Variant report

Variant	nsv889741
Chromosome Location	chr8:1916347-1955283
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:716)
CpG islands
(count:2443)
Chromatin interactive
region (count:17)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:716 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr8:1949444-1949648	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr8:1921474-1922031	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr8:1949877-1951075	H1-hESC	embryonic stem cell:	n/a	n/a
4	CCNT2	chr8:1921657-1922031	K562	blood:	n/a	n/a
5	CEBPB	chr8:1942047-1942403	A549	lung:	n/a	chr8:1942226-1942239 chr8:1942226-1942237 chr8:1942226-1942239
6	CEBPB	chr8:1917852-1918103	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr8:1942047-1942399	HepG2	liver:	n/a	chr8:1942226-1942239 chr8:1942226-1942237 chr8:1942226-1942239
8	CEBPB	chr8:1942036-1942796	IMR90	lung:	n/a	chr8:1942226-1942239 chr8:1942226-1942237 chr8:1942226-1942239
9	CEBPB	chr8:1942103-1942376	H1-hESC	embryonic stem cell:	n/a	chr8:1942226-1942239 chr8:1942226-1942237 chr8:1942226-1942239
10	CEBPB	chr8:1917911-1918068	A549	lung:	n/a	n/a
11	CEBPB	chr8:1942182-1942295	Hela-S3	cervix:	n/a	chr8:1942226-1942239 chr8:1942226-1942237 chr8:1942226-1942239
12	CEBPB	chr8:1931727-1931927	HepG2	liver:	n/a	n/a
13	CEBPB	chr8:1942051-1942407	K562	blood:	n/a	chr8:1942226-1942239 chr8:1942226-1942237 chr8:1942226-1942239
14	CEBPB	chr8:1917870-1918070	K562	blood:	n/a	n/a
15	CEBPB	chr8:1941969-1942515	A549	lung:	n/a	chr8:1942226-1942239 chr8:1942226-1942237 chr8:1942226-1942239
16	CEBPB	chr8:1927713-1927808	HepG2	liver:	n/a	chr8:1927745-1927756
17	CHD1	chr8:1950968-1950973	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD2	chr8:1949818-1950108	H1-hESC	embryonic stem cell:	n/a	n/a
19	CREB1	chr8:1949613-1950373	A549	lung:	n/a	n/a
20	CTBP2	chr8:1949754-1951026	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr8:1948600-1948750	HBMEC	blood vessel:	n/a	chr8:1948693-1948711
22	CTCF	chr8:1921200-1921350	BJ	skin:	n/a	chr8:1921313-1921322
23	CTCF	chr8:1926240-1926390	NB4	blood:	n/a	n/a
24	CTCF	chr8:1942380-1942530	AG04449	skin:	n/a	n/a
25	CTCF	chr8:1926221-1926440	Hela-S3	cervix:	n/a	n/a
26	CTCF	chr8:1926160-1926310	A549	lung:	n/a	n/a
27	CTCF	chr8:1948500-1948650	BE2_C	brain:	n/a	n/a
28	CTCF	chr8:1926020-1926310	NHEK	skin:	n/a	n/a
29	CTCF	chr8:1949517-1949543	LNCaP	prostate:	n/a	n/a
30	CTCF	chr8:1948600-1948750	SK-N-SH_RA	brain:	n/a	chr8:1948693-1948711
31	CTCF	chr8:1948540-1948690	HPF	lung:	n/a	n/a
32	CTCF	chr8:1949420-1949570	HEK293	kidney:	n/a	n/a
33	CTCF	chr8:1921200-1921350	HPAF	blood vessel:	n/a	chr8:1921313-1921322
34	CTCF	chr8:1942340-1942490	HRPEpiC	eye:	n/a	n/a
35	CTCF	chr8:1948653-1948666	Gliobla	brain:	n/a	n/a
36	CTCF	chr8:1948660-1948810	HRPEpiC	eye:	n/a	chr8:1948693-1948711
37	CTCF	chr8:1926180-1926330	GM12875	blood:	n/a	n/a
38	CTCF	chr8:1926280-1926430	GM12870	blood:	n/a	n/a
39	CTCF	chr8:1926280-1926430	AG09319	gingival:	n/a	n/a
40	CTCF	chr8:1942500-1942650	RPTEC	kidney:	n/a	n/a
41	CTCF	chr8:1926300-1926450	AG04450	lung:	n/a	n/a
42	CTCF	chr8:1949440-1949590	AoAF	blood vessel:	n/a	n/a
43	CTCF	chr8:1924100-1924250	AG04449	skin:	n/a	n/a
44	CTCF	chr8:1950044-1950195	ProgFib	skin:	n/a	n/a
45	CTCF	chr8:1926200-1926350	BE2_C	brain:	n/a	n/a
46	CTCF	chr8:1924060-1924210	WERI-Rb-1	eye:	n/a	chr8:1924088-1924096
47	CTCF	chr8:1926260-1926410	HPAF	blood vessel:	n/a	n/a
48	CTCF	chr8:1924040-1924190	AG09319	gingival:	n/a	chr8:1924088-1924096
49	CTCF	chr8:1950837-1951115	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr8:1949820-1949970	SK-N-SH_RA	brain:	n/a	n/a

