Variant report

Variant	nsv981330
Chromosome Location	chr6:79781902-79785177
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:48)
CpG islands
(count:0)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:48 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr6:79782402-79782936	GM12878	blood:	n/a	n/a
2	ATF2	chr6:79782316-79782849	GM12878	blood:	n/a	n/a
3	BATF	chr6:79782569-79782809	GM12878	blood:	n/a	n/a
4	BATF	chr6:79782513-79782920	GM12878	blood:	n/a	n/a
5	BCL11A	chr6:79782471-79782847	GM12878	blood:	n/a	n/a
6	CUX1	chr6:79784220-79784221	GM12878	blood:	n/a	n/a
7	EBF1	chr6:79785015-79785024	GM12878	blood:	n/a	n/a
8	EBF1	chr6:79782766-79782824	GM12878	blood:	n/a	n/a
9	EP300	chr6:79784807-79784808	K562	blood:	n/a	n/a
10	FOS	chr6:79782644-79782842	MCF10A-Er-Src	breast:	n/a	n/a
11	FOXM1	chr6:79782376-79782952	GM12878	blood:	n/a	n/a
12	IKZF1	chr6:79782400-79782865	GM12878	blood:	n/a	chr6:79782801-79782809
13	IRF1	chr6:79783961-79784646	K562	blood:	n/a	n/a
14	IRF1	chr6:79783652-79783802	K562	blood:	n/a	n/a
15	MEF2A	chr6:79782410-79782896	GM12878	blood:	n/a	chr6:79782631-79782652
16	MEF2A	chr6:79782317-79782850	GM12878	blood:	n/a	chr6:79782631-79782652
17	MEF2C	chr6:79782382-79782906	GM12878	blood:	n/a	chr6:79782631-79782652
18	MYC	chr6:79782247-79782322	MCF-7	breast:	n/a	n/a
19	NFATC1	chr6:79782132-79782904	GM12878	blood:	n/a	n/a
20	NFATC1	chr6:79782114-79782986	GM12878	blood:	n/a	n/a
21	NFIC	chr6:79782212-79783054	GM12878	blood:	n/a	n/a
22	NFYA	chr6:79784329-79784552	Hela-S3	cervix:	n/a	n/a
23	POLR2A	chr6:79785139-79785151	MCF-7	breast:	n/a	n/a
24	POLR2A	chr6:79783925-79784021	MCF10A-Er-Src	breast:	n/a	n/a
25	POLR2A	chr6:79782216-79782343	GM12878	blood:	n/a	n/a
26	POLR2A	chr6:79782193-79782358	H1-hESC	embryonic stem cell:	n/a	n/a
27	POLR2A	chr6:79781713-79781913	MCF10A-Er-Src	breast:	n/a	n/a
28	POLR2A	chr6:79779097-79782230	K562	blood:	n/a	n/a
29	POLR2A	chr6:79781829-79782008	ProgFib	skin:	n/a	n/a
30	POLR2A	chr6:79782031-79782409	GM12892	blood:	n/a	n/a
31	POLR2A	chr6:79782178-79782390	H1-hESC	embryonic stem cell:	n/a	n/a
32	POLR2A	chr6:79783191-79783539	MCF10A-Er-Src	breast:	n/a	n/a
33	POLR2A	chr6:79782106-79782500	GM12878	blood:	n/a	n/a
34	POLR2A	chr6:79785088-79785138	MCF-7	breast:	n/a	n/a
35	POLR2A	chr6:79784737-79785098	MCF10A-Er-Src	breast:	n/a	n/a
36	POLR2A	chr6:79782127-79782472	GM12892	blood:	n/a	n/a
37	POLR2A	chr6:79782267-79782336	MCF-7	breast:	n/a	n/a
38	POLR2A	chr6:79782409-79782420	H1-hESC	embryonic stem cell:	n/a	n/a
39	POLR2A	chr6:79782185-79782878	GM12892	blood:	n/a	n/a
40	POLR2A	chr6:79784256-79785324	K562	blood:	n/a	n/a
41	POLR2A	chr6:79782281-79782355	H1-hESC	embryonic stem cell:	n/a	n/a
42	POLR2A	chr6:79784830-79785264	MCF10A-Er-Src	breast:	n/a	n/a
43	RCOR1	chr6:79785109-79785116	HepG2	liver:	n/a	n/a
44	RUNX3	chr6:79782144-79782877	GM12878	blood:	n/a	n/a
45	RUNX3	chr6:79782160-79782946	GM12878	blood:	n/a	n/a
46	STAT3	chr6:79783523-79783921	MCF10A-Er-Src	breast:	n/a	n/a
47	STAT3	chr6:79784664-79784856	MCF10A-Er-Src	breast:	n/a	n/a
48	ZNF143	chr6:79782648-79782822	GM12878	blood:	n/a	n/a

