	n/a
30	chr11:3744085-3744135	NHDF-neo	bronchial:	n/a
31	chr11:3744085-3744135	SK-N-SH	brain:	n/a
32	chr11:3744085-3744135	ProgFib	skin:	n/a
33	chr11:3744085-3744135	HPAEpiC	pulmonary alveolar:	n/a
34	chr11:3744085-3744135	PANC-1	pancreas:	n/a
35	chr11:3744085-3744135	GM12878	blood:	n/a
36	chr11:3744085-3744135	GM12891	blood:	n/a
37	chr11:3744085-3744135	HEEpiC	esophagus:	n/a
38	chr11:3744085-3744135	NT2-D1	testis:	n/a
39	chr11:3744085-3744135	HNPCEpiC	eye:	n/a
40	chr11:3744085-3744135	HRPEpiC	eye:	n/a
41	chr11:3744085-3744135	HL-60	blood:	n/a
42	chr11:3744085-3744135	HCT-116	colon:	n/a
43	chr11:3744085-3744135	NH-A	brain:	n/a
44	chr11:3744085-3744135	HCM	heart:	n/a
45	chr11:3744085-3744135	HIPEpiC	eye:	n/a
46	chr11:3744085-3744135	AG04450	lung:	fetal
47	chr11:3744085-3744135	CMK	blood:	n/a
48	chr11:3744085-3744135	MCF10A-Er-Src	breast:	n/a
49	chr11:3744085-3744135	Jurkat	blood:	n/a
50	chr11:3744085-3744135	HRE	kidney:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:3727085..3729822-chr11:3743744..3745444,2	MCF-7	breast:
2	chr11:3764124..3767130-chr11:3771414..3774261,3	K562	blood:
3	chr11:3728202..3731032-chr11:3737163..3739664,2	MCF-7	breast:
4	chr11:3764124..3767130-chr11:3771414..3774261,3	K562	blood:
5	chr11:3726751..3729655-chr11:3738609..3740778,2	K562	blood:
6	chr11:3769093..3770823-chr11:3816155..3819010,2	K562	blood:
7	chr11:3732805..3734447-chr11:3756261..3757990,2	K562	blood:
8	chr11:3732732..3736237-chr11:3737365..3740314,3	K562	blood:

No data

Variant related genes	Relation type
NUP98	TF binding region
RNU6-1143P	TF binding region
NUP98	CpG island
RNU6-1143P	CpG island
ENSG00000110713	chromatin interactions
ENSG00000251934	chromatin interactions
ENSG00000148985	chromatin interactions

Extended variants
information (count: 1935 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:1935 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs619479	chr11:3737398-3737399	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs559988061	chr11:3737489-3737490	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs181363795	chr11:3737496-3737497	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs143736957	chr11:3737501-3737502	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs79528150	chr11:3737503-3737504	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs146804195	chr11:3737527-3737528	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs530533000	chr11:3737566-3737567	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs544068732	chr11:3737569-3737570	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs78559016	chr11:3737581-3737582	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs75134905	chr11:3737592-3737593	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs570666433	chr11:3737594-3737595	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs77364309	chr11:3737605-3737606	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs548941433	chr11:3737628-3737629	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs184571602	chr11:3737635-3737636	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs61879800	chr11:3737639-3737640	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs150341653	chr11:3737649-3737650	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs596269	chr11:3737666-3737667	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs537158189	chr11:3737739-3737740	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs558673500	chr11:3737796-3737797	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs551413182	chr11:3737861-3737862	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs200866785	chr11:3737871-3737872	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs571276398	chr11:3737889-3737890	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs541261182	chr11:3737899-3737900	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs144994212	chr11:3737913-3737914	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs111339240	chr11:3737946-3737947	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs144159455	chr11:3737978-3737979	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs375171020	chr11:3737980-3737981	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs541772037	chr11:3738017-3738018	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs181502754	chr11:3738087-3738088	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs530577534	chr11:3738100-3738101	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs545913702	chr11:3738110-3738111	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs113827782	chr11:3738120-3738121	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs564212385	chr11:3738166-3738167	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs623056	chr11:3738167-3738168	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs77992314	chr11:3738233-3738234	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs568317484	chr11:3738256-3738257	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs529191031	chr11:3738295-3738296	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs553778827	chr11:3738343-3738344	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs569947366	chr11:3738344-3738345	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs186497634	chr11:3738345-3738346	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs558610317	chr11:3738349-3738350	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs149119758	chr11:3738371-3738372	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs534859876	chr11:3738373-3738374	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs143184594	chr11:3738381-3738382	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs190940695	chr11:3738386-3738387	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs376319893	chr11:3738389-3738390	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs138691167	chr11:3738404-3738405	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs180988221	chr11:3738474-3738475	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs556525135	chr11:3738475-3738476	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs186040166	chr11:3738510-3738511	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:68)

