Variant report

Variant	nsv609526
Chromosome Location	chr8:1595450-1640790
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	chr8:1612841-1613066	K562	blood:	n/a	n/a
2	ATF1	chr8:1631106-1631363	K562	blood:	n/a	n/a
3	ATF2	chr8:1606188-1606635	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF3	chr8:1631111-1631356	K562	blood:	n/a	n/a
5	BACH1	chr8:1600054-1600554	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL3	chr8:1613411-1613643	GM12878	blood:	n/a	chr8:1613634-1613643
7	BHLHE40	chr8:1610754-1610850	GM12878	blood:	n/a	n/a
8	BHLHE40	chr8:1598474-1598541	GM12878	blood:	n/a	n/a
9	CEBPB	chr8:1598267-1598411	HepG2	liver:	n/a	chr8:1598339-1598350 chr8:1598339-1598348
10	CEBPB	chr8:1600968-1601172	MCF-7	breast:	n/a	chr8:1601081-1601090 chr8:1601081-1601090 chr8:1601081-1601090 chr8:1601079-1601092 chr8:1601079-1601090 chr8:1601080-1601091 chr8:1601081-1601090
11	CEBPB	chr8:1631054-1631361	K562	blood:	n/a	chr8:1631220-1631231
12	CEBPB	chr8:1628099-1628437	HepG2	liver:	n/a	chr8:1628260-1628269 chr8:1628260-1628269 chr8:1628260-1628271 chr8:1628258-1628269 chr8:1628260-1628269 chr8:1628260-1628269
13	CEBPB	chr8:1628133-1628450	K562	blood:	n/a	chr8:1628260-1628269 chr8:1628260-1628269 chr8:1628260-1628271 chr8:1628258-1628269 chr8:1628260-1628269 chr8:1628260-1628269
14	CEBPB	chr8:1631078-1631329	K562	blood:	n/a	chr8:1631220-1631231
15	CEBPB	chr8:1628117-1628387	Hela-S3	cervix:	n/a	chr8:1628260-1628269 chr8:1628260-1628269 chr8:1628260-1628271 chr8:1628258-1628269 chr8:1628260-1628269 chr8:1628260-1628269
16	CEBPB	chr8:1600966-1601219	HepG2	liver:	n/a	chr8:1601081-1601090 chr8:1601081-1601090 chr8:1601081-1601090 chr8:1601079-1601092 chr8:1601079-1601090 chr8:1601080-1601091 chr8:1601081-1601090
17	CEBPB	chr8:1631129-1631386	IMR90	lung:	n/a	chr8:1631220-1631231
18	CEBPB	chr8:1630919-1631593	HCT-116	colon:	n/a	chr8:1631220-1631231
19	CEBPB	chr8:1631051-1631490	K562	blood:	n/a	chr8:1631220-1631231
20	CEBPB	chr8:1601039-1601179	IMR90	lung:	n/a	chr8:1601081-1601090 chr8:1601081-1601090 chr8:1601081-1601090 chr8:1601079-1601092 chr8:1601079-1601090 chr8:1601080-1601091 chr8:1601081-1601090
21	CEBPB	chr8:1628110-1628439	IMR90	lung:	n/a	chr8:1628260-1628269 chr8:1628260-1628269 chr8:1628260-1628271 chr8:1628258-1628269 chr8:1628260-1628269 chr8:1628260-1628269
22	CEBPB	chr8:1631113-1631408	A549	lung:	n/a	chr8:1631220-1631231
23	CEBPB	chr8:1631046-1631432	Hela-S3	cervix:	n/a	chr8:1631220-1631231
24	CEBPB	chr8:1628240-1628361	H1-hESC	embryonic stem cell:	n/a	chr8:1628260-1628269 chr8:1628260-1628269 chr8:1628260-1628271 chr8:1628258-1628269 chr8:1628260-1628269 chr8:1628260-1628269
25	CEBPB	chr8:1631004-1631475	HCT-116	colon:	n/a	chr8:1631220-1631231
26	CEBPB	chr8:1601046-1601180	K562	blood:	n/a	chr8:1601081-1601090 chr8:1601081-1601090 chr8:1601081-1601090 chr8:1601079-1601092 chr8:1601079-1601090 chr8:1601080-1601091 chr8:1601081-1601090
27	CEBPB	chr8:1631047-1631403	HepG2	liver:	n/a	chr8:1631220-1631231
28	CEBPB	chr8:1628160-1628398	A549	lung:	n/a	chr8:1628260-1628269 chr8:1628260-1628269 chr8:1628260-1628271 chr8:1628258-1628269 chr8:1628260-1628269 chr8:1628260-1628269
29	CHD2	chr8:1606162-1606617	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr8:1628751-1628810	MCF-7	breast:	n/a	n/a
31	CTCF	chr8:1595780-1595930	HepG2	liver:	n/a	n/a
32	CTCF	chr8:1614240-1614390	GM12872	blood:	n/a	n/a
33	CTCF	chr8:1616615-1616757	HepG2	liver:	n/a	n/a
34	CTCF	chr8:1611313-1611348	GM19239	blood:	n/a	n/a
35	CTCF	chr8:1616699-1616794	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr8:1610925-1611115	GM19239	blood:	n/a	n/a
37	CTCF	chr8:1609079-1609141	Pancreas_OC	pancreas:	n/a	n/a
38	CTCF	chr8:1624240-1624390	GM12865	blood:	n/a	n/a
39	CTCF	chr8:1616699-1616780	MCF-7	breast:	n/a	n/a
40	CTCF	chr8:1595860-1596010	A549	lung:	n/a	n/a
41	CTCF	chr8:1595864-1595915	MCF-7	breast:	n/a	n/a
42	CTCF	chr8:1616651-1616818	MCF-7	breast:	n/a	n/a
