Variant report

Variant	nsv540926
Chromosome Location	chr11:4621196-4639254
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:367)
CpG islands
(count:917)
Chromatin interactive
region (count:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

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	BHLHE40	chr11:4629164-4629819	K562	blood:	n/a	chr11:4629490-4629506
3	BRCA1	chr11:4629133-4629295	Hela-S3	cervix:	n/a	n/a
4	CBX3	chr11:4628967-4630004	K562	blood:	n/a	n/a
5	CCNT2	chr11:4629051-4629981	K562	blood:	n/a	chr11:4629061-4629070
6	CEBPB	chr11:4629219-4629669	Hela-S3	cervix:	n/a	chr11:4629483-4629491 chr11:4629547-4629555
7	CHD2	chr11:4629007-4629765	H1-hESC	embryonic stem cell:	n/a	n/a
8	CHD2	chr11:4629071-4629849	K562	blood:	n/a	n/a
9	CHD2	chr11:4629022-4629829	GM12878	blood:	n/a	n/a
10	CHD2	chr11:4628967-4629798	Hela-S3	cervix:	n/a	n/a
11	CREB1	chr11:4628953-4629773	A549	lung:	n/a	n/a
12	CTCF	chr11:4629040-4629190	GM12865	blood:	n/a	n/a
13	CTCF	chr11:4629380-4629530	NHEK	skin:	n/a	chr11:4629520-4629530
14	CTCF	chr11:4631653-4631704	Kidney_OC	kidney:	n/a	n/a
15	CTCF	chr11:4629480-4629630	Caco-2	colon:	n/a	chr11:4629518-4629531 chr11:4629520-4629530
16	CTCF	chr11:4629460-4629610	AG09319	gingival:	n/a	chr11:4629518-4629531 chr11:4629520-4629530
17	CTCF	chr11:4629060-4629210	AG10803	skin:	n/a	n/a
18	CTCF	chr11:4631120-4631270	K562	blood:	n/a	n/a
19	CTCF	chr11:4629100-4629250	NHLF	lung:	n/a	n/a
20	CTCF	chr11:4629020-4629170	GM12875	blood:	n/a	n/a
21	CTCF	chr11:4629120-4629270	GM12864	blood:	n/a	n/a
22	CTCF	chr11:4629120-4629270	HMEC	breast:	n/a	n/a
23	CTCF	chr11:4629400-4629550	Caco-2	colon:	n/a	chr11:4629518-4629531 chr11:4629520-4629530
24	CTCF	chr11:4629560-4629710	SK-N-SH_RA	brain:	n/a	n/a
25	CTCF	chr11:4629100-4629250	AG04449	skin:	n/a	n/a
26	CTCF	chr11:4631520-4631670	GM12872	blood:	n/a	n/a
27	CTCF	chr11:4629020-4629170	Hela-S3	cervix:	n/a	n/a
28	CTCF	chr11:4633120-4633270	GM12872	blood:	n/a	n/a
29	CTCF	chr11:4629100-4629250	GM12870	blood:	n/a	n/a
30	CTCF	chr11:4623515-4623545	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr11:4629455-4629629	Spleen_OC	spleen:	n/a	chr11:4629518-4629531 chr11:4629520-4629530
32	CTCF	chr11:4628906-4629502	K562	blood:	n/a	n/a
33	CTCF	chr11:4629120-4629270	SK-N-SH_RA	brain:	n/a	n/a
34	CTCF	chr11:4629440-4629590	HUVEC	blood vessel:	n/a	chr11:4629518-4629531 chr11:4629520-4629530
35	CTCF	chr11:4629560-4629710	HEEpiC	esophagus:	n/a	n/a
36	CTCF	chr11:4629140-4629290	HBMEC	blood vessel:	n/a	n/a
37	CTCF	chr11:4629140-4629290	AoAF	blood vessel:	n/a	n/a
38	CTCF	chr11:4629340-4629490	AG04449	skin:	n/a	n/a
39	CTCF	chr11:4621120-4621270	GM12864	blood:	n/a	n/a
40	CTCF	chr11:4629080-4629230	AoAF	blood vessel:	n/a	n/a
41	CTCF	chr11:4629460-4629610	AG04449	skin:	n/a	chr11:4629518-4629531 chr11:4629520-4629530
42	CTCF	chr11:4629420-4629570	SAEC	small airway:	n/a	chr11:4629518-4629531 chr11:4629520-4629530
43	CTCF	chr11:4629200-4629350	Caco-2	colon:	n/a	n/a
44	CTCF	chr11:4628940-4629090	HCFaa	heart:	n/a	n/a
45	CTCF	chr11:4629140-4629410	K562	blood:	n/a	n/a
46	CTCF	chr11:4629125-4629238	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr11:4629060-4629210	AG04449	skin:	n/a	n/a
48	CTCF	chr11:4629120-4629270	SAEC	small airway:	n/a	n/a
49	CTCF	chr11:4631560-4631710	HPAF	blood vessel:	n/a	n/a
50	CTCF	chr11:4629100-4629250	GM12864	blood:	n/a	n/a