(count:2443 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:1922165-1922215	AG09309	skin:	n/a
2	chr8:1921369-1921419	GM12892	blood:	n/a
3	chr8:1942462-1942512	MCF-7	breast:	n/a
4	chr8:1922165-1922215	AG09309	skin:	n/a
5	chr8:1921369-1921419	GM12892	blood:	n/a
6	chr8:1942462-1942512	MCF-7	breast:	n/a
7	chr8:1923052-1923102	GM12878	blood:	n/a
8	chr8:1933522-1933572	CMK	blood:	n/a
9	chr8:1955069-1955119	GM12878	blood:	n/a
10	chr8:1955196-1955246	A549	lung:	n/a
11	chr8:1949329-1949379	Caco-2	colon:	n/a
12	chr8:1950120-1950170	HL-60	blood:	n/a
13	chr8:1950120-1950170	HUVEC	blood vessel:	n/a
14	chr8:1937676-1937726	BJ	skin:	n/a
15	chr8:1940523-1940573	HCM	heart:	n/a
16	chr8:1921740-1921790	SK-N-SH	brain:	n/a
17	chr8:1948999-1949049	MCF10A-Er-Src	breast:	n/a
18	chr8:1923115-1923165	GM19239	blood:	n/a
19	chr8:1949342-1949392	SK-N-SH_RA	brain:	n/a
20	chr8:1955117-1955167	HepG2	liver:	n/a
21	chr8:1955196-1955246	U87	brain:	n/a
22	chr8:1938530-1938580	BJ	skin:	n/a
23	chr8:1955196-1955246	Hela-S3	cervix:	n/a
24	chr8:1949342-1949392	LNCaP	prostate:	n/a
25	chr8:1933522-1933572	SAEC	small airway:	n/a
26	chr8:1922165-1922215	HCT-116	colon:	n/a
27	chr8:1954777-1954827	AG09309	skin:	n/a
28	chr8:1942462-1942512	HIPEpiC	eye:	n/a
29	chr8:1935720-1935770	HCPEpiC	choroid plexus:	n/a
30	chr8:1955069-1955119	HRE	kidney:	n/a
31	chr8:1948999-1949049	HAEpiC	amniotic membrane:	n/a
32	chr8:1949342-1949392	NB4	blood:	n/a
33	chr8:1935720-1935770	HNPCEpiC	eye:	n/a
34	chr8:1922372-1922422	NH-A	brain:	n/a
35	chr8:1950112-1950162	AoSMC	blood vessel:	n/a
36	chr8:1924394-1924444	BJ	skin:	n/a
37	chr8:1951383-1951433	LNCaP	prostate:	n/a
38	chr8:1921410-1921460	SK-N-MC	brain:	n/a
39	chr8:1921165-1921215	ovcar-3	ovarian:	n/a
40	chr8:1949246-1949296	AG04450	lung:	fetal
41	chr8:1949246-1949296	RPTEC	kidney:	n/a
42	chr8:1935720-1935770	NHBE	bronchial:	n/a
43	chr8:1933651-1933701	SK-N-SH_RA	brain:	n/a
44	chr8:1923115-1923165	SAEC	small airway:	n/a
45	chr8:1922372-1922422	MCF10A-Er-Src	breast:	n/a
46	chr8:1923052-1923102	ProgFib	skin:	n/a
47	chr8:1948874-1948924	HNPCEpiC	eye:	n/a
48	chr8:1921369-1921419	K562	blood:	n/a
49	chr8:1933522-1933572	MCF10A-Er-Src	breast:	n/a
50	chr8:1923115-1923165	SK-N-SH	brain:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:1945649..1948332-chr8:1948376..1949994,2	MCF-7	breast:
2	chr8:1862307..1864338-chr8:1926078..1927839,2	K562	blood:
3	chr8:1947283..1948870-chr8:1955148..1956732,2	MCF-7	breast:
4	chr8:1906659..1908488-chr8:1948019..1949630,2	MCF-7	breast:
5	chr8:1953398..1956111-chr8:1957370..1959528,2	MCF-7	breast:
6	chr8:1877543..1880354-chr8:1915068..1917833,2	K562	blood:
7	chr17:8339151..8339685-chr8:1949081..1949841,2	Hela-S3	cervix:
8	chr8:1920209..1923568-chr8:1948553..1950993,3	MCF-7	breast:
9	chr8:1939104..1942044-chr8:1945221..1947708,2	MCF-7	breast:
10	chr1:8021103..8021603-chr8:1931796..1932353,2	HCT-116	colon:
11	chr8:1947283..1948870-chr8:1955148..1956732,2	MCF-7	breast:
12	chr8:1945649..1948332-chr8:1948376..1949994,2	MCF-7	breast:
13	chr8:1920801..1923588-chr8:1929639..1933248,3	MCF-7	breast:
14	chr8:1939104..1942044-chr8:1945221..1947708,2	MCF-7	breast:
15	chr8:1923575..1926096-chr8:1929371..1931428,2	K562	blood:
16	chr8:1920180..1923138-chr8:1945737..1947399,2	MCF-7	breast:
17	chr8:1923575..1926096-chr8:1929371..1931428,2	K562	blood:

(count:15 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KBTBD11-1	chr8:1919563-1919684	ENSG00000253696.2
2	lnc-KBTBD11-1	chr8:1919296-1920689	NONHSAT124692
3	lnc-KBTBD11-1	chr8:1924065-1924644	ENSG00000253696.2
4	lnc-CSMD1-7	chr8:1921314-1921511	ENSG00000253764.1
5	lnc-CSMD1-7	chr8:1920987-1921202	ENSG00000253764.1
6	lnc-KBTBD11-1	chr8:1924065-1924610	ENSG00000253696.1
7	lnc-KBTBD11-1	chr8:1919427-1919611	NONHSAT124693
8	lnc-KBTBD11-1	chr8:1920091-1920203	ENSG00000253696.2
9	lnc-CSMD1-7	chr8:1921314-1921776	ENSG00000253764.1
10	lnc-CSMD1-7	chr8:1922773-1922803	ENSG00000253764.1
11	lnc-KBTBD11-1	chr8:1919563-1919684	ENSG00000253696.1
12	lnc-KBTBD11-1	chr8:1920091-1920518	NONHSAT124693
13	lnc-KBTBD11-1	chr8:1920091-1920203	ENSG00000253696.1
14	lnc-ARHGEF10-1	chr8:1922984-1923480	ENSG00000270988.1
15	lnc-CSMD1-7	chr8:1920736-1920829	ENSG00000253764.1