No data

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:79782683..79789958-chr6:79939846..79945776,22	MCF-7	breast:
2	chr6:79784764..79788097-chr6:80246158..80249987,4	MCF-7	breast:
3	chr6:79780063..79782220-chr6:79942614..79944561,2	K562	blood:
4	chr6:79780063..79782941-chr6:79943061..79945739,2	K562	blood:
5	chr6:76311195..76314195-chr6:79782356..79784947,3	K562	blood:
6	chr6:79780917..79783210-chr6:79805611..79807685,2	K562	blood:
7	chr6:79721662..79723988-chr6:79780005..79781950,2	K562	blood:
8	chr6:79577225..79578806-chr6:79784648..79786637,2	K562	blood:
9	chr6:79781654..79785263-chr6:79942636..79944912,3	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000217512	TF binding region
ENSG00000270362	chromatin interactions
ENSG00000118418	chromatin interactions
ENSG00000146243	chromatin interactions
ENSG00000135338	chromatin interactions
ENSG00000112701	chromatin interactions

Extended variants
information (count: 138 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:138 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs149277668	chr6:79781905-79781906	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs566209642	chr6:79781906-79781907	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs377653129	chr6:79781953-79781954	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs533701171	chr6:79782001-79782002	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs114363394	chr6:79782010-79782011	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs76521028	chr6:79782053-79782054	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs570620793	chr6:79782084-79782085	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs186769429	chr6:79782105-79782106	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs191238750	chr6:79782108-79782109	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs576093124	chr6:79782155-79782156	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs144768962	chr6:79782167-79782168	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs541888926	chr6:79782193-79782194	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs138687566	chr6:79782194-79782195	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs66481367	chr6:79782198-79782199	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs559569038	chr6:79782199-79782200	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs398002059	chr6:79782208-79782209	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs200774037	chr6:79782209-79782210	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs202048645	chr6:79782210-79782211	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs572111578	chr6:79782233-79782234	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs541228107	chr6:79782289-79782290	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs564720926	chr6:79782304-79782305	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs187025248	chr6:79782324-79782325	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs55696019	chr6:79782332-79782333	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs370223975	chr6:79782356-79782357	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs563676931	chr6:79782357-79782358	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs73466210	chr6:79782360-79782361	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs574365478	chr6:79782363-79782364	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs111254564	chr6:79782455-79782456	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs140094972	chr6:79782457-79782458	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs528601774	chr6:79782515-79782516	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs547248109	chr6:79782517-79782518	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs145614593	chr6:79782536-79782537	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs147338526	chr6:79782608-79782609	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs56386305	chr6:79782616-79782617	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs556489679	chr6:79782740-79782741	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs570014645	chr6:79782763-79782764	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs9352689	chr6:79782814-79782815	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs140703698	chr6:79782818-79782819	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs145546623	chr6:79782833-79782834	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs142292039	chr6:79782841-79782842	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs571844957	chr6:79782842-79782843	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs151268404	chr6:79782843-79782844	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs557600450	chr6:79782857-79782858	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs9361488	chr6:79782874-79782875	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs553449902	chr6:79782895-79782896	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs111723831	chr6:79782914-79782915	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs565388442	chr6:79782930-79782931	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs563591218	chr6:79782943-79782944	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs376934068	chr6:79782951-79782952	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs370316701	chr6:79782994-79782995	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:104)