(count:917 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:4629667-4629717	ECC-1	luminal epithelium:	n/a
2	chr11:4629597-4629647	ovcar-3	ovarian:	n/a
3	chr11:4629667-4629717	ECC-1	luminal epithelium:	n/a
4	chr11:4629597-4629647	ovcar-3	ovarian:	n/a
5	chr11:4629195-4629245	HCT-116	colon:	n/a
6	chr11:4629749-4629799	HUVEC	blood vessel:	n/a
7	chr11:4629432-4629482	ovcar-3	ovarian:	n/a
8	chr11:4629606-4629656	GM12878	blood:	n/a
9	chr11:4629034-4629084	AG04449	skin:	fetal
10	chr11:4629667-4629717	H1-hESC	embryonic stem cell:	embryo
11	chr11:4629432-4629482	BE2_C	brain:	n/a
12	chr11:4628823-4628873	HEK293	kidney:	embryo
13	chr11:4621440-4621490	HMEC	breast:	n/a
14	chr11:4629667-4629717	NHBE	bronchial:	n/a
15	chr11:4629195-4629245	ProgFib	skin:	n/a
16	chr11:4629357-4629407	HNPCEpiC	eye:	n/a
17	chr11:4629667-4629717	SK-N-MC	brain:	n/a
18	chr11:4629195-4629245	HRPEpiC	eye:	n/a
19	chr11:4629432-4629482	AG09319	gingival:	n/a
20	chr11:4629667-4629717	HRE	kidney:	n/a
21	chr11:4628823-4628873	HPAEpiC	pulmonary alveolar:	n/a
22	chr11:4629606-4629656	MCF-7	breast:	n/a
23	chr11:4629034-4629084	NB4	blood:	n/a
24	chr11:4628823-4628873	H1-hESC	embryonic stem cell:	embryo
25	chr11:4629912-4629962	GM12891	blood:	n/a
26	chr11:4629597-4629647	PrEC	prostate:	n/a
27	chr11:4629597-4629647	AG09309	skin:	n/a
28	chr11:4631906-4631956	PrEC	prostate:	n/a
29	chr11:4626526-4626576	U87	brain:	n/a
30	chr11:4629432-4629482	Caco-2	colon:	n/a
31	chr11:4629606-4629656	NB4	blood:	n/a
32	chr11:4629195-4629245	AG10803	skin:	n/a
33	chr11:4629606-4629656	NHBE	bronchial:	n/a
34	chr11:4629034-4629084	Hela-S3	cervix:	n/a
35	chr11:4626526-4626576	NHBE	bronchial:	n/a
36	chr11:4629195-4629245	SK-N-MC	brain:	n/a
37	chr11:4629597-4629647	NB4	blood:	n/a
38	chr11:4621440-4621490	ovcar-3	ovarian:	n/a
39	chr11:4629749-4629799	HMEC	breast:	n/a
40	chr11:4621440-4621490	PANC-1	pancreas:	n/a
41	chr11:4629034-4629084	NH-A	brain:	n/a
42	chr11:4631906-4631956	NT2-D1	testis:	n/a
43	chr11:4631906-4631956	NHBE	bronchial:	n/a
44	chr11:4629597-4629647	IMR90	lung:	fetal
45	chr11:4621713-4621763	MCF-7	breast:	n/a
46	chr11:4629749-4629799	HL-60	blood:	n/a
47	chr11:4629357-4629407	Hela-S3	cervix:	n/a
48	chr11:4629912-4629962	LNCaP	prostate:	n/a
49	chr11:4629195-4629245	AG09309	skin:	n/a
50	chr11:4629609-4629659	NHBE	bronchial:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:4623447..4627456-chr11:4629484..4632827,3	K562	blood:
2	chr11:4620058..4622735-chr11:4626222..4629091,3	K562	blood:
3	chr11:4623027..4625969-chr11:4627672..4630327,2	MCF-7	breast:
4	chr11:4622993..4626979-chr11:4627107..4631153,5	K562	blood:
5	chr11:4626393..4630553-chr11:4632444..4636618,6	K562	blood:
6	chr11:4625479..4627156-chr11:4627233..4629279,2	K562	blood:
7	chr11:4625479..4627156-chr11:4627233..4629279,2	K562	blood:
8	chr11:4619365..4621558-chr11:4626252..4629277,3	K562	blood:
9	chr11:4619365..4621558-chr11:4626252..4629277,3	K562	blood:
10	chr11:4619771..4622013-chr11:4626774..4630457,4	MCF-7	breast:
11	chr11:4620058..4622735-chr11:4626222..4629091,3	K562	blood:

No data

Variant related genes	Relation type
TRIM68	TF binding region
TRIM68	CpG island
ENSG00000167333	chromatin interactions

Extended variants
information (count: 846 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:846 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs556586865	chr11:4621207-4621208	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs188231464	chr11:4621215-4621216	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs538977027	chr11:4621231-4621232	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs115038309	chr11:4621232-4621233	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs572766515	chr11:4621258-4621259	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs541111695	chr11:4621275-4621276	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs78700188	chr11:4621276-4621277	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs561443068	chr11:4621304-4621305	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs145338763	chr11:4621315-4621316	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs199573844	chr11:4621317-4621318	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs200640502	chr11:4621320-4621321	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs3750992	chr11:4621323-4621324	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs73399628	chr11:4621349-4621350	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs564949542	chr11:4621354-4621355	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs552531526	chr11:4621389-4621390	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs113095095	chr11:4621440-4621441	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs375887655	chr11:4621458-4621459	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs370158262	chr11:4621464-4621465	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs2231978	chr11:4621485-4621486	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs2231977	chr11:4621486-4621487	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs7109316	chr11:4621567-4621568	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs370899409	chr11:4621591-4621592	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs2231976	chr11:4621594-4621595	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs187005657	chr11:4621595-4621596	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs146764591	chr11:4621596-4621597	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs139088568	chr11:4621600-4621601	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs144009048	chr11:4621611-4621612	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs144925338	chr11:4621612-4621613	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs201728210	chr11:4621613-4621614	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs368137460	chr11:4621626-4621627	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs146057620	chr11:4621638-4621639	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs2231975	chr11:4621639-4621640	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs372093266	chr11:4621647-4621648	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs375064749	chr11:4621651-4621652	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs200332840	chr11:4621681-4621682	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs149059447	chr11:4621686-4621687	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs200700449	chr11:4621690-4621691	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs371696653	chr11:4621700-4621701	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs143749633	chr11:4621702-4621703	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs375970946	chr11:4621723-4621724	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs199866771	chr11:4621755-4621756	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs151094505	chr11:4621764-4621765	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs142575508	chr11:4621783-4621784	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs368773254	chr11:4621792-4621793	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs146898853	chr11:4621796-4621797	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs372144915	chr11:4621807-4621808	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs572500115	chr11:4621822-4621823	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs571003671	chr11:4621835-4621836	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs375151620	chr11:4621842-4621843	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs369399460	chr11:4621848-4621849	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:60)

