Variant report

Variant	nsv5183
Chromosome Location	chr6:5821731-5866796
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:240)
CpG islands
(count:611)
Chromatin interactive
region (count:2)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:240 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr6:5850966-5852068	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr6:5851393-5851850	GM12878	blood:	n/a	n/a
3	ATF2	chr6:5851385-5851858	GM12878	blood:	n/a	n/a
4	ATF2	chr6:5850961-5852209	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr6:5851672-5851905	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr6:5850971-5851313	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr6:5847115-5847430	GM12878	blood:	n/a	n/a
8	BHLHE40	chr6:5822058-5822298	HepG2	liver:	n/a	n/a
9	CCNT2	chr6:5851721-5851867	K562	blood:	n/a	n/a
10	CEBPB	chr6:5851181-5851786	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr6:5827736-5828280	HepG2	liver:	n/a	chr6:5828089-5828100 chr6:5828090-5828101
12	CEBPB	chr6:5827963-5828215	H1-hESC	embryonic stem cell:	n/a	chr6:5828089-5828100 chr6:5828090-5828101
13	CEBPB	chr6:5828048-5828161	K562	blood:	n/a	chr6:5828089-5828100 chr6:5828090-5828101
14	CHD2	chr6:5851127-5851863	H1-hESC	embryonic stem cell:	n/a	chr6:5851693-5851703
15	CREB1	chr6:5851523-5851809	A549	lung:	n/a	n/a
16	CTBP2	chr6:5851148-5851686	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr6:5839407-5839479	GM12891	blood:	n/a	n/a
18	CTCF	chr6:5855293-5855392	MCF-7	breast:	n/a	n/a
19	CTCF	chr6:5828729-5828837	GM12878	blood:	n/a	chr6:5828756-5828769
20	CTCF	chr6:5855240-5855390	GM06990	blood:	n/a	n/a
21	CTCF	chr6:5855100-5855250	GM06990	blood:	n/a	n/a
22	CTCF	chr6:5831796-5831915	Spleen_OC	spleen:	n/a	n/a
23	CTCF	chr6:5828795-5828888	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr6:5856060-5856210	K562	blood:	n/a	n/a
25	CTCF	chr6:5859471-5859475	GM10248	blood:	n/a	n/a
26	CTCF	chr6:5855240-5855390	HMF	breast:	n/a	n/a
27	CTCF	chr6:5832460-5832507	LNCaP	prostate:	n/a	n/a
28	CTCF	chr6:5828810-5828844	GM12892	blood:	n/a	n/a
29	CTCF	chr6:5855280-5855430	HMF	breast:	n/a	n/a
30	CTCF	chr6:5855280-5855430	Caco-2	colon:	n/a	n/a
31	CTCF	chr6:5828707-5828840	GM19240	blood:	n/a	chr6:5828756-5828769
32	CTCF	chr6:5855300-5855450	WERI-Rb-1	eye:	n/a	n/a
33	CTCF	chr6:5828756-5828807	GM12892	blood:	n/a	chr6:5828756-5828769
34	CTCF	chr6:5828710-5828836	GM12891	blood:	n/a	chr6:5828756-5828769
35	CTCF	chr6:5828806-5828868	MCF-7	breast:	n/a	n/a
36	CTCF	chr6:5855480-5855630	A549	lung:	n/a	n/a
37	CTCF	chr6:5831739-5831832	GM12891	blood:	n/a	n/a
38	CTCF	chr6:5839427-5839458	GM19239	blood:	n/a	n/a
39	CTCF	chr6:5832460-5832610	HEK293	kidney:	n/a	n/a
40	CTCF	chr6:5831940-5832090	GM12873	blood:	n/a	chr6:5831993-5832006 chr6:5831997-5832006
41	CTCF	chr6:5855240-5855390	GM12865	blood:	n/a	n/a
42	CTCF	chr6:5855251-5855400	HepG2	liver:	n/a	n/a
43	CTCF	chr6:5828828-5828856	K562	blood:	n/a	n/a
44	CTCF	chr6:5840820-5840970	WERI-Rb-1	eye:	n/a	n/a
45	CTCF	chr6:5855338-5855345	MCF-7	breast:	n/a	n/a
46	CTCF	chr6:5855280-5855430	HEK293	kidney:	n/a	n/a
47	CTCF	chr6:5846270-5846321	GM13976	blood:	n/a	n/a
48	CTCF	chr6:5823840-5823990	HepG2	liver:	n/a	n/a
49	CTCF	chr6:5855289-5855383	HepG2	liver:	n/a	n/a
50	CTCF	chr6:5828692-5828889	GM12878	blood:	n/a	chr6:5828756-5828769

