Variant report

Variant	nsv5436
Chromosome Location	chr6:110052812-110097662
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:198)
CpG islands
(count:183)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:198 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr6:110093229-110093466	K562	blood:	n/a	n/a
2	ATF2	chr6:110090390-110090870	GM12878	blood:	n/a	n/a
3	ATF2	chr6:110090341-110090948	GM12878	blood:	n/a	n/a
4	BATF	chr6:110090504-110090663	GM12878	blood:	n/a	n/a
5	BATF	chr6:110093219-110093492	GM12878	blood:	n/a	n/a
6	BCL11A	chr6:110090503-110090669	GM12878	blood:	n/a	n/a
7	BHLHE40	chr6:110094072-110094089	K562	blood:	n/a	n/a
8	CEBPB	chr6:110093223-110093453	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr6:110062108-110062332	A549	lung:	n/a	n/a
10	CEBPB	chr6:110093176-110093466	K562	blood:	n/a	n/a
11	CEBPB	chr6:110062154-110062387	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr6:110093233-110093457	HepG2	liver:	n/a	n/a
13	CEBPB	chr6:110093203-110093753	IMR90	lung:	n/a	n/a
14	CEBPB	chr6:110097544-110097759	HepG2	liver:	n/a	chr6:110097669-110097680 chr6:110097671-110097680 chr6:110097670-110097681
15	CEBPB	chr6:110093139-110093553	K562	blood:	n/a	n/a
16	CEBPB	chr6:110093199-110093496	K562	blood:	n/a	n/a
17	CEBPB	chr6:110062120-110062336	K562	blood:	n/a	n/a
18	CTCF	chr6:110089720-110089870	HMF	breast:	n/a	n/a
19	CTCF	chr6:110067238-110067272	Medullo	brain:	n/a	n/a
20	CTCF	chr6:110064840-110065110	HMF	breast:	n/a	n/a
21	CTCF	chr6:110089740-110089890	HBMEC	blood vessel:	n/a	n/a
22	CTCF	chr6:110058920-110059070	HCPEpiC	choroid plexus:	n/a	n/a
23	CTCF	chr6:110064960-110065110	HBMEC	blood vessel:	n/a	n/a
24	CTCF	chr6:110078714-110078776	Spleen_OC	spleen:	n/a	n/a
25	CTCF	chr6:110092820-110092970	HL-60	blood:	n/a	n/a
26	CTCF	chr6:110068700-110068850	GM12866	blood:	n/a	n/a
27	CTCF	chr6:110078487-110078543	Lung_OC	lung:	n/a	n/a
28	CTCF	chr6:110064960-110065110	HAc	cerebellar:	n/a	n/a
29	CTCF	chr6:110059000-110059150	HEK293	kidney:	n/a	n/a
30	CTCF	chr6:110064940-110065090	AG04449	skin:	n/a	n/a
31	CTCF	chr6:110058920-110059070	HEK293	kidney:	n/a	n/a
32	CTCF	chr6:110057660-110057810	HEK293	kidney:	n/a	n/a
33	CUX1	chr6:110093300-110093623	K562	blood:	n/a	n/a
34	E2F4	chr6:110060071-110060207	MCF10A-Er-Src	breast:	n/a	n/a
35	E2F4	chr6:110092075-110092275	MCF10A-Er-Src	breast:	n/a	n/a
36	E2F4	chr6:110064995-110065203	MCF10A-Er-Src	breast:	n/a	n/a
37	E2F4	chr6:110058784-110059078	MCF10A-Er-Src	breast:	n/a	n/a
38	EBF1	chr6:110093147-110093387	GM12878	blood:	n/a	n/a
39	EP300	chr6:110093230-110093515	K562	blood:	n/a	n/a
40	EP300	chr6:110060540-110060586	K562	blood:	n/a	n/a
41	EP300	chr6:110081473-110081748	SK-N-SH_RA	brain:	n/a	n/a
42	EP300	chr6:110081451-110081753	SK-N-SH_RA	brain:	n/a	n/a
43	FOS	chr6:110093099-110093471	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr6:110081471-110081755	MCF10A-Er-Src	breast:	n/a	chr6:110081685-110081694
45	FOS	chr6:110064984-110065394	MCF10A-Er-Src	breast:	n/a	chr6:110065124-110065134 chr6:110065124-110065134 chr6:110065124-110065134 chr6:110065125-110065133 chr6:110065243-110065252 chr6:110065123-110065134