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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:908 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:4611600-4621400	Weak transcription	Stomach Mucosa	stomach
2	chr11:4612000-4622400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr11:4612400-4621400	Weak transcription	Small Intestine	intestine
4	chr11:4614600-4621200	Weak transcription	NHDF-Ad	bronchial
5	chr11:4614600-4622200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr11:4614800-4621400	Weak transcription	HMEC	breast
7	chr11:4615000-4621200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
8	chr11:4615200-4627400	Strong transcription	Primary T cells from cord blood	blood
9	chr11:4616200-4626800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chr11:4617000-4622600	Weak transcription	HUVEC	blood vessel
11	chr11:4617400-4621200	Weak transcription	Pancreatic Islets	Pancreatic Islet
12	chr11:4618000-4626800	Strong transcription	Liver	Liver
13	chr11:4618000-4627000	Strong transcription	Rectal Mucosa Donor 29	rectum
14	chr11:4618000-4627200	Strong transcription	Primary B cells from cord blood	blood
15	chr11:4618000-4628000	Weak transcription	K562	blood
16	chr11:4618200-4625600	Weak transcription	HSMM	muscle
17	chr11:4618200-4626800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr11:4618400-4622000	Weak transcription	HUES64 Cell Line	embryonic stem cell
19	chr11:4618400-4626600	Strong transcription	Primary B cells from peripheral blood	blood
20	chr11:4618400-4626600	Strong transcription	Primary T helper cells fromperipheralblood	blood
21	chr11:4618400-4626800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr11:4618400-4626800	Strong transcription	Brain Inferior Temporal Lobe	brain
23	chr11:4618400-4627600	Weak transcription	Fetal Heart	heart
24	chr11:4618600-4621600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
25	chr11:4618600-4625000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
26	chr11:4618600-4626200	Strong transcription	Primary T cells fromperipheralblood	blood
27	chr11:4618600-4626400	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
28	chr11:4618600-4626600	Strong transcription	Aorta	Aorta
29	chr11:4618600-4626600	Strong transcription	Brain Anterior Caudate	brain
30	chr11:4618600-4626600	Strong transcription	Brain Hippocampus Middle	brain
31	chr11:4618600-4626600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
32	chr11:4618600-4626800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr11:4618600-4626800	Strong transcription	Brain Cingulate Gyrus	brain
34	chr11:4618600-4626800	Strong transcription	Duodenum Smooth Muscle	Duodenum
35	chr11:4618600-4626800	Strong transcription	Fetal Muscle Trunk	muscle
36	chr11:4618600-4626800	Strong transcription	Fetal Stomach	stomach
37	chr11:4618600-4626800	Strong transcription	Sigmoid Colon	Sigmoid Colon
38	chr11:4618600-4627000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
39	chr11:4618600-4627000	Strong transcription	Monocytes-CD14+_RO01746	blood
40	chr11:4618600-4627800	Strong transcription	Fetal Muscle Leg	muscle
41	chr11:4618600-4628400	Weak transcription	H9 Cell Line	embryonic stem cell
42	chr11:4618800-4622200	Weak transcription	HUES48 Cell Line	embryonic stem cell
43	chr11:4618800-4624600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr11:4618800-4624800	Strong transcription	Gastric	stomach
45	chr11:4618800-4625000	Strong transcription	Duodenum Mucosa	Duodenum
46	chr11:4618800-4626400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr11:4618800-4626800	Strong transcription	Primary hematopoietic stem cells	blood
48	chr11:4618800-4627000	Strong transcription	Stomach Smooth Muscle	stomach
49	chr11:4619000-4623600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
50	chr11:4619000-4624800	Strong transcription	Fetal Intestine Small	intestine

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