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
Endometrioid adenocarcinoma	16974079	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
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Systemic lupus erythematosus	17503323	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	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
Prostate cancer	16573809	CNVD
Breast cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Follicular lymphoma	17699855	CNVD
Breast cancer	17133270	CNVD
Leukemia	18688285	CNVD
Prostate cancer	19242612	CNVD
Developmental delay	21147756	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
low-grade B-cell lymphoma tumor	18367492	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Salivary gland tumor	18059337	CNVD
Lung cancer	16773561	CNVD
Glioblastoma multiforme	22286061	CNVD
Urothelial cell carcinoma	18451213	CNVD
Prostate cancer	16461572	CNVD
Mental retardation	21045960	CNVD
Obesity	21045960	CNVD
learning difficulties	21045960	CNVD
Prostate cancer	17245344	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Cancer	20164920	CNVD
Burkitt''s lymphoma	20823134	CNVD
Ductal carcinoma	22052326	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Acute lymphoblastic leukemia	17640729	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:330 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:79704600-79786600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr6:79707400-79786000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr6:79707400-79786600	Weak transcription	Esophagus	oesophagus
4	chr6:79730000-79786600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr6:79742000-79785400	Weak transcription	HSMMtube	muscle
6	chr6:79755000-79785400	Weak transcription	Colonic Mucosa	Colon
7	chr6:79760600-79785400	Weak transcription	Right Ventricle	heart
8	chr6:79760600-79786800	Weak transcription	Spleen	Spleen
9	chr6:79764000-79782200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr6:79766400-79782000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
11	chr6:79768600-79786400	Weak transcription	Placenta Amnion	Placenta Amnion
12	chr6:79769800-79785400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr6:79770400-79784400	Weak transcription	Fetal Brain Male	brain
14	chr6:79770400-79784600	Weak transcription	NHEK	skin
15	chr6:79770400-79784800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr6:79770400-79784800	Weak transcription	HMEC	breast
17	chr6:79770400-79785000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr6:79770400-79785400	Weak transcription	Thymus	Thymus
19	chr6:79770400-79786600	Weak transcription	Lung	lung
20	chr6:79770600-79782000	Weak transcription	Fetal Intestine Large	intestine
21	chr6:79770600-79782000	Weak transcription	Placenta	Placenta
22	chr6:79770600-79782600	Weak transcription	A549	lung
23	chr6:79770600-79783800	Weak transcription	Cortex derived primary cultured neurospheres	brain
24	chr6:79770600-79785000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr6:79770600-79785000	Weak transcription	Hela-S3	cervix
26	chr6:79770600-79785400	Weak transcription	Liver	Liver
27	chr6:79770600-79785800	Weak transcription	Fetal Muscle Trunk	muscle
28	chr6:79770600-79786000	Weak transcription	H9 Cell Line	embryonic stem cell
29	chr6:79771000-79782800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr6:79772000-79784800	Weak transcription	H1 Cell Line	embryonic stem cell
31	chr6:79773000-79782200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr6:79773400-79785400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
33	chr6:79774200-79783400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr6:79774800-79782200	Weak transcription	Rectal Smooth Muscle	rectum
35	chr6:79774800-79783400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr6:79775000-79785400	Weak transcription	Fetal Stomach	stomach
37	chr6:79775200-79785800	Weak transcription	Fetal Muscle Leg	muscle
38	chr6:79775200-79786600	Weak transcription	Pancreas	Pancrea
39	chr6:79775400-79783000	Weak transcription	Brain Inferior Temporal Lobe	brain
40	chr6:79775400-79783600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
41	chr6:79775400-79783800	Weak transcription	Fetal Heart	heart
42	chr6:79775400-79785000	Weak transcription	Adipose Nuclei	Adipose
43	chr6:79775400-79786600	Weak transcription	Gastric	stomach
44	chr6:79776000-79782000	Weak transcription	Primary neutrophils fromperipheralblood	blood
45	chr6:79776800-79782800	Strong transcription	Monocytes-CD14+_RO01746	blood
46	chr6:79777000-79786000	Weak transcription	Left Ventricle	heart
47	chr6:79777800-79782800	Strong transcription	Primary monocytes fromperipheralblood	blood
48	chr6:79777800-79784800	Weak transcription	NH-A	brain
49	chr6:79777800-79785600	Weak transcription	Fetal Thymus	thymus
50	chr6:79778000-79784000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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