46	FOS	chr6:110064977-110065369	MCF10A-Er-Src	breast:	n/a	chr6:110065124-110065134 chr6:110065124-110065134 chr6:110065124-110065134 chr6:110065125-110065133 chr6:110065243-110065252 chr6:110065123-110065134
47	FOS	chr6:110093208-110093480	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr6:110089701-110090100	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr6:110089626-110090174	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr6:110093211-110093460	MCF10A-Er-Src	breast:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:110094833-110094883	NT2-D1	testis:	n/a
2	chr6:110057745-110057795	HEK293	kidney:	embryo
3	chr6:110057745-110057795	HNPCEpiC	eye:	n/a
4	chr6:110094833-110094883	AG09319	gingival:	n/a
5	chr6:110094833-110094883	HUVEC	blood vessel:	n/a
6	chr6:110057745-110057795	AG04450	lung:	fetal
7	chr6:110057745-110057795	CMK	blood:	n/a
8	chr6:110057745-110057795	Jurkat	blood:	n/a
9	chr6:110057745-110057795	HPAEpiC	pulmonary alveolar:	n/a
10	chr6:110094833-110094883	U87	brain:	n/a
11	chr6:110057745-110057795	SK-N-SH_RA	brain:	n/a
12	chr6:110057745-110057795	A549	lung:	n/a
13	chr6:110094833-110094883	LNCaP	prostate:	n/a
14	chr6:110094833-110094883	Jurkat	blood:	n/a
15	chr6:110094833-110094883	IMR90	lung:	fetal
16	chr6:110059611-110059661	HMEC	breast:	n/a
17	chr6:110057745-110057795	HCPEpiC	choroid plexus:	n/a
18	chr6:110057745-110057795	Caco-2	colon:	n/a
19	chr6:110094833-110094883	ovcar-3	ovarian:	n/a
20	chr6:110057745-110057795	AoSMC	blood vessel:	n/a
21	chr6:110057745-110057795	PrEC	prostate:	n/a
22	chr6:110057745-110057795	H1-hESC	embryonic stem cell:	embryo
23	chr6:110059611-110059661	AG09319	gingival:	n/a
24	chr6:110059611-110059661	RPTEC	kidney:	n/a
25	chr6:110094833-110094883	AG10803	skin:	n/a
26	chr6:110057745-110057795	HCF	heart:	n/a
27	chr6:110057745-110057795	GM19239	blood:	n/a
28	chr6:110057745-110057795	HepG2	liver:	n/a
29	chr6:110094833-110094883	GM19239	blood:	n/a
30	chr6:110059611-110059661	NT2-D1	testis:	n/a
31	chr6:110059611-110059661	A549	lung:	n/a
32	chr6:110059611-110059661	PFSK-1	brain:	n/a
33	chr6:110094833-110094883	HRE	kidney:	n/a
34	chr6:110094833-110094883	H1-hESC	embryonic stem cell:	embryo
35	chr6:110057745-110057795	AG09309	skin:	n/a
36	chr6:110094833-110094883	NHBE	bronchial:	n/a
37	chr6:110057745-110057795	HRCEpiC	kidney:	n/a
38	chr6:110059611-110059661	MCF-7	breast:	n/a
39	chr6:110057745-110057795	K562	blood:	n/a
40	chr6:110057745-110057795	SKMC	muscle:	n/a
41	chr6:110057745-110057795	HRE	kidney:	n/a
42	chr6:110057745-110057795	SK-N-MC	brain:	n/a
43	chr6:110059611-110059661	HL-60	blood:	n/a
44	chr6:110059611-110059661	AG10803	skin:	n/a
45	chr6:110094833-110094883	ECC-1	luminal epithelium:	n/a
46	chr6:110094833-110094883	HL-60	blood:	n/a
47	chr6:110059611-110059661	LNCaP	prostate:	n/a
48	chr6:110094833-110094883	AG09309	skin:	n/a
49	chr6:110057745-110057795	BE2_C	brain:	n/a
50	chr6:110059611-110059661	AG04450	lung:	fetal