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:5851330-5851380	A549	lung:	n/a
2	chr6:5851330-5851380	A549	lung:	n/a
3	chr6:5851436-5851486	GM12878	blood:	n/a
4	chr6:5849049-5849099	AG09309	skin:	n/a
5	chr6:5851330-5851380	BE2_C	brain:	n/a
6	chr6:5851840-5851890	NT2-D1	testis:	n/a
7	chr6:5851644-5851694	ECC-1	luminal epithelium:	n/a
8	chr6:5849049-5849099	A549	lung:	n/a
9	chr6:5849049-5849099	NB4	blood:	n/a
10	chr6:5850005-5850055	BJ	skin:	n/a
11	chr6:5851436-5851486	RPTEC	kidney:	n/a
12	chr6:5850005-5850055	ProgFib	skin:	n/a
13	chr6:5849049-5849099	HNPCEpiC	eye:	n/a
14	chr6:5851436-5851486	NB4	blood:	n/a
15	chr6:5851912-5851962	U87	brain:	n/a
16	chr6:5851644-5851694	BE2_C	brain:	n/a
17	chr6:5851436-5851486	LNCaP	prostate:	n/a
18	chr6:5850005-5850055	SAEC	small airway:	n/a
19	chr6:5849049-5849099	PANC-1	pancreas:	n/a
20	chr6:5851644-5851694	GM12892	blood:	n/a
21	chr6:5849049-5849099	GM19239	blood:	n/a
22	chr6:5850005-5850055	NHDF-neo	bronchial:	n/a
23	chr6:5851757-5851807	NB4	blood:	n/a
24	chr6:5851757-5851807	SKMC	muscle:	n/a
25	chr6:5851912-5851962	GM12892	blood:	n/a
26	chr6:5851757-5851807	GM12878	blood:	n/a
27	chr6:5851840-5851890	AG04450	lung:	fetal
28	chr6:5851330-5851380	HCM	heart:	n/a
29	chr6:5849049-5849099	HCT-116	colon:	n/a
30	chr6:5850005-5850055	HPAEpiC	pulmonary alveolar:	n/a
31	chr6:5851644-5851694	GM12878	blood:	n/a
32	chr6:5851644-5851694	MCF10A-Er-Src	breast:	n/a
33	chr6:5851757-5851807	CMK	blood:	n/a
34	chr6:5851644-5851694	HepG2	liver:	n/a
35	chr6:5851031-5851081	GM19239	blood:	n/a
36	chr6:5851330-5851380	SK-N-MC	brain:	n/a
37	chr6:5851840-5851890	HCPEpiC	choroid plexus:	n/a
38	chr6:5851757-5851807	HNPCEpiC	eye:	n/a
39	chr6:5851031-5851081	HPAEpiC	pulmonary alveolar:	n/a
40	chr6:5850005-5850055	HNPCEpiC	eye:	n/a
41	chr6:5851031-5851081	HUVEC	blood vessel:	n/a
42	chr6:5851031-5851081	A549	lung:	n/a
43	chr6:5851912-5851962	NT2-D1	testis:	n/a
44	chr6:5851436-5851486	K562	blood:	n/a
45	chr6:5851840-5851890	K562	blood:	n/a
46	chr6:5851994-5852044	ECC-1	luminal epithelium:	n/a
47	chr6:5849049-5849099	Jurkat	blood:	n/a
48	chr6:5851994-5852044	AG09309	skin:	n/a
49	chr6:5851840-5851890	HRE	kidney:	n/a
50	chr6:5851840-5851890	HCF	heart:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:5860915..5862515-chr6:5878997..5881737,2	MCF-7	breast:
2	chr6:5866299..5868862-chr6:5869895..5873269,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FARS2-1	chr6:5851739-5851895	ENSG00000233064.2
2	lnc-FARS2-1	chr6:5852296-5852369	ENSG00000233064.2
3	lnc-FARS2-1	chr6:5852296-5852370	XLOC_005144
4	lnc-FARS2-1	chr6:5851739-5851895	XLOC_005144

No data

Variant related genes	Relation type
ENSG00000233064	TF binding region
ENSG00000216360	TF binding region
ENSG00000233064	CpG island
ENSG00000216360	CpG island
NACC2	miRNA target sites

Extended variants
information (count: 1607 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:1607 , 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	rs57258690	chr6:5821732-5821733	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs11969751	chr6:5821742-5821743	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs11964932	chr6:5821783-5821784	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs1830689	chr6:5821801-5821802	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs148322164	chr6:5821827-5821828	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs569690783	chr6:5821886-5821887	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs537307230	chr6:5821887-5821888	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs36105419	chr6:5821918-5821919	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs558822060	chr6:5821934-5821935	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs143147060	chr6:5821968-5821969	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs184492806	chr6:5822006-5822007	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs552929793	chr6:5822036-5822037	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs568582316	chr6:5822038-5822039	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs4370407	chr6:5822043-5822044	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs541945247	chr6:5822044-5822045	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs1830688	chr6:5822049-5822050	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs530832646	chr6:5822066-5822067	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs527770649	chr6:5822067-5822068	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs147451472	chr6:5822073-5822074	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs114747965	chr6:5822121-5822122	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs1830687	chr6:5822122-5822123	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs562179509	chr6:5822124-5822125	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs138268041	chr6:5822134-5822135	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs1830686	chr6:5822142-5822143	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs114662942	chr6:5822155-5822156	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs537045263	chr6:5822179-5822180	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs1407795	chr6:5822192-5822193	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs143850229	chr6:5822193-5822194	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs372411662	chr6:5822195-5822196	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs4604310	chr6:5822232-5822233	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs553108204	chr6:5822302-5822303	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs574311729	chr6:5822325-5822326	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs143113308	chr6:5822361-5822362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs13218554	chr6:5822362-5822363	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs189171826	chr6:5822383-5822384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs13219593	chr6:5822414-5822415	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs9504532	chr6:5822430-5822431	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs13218657	chr6:5822436-5822437	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs540598302	chr6:5822458-5822459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs58818464	chr6:5822471-5822472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs13208150	chr6:5822476-5822477	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs181848052	chr6:5822488-5822489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs563368342	chr6:5822499-5822500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs530559346	chr6:5822509-5822510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs552133429	chr6:5822530-5822531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs13204941	chr6:5822534-5822535	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs13218815	chr6:5822551-5822552	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs546595893	chr6:5822555-5822556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs13205062	chr6:5822634-5822635	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs184868492	chr6:5822646-5822647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:100)

