Variant report

Variant	nsv524631
Chromosome Location	chr8:1907855-1916144
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	chr8:1908240-1908440	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chr8:1911161-1911462	K562	blood:	n/a	n/a
3	CEBPB	chr8:1908171-1908466	HepG2	liver:	n/a	n/a
4	CEBPB	chr8:1908125-1908384	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr8:1907993-1908601	HCT-116	colon:	n/a	n/a
6	CEBPB	chr8:1914793-1914975	K562	blood:	n/a	chr8:1914929-1914940 chr8:1914954-1914966 chr8:1914924-1914941 chr8:1914929-1914940
7	CEBPB	chr8:1908101-1908510	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr8:1908196-1908486	MCF-7	breast:	n/a	n/a
9	CEBPB	chr8:1908278-1908309	K562	blood:	n/a	n/a
10	CEBPB	chr8:1914751-1915120	IMR90	lung:	n/a	chr8:1914929-1914940 chr8:1914954-1914966 chr8:1914924-1914941 chr8:1914929-1914940
11	CREB1	chr8:1916103-1916317	A549	lung:	n/a	chr8:1916249-1916262
12	CTCF	chr8:1908604-1908632	Lung_OC	lung:	n/a	n/a
13	CTCF	chr8:1908380-1908530	SAEC	small airway:	n/a	n/a
14	EP300	chr8:1908328-1908355	K562	blood:	n/a	n/a
15	FOS	chr8:1908198-1908727	MCF10A-Er-Src	breast:	n/a	n/a
16	FOS	chr8:1908156-1908649	MCF10A-Er-Src	breast:	n/a	n/a
17	FOS	chr8:1908169-1908531	MCF10A-Er-Src	breast:	n/a	n/a
18	FOS	chr8:1908198-1908414	MCF10A-Er-Src	breast:	n/a	n/a
19	FOXA1	chr8:1911369-1911679	T-47D	breast:	n/a	chr8:1911533-1911545
20	FOXP2	chr8:1908102-1908635	PFSK-1	brain:	n/a	n/a
21	FOXP2	chr8:1914179-1914796	PFSK-1	brain:	n/a	n/a
22	HA-E2F1	chr8:1911444-1912022	MCF-7	breast:	n/a	n/a
23	HDAC2	chr8:1911438-1911872	MCF-7	breast:	n/a	n/a
24	KAP1	chr8:1908756-1909170	U2OS	brain:	n/a	n/a
25	MAFF	chr8:1908335-1908488	HepG2	liver:	n/a	chr8:1908378-1908396
26	MAFK	chr8:1908243-1908443	H1-hESC	embryonic stem cell:	n/a	chr8:1908379-1908394
27	MAFK	chr8:1908330-1908512	HepG2	liver:	n/a	chr8:1908379-1908394
28	MAFK	chr8:1909943-1910174	HepG2	liver:	n/a	chr8:1910043-1910052 chr8:1910042-1910056 chr8:1910041-1910057
29	MAFK	chr8:1908905-1909289	IMR90	lung:	n/a	n/a
30	MAFK	chr8:1909943-1910174	H1-hESC	embryonic stem cell:	n/a	chr8:1910043-1910052 chr8:1910042-1910056 chr8:1910041-1910057
31	MAFK	chr8:1909927-1910160	HepG2	liver:	n/a	chr8:1910043-1910052 chr8:1910042-1910056 chr8:1910041-1910057
32	MAX	chr8:1911120-1911538	NB4	blood:	n/a	chr8:1911380-1911389 chr8:1911379-1911390 chr8:1911381-1911388 chr8:1911379-1911390 chr8:1911380-1911390 chr8:1911380-1911389
33	MAX	chr8:1916001-1916806	A549	lung:	n/a	n/a
34	MAX	chr8:1913318-1913345	NB4	blood:	n/a	n/a
35	MAX	chr8:1911207-1911669	MCF-7	breast:	n/a	chr8:1911380-1911389 chr8:1911379-1911390 chr8:1911381-1911388 chr8:1911379-1911390 chr8:1911380-1911390 chr8:1911380-1911389
36	MYC	chr8:1908242-1908491	MCF10A-Er-Src	breast:	n/a	n/a
37	MYC	chr8:1908202-1908402	MCF10A-Er-Src	breast:	n/a	n/a
38	MYC	chr8:1911123-1911250	MCF-7	breast:	n/a	n/a
39	MYC	chr8:1911255-1911268	MCF-7	breast:	n/a	n/a
40	MYC	chr8:1911102-1911515	MCF-7	breast:	n/a	chr8:1911380-1911389 chr8:1911379-1911390 chr8:1911381-1911388 chr8:1911379-1911390 chr8:1911380-1911390 chr8:1911380-1911389
41	MYC	chr8:1911197-1911458	MCF-7	breast:	n/a	chr8:1911380-1911389 chr8:1911379-1911390 chr8:1911381-1911388 chr8:1911379-1911390 chr8:1911380-1911390 chr8:1911380-1911389
42	MYC	chr8:1911253-1911452	NB4	blood:	n/a	chr8:1911380-1911389 chr8:1911379-1911390 chr8:1911381-1911388 chr8:1911379-1911390 chr8:1911380-1911390 chr8:1911380-1911389
43	NRF1	chr8:1912737-1912817	H1-hESC	embryonic stem cell:	n/a	n/a
44	POLR2A	chr8:1907775-1908468	HL-60	blood:	n/a	n/a
45	POLR2A	chr8:1909164-1909329	H1-hESC	embryonic stem cell:	n/a	n/a
46	POLR2A	chr8:1908155-1908461	H1-hESC	embryonic stem cell:	n/a	n/a
47	POLR2A	chr8:1907590-1908058	H1-hESC	embryonic stem cell:	n/a	n/a
48	POLR2A	chr8:1908684-1908703	H1-hESC	embryonic stem cell:	n/a	n/a
49	POLR2A	chr8:1911105-1911326	MCF-7	breast:	n/a	n/a
50	POLR2A	chr8:1908337-1908338	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:1910300-1910350	HEK293	kidney:	embryo
2	chr8:1910300-1910350	HEK293	kidney:	embryo
3	chr8:1913424-1913474	Caco-2	colon:	n/a
4	chr8:1913424-1913474	GM12892	blood:	n/a
5	chr8:1913086-1913136	SAEC	small airway:	n/a