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
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Cancer	17440070	CNVD

Chromatin state (count:1263 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:3685000-3743800	Strong transcription	Duodenum Mucosa	Duodenum
2	chr11:3685200-3766800	Strong transcription	Placenta	Placenta
3	chr11:3685400-3739000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr11:3685400-3741600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chr11:3685400-3743800	Strong transcription	Primary monocytes fromperipheralblood	blood
6	chr11:3685400-3802600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr11:3685600-3805600	Strong transcription	Fetal Thymus	thymus
8	chr11:3685800-3754200	Strong transcription	Primary T helper cells fromperipheralblood	blood
9	chr11:3685800-3776200	Strong transcription	Primary B cells from peripheral blood	blood
10	chr11:3685800-3779800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr11:3686000-3779800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr11:3686600-3802600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
13	chr11:3686800-3757400	Strong transcription	Duodenum Smooth Muscle	Duodenum
14	chr11:3687000-3805600	Strong transcription	Dnd41	blood
15	chr11:3687200-3767000	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
16	chr11:3687600-3743800	Strong transcription	Monocytes-CD14+_RO01746	blood
17	chr11:3687600-3802200	Strong transcription	Primary T cells fromperipheralblood	blood
18	chr11:3687600-3802200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
19	chr11:3687800-3801400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr11:3696200-3779800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr11:3696800-3766800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr11:3705800-3742600	Strong transcription	Rectal Mucosa Donor 31	rectum
23	chr11:3705800-3802400	Strong transcription	Rectal Mucosa Donor 29	rectum
24	chr11:3706200-3757800	Strong transcription	Fetal Muscle Leg	muscle
25	chr11:3707400-3758000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
26	chr11:3709400-3753800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr11:3714000-3744800	Strong transcription	Primary B cells from cord blood	blood
28	chr11:3715800-3745000	Strong transcription	Hela-S3	cervix
29	chr11:3716000-3744200	Strong transcription	HSMM	muscle
30	chr11:3716200-3744400	Strong transcription	HUVEC	blood vessel
31	chr11:3718000-3751600	Strong transcription	K562	blood
32	chr11:3719000-3779800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr11:3719800-3753800	Strong transcription	Primary T helper cells PMA-I stimulated	--
34	chr11:3719800-3758000	Strong transcription	Primary T cells from cord blood	blood
35	chr11:3720000-3803000	Strong transcription	Sigmoid Colon	Sigmoid Colon
36	chr11:3720600-3739200	Weak transcription	Pancreatic Islets	Pancreatic Islet
37	chr11:3722000-3802400	Strong transcription	Fetal Stomach	stomach
38	chr11:3725600-3744800	Strong transcription	Cortex derived primary cultured neurospheres	brain
39	chr11:3727200-3742400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr11:3728200-3743800	Weak transcription	Stomach Mucosa	stomach
41	chr11:3729000-3757800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr11:3729200-3745000	Strong transcription	GM12878-XiMat	blood
43	chr11:3729200-3751000	Strong transcription	Primary hematopoietic stem cells	blood
44	chr11:3729400-3752600	Strong transcription	Fetal Lung	lung
45	chr11:3729400-3758200	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
46	chr11:3729600-3744600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr11:3729800-3757200	Strong transcription	Fetal Brain Female	brain
48	chr11:3730400-3753800	Strong transcription	Left Ventricle	heart
49	chr11:3731000-3744200	Strong transcription	HMEC	breast
50	chr11:3731200-3779800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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