43	CTCF	chr8:1607807-1607898	Lung_OC	lung:	n/a	n/a
44	CTCF	chr8:1627606-1627668	GM13977	blood:	n/a	n/a
45	CTCF	chr8:1627660-1627810	K562	blood:	n/a	n/a
46	CUX1	chr8:1630984-1631321	K562	blood:	n/a	n/a
47	E2F6	chr8:1630296-1630411	K562	blood:	n/a	n/a
48	E2F6	chr8:1639851-1639984	K562	blood:	n/a	chr8:1639930-1639942
49	EP300	chr8:1628247-1628270	HepG2	liver:	n/a	n/a
50	EP300	chr8:1606113-1606596	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:1614107-1614157	BE2_C	brain:	n/a
2	chr8:1616381-1616431	ECC-1	luminal epithelium:	n/a
3	chr8:1639573-1639623	GM06990	blood:	n/a
4	chr8:1623303-1623353	H1-hESC	embryonic stem cell:	embryo
5	chr8:1623378-1623428	RPTEC	kidney:	n/a
6	chr8:1626419-1626469	HL-60	blood:	n/a
7	chr8:1639563-1639613	Hepatocyte	liver:	n/a
8	chr8:1614107-1614157	BE2_C	brain:	n/a
9	chr8:1616381-1616431	ECC-1	luminal epithelium:	n/a
10	chr8:1639573-1639623	GM06990	blood:	n/a
11	chr8:1623303-1623353	H1-hESC	embryonic stem cell:	embryo
12	chr8:1623378-1623428	RPTEC	kidney:	n/a
13	chr8:1626419-1626469	HL-60	blood:	n/a
14	chr8:1639563-1639613	Hepatocyte	liver:	n/a
15	chr8:1616209-1616259	AG09309	skin:	n/a
16	chr8:1614182-1614232	Hepatocyte	liver:	n/a
17	chr8:1601314-1601364	IMR90	lung:	fetal
18	chr8:1617756-1617806	HRPEpiC	eye:	n/a
19	chr8:1624741-1624791	SK-N-SH	brain:	n/a
20	chr8:1616767-1616817	PANC-1	pancreas:	n/a
21	chr8:1605546-1605596	GM06990	blood:	n/a
22	chr8:1639909-1639959	HEK293	kidney:	embryo
23	chr8:1616622-1616672	AG09319	gingival:	n/a
24	chr8:1617616-1617666	HEK293	kidney:	embryo
25	chr8:1617868-1617918	HMEC	breast:	n/a
26	chr8:1616111-1616161	H1-hESC	embryonic stem cell:	embryo
27	chr8:1626697-1626747	HNPCEpiC	eye:	n/a
28	chr8:1640712-1640762	SAEC	small airway:	n/a
29	chr8:1639563-1639613	PANC-1	pancreas:	n/a
30	chr8:1623483-1623533	HPAEpiC	pulmonary alveolar:	n/a
31	chr8:1613877-1613927	Hela-S3	cervix:	n/a
32	chr8:1614053-1614103	RPTEC	kidney:	n/a
33	chr8:1623378-1623428	A549	lung:	n/a
34	chr8:1623483-1623533	GM12892	blood:	n/a
35	chr8:1626419-1626469	MCF10A-Er-Src	breast:	n/a
36	chr8:1626697-1626747	AG10803	skin:	n/a
37	chr8:1626419-1626469	GM12892	blood:	n/a
38	chr8:1617756-1617806	AG10803	skin:	n/a
39	chr8:1639563-1639613	BE2_C	brain:	n/a
40	chr8:1638304-1638354	GM12892	blood:	n/a
41	chr8:1624822-1624872	AG04449	skin:	fetal
42	chr8:1639909-1639959	H1-hESC	embryonic stem cell:	embryo
43	chr8:1615080-1615130	BJ	skin:	n/a
44	chr8:1623483-1623533	HRPEpiC	eye:	n/a
45	chr8:1626419-1626469	LNCaP	prostate:	n/a
46	chr8:1615080-1615130	NB4	blood:	n/a
47	chr8:1617616-1617666	Caco-2	colon:	n/a
48	chr8:1626419-1626469	IMR90	lung:	fetal
49	chr8:1615080-1615130	HL-60	blood:	n/a
50	chr8:1618448-1618498	HepG2	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:1584132..1586956-chr8:1595846..1598280,3	K562	blood:
2	chr8:1578132..1580473-chr8:1601540..1604510,2	K562	blood:
3	chr8:1627163..1629357-chr8:1633786..1636690,2	K562	blood:
4	chr8:1599745..1602131-chr8:1603017..1606467,3	K562	blood:
5	chr8:1615891..1617815-chr8:1624787..1626742,2	K562	blood:
6	chr8:1627163..1629357-chr8:1633786..1636690,2	K562	blood:
7	chr8:1593850..1596302-chr8:1622198..1625044,2	K562	blood:
8	chr8:1639712..1642185-chr8:1645555..1647369,2	K562	blood:
9	chr8:1599745..1602131-chr8:1603017..1606467,3	K562	blood:
10	chr8:1621344..1623146-chr8:1688699..1690451,2	K562	blood:

Variant related genes	Relation type
DLGAP2	TF binding region
DLGAP2	CpG island
ENSG00000198010	chromatin interactions

Extended variants
information (count: 2766 )
Associated
traits (count: 116 )

