Variant report

Variant	nsv886826
Chromosome Location	chr6:162032087-162146333
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr6:162140696-162140749	K562	blood:	n/a	n/a
2	ATF1	chr6:162132283-162132287	K562	blood:	n/a	n/a
3	ATF1	chr6:162131444-162131661	K562	blood:	n/a	n/a
4	ATF3	chr6:162040045-162040462	K562	blood:	n/a	n/a
5	BACH1	chr6:162062267-162062596	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr6:162053102-162053295	H1-hESC	embryonic stem cell:	n/a	chr6:162053163-162053177
7	BACH1	chr6:162051173-162051178	K562	blood:	n/a	n/a
8	BACH1	chr6:162104075-162104373	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr6:162040099-162040427	K562	blood:	n/a	chr6:162040293-162040304 chr6:162040292-162040305
10	CEBPB	chr6:162091000-162091232	A549	lung:	n/a	chr6:162091106-162091117 chr6:162091108-162091119
11	CEBPB	chr6:162073871-162074166	A549	lung:	n/a	n/a
12	CEBPB	chr6:162070270-162070519	HepG2	liver:	n/a	chr6:162070379-162070390
13	CEBPB	chr6:162127580-162127812	HepG2	liver:	n/a	chr6:162127670-162127681
14	CEBPB	chr6:162070447-162070488	A549	lung:	n/a	n/a
15	CEBPB	chr6:162086304-162086601	K562	blood:	n/a	chr6:162086444-162086457 chr6:162086444-162086455
16	CEBPB	chr6:162040089-162040485	K562	blood:	n/a	chr6:162040293-162040304 chr6:162040292-162040305
17	CEBPB	chr6:162039951-162040486	H1-hESC	embryonic stem cell:	n/a	chr6:162040293-162040304 chr6:162040292-162040305
18	CEBPB	chr6:162040075-162040483	HepG2	liver:	n/a	chr6:162040293-162040304 chr6:162040292-162040305
19	CEBPB	chr6:162073884-162074194	A549	lung:	n/a	n/a
20	CEBPB	chr6:162090972-162091261	HepG2	liver:	n/a	chr6:162091106-162091117 chr6:162091108-162091119
21	CEBPB	chr6:162040153-162040413	K562	blood:	n/a	chr6:162040293-162040304 chr6:162040292-162040305
22	CEBPB	chr6:162040141-162040465	IMR90	lung:	n/a	chr6:162040293-162040304 chr6:162040292-162040305
23	CEBPB	chr6:162086348-162086600	HepG2	liver:	n/a	chr6:162086444-162086457 chr6:162086444-162086455
24	CEBPB	chr6:162039960-162040482	MCF-7	breast:	n/a	chr6:162040293-162040304 chr6:162040292-162040305
25	CEBPB	chr6:162039972-162040478	A549	lung:	n/a	chr6:162040293-162040304 chr6:162040292-162040305
26	CEBPB	chr6:162039877-162040568	A549	lung:	n/a	chr6:162040293-162040304 chr6:162040292-162040305
27	CEBPB	chr6:162040128-162040496	A549	lung:	n/a	chr6:162040293-162040304 chr6:162040292-162040305
28	CEBPB	chr6:162039967-162040513	MCF-7	breast:	n/a	chr6:162040293-162040304 chr6:162040292-162040305
29	CEBPB	chr6:162039941-162040487	Hela-S3	cervix:	n/a	chr6:162040293-162040304 chr6:162040292-162040305
30	CEBPB	chr6:162091042-162091242	K562	blood:	n/a	chr6:162091106-162091117 chr6:162091108-162091119
31	CEBPB	chr6:162129712-162129932	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD2	chr6:162039900-162040223	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD2	chr6:162053772-162053995	K562	blood:	n/a	n/a
34	CTCF	chr6:162039920-162040150	GM12868	blood:	n/a	chr6:162040039-162040057
35	CTCF	chr6:162116114-162116366	LNCaP	prostate:	n/a	chr6:162116227-162116248 chr6:162116232-162116250 chr6:162116234-162116247
36	CTCF	chr6:162039960-162040110	BE2_C	brain:	n/a	chr6:162040039-162040057
37	CTCF	chr6:162082553-162082607	GM13976	blood:	n/a	n/a
38	CTCF	chr6:162039980-162040130	NHDF-neo	bronchial:	n/a	chr6:162040039-162040057
39	CTCF	chr6:162116140-162116290	AG04450	lung:	n/a	chr6:162116227-162116248 chr6:162116232-162116250 chr6:162116234-162116247
40	CTCF	chr6:162116160-162116310	A549	lung:	n/a	chr6:162116227-162116248 chr6:162116232-162116250 chr6:162116234-162116247
41	CTCF	chr6:162116130-162116319	GM20000	blood:	n/a	chr6:162116227-162116248 chr6:162116232-162116250 chr6:162116234-162116247
42	CTCF	chr6:162039920-162040070	GM12873	blood:	n/a	chr6:162040039-162040057
43	CTCF	chr6:162039940-162040090	AG09309	skin:	n/a	chr6:162040039-162040057
44	CTCF	chr6:162040000-162040150	HCT-116	colon:	n/a	chr6:162040039-162040057
45	CTCF	chr6:162116120-162116270	HRPEpiC	eye:	n/a	chr6:162116227-162116248 chr6:162116232-162116250 chr6:162116234-162116247
46	CTCF	chr6:162116160-162116310	AG04450	lung:	n/a	chr6:162116227-162116248 chr6:162116232-162116250 chr6:162116234-162116247
47	CTCF	chr6:162082020-162082170	AG09319	gingival:	n/a	n/a
48	CTCF	chr6:162039980-162040130	HCPEpiC	choroid plexus:	n/a	chr6:162040039-162040057
49	CTCF	chr6:162039594-162040558	A549	lung:	n/a	chr6:162040039-162040057
50	CTCF	chr6:162116102-162116307	A549	lung:	n/a	chr6:162116227-162116248 chr6:162116232-162116250 chr6:162116234-162116247

