Variant report

Variant	nsv970379
Chromosome Location	chr6:79571879-79578296
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:574)
CpG islands
(count:976)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:574 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:79575799-79575832	K562	blood:	n/a	n/a
2	ARID3A	chr6:79577598-79577777	K562	blood:	n/a	n/a
3	ARID3A	chr6:79576806-79577041	K562	blood:	n/a	n/a
4	ATF2	chr6:79576885-79577787	GM12878	blood:	n/a	n/a
5	ATF2	chr6:79577087-79577782	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr6:79576934-79577738	GM12878	blood:	n/a	n/a
7	ATF2	chr6:79577022-79577772	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr6:79577371-79577697	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF3	chr6:79577395-79577639	K562	blood:	n/a	n/a
10	BACH1	chr6:79577037-79577147	K562	blood:	n/a	n/a
11	BACH1	chr6:79577206-79577978	H1-hESC	embryonic stem cell:	n/a	n/a
12	BCLAF1	chr6:79576821-79577785	GM12878	blood:	n/a	n/a
13	BHLHE40	chr6:79576822-79577745	GM12878	blood:	n/a	chr6:79577246-79577262
14	BHLHE40	chr6:79577157-79577772	K562	blood:	n/a	chr6:79577246-79577262
15	BRCA1	chr6:79577109-79577326	H1-hESC	embryonic stem cell:	n/a	n/a
16	BRCA1	chr6:79577623-79577681	H1-hESC	embryonic stem cell:	n/a	n/a
17	BRCA1	chr6:79577448-79577864	Hela-S3	cervix:	n/a	n/a
18	CBX3	chr6:79576917-79577316	K562	blood:	n/a	n/a
19	CBX3	chr6:79577390-79577772	K562	blood:	n/a	n/a
20	CCNT2	chr6:79577088-79577612	K562	blood:	n/a	n/a
21	CEBPB	chr6:79576983-79577921	Hela-S3	cervix:	n/a	chr6:79577904-79577917
22	CEBPB	chr6:79577027-79577929	H1-hESC	embryonic stem cell:	n/a	chr6:79577904-79577917
23	CEBPB	chr6:79577057-79577817	MCF-7	breast:	n/a	n/a
24	CEBPB	chr6:79576937-79577829	K562	blood:	n/a	n/a
25	CEBPB	chr6:79577090-79577939	HepG2	liver:	n/a	chr6:79577904-79577917
26	CHD1	chr6:79577672-79578053	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD1	chr6:79576919-79577235	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr6:79576921-79577144	K562	blood:	n/a	n/a
29	CHD2	chr6:79576913-79577825	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD2	chr6:79577660-79577766	K562	blood:	n/a	n/a
31	CHD2	chr6:79577215-79577380	HepG2	liver:	n/a	n/a
32	CHD2	chr6:79576791-79577749	GM12878	blood:	n/a	n/a
33	CHD2	chr6:79577019-79577828	Hela-S3	cervix:	n/a	n/a
34	CHD2	chr6:79577430-79577442	K562	blood:	n/a	n/a
35	CREB1	chr6:79577243-79577854	K562	blood:	n/a	n/a
36	CREB1	chr6:79577301-79577815	K562	blood:	n/a	n/a
37	CREB1	chr6:79577060-79577825	H1-hESC	embryonic stem cell:	n/a	n/a
38	CREB1	chr6:79576938-79577843	H1-hESC	embryonic stem cell:	n/a	n/a
39	CREB1	chr6:79576734-79577856	GM12878	blood:	n/a	n/a
40	CREB1	chr6:79576952-79577838	HepG2	liver:	n/a	n/a
41	CREB1	chr6:79577086-79577740	A549	lung:	n/a	n/a
42	CTBP2	chr6:79576808-79577846	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr6:79577600-79577750	HMF	breast:	n/a	n/a
44	CTCF	chr6:79577486-79577706	NHEK	skin:	n/a	n/a
45	CTCF	chr6:79577560-79577710	GM12864	blood:	n/a	n/a
46	CTCF	chr6:79576900-79577050	RPTEC	kidney:	n/a	n/a
47	CTCF	chr6:79577560-79577710	SAEC	small airway:	n/a	n/a
48	CTCF	chr6:79577560-79577710	GM12873	blood:	n/a	n/a
49	CTCF	chr6:79577623-79577733	GM13977	blood:	n/a	n/a
50	CTCF	chr6:79577580-79577730	SK-N-SH_RA	brain:	n/a	n/a

(count:976 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:79577175-79577225	ProgFib	skin:	n/a
2	chr6:79577539-79577589	A549	lung:	n/a
3	chr6:79577175-79577225	AG09309	skin:	n/a
4	chr6:79577177-79577227	A549	lung:	n/a
5	chr6:79577232-79577282	HCT-116	colon:	n/a
6	chr6:79577260-79577310	AG10803	skin:	n/a
7	chr6:79577069-79577119	ovcar-3	ovarian:	n/a
8	chr6:79577539-79577589	NT2-D1	testis:	n/a
9	chr6:79577232-79577282	SK-N-SH_RA	brain:	n/a
10	chr6:79577110-79577160	T-47D	breast:	n/a
11	chr6:79574843-79574893	GM12878	blood:	n/a
12	chr6:79577069-79577119	HEEpiC	esophagus:	n/a
13	chr6:79577110-79577160	A549	lung:	n/a
14	chr6:79574843-79574893	PrEC	prostate:	n/a
15	chr6:79577539-79577589	HRE	kidney:	n/a
16	chr6:79577175-79577225	NT2-D1	testis:	n/a
17	chr6:79576881-79576931	GM12892	blood:	n/a
18	chr6:79577007-79577057	HL-60	blood:	n/a
19	chr6:79577539-79577589	HAEpiC	amniotic membrane:	n/a
20	chr6:79577801-79577851	T-47D	breast:	n/a
21	chr6:79577195-79577245	PFSK-1	brain:	n/a
22	chr6:79577177-79577227	AG09319	gingival:	n/a
23	chr6:79577175-79577225	PANC-1	pancreas:	n/a
24	chr6:79574843-79574893	SK-N-MC	brain:	n/a
25	chr6:79577691-79577741	AoSMC	blood vessel:	n/a
26	chr6:79577539-79577589	SK-N-MC	brain:	n/a
27	chr6:79576994-79577044	H1-hESC	embryonic stem cell:	embryo
28	chr6:79577195-79577245	SK-N-SH	brain:	n/a
29	chr6:79577007-79577057	SAEC	small airway:	n/a
30	chr6:79576851-79576901	HIPEpiC	eye:	n/a
31	chr6:79577175-79577225	GM12892	blood:	n/a
32	chr6:79577177-79577227	HCT-116	colon:	n/a
33	chr6:79577177-79577227	GM19239	blood:	n/a
34	chr6:79576881-79576931	HRCEpiC	kidney:	n/a
35	chr6:79577539-79577589	U87	brain:	n/a
36	chr6:79577177-79577227	MCF10A-Er-Src	breast:	n/a
37	chr6:79577175-79577225	SK-N-SH_RA	brain:	n/a
38	chr6:79577110-79577160	HPAEpiC	pulmonary alveolar:	n/a
39	chr6:79577110-79577160	H1-hESC	embryonic stem cell:	embryo
40	chr6:79577175-79577225	HL-60	blood:	n/a
41	chr6:79577260-79577310	HIPEpiC	eye:	n/a
42	chr6:79577177-79577227	MCF-7	breast:	n/a
43	chr6:79577069-79577119	NT2-D1	testis:	n/a
44	chr6:79577691-79577741	H1-hESC	embryonic stem cell:	embryo
45	chr6:79576994-79577044	CMK	blood:	n/a
46	chr6:79577069-79577119	BJ	skin:	n/a
47	chr6:79577175-79577225	U87	brain:	n/a
48	chr6:79577177-79577227	HL-60	blood:	n/a
49	chr6:79577640-79577690	AG09319	gingival:	n/a
50	chr6:79576994-79577044	HAEpiC	amniotic membrane:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:79576198..79578688-chr6:79580398..79583072,2	K562	blood:
2	chr6:79575390..79577053-chr6:79941953..79944016,2	K562	blood:
3	chr6:79568772..79571138-chr6:79573163..79575541,2	K562	blood:
4	chr6:79575800..79578597-chr6:79786334..79789260,2	MCF-7	breast:
5	chr6:79572341..79575161-chr6:79575433..79577660,3	K562	blood:

No data

Variant related genes	Relation type
IRAK1BP1	TF binding region
IRAK1BP1	CpG island
ENSG00000270362	chromatin interactions
ENSG00000146247	chromatin interactions
ENSG00000146243	chromatin interactions

Extended variants
information (count: 249 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:249 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs539646915	chr6:79571924-79571925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs556384072	chr6:79571942-79571943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs143444668	chr6:79571960-79571961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs182839351	chr6:79571978-79571979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs555706549	chr6:79571985-79571986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs572368251	chr6:79572038-79572039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs541474592	chr6:79572145-79572146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs189240237	chr6:79572152-79572153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs9352666	chr6:79572184-79572185	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs546011875	chr6:79572207-79572208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs117443891	chr6:79572273-79572274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs9352667	chr6:79572296-79572297	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs181465239	chr6:79572312-79572313	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs372472319	chr6:79572324-79572325	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs564459703	chr6:79572380-79572381	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs57023887	chr6:79572381-79572382	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs148648372	chr6:79572420-79572421	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs547420421	chr6:79572443-79572444	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs549312319	chr6:79572518-79572519	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs201534937	chr6:79572519-79572520	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs193081089	chr6:79572554-79572555	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs79030950	chr6:79572562-79572563	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs375176107	chr6:79572647-79572648	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs183893416	chr6:79572661-79572662	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs9352668	chr6:79572678-79572679	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs142401680	chr6:79572698-79572699	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs150878638	chr6:79572732-79572733	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs9448584	chr6:79572799-79572800	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs576502408	chr6:79572821-79572822	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs9448585	chr6:79572841-79572842	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs553602370	chr6:79572856-79572857	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs371243881	chr6:79572858-79572859	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs187603974	chr6:79572878-79572879	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs113935959	chr6:79572919-79572920	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs9361459	chr6:79572922-79572923	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs576319491	chr6:79572940-79572941	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs112763473	chr6:79572969-79572970	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs369166097	chr6:79573001-79573002	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs561836073	chr6:79573085-79573086	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs75450257	chr6:79573194-79573195	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs372180699	chr6:79573233-79573234	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs555856904	chr6:79573240-79573241	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs184224107	chr6:79573321-79573322	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs563768909	chr6:79573335-79573336	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs144530988	chr6:79573364-79573365	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs549483327	chr6:79573373-79573374	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs573930873	chr6:79573375-79573376	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs565371720	chr6:79573384-79573385	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs563502596	chr6:79573404-79573405	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs117355345	chr6:79573437-79573438	Weak transcription Enhancers	Chromatin interactive region	1 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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:341 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:79555800-79576400	Weak transcription	Left Ventricle	heart
2	chr6:79563000-79576200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr6:79564200-79576200	Weak transcription	Right Ventricle	heart
4	chr6:79566200-79576400	Weak transcription	Gastric	stomach
5	chr6:79568800-79576400	Weak transcription	Pancreas	Pancrea
6	chr6:79569800-79576800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr6:79571600-79576400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr6:79573000-79576400	Weak transcription	Primary B cells from cord blood	blood
9	chr6:79573400-79574600	Enhancers	K562	blood
10	chr6:79573600-79574000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr6:79573600-79576400	Weak transcription	Small Intestine	intestine
12	chr6:79574600-79578400	Active TSS	K562	blood
13	chr6:79574800-79575000	Enhancers	Brain Anterior Caudate	brain
14	chr6:79575000-79576200	Weak transcription	Brain Anterior Caudate	brain
15	chr6:79575800-79576000	Enhancers	Dnd41	blood
16	chr6:79576000-79576200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr6:79576000-79576200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr6:79576000-79576200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr6:79576000-79576200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr6:79576000-79576200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr6:79576000-79576200	Enhancers	GM12878-XiMat	blood
22	chr6:79576000-79576600	Flanking Active TSS	Dnd41	blood
23	chr6:79576000-79576800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr6:79576000-79576800	Enhancers	Primary T helper naive cells from peripheral blood	blood
25	chr6:79576000-79578600	Active TSS	ES-I3 Cell Line	embryonic stem cell
26	chr6:79576200-79576400	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr6:79576200-79576400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr6:79576200-79576400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr6:79576200-79576400	Enhancers	Brain Angular Gyrus	brain
30	chr6:79576200-79576400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
31	chr6:79576200-79576400	Enhancers	Fetal Lung	lung
32	chr6:79576200-79576400	Enhancers	Right Ventricle	heart
33	chr6:79576200-79576400	Enhancers	Skeletal Muscle Male	skeletal muscle
34	chr6:79576200-79576400	Enhancers	Thymus	Thymus
35	chr6:79576200-79576400	Enhancers	HepG2	liver
36	chr6:79576200-79576600	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr6:79576200-79576600	Enhancers	Primary T helper cells PMA-I stimulated	--
38	chr6:79576200-79576600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
39	chr6:79576200-79576600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr6:79576200-79576600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr6:79576200-79576600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr6:79576200-79576600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
43	chr6:79576200-79576600	Flanking Active TSS	Brain Anterior Caudate	brain
44	chr6:79576200-79576600	Enhancers	Colonic Mucosa	Colon
45	chr6:79576200-79576600	Enhancers	Fetal Heart	heart
46	chr6:79576200-79576600	Enhancers	Fetal Muscle Leg	muscle
47	chr6:79576200-79576600	Enhancers	Fetal Stomach	stomach
48	chr6:79576200-79576600	Flanking Active TSS	GM12878-XiMat	blood
49	chr6:79576200-79576800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
50	chr6:79576200-79576800	Enhancers	Primary T killer naive cells fromperipheralblood	blood

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