Variant overlapped rSNPs/rCNVs (count:2766 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4876115	chr8:1595450-1595451	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs191323514	chr8:1595480-1595481	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs4445252	chr8:1595484-1595485	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs573202703	chr8:1595492-1595493	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs183159720	chr8:1595515-1595516	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs555103021	chr8:1595529-1595530	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs373439899	chr8:1595547-1595548	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs188384047	chr8:1595585-1595586	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs144919506	chr8:1595603-1595604	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs557851848	chr8:1595610-1595611	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs141297711	chr8:1595611-1595612	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs567451595	chr8:1595677-1595678	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs540434387	chr8:1595738-1595739	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs145255771	chr8:1595754-1595755	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs529241745	chr8:1595758-1595759	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs147621696	chr8:1595767-1595768	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs141631548	chr8:1595772-1595773	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs575796890	chr8:1595781-1595782	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs550665651	chr8:1595785-1595786	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs182995785	chr8:1595796-1595797	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs570621167	chr8:1595813-1595814	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs5029058	chr8:1595822-1595823	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs188071123	chr8:1595864-1595865	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs546837241	chr8:1595893-1595894	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs566708497	chr8:1595894-1595895	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs6558503	chr8:1595901-1595902	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs556048610	chr8:1595940-1595941	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs2472091	chr8:1595962-1595963	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs2469678	chr8:1595964-1595965	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs569417286	chr8:1595968-1595969	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs2469679	chr8:1596015-1596016	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs192440751	chr8:1596016-1596017	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs2472092	chr8:1596024-1596025	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs557425101	chr8:1596040-1596041	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs577861897	chr8:1596054-1596055	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs117226074	chr8:1596066-1596067	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs533665468	chr8:1596080-1596081	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs6558504	chr8:1596082-1596083	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs542427541	chr8:1596089-1596090	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs371681341	chr8:1596092-1596093	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs562815729	chr8:1596095-1596096	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs548841387	chr8:1596097-1596098	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs183911679	chr8:1596116-1596117	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs142516019	chr8:1596147-1596148	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs544597037	chr8:1596151-1596152	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs189330757	chr8:1596154-1596155	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs564137065	chr8:1596171-1596172	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs533290925	chr8:1596174-1596175	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs546668079	chr8:1596179-1596180	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs192754499	chr8:1596183-1596184	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:116)