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:110096762..110098535-chr6:110100330..110101952,2	K562	blood:
2	chr6:110096444..110098680-chr6:110099797..110102470,2	K562	blood:
3	chr6:110047914..110050234-chr6:110051143..110053248,2	MCF-7	breast:
4	chr6:110011565..110014032-chr6:110081170..110083207,2	MCF-7	breast:

No data

Variant related genes	Relation type
FIG4	TF binding region
FIG4	CpG island
ENSG00000155085	chromatin interactions
ENSG00000112367	chromatin interactions

Extended variants
information (count: 1637 )
Associated
traits (count: 114 )

Variant overlapped rSNPs/rCNVs (count:1637 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs377438647	chr6:110052839-110052840	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs545761474	chr6:110052855-110052856	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs374586700	chr6:110052859-110052860	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs12215077	chr6:110052880-110052881	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs181865038	chr6:110052886-110052887	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs540282349	chr6:110052891-110052892	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs541476125	chr6:110052920-110052921	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs150822732	chr6:110052965-110052966	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs56138799	chr6:110052971-110052972	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs139260232	chr6:110053026-110053027	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs560814326	chr6:110053031-110053032	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs144245909	chr6:110053073-110053074	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs185234161	chr6:110053093-110053094	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs530348105	chr6:110053094-110053095	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs569119876	chr6:110053179-110053180	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs191063665	chr6:110053200-110053201	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs12661287	chr6:110053250-110053251	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs180683276	chr6:110053265-110053266	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs6568602	chr6:110053276-110053277	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs533960435	chr6:110053277-110053278	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs186649305	chr6:110053285-110053286	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs570647173	chr6:110053329-110053330	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs115112683	chr6:110053349-110053350	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs111500360	chr6:110053381-110053382	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs12215385	chr6:110053456-110053457	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs112413315	chr6:110053479-110053480	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs541463757	chr6:110053505-110053506	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs555027648	chr6:110053542-110053543	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs191040443	chr6:110053592-110053593	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs35261023	chr6:110053595-110053596	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs78373086	chr6:110053643-110053644	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs79548908	chr6:110053670-110053671	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs11153215	chr6:110053721-110053722	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs376090038	chr6:110053729-110053730	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs183146629	chr6:110053742-110053743	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs80071666	chr6:110053747-110053748	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs531729825	chr6:110053776-110053777	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs575092155	chr6:110053810-110053811	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs200890189	chr6:110053824-110053825	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs570174858	chr6:110053825-110053826	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs398110541	chr6:110053837-110053838	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs140111950	chr6:110053897-110053898	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs118056228	chr6:110053920-110053921	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs527757846	chr6:110053950-110053951	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs115467680	chr6:110053951-110053952	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs570506258	chr6:110053997-110053998	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs529539750	chr6:110054020-110054021	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs111759494	chr6:110054065-110054066	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs569648200	chr6:110054074-110054075	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs187441334	chr6:110054114-110054115	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:114)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	22495311	CNVD