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:162067177-162067227	HRE	kidney:	n/a
2	chr6:162064339-162064389	ProgFib	skin:	n/a
3	chr6:162067688-162067738	U87	brain:	n/a
4	chr6:162066927-162066977	Caco-2	colon:	n/a
5	chr6:162060886-162060936	HCT-116	colon:	n/a
6	chr6:162067177-162067227	HUVEC	blood vessel:	n/a
7	chr6:162067688-162067738	GM06990	blood:	n/a
8	chr6:162060886-162060936	IMR90	lung:	fetal
9	chr6:162067688-162067738	RPTEC	kidney:	n/a
10	chr6:162065571-162065621	HIPEpiC	eye:	n/a
11	chr6:162066927-162066977	HCF	heart:	n/a
12	chr6:162065571-162065621	HCT-116	colon:	n/a
13	chr6:162064339-162064389	NH-A	brain:	n/a
14	chr6:162071140-162071190	HCM	heart:	n/a
15	chr6:162060886-162060936	GM12891	blood:	n/a
16	chr6:162067688-162067738	PrEC	prostate:	n/a
17	chr6:162067688-162067738	GM19239	blood:	n/a
18	chr6:162060886-162060936	SK-N-MC	brain:	n/a
19	chr6:162064339-162064389	HEK293	kidney:	embryo
20	chr6:162066927-162066977	Jurkat	blood:	n/a
21	chr6:162066927-162066977	AG10803	skin:	n/a
22	chr6:162060886-162060936	AG04450	lung:	fetal
23	chr6:162065571-162065621	NT2-D1	testis:	n/a
24	chr6:162068382-162068432	HMEC	breast:	n/a
25	chr6:162067177-162067227	GM12891	blood:	n/a
26	chr6:162065571-162065621	HUVEC	blood vessel:	n/a
27	chr6:162060886-162060936	Hela-S3	cervix:	n/a
28	chr6:162064339-162064389	HRCEpiC	kidney:	n/a
29	chr6:162064339-162064389	Caco-2	colon:	n/a
30	chr6:162071140-162071190	ovcar-3	ovarian:	n/a
31	chr6:162067688-162067738	SK-N-SH	brain:	n/a
32	chr6:162071140-162071190	BE2_C	brain:	n/a
33	chr6:162071140-162071190	HAEpiC	amniotic membrane:	n/a
34	chr6:162066927-162066977	GM12878	blood:	n/a
35	chr6:162068382-162068432	H1-hESC	embryonic stem cell:	embryo
36	chr6:162065571-162065621	HepG2	liver:	n/a
37	chr6:162071140-162071190	IMR90	lung:	fetal
38	chr6:162071140-162071190	Hepatocyte	liver:	n/a
39	chr6:162066927-162066977	SKMC	muscle:	n/a
40	chr6:162068382-162068432	SAEC	small airway:	n/a
41	chr6:162065571-162065621	SAEC	small airway:	n/a
42	chr6:162067688-162067738	HEEpiC	esophagus:	n/a
43	chr6:162071140-162071190	ECC-1	luminal epithelium:	n/a
44	chr6:162066927-162066977	HRE	kidney:	n/a
45	chr6:162065571-162065621	HPAEpiC	pulmonary alveolar:	n/a
46	chr6:162060886-162060936	Jurkat	blood:	n/a
47	chr6:162068382-162068432	AG10803	skin:	n/a
48	chr6:162066927-162066977	ECC-1	luminal epithelium:	n/a
49	chr6:162067177-162067227	AG09319	gingival:	n/a
50	chr6:162064339-162064389	ECC-1	luminal epithelium:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:162057469..162059362-chr6:162068678..162070292,2	K562	blood:
2	chr6:162052847..162055292-chr6:162059575..162062461,2	MCF-7	breast:
3	chr6:162111336..162114011-chr6:162137192..162139483,2	K562	blood:
4	chr6:162080897..162083173-chr6:162084992..162086582,2	K562	blood:
5	chr6:162115124..162116676-chr6:162119287..162121862,2	K562	blood:
6	chr6:162135808..162138276-chr6:162142475..162145172,2	K562	blood:
7	chr6:162041107..162043997-chr6:162053743..162055556,2	K562	blood:
8	chr6:162039551..162040468-chr6:162115665..162116674,7	MCF-7	breast:
9	chr6:162057469..162059362-chr6:162068678..162070292,2	K562	blood:
10	chr6:162115124..162116676-chr6:162119287..162121862,2	K562	blood:
11	chr6:162075282..162077598-chr6:162078551..162080758,2	K562	blood:
12	chr6:162041107..162043997-chr6:162053743..162055556,2	K562	blood:
13	chr6:162052847..162055292-chr6:162059575..162062461,2	MCF-7	breast:
14	chr6:162111336..162114011-chr6:162137192..162139483,2	K562	blood:
15	chr6:162064140..162064803-chr7:123198816..123199394,2	MCF-7	breast:
16	chr6:162039551..162040468-chr6:162115665..162116674,7	MCF-7	breast:
17	chr6:162135808..162138276-chr6:162142475..162145172,2	K562	blood:
18	chr19:35885081..35886581-chr6:162062521..162064392,2	K562	blood:
19	chr6:162056640..162058918-chr6:162062226..162064429,2	K562	blood:
20	chr6:161813445..161815530-chr6:162115453..162117705,2	MCF-7	breast:
21	chr6:162075282..162077598-chr6:162078551..162080758,2	K562	blood:
22	chr6:162080897..162083173-chr6:162084992..162086582,2	K562	blood:
23	chr6:162056640..162058918-chr6:162062226..162064429,2	K562	blood:

Variant related genes	Relation type
ENSG00000221021	TF binding region
ENSG00000221021	CpG island

Extended variants
information (count: 4043 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:4043 , 50 per page) page: 1 2 3 4 5 6 7 ... 81

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6924602	chr6:162032087-162032088	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs539040684	chr6:162032088-162032089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs10945759	chr6:162032127-162032128	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs117508373	chr6:162032163-162032164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs368003004	chr6:162032229-162032230	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs2206950	chr6:162032238-162032239	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs558801211	chr6:162032327-162032328	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs376095821	chr6:162032373-162032374	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs570999380	chr6:162032380-162032381	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs573547477	chr6:162032491-162032492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs542369086	chr6:162032498-162032499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs148646293	chr6:162032512-162032513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs9458318	chr6:162032593-162032594	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs553972038	chr6:162032634-162032635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs79176798	chr6:162032668-162032669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs564760068	chr6:162032717-162032718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs367773903	chr6:162032750-162032751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs530517144	chr6:162032766-162032767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs551342755	chr6:162032784-162032785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs185775581	chr6:162032788-162032789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs561517964	chr6:162032793-162032794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs530325169	chr6:162032857-162032858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs141190694	chr6:162032919-162032920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs566978803	chr6:162033003-162033004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs573879485	chr6:162033006-162033007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs530264080	chr6:162033010-162033011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs552625803	chr6:162033013-162033014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs150883226	chr6:162033035-162033036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs11965612	chr6:162033088-162033089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs538237796	chr6:162033091-162033092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs556841963	chr6:162033117-162033118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs9347525	chr6:162033143-162033144	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs536062762	chr6:162033145-162033146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs552775147	chr6:162033201-162033202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs572976376	chr6:162033206-162033207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs544816570	chr6:162033283-162033284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs373347439	chr6:162033295-162033296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs78804346	chr6:162033344-162033345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs191020044	chr6:162033364-162033365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs575133983	chr6:162033447-162033448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs181841498	chr6:162033478-162033479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs561585272	chr6:162033479-162033480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs530391705	chr6:162033496-162033497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs376430338	chr6:162033527-162033528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs139338594	chr6:162033552-162033553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs560556853	chr6:162033614-162033615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs186133812	chr6:162033622-162033623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs368127663	chr6:162033654-162033655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs565108497	chr6:162033712-162033713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs569290147	chr6:162033713-162033714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

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
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
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
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	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
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Testicular germ cell tumor	18059402	CNVD
Developmental delay	21147756	CNVD
Chordoma	18071362	CNVD
Myelofibrosis	22110671	CNVD
Autism	22241247	CNVD
Breast cancer	16397240	CNVD
Atherosclerosis	21956041	CNVD
Maculopathy	20981449	CNVD
Retinoblastoma	22278416	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Ovarian cancer	20844748	CNVD
Uveal melanoma	20484589	CNVD
Glioblastoma multiforme	19435819	CNVD
Astrocytoma	16205629	CNVD
Parkinson disease	17160897	CNVD
Cancer	20164920	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	20838587	CNVD
Early-onset parkinson disease	21993715	CNVD
Glioblastoma	18772890	CNVD
Pancreatic cancer	20981101	CNVD
Autism	21360662	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Intellectual disability	22102821	CNVD
Parkinson disease	0	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Bipolar disorder	19114987	CNVD
Cancer	20164919	CNVD
Ovarian cancer	21720365	CNVD

Chromatin state (count:323 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:162013800-162036600	Weak transcription	Left Ventricle	heart
2	chr6:162017000-162045400	Weak transcription	Ovary	ovary
3	chr6:162028400-162033200	Weak transcription	Gastric	stomach
4	chr6:162031600-162032200	Weak transcription	Aorta	Aorta
5	chr6:162032200-162032400	ZNF genes & repeats	Aorta	Aorta
6	chr6:162032200-162036800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr6:162035600-162036600	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr6:162035800-162036000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr6:162035800-162036200	Enhancers	HSMMtube	muscle
10	chr6:162035800-162037200	Enhancers	Psoas Muscle	Psoas
11	chr6:162036000-162036800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr6:162036200-162036600	Weak transcription	HSMMtube	muscle
13	chr6:162036400-162037000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr6:162036600-162036800	Enhancers	HSMMtube	muscle
15	chr6:162036600-162037000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr6:162036600-162037000	Weak transcription	Cortex derived primary cultured neurospheres	brain
17	chr6:162036600-162037000	Active TSS	Brain Hippocampus Middle	brain
18	chr6:162036600-162037200	Enhancers	Left Ventricle	heart
19	chr6:162036600-162037200	Enhancers	Right Atrium	heart
20	chr6:162036800-162037000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr6:162036800-162037200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr6:162036800-162037200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr6:162036800-162037200	Enhancers	Brain Anterior Caudate	brain
24	chr6:162036800-162037200	Enhancers	Brain Substantia Nigra	brain
25	chr6:162036800-162037200	Enhancers	Right Ventricle	heart
26	chr6:162036800-162037200	Enhancers	Skeletal Muscle Female	skeletal muscle
27	chr6:162036800-162040000	Weak transcription	HSMMtube	muscle
28	chr6:162037000-162037200	Enhancers	Cortex derived primary cultured neurospheres	brain
29	chr6:162037000-162039200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr6:162037000-162039600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr6:162037000-162039800	Weak transcription	Brain Hippocampus Middle	brain
32	chr6:162037200-162038800	Weak transcription	Cortex derived primary cultured neurospheres	brain
33	chr6:162037200-162039600	Weak transcription	Brain Anterior Caudate	brain
34	chr6:162037200-162040000	Weak transcription	Brain Substantia Nigra	brain
35	chr6:162037200-162040000	Weak transcription	Skeletal Muscle Female	skeletal muscle
36	chr6:162038800-162040800	Enhancers	Cortex derived primary cultured neurospheres	brain
37	chr6:162039000-162040000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr6:162039200-162039600	Enhancers	Brain Germinal Matrix	brain
39	chr6:162039200-162040400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr6:162039600-162039800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr6:162039600-162039800	Enhancers	Brain Anterior Caudate	brain
42	chr6:162039600-162039800	Flanking Active TSS	Brain Germinal Matrix	brain
43	chr6:162039600-162039800	Enhancers	Fetal Brain Female	brain
44	chr6:162039600-162040000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr6:162039600-162040000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr6:162039600-162040000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
47	chr6:162039800-162040000	Enhancers	Muscle Satellite Cultured Cells	--
48	chr6:162039800-162040000	Weak transcription	Brain Anterior Caudate	brain
49	chr6:162039800-162040000	Flanking Active TSS	Fetal Brain Female	brain
50	chr6:162039800-162040200	Active TSS	Brain Germinal Matrix	brain

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