Variant report

Variant	nsv429914
Chromosome Location	chr8:51371447-51617647
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	BACH1	chr8:51551406-51551486	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr8:51380375-51380444	K562	blood:	n/a	n/a
3	BACH1	chr8:51448363-51448441	K562	blood:	n/a	n/a
4	BACH1	chr8:51549746-51549863	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr8:51553900-51554065	GM12878	blood:	n/a	n/a
6	CEBPB	chr8:51379026-51379129	A549	lung:	n/a	n/a
7	CEBPB	chr8:51417314-51417678	A549	lung:	n/a	chr8:51417510-51417521 chr8:51417479-51417490
8	CEBPB	chr8:51417307-51417674	H1-hESC	embryonic stem cell:	n/a	chr8:51417510-51417521 chr8:51417479-51417490
9	CEBPB	chr8:51417321-51417664	Hela-S3	cervix:	n/a	chr8:51417510-51417521 chr8:51417479-51417490
10	CEBPB	chr8:51590751-51591040	HepG2	liver:	n/a	chr8:51590858-51590871 chr8:51590858-51590869
11	CEBPB	chr8:51442889-51443030	H1-hESC	embryonic stem cell:	n/a	chr8:51442918-51442929 chr8:51442920-51442931 chr8:51442918-51442931
12	CEBPB	chr8:51544182-51544382	IMR90	lung:	n/a	chr8:51544270-51544279 chr8:51544268-51544279
13	CEBPB	chr8:51388326-51388344	A549	lung:	n/a	n/a
14	CEBPB	chr8:51463003-51463270	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr8:51440554-51440643	HepG2	liver:	n/a	chr8:51440566-51440577
16	CEBPB	chr8:51417303-51417661	K562	blood:	n/a	chr8:51417510-51417521 chr8:51417479-51417490
17	CEBPB	chr8:51442567-51443109	Hela-S3	cervix:	n/a	chr8:51442578-51442589 chr8:51442918-51442929 chr8:51442920-51442931 chr8:51442918-51442931
18	CEBPB	chr8:51384894-51385137	IMR90	lung:	n/a	n/a
19	CEBPB	chr8:51463151-51463193	HepG2	liver:	n/a	n/a
20	CEBPB	chr8:51576308-51576662	IMR90	lung:	n/a	n/a
21	CEBPB	chr8:51417299-51417672	IMR90	lung:	n/a	chr8:51417510-51417521 chr8:51417479-51417490
22	CEBPB	chr8:51594361-51594688	IMR90	lung:	n/a	n/a
23	CEBPB	chr8:51417365-51417636	A549	lung:	n/a	chr8:51417510-51417521 chr8:51417479-51417490
24	CEBPB	chr8:51483855-51484159	HepG2	liver:	n/a	chr8:51483989-51484000
25	CEBPB	chr8:51417301-51417674	HepG2	liver:	n/a	chr8:51417510-51417521 chr8:51417479-51417490
26	CEBPB	chr8:51442847-51443072	HepG2	liver:	n/a	chr8:51442918-51442929 chr8:51442920-51442931 chr8:51442918-51442931
27	CEBPZ	chr8:51529649-51529754	HepG2	liver:	n/a	n/a
28	CTCF	chr8:51438600-51438750	HEK293	kidney:	n/a	chr8:51438697-51438705
29	CTCF	chr8:51438560-51438710	AG04450	lung:	n/a	chr8:51438697-51438705
30	CTCF	chr8:51501714-51501780	LNCaP	prostate:	n/a	n/a
31	CTCF	chr8:51475054-51475115	HUVEC	blood vessel:	n/a	n/a
32	CTCF	chr8:51426000-51426150	GM12864	blood:	n/a	n/a
33	CTCF	chr8:51438600-51438750	HRPEpiC	eye:	n/a	chr8:51438697-51438705
34	CTCF	chr8:51372276-51372364	GM13977	blood:	n/a	n/a
35	CTCF	chr8:51408280-51408430	MCF-7	breast:	n/a	chr8:51408333-51408341
36	CTCF	chr8:51408333-51408408	MCF-7	breast:	n/a	chr8:51408333-51408341
37	CTCF	chr8:51518296-51518331	GM20000	blood:	n/a	n/a
38	CTCF	chr8:51438600-51438750	HPAF	blood vessel:	n/a	chr8:51438697-51438705
39	CTCF	chr8:51426020-51426170	NB4	blood:	n/a	n/a
40	CTCF	chr8:51438580-51438730	HPF	lung:	n/a	chr8:51438697-51438705
41	CTCF	chr8:51548842-51548909	GM20000	blood:	n/a	n/a
42	CTCF	chr8:51438480-51438630	MCF-7	breast:	n/a	n/a
43	CTCF	chr8:51438620-51438770	MCF-7	breast:	n/a	chr8:51438697-51438705
44	CTCF	chr8:51438640-51438790	NHEK	skin:	n/a	chr8:51438697-51438705
45	CTCF	chr8:51408340-51408402	MCF-7	breast:	n/a	n/a
46	CTCF	chr8:51426060-51426210	SK-N-SH_RA	brain:	n/a	n/a
47	CTCF	chr8:51426120-51426270	GM12874	blood:	n/a	n/a
48	CTCF	chr8:51429179-51429252	Kidney_OC	kidney:	n/a	n/a
49	CTCF	chr8:51438580-51438730	WERI-Rb-1	eye:	n/a	chr8:51438697-51438705
50	CTCF	chr8:51438560-51438710	SK-N-SH_RA	brain:	n/a	chr8:51438697-51438705

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:51528401-51528451	LNCaP	prostate:	n/a
2	chr8:51576109-51576159	ProgFib	skin:	n/a
3	chr8:51404066-51404116	ovcar-3	ovarian:	n/a
4	chr8:51555740-51555790	PANC-1	pancreas:	n/a
5	chr8:51555740-51555790	NH-A	brain:	n/a
6	chr8:51528401-51528451	BJ	skin:	n/a
7	chr8:51555740-51555790	PrEC	prostate:	n/a
8	chr8:51576109-51576159	GM19239	blood:	n/a
9	chr8:51404106-51404156	A549	lung:	n/a
10	chr8:51404066-51404116	MCF-7	breast:	n/a
11	chr8:51576109-51576159	HCF	heart:	n/a
12	chr8:51404106-51404156	GM12878	blood:	n/a
13	chr8:51449266-51449316	PrEC	prostate:	n/a
14	chr8:51404179-51404229	AG09309	skin:	n/a
15	chr8:51555740-51555790	ovcar-3	ovarian:	n/a
16	chr8:51404179-51404229	HNPCEpiC	eye:	n/a
17	chr8:51553739-51553789	PrEC	prostate:	n/a
18	chr8:51528401-51528451	K562	blood:	n/a
19	chr8:51404066-51404116	HL-60	blood:	n/a
20	chr8:51528401-51528451	HCF	heart:	n/a
21	chr8:51449266-51449316	HMEC	breast:	n/a
22	chr8:51553739-51553789	HNPCEpiC	eye:	n/a
23	chr8:51576109-51576159	HRCEpiC	kidney:	n/a
24	chr8:51449266-51449316	Hela-S3	cervix:	n/a
25	chr8:51555740-51555790	MCF-7	breast:	n/a
26	chr8:51404179-51404229	PANC-1	pancreas:	n/a
27	chr8:51555740-51555790	RPTEC	kidney:	n/a
28	chr8:51576109-51576159	HMEC	breast:	n/a
29	chr8:51553739-51553789	AG09319	gingival:	n/a
30	chr8:51449266-51449316	HUVEC	blood vessel:	n/a
31	chr8:51576109-51576159	Jurkat	blood:	n/a
32	chr8:51553739-51553789	AG04450	lung:	fetal
33	chr8:51528401-51528451	HUVEC	blood vessel:	n/a
34	chr8:51404106-51404156	AoSMC	blood vessel:	n/a
35	chr8:51404179-51404229	AG04449	skin:	fetal
36	chr8:51449266-51449316	GM06990	blood:	n/a
37	chr8:51553739-51553789	HRE	kidney:	n/a
38	chr8:51404106-51404156	MCF10A-Er-Src	breast:	n/a
39	chr8:51553739-51553789	HRCEpiC	kidney:	n/a
40	chr8:51528401-51528451	AG09319	gingival:	n/a
41	chr8:51404179-51404229	K562	blood:	n/a
42	chr8:51576109-51576159	MCF-7	breast:	n/a
43	chr8:51404066-51404116	IMR90	lung:	fetal
44	chr8:51528401-51528451	PrEC	prostate:	n/a
45	chr8:51404179-51404229	AoSMC	blood vessel:	n/a
46	chr8:51553739-51553789	AG09309	skin:	n/a
47	chr8:51449266-51449316	T-47D	breast:	n/a
48	chr8:51555740-51555790	AG09309	skin:	n/a
49	chr8:51404106-51404156	NHBE	bronchial:	n/a
50	chr8:51404179-51404229	SK-N-SH	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:51590048..51591794-chr8:51592149..51596284,3	K562	blood:
2	chr7:135846774..135848617-chr8:51481190..51483855,2	MCF-7	breast:
3	chr1:116959143..116962126-chr8:51573809..51576471,2	MCF-7	breast:
4	chr8:51372315..51374214-chr8:51375832..51377998,2	K562	blood:
5	chr8:51372315..51374214-chr8:51375832..51377998,2	K562	blood:
6	chr8:51464363..51466671-chr8:51475999..51477985,2	K562	blood:
7	chr8:51590048..51591794-chr8:51592149..51596284,3	K562	blood:

Variant related genes	Relation type
ENSG00000254392	TF binding region
SNTG1	TF binding region
ENSG00000254392	CpG island
SNTG1	CpG island
ENSG00000147481	chromatin interactions
ENSG00000203865	chromatin interactions

Extended variants
information (count: 7166 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:7166 , 50 per page) page: 1 2 3 4 5 6 7 ... 144

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1383819	chr8:51371466-51371467	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs117319466	chr8:51371508-51371509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs561017265	chr8:51371511-51371512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs529324409	chr8:51371563-51371564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs181002971	chr8:51371579-51371580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs541048115	chr8:51371580-51371581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs75614925	chr8:51371614-51371615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs185145766	chr8:51371641-51371642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs11775411	chr8:51371650-51371651	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs141758155	chr8:51371767-51371768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs531008488	chr8:51371792-51371793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs370632817	chr8:51371834-51371835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs567845303	chr8:51371858-51371859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs12545273	chr8:51371910-51371911	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
15	rs147078673	chr8:51371936-51371937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs571187280	chr8:51371951-51371952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs572743836	chr8:51371953-51371954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs538747261	chr8:51372002-51372003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs189956203	chr8:51372053-51372054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs182545752	chr8:51372054-51372055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs541653054	chr8:51372077-51372078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs116095737	chr8:51372130-51372131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs554877469	chr8:51372165-51372166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs76690828	chr8:51372179-51372180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs532784940	chr8:51372195-51372196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs540489741	chr8:51372210-51372211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs12542193	chr8:51372245-51372246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs559500804	chr8:51372310-51372311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs138567599	chr8:51372323-51372324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs545146564	chr8:51372361-51372362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs7836540	chr8:51372376-51372377	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs201266757	chr8:51372401-51372402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs113017518	chr8:51372405-51372406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs13274680	chr8:51372406-51372407	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs576005762	chr8:51372442-51372443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs549287927	chr8:51372444-51372445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs78928580	chr8:51372479-51372480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs367922542	chr8:51372503-51372504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs528798380	chr8:51372540-51372541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs142659919	chr8:51372550-51372551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs368743060	chr8:51372560-51372561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs535261601	chr8:51372582-51372583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs78827233	chr8:51372594-51372595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs187364129	chr8:51372603-51372604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs550731600	chr8:51372605-51372606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs568952930	chr8:51372624-51372625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs373429507	chr8:51372627-51372628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs192048488	chr8:51372640-51372641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs554483934	chr8:51372681-51372682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs572403321	chr8:51372707-51372708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	22286061	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Melanoma	17363583	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Sezary syndrome	18413736	CNVD
Ovarian cancer	22174824	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
22q11 deletion syndrome	20357662	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Medulloblastoma	21163964	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:221 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:51365800-51375800	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr8:51370600-51374400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr8:51374400-51375000	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr8:51381200-51381400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr8:51382000-51382200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr8:51385600-51386000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr8:51389000-51394600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr8:51393000-51393200	Enhancers	Brain Germinal Matrix	brain
9	chr8:51393000-51393200	Enhancers	Fetal Brain Female	brain
10	chr8:51393400-51394600	Weak transcription	Brain Germinal Matrix	brain
11	chr8:51393400-51394600	Weak transcription	Fetal Brain Female	brain
12	chr8:51393800-51394400	Enhancers	Dnd41	blood
13	chr8:51394400-51394600	Active TSS	Fetal Brain Male	brain
14	chr8:51394400-51394800	Flanking Active TSS	Dnd41	blood
15	chr8:51394600-51394800	Flanking Active TSS	Fetal Brain Male	brain
16	chr8:51394600-51395000	Enhancers	Brain Germinal Matrix	brain
17	chr8:51394600-51395000	Enhancers	Ovary	ovary
18	chr8:51394600-51395200	Enhancers	Fetal Brain Female	brain
19	chr8:51394600-51395400	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr8:51394800-51395200	Enhancers	Fetal Brain Male	brain
21	chr8:51394800-51395400	Enhancers	Dnd41	blood
22	chr8:51395400-51403000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr8:51402600-51403200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr8:51403000-51404200	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr8:51403200-51403400	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr8:51403200-51404200	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
27	chr8:51403400-51404000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr8:51403600-51404200	ZNF genes & repeats	Fetal Brain Female	brain
29	chr8:51404000-51404200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr8:51404200-51407400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr8:51413400-51413800	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr8:51426400-51427200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
33	chr8:51428400-51429800	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr8:51441000-51469200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr8:51444200-51444400	Enhancers	Gastric	stomach
36	chr8:51451200-51452000	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr8:51452000-51452200	Enhancers	Spleen	Spleen
38	chr8:51452000-51452400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr8:51457200-51457400	Enhancers	Brain Germinal Matrix	brain
40	chr8:51457400-51469400	Weak transcription	Brain Germinal Matrix	brain
41	chr8:51458200-51469400	Weak transcription	Cortex derived primary cultured neurospheres	brain
42	chr8:51469200-51470200	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr8:51469400-51470400	Strong transcription	Cortex derived primary cultured neurospheres	brain
44	chr8:51470200-51471200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr8:51470400-51472000	Weak transcription	Cortex derived primary cultured neurospheres	brain
46	chr8:51471200-51489400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr8:51483600-51484000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr8:51483600-51484200	Enhancers	Liver	Liver
49	chr8:51491800-51493200	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr8:51492200-51493200	ZNF genes & repeats	Brain Germinal Matrix	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links