Disease	PMID	Source
Developmental delay	19490664	CNVD
Cancer	21183584	CNVD
Multiple Epiphyseal Dysplasia	20877625	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Glaucoma	18694899	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	17603634	CNVD
Cancer	20164920	CNVD
Colorectal cancer	21297112	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Myelodysplastic syndrome	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Bladder cancer	21909424	CNVD
Multiple myeloma	17550852	CNVD
Ewing''s sarcoma	17952124	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
Autism	22495311	CNVD
Autism	21448237	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ependymoma	19289631	CNVD
small cell lung cancer	20016488	CNVD
Gestational infection	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
dysmorphism	22105932	CNVD
psychomotor delay	22105932	CNVD
Ovarian cancer	19193619	CNVD
Osteosarcoma	16790693	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21364760	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:581 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:5817200-5828000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr6:5821600-5822200	Enhancers	Duodenum Mucosa	Duodenum
3	chr6:5823600-5825600	Enhancers	Primary T cells fromperipheralblood	blood
4	chr6:5823600-5825600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
5	chr6:5823800-5825400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
6	chr6:5823800-5825600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
7	chr6:5824200-5825200	Enhancers	Primary T helper cells PMA-I stimulated	--
8	chr6:5824200-5825400	Enhancers	Primary T helper naive cells from peripheral blood	blood
9	chr6:5824200-5825600	Enhancers	Fetal Thymus	thymus
10	chr6:5824400-5825000	Enhancers	Primary T cells from cord blood	blood
11	chr6:5824400-5825000	Enhancers	Primary T helper cells fromperipheralblood	blood
12	chr6:5824400-5825000	Enhancers	Primary T killer memory cells from peripheral blood	blood
13	chr6:5824400-5825400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
14	chr6:5824600-5825000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
15	chr6:5824600-5825000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
16	chr6:5824600-5825000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
17	chr6:5825000-5827600	Weak transcription	Primary T cells from cord blood	blood
18	chr6:5825000-5828800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
19	chr6:5825000-5829000	Weak transcription	Primary T helper cells fromperipheralblood	blood
20	chr6:5825000-5829400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
21	chr6:5825000-5832000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
22	chr6:5825200-5828800	Weak transcription	Primary T helper cells PMA-I stimulated	--
23	chr6:5825400-5827200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
24	chr6:5825400-5830600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
25	chr6:5825400-5830600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
26	chr6:5825600-5827400	Weak transcription	Fetal Thymus	thymus
27	chr6:5825600-5828000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
28	chr6:5825600-5828600	Weak transcription	Primary T cells fromperipheralblood	blood
29	chr6:5825600-5828800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
30	chr6:5826600-5826800	Enhancers	Fetal Brain Female	brain
31	chr6:5826600-5831600	Enhancers	Primary neutrophils fromperipheralblood	blood
32	chr6:5826800-5827400	Weak transcription	Fetal Brain Female	brain
33	chr6:5827200-5827400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr6:5827200-5827600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
35	chr6:5827200-5827600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr6:5827200-5827600	Enhancers	Brain Germinal Matrix	brain
37	chr6:5827200-5829400	Enhancers	Fetal Brain Male	brain
38	chr6:5827200-5829600	Enhancers	Primary monocytes fromperipheralblood	blood
39	chr6:5827200-5829600	Enhancers	Cortex derived primary cultured neurospheres	brain
40	chr6:5827400-5827600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr6:5827400-5828200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr6:5827400-5828400	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr6:5827400-5828400	Enhancers	Fetal Muscle Trunk	muscle
44	chr6:5827400-5829000	Enhancers	Monocytes-CD14+_RO01746	blood
45	chr6:5827400-5829200	Enhancers	Fetal Brain Female	brain
46	chr6:5827400-5835000	Enhancers	Fetal Thymus	thymus
47	chr6:5827600-5828000	Flanking Active TSS	Brain Germinal Matrix	brain
48	chr6:5827600-5828200	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr6:5827600-5828200	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr6:5827600-5828400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood

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