6	chr8:1910300-1910350	MCF-7	breast:	n/a
7	chr8:1911588-1911638	GM12891	blood:	n/a
8	chr8:1913217-1913267	HRCEpiC	kidney:	n/a
9	chr8:1910300-1910350	SKMC	muscle:	n/a
10	chr8:1913086-1913136	U87	brain:	n/a
11	chr8:1913132-1913182	ovcar-3	ovarian:	n/a
12	chr8:1911588-1911638	BJ	skin:	n/a
13	chr8:1911588-1911638	NT2-D1	testis:	n/a
14	chr8:1913086-1913136	HepG2	liver:	n/a
15	chr8:1913217-1913267	HCT-116	colon:	n/a
16	chr8:1910300-1910350	SK-N-MC	brain:	n/a
17	chr8:1913217-1913267	A549	lung:	n/a
18	chr8:1914991-1915041	HNPCEpiC	eye:	n/a
19	chr8:1911588-1911638	H1-hESC	embryonic stem cell:	embryo
20	chr8:1914991-1915041	LNCaP	prostate:	n/a
21	chr8:1915004-1915054	BE2_C	brain:	n/a
22	chr8:1913424-1913474	SK-N-MC	brain:	n/a
23	chr8:1910300-1910350	LNCaP	prostate:	n/a
24	chr8:1913132-1913182	GM12892	blood:	n/a
25	chr8:1913217-1913267	Caco-2	colon:	n/a
26	chr8:1913132-1913182	MCF10A-Er-Src	breast:	n/a
27	chr8:1914262-1914312	BE2_C	brain:	n/a
28	chr8:1915004-1915054	Hela-S3	cervix:	n/a
29	chr8:1913086-1913136	A549	lung:	n/a
30	chr8:1908301-1908351	IMR90	lung:	fetal
31	chr8:1913217-1913267	U87	brain:	n/a
32	chr8:1913132-1913182	SAEC	small airway:	n/a
33	chr8:1914991-1915041	HCM	heart:	n/a
34	chr8:1915004-1915054	MCF10A-Er-Src	breast:	n/a
35	chr8:1915076-1915126	NH-A	brain:	n/a
36	chr8:1915004-1915054	HMEC	breast:	n/a
37	chr8:1914262-1914312	HepG2	liver:	n/a
38	chr8:1915076-1915126	HRPEpiC	eye:	n/a
39	chr8:1913269-1913319	H1-hESC	embryonic stem cell:	embryo
40	chr8:1914991-1915041	NHDF-neo	bronchial:	n/a
41	chr8:1913132-1913182	AG09319	gingival:	n/a
42	chr8:1915076-1915126	Caco-2	colon:	n/a
43	chr8:1908301-1908351	HEEpiC	esophagus:	n/a
44	chr8:1915004-1915054	HL-60	blood:	n/a
45	chr8:1914262-1914312	HCF	heart:	n/a
46	chr8:1914262-1914312	Caco-2	colon:	n/a
47	chr8:1910190-1910240	SK-N-SH_RA	brain:	n/a
48	chr8:1915004-1915054	ECC-1	luminal epithelium:	n/a
49	chr8:1913132-1913182	AG10803	skin:	n/a
50	chr8:1910190-1910240	HCT-116	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:1905928..1907788-chr8:1909949..1911807,2	MCF-7	breast:
2	chr8:1904438..1906943-chr8:1908364..1910920,2	K562	blood:
3	chr8:1911383..1914358-chr8:1918883..1921800,2	MCF-7	breast:
4	chr8:1907491..1909196-chr8:1911477..1913920,2	K562	blood:
5	chr8:1907491..1909196-chr8:1911477..1913920,2	K562	blood:
6	chr8:1902551..1904412-chr8:1906073..1908055,2	K562	blood:
7	chr8:1906659..1908488-chr8:1948019..1949630,2	MCF-7	breast:
8	chr8:1877543..1880354-chr8:1915068..1917833,2	K562	blood:
9	chr8:1910618..1913298-chr8:1921170..1922936,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CSMD1-18	chr8:1906704-1908609	l_3533_chr8:1906703-1909044_brain
2	lnc-CSMD1-18	chr8:1908721-1909149	l_3533_chr8:1906703-1909044_brain

Variant related genes	Relation type
KBTBD11-OT1	TF binding region
KBTBD11-OT1	CpG island
ENSG00000176595	chromatin interactions
ENSG00000253696	chromatin interactions
ENSG00000253764	chromatin interactions

Extended variants
information (count: 484 )
Associated
traits (count: 115 )

Variant overlapped rSNPs/rCNVs (count:484 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6981540	chr8:1907855-1907856	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs538171565	chr8:1907856-1907857	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
3	rs137951165	chr8:1907869-1907870	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
4	rs377765598	chr8:1907873-1907874	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
5	rs545297896	chr8:1907904-1907905	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
6	rs193261491	chr8:1907931-1907932	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
7	rs7006457	chr8:1907935-1907936	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs541098890	chr8:1907956-1907957	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
9	rs560866251	chr8:1907962-1907963	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
10	rs13272508	chr8:1907973-1907974	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs373301177	chr8:1907982-1907983	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
12	rs116613510	chr8:1908006-1908007	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