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
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:292 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:1575200-1599400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr8:1595800-1596800	Enhancers	Gastric	stomach
3	chr8:1596000-1596200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr8:1596800-1598000	Weak transcription	Gastric	stomach
5	chr8:1599400-1599600	Bivalent Enhancer	Brain Substantia Nigra	brain
6	chr8:1599400-1600000	Enhancers	H9 Cell Line	embryonic stem cell
7	chr8:1599400-1600200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr8:1599400-1601200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr8:1599600-1599800	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
10	chr8:1599600-1600400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr8:1599600-1600600	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
12	chr8:1599600-1601000	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr8:1599600-1601600	Enhancers	H1 Cell Line	embryonic stem cell
14	chr8:1599800-1600000	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
15	chr8:1599800-1600400	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr8:1599800-1600800	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr8:1599800-1601200	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr8:1600000-1601000	Weak transcription	H9 Cell Line	embryonic stem cell
19	chr8:1600000-1601200	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
20	chr8:1600200-1600400	Enhancers	Fetal Kidney	kidney
21	chr8:1600200-1600800	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr8:1600200-1601200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr8:1600400-1601000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
24	chr8:1600400-1601000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
25	chr8:1600400-1601000	Bivalent Enhancer	Fetal Kidney	kidney
26	chr8:1600400-1604800	Weak transcription	HUES48 Cell Line	embryonic stem cell
27	chr8:1600800-1604800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
28	chr8:1600800-1605000	Weak transcription	HUES64 Cell Line	embryonic stem cell
29	chr8:1601000-1601200	Enhancers	H9 Cell Line	embryonic stem cell
30	chr8:1601000-1603400	Weak transcription	Gastric	stomach
31	chr8:1601000-1604800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
32	chr8:1601200-1601800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr8:1601200-1604600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr8:1601800-1605600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr8:1602000-1604800	Weak transcription	H1 Cell Line	embryonic stem cell
36	chr8:1604000-1604200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr8:1604000-1604200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr8:1604000-1604200	Enhancers	Gastric	stomach
39	chr8:1604600-1605400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
40	chr8:1604800-1605000	Enhancers	iPS-20b Cell Line	embryonic stem cell
41	chr8:1604800-1605000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr8:1604800-1605800	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr8:1604800-1605800	Enhancers	HUES48 Cell Line	embryonic stem cell
44	chr8:1604800-1605800	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr8:1604800-1605800	Enhancers	iPS-15b Cell Line	embryonic stem cell
46	chr8:1604800-1605800	Enhancers	iPS-18 Cell Line	embryonic stem cell
47	chr8:1604800-1607600	Enhancers	H1 Cell Line	embryonic stem cell
48	chr8:1605000-1605800	Enhancers	HUES64 Cell Line	embryonic stem cell
49	chr8:1605800-1606000	Weak transcription	HUES6 Cell Line	embryonic stem cell
50	chr8:1605800-1606000	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell

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