No data

Variant related genes	Relation type
KBTBD11-OT1	TF binding region
KBTBD11	TF binding region
ENSG00000270988	TF binding region
ENSG00000253764	TF binding region
KBTBD11-OT1	CpG island
KBTBD11	CpG island
ENSG00000270988	CpG island
ENSG00000253764	CpG island
ENSG00000176595	chromatin interactions
ENSG00000270988	chromatin interactions
ENSG00000253764	chromatin interactions
ENSG00000166579	chromatin interactions

Extended variants
information (count: 2383 )
Associated
traits (count: 117 )

Variant overlapped rSNPs/rCNVs (count:2383 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4876265	chr8:1916347-1916348	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs115434390	chr8:1916357-1916358	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs554587503	chr8:1916384-1916385	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs4876264	chr8:1916421-1916422	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs368725991	chr8:1916426-1916427	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs191373610	chr8:1916429-1916430	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs182652484	chr8:1916455-1916456	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs545935047	chr8:1916467-1916468	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs559300858	chr8:1916496-1916497	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs4876263	chr8:1916499-1916500	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs547513179	chr8:1916583-1916584	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs560943682	chr8:1916596-1916597	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs530079159	chr8:1916601-1916602	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs186137022	chr8:1916649-1916650	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs570284638	chr8:1916657-1916658	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs538983787	chr8:1916676-1916677	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs572013191	chr8:1916691-1916692	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs59318872	chr8:1916703-1916704	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs566174152	chr8:1916773-1916774	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs7001374	chr8:1916777-1916778	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs6988018	chr8:1916778-1916779	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs6983993	chr8:1916808-1916809	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs6988152	chr8:1916837-1916838	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs574475004	chr8:1916850-1916851	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs190463194	chr8:1916874-1916875	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs556684116	chr8:1916881-1916882	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs367553882	chr8:1916959-1916960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs56291843	chr8:1917000-1917001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs56173433	chr8:1917109-1917110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs35229570	chr8:1917142-1917143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs62478189	chr8:1917176-1917177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs139608398	chr8:1917233-1917234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs28406150	chr8:1917234-1917235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs77123957	chr8:1917249-1917250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs200258332	chr8:1917262-1917263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs28574749	chr8:1917263-1917264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs79204916	chr8:1917271-1917272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs34870329	chr8:1917278-1917279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs545814714	chr8:1917291-1917292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs559477647	chr8:1917292-1917293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs572748619	chr8:1917295-1917296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs543246548	chr8:1917300-1917301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs541120381	chr8:1917307-1917308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs576698042	chr8:1917319-1917320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs112456784	chr8:1917320-1917321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs188651475	chr8:1917321-1917322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs201138091	chr8:1917338-1917339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs193228888	chr8:1917365-1917366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs182748007	chr8:1917392-1917393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs71211536	chr8:1917413-1917414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:117)

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
Non-syndromic sensorineural hearing loss	22297974	CNVD

Chromatin state (count:1596 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:1905600-1921000	Weak transcription	Aorta	Aorta
2	chr8:1905800-1916800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr8:1906600-1921000	Weak transcription	Right Ventricle	heart
4	chr8:1909000-1919000	Weak transcription	Fetal Kidney	kidney
5	chr8:1911600-1919200	Weak transcription	Brain Germinal Matrix	brain
6	chr8:1912000-1920600	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr8:1912200-1918800	Weak transcription	Liver	Liver
8	chr8:1912200-1920800	Weak transcription	Brain Hippocampus Middle	brain
9	chr8:1913600-1916600	Enhancers	Fetal Muscle Leg	muscle
10	chr8:1913600-1921200	Weak transcription	Esophagus	oesophagus
11	chr8:1913800-1916600	Enhancers	HSMMtube	muscle
12	chr8:1914400-1916600	Enhancers	Psoas Muscle	Psoas
13	chr8:1914600-1918200	Weak transcription	Small Intestine	intestine
14	chr8:1914600-1921200	Weak transcription	Left Ventricle	heart
15	chr8:1914800-1916400	Enhancers	Fetal Muscle Trunk	muscle
16	chr8:1914800-1916800