13	rs569635064	chr8:1908015-1908016	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
14	rs76146413	chr8:1908030-1908031	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
15	rs539116697	chr8:1908051-1908052	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
16	rs13281187	chr8:1908052-1908053	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs565862437	chr8:1908071-1908072	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
18	rs572892956	chr8:1908084-1908085	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
19	rs375494818	chr8:1908138-1908139	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
20	rs547862168	chr8:1908174-1908175	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
21	rs138962288	chr8:1908184-1908185	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
22	rs536755832	chr8:1908221-1908222	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
23	rs76266622	chr8:1908228-1908229	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
24	rs114112935	chr8:1908231-1908232	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
25	rs142187625	chr8:1908242-1908243	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
26	rs558850184	chr8:1908301-1908302	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
27	rs528731317	chr8:1908302-1908303	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
28	rs572302467	chr8:1908305-1908306	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
29	rs541303203	chr8:1908330-1908331	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
30	rs561539510	chr8:1908345-1908346	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
31	rs146209374	chr8:1908385-1908386	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
32	rs575575490	chr8:1908390-1908391	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
33	rs386720726	chr8:1908391-1908392	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
34	rs115009195	chr8:1908393-1908394	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
35	rs78666178	chr8:1908408-1908409	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
36	rs377018652	chr8:1908416-1908417	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
37	rs552500221	chr8:1908447-1908448	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
38	rs559728284	chr8:1908453-1908454	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
39	rs528398457	chr8:1908460-1908461	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
40	rs548035081	chr8:1908475-1908476	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
41	rs13271878	chr8:1908476-1908477	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs372960273	chr8:1908484-1908485	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
43	rs566473661	chr8:1908502-1908503	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
44	rs139167459	chr8:1908503-1908504	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
45	rs535520303	chr8:1908508-1908509	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
46	rs74532697	chr8:1908511-1908512	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
47	rs202044478	chr8:1908575-1908576	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
48	rs60098078	chr8:1908592-1908593	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs141690483	chr8:1908616-1908617	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs558814704	chr8:1908635-1908636	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:115)

Disease	PMID	Source
Ovarian cancer	21720365	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Congenital diaphragmatic hernia	21341218	CNVD
Cancer	18840272	CNVD
Pilocytic astrocytoma	18622384	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	16573809	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
abnormal development	18461090	CNVD
Crohn''s disease	19220326	CNVD
Psoriasis	19220326	CNVD
Prostate cancer	21965145	CNVD
Prostate cancer	18515986	CNVD
Chronic obstructive pulmonary disease	20378733	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17603634	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Ovarian cancer	20844748	CNVD
Cervical cancer	17311676	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Schizophrenia	20877625	CNVD
Disorders of sex development	21048976	CNVD
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	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
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	20729466	CNVD
Ductal carcinoma	22052326	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Epilepsy	22083797	CNVD
Acute myeloid leukemia	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Breast cancer	20932292	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Ependymoma	20639864	CNVD
Ovarian cancer	22355333	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:266 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:1845400-1908000	Weak transcription	Right Atrium	heart
2	chr8:1889400-1910000	Weak transcription	HUVEC	blood vessel
3	chr8:1890000-1911000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr8:1898400-1908600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr8:1900200-1909000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr8:1903600-1908200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr8:1903600-1908400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr8:1903600-1909400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr8:1904000-1908000	Weak transcription	NHEK	skin
10	chr8:1904400-1908000	Strong transcription	Dnd41	blood
11	chr8:1905000-1909600	Enhancers	Liver	Liver
12	chr8:1905200-1908800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr8:1905400-1909000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
14	chr8:1905600-1908000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr8:1905600-1908400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr8:1905600-1910800	Weak transcription	Gastric	stomach
17	chr8:1905600-1921000	Weak transcription	Aorta	Aorta
18	chr8:1905800-1908200	Weak transcription	H1 Cell Line	embryonic stem cell
19	chr8:1905800-1916800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
20	chr8:1906000-1911200	Weak transcription	HMEC	breast
21	chr8:1906000-1914200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr8:1906400-1908000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr8:1906400-1908400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr8:1906400-1909200	Weak transcription	Thymus	Thymus
25	chr8:1906400-1910600	Weak transcription	Lung	lung
26	chr8:1906400-1911200	Weak transcription	Psoas Muscle	Psoas
27	chr8:1906400-1911400	Weak transcription	Placenta Amnion	Placenta Amnion
28	chr8:1906600-1908000	Weak transcription	NH-A	brain
29	chr8:1906600-1908200	Weak transcription	A549	lung
30	chr8:1906600-1908400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr8:1906600-1908400	Weak transcription	Rectal Mucosa Donor 31	rectum
32	chr8:1906600-1908600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
33	chr8:1906600-1908800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
34	chr8:1906600-1910400	Weak transcription	HUES64 Cell Line	embryonic stem cell
35	chr8:1906600-1910800	Weak transcription	Brain Angular Gyrus	brain
36	chr8:1906600-1911000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr8:1906600-1911200	Weak transcription	H9 Cell Line	embryonic stem cell
38	chr8:1906600-1911200	Weak transcription	Brain Germinal Matrix	brain
39	chr8:1906600-1911400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr8:1906600-1914200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr8:1906600-1914200	Weak transcription	Colonic Mucosa	Colon
42	chr8:1906600-1914600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr8:1906600-1921000	Weak transcription	Right Ventricle	heart
44	chr8:1906800-1908200	Weak transcription	Muscle Satellite Cultured Cells	--
45	chr8:1906800-1908400	Weak transcription	Fetal Heart	heart
46	chr8:1906800-1908400	Strong transcription	Stomach Smooth Muscle	stomach
47	chr8:1906800-1908800	Weak transcription	HUES48 Cell Line	embryonic stem cell
48	chr8:1906800-1910200	Weak transcription	HUES6 Cell Line	embryonic stem cell
49	chr8:1906800-1910600	Weak transcription	Brain Anterior Caudate	brain
50	chr8:1906800-1910600	Weak transcription	Brain Hippocampus Middle	brain

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