Gastric cancer	17908304	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Ependymoma	16718352	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Leukemia	18688285	CNVD
Prostate cancer	19242612	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Lung adenocarcinoma	21935476	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Burkitt''s lymphoma	18698080	CNVD
Ovarian cancer	21720365	CNVD
Basal cell lymphoma	17170743	CNVD
Prostate cancer	16573809	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21785460	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16461572	CNVD
Neurocytoma	17123091	CNVD
Cancer	20164920	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	17805327	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Autism	17483303	CNVD
Chordoma	21602918	CNVD
Kartagener syndrome	16639409	CNVD
abnormal development	18461090	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Systemic lupus erythematosus	19220326	CNVD
Cancer	17160897	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Acute lymphoblastic leukemia	17229543	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17133270	CNVD
Follicular lymphoma	18703704	CNVD
Mental retardation	17621639	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:939 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:110013000-110057000	Weak transcription	Left Ventricle	heart
2	chr6:110013000-110114400	Weak transcription	Right Ventricle	heart
3	chr6:110013200-110057000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr6:110013200-110057000	Weak transcription	Aorta	Aorta
5	chr6:110013600-110056000	Weak transcription	Rectal Mucosa Donor 31	rectum
6	chr6:110013600-110056800	Weak transcription	Rectal Mucosa Donor 29	rectum
7	chr6:110024200-110056400	Weak transcription	Skeletal Muscle Male	skeletal muscle
8	chr6:110025000-110057000	Weak transcription	Fetal Thymus	thymus
9	chr6:110027000-110056400	Weak transcription	Duodenum Smooth Muscle	Duodenum
10	chr6:110028000-110071200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr6:110028200-110057200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
12	chr6:110028200-110080800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
13	chr6:110034400-110060800	Weak transcription	Fetal Stomach	stomach
14	chr6:110034600-110056400	Weak transcription	Fetal Brain Female	brain
15	chr6:110034600-110057000	Weak transcription	Brain Inferior Temporal Lobe	brain
16	chr6:110034800-110059000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr6:110035000-110071400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr6:110035000-110084000	Weak transcription	GM12878-XiMat	blood
19	chr6:110035200-110056200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
20	chr6:110035200-110065000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr6:110035200-110094200	Weak transcription	Cortex derived primary cultured neurospheres	brain
22	chr6:110035400-110057800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr6:110035400-110083000	Weak transcription	Brain Germinal Matrix	brain
24	chr6:110035600-110056400	Weak transcription	Ovary	ovary
25	chr6:110035600-110057000	Weak transcription	Pancreas	Pancrea
26	chr6:110035600-110089000	Weak transcription	Spleen	Spleen
27	chr6:110035800-110057000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
28	chr6:110035800-110065000	Weak transcription	HSMM	muscle
29	chr6:110036200-110056200	Weak transcription	Duodenum Mucosa	Duodenum
30	chr6:110036600-110057000	Weak transcription	Fetal Muscle Trunk	muscle
31	chr6:110036800-110115600	Weak transcription	Colonic Mucosa	Colon
32	chr6:110037200-110056000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr6:110037200-110056000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
34	chr6:110037600-110057000	Weak transcription	Psoas Muscle	Psoas
35	chr6:110038000-110056400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr6:110038000-110057000	Weak transcription	Fetal Intestine Large	intestine
37	chr6:110038400-110056400	Weak transcription	HUES64 Cell Line	embryonic stem cell
38	chr6:110039000-110054600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr6:110039000-110056400	Weak transcription	Placenta	Placenta
40	chr6:110039000-110081000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
41	chr6:110039200-110057000	Weak transcription	Skeletal Muscle Female	skeletal muscle
42	chr6:110039200-110058800	Weak transcription	Colon Smooth Muscle	Colon
43	chr6:110039600-110053400	Weak transcription	Stomach Smooth Muscle	stomach
44	chr6:110039600-110056400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr6:110039600-110057000	Weak transcription	Brain Hippocampus Middle	brain
46	chr6:110039800-110062000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
47	chr6:110040400-110056400	Weak transcription	Rectal Smooth Muscle	rectum
48	chr6:110040800-110062000	Weak transcription	Thymus	Thymus
49	chr6:110041000-110056000	Weak transcription	Primary T helper cells fromperipheralblood	blood
50	chr6:110041000-110057000	Weak transcription	Esophagus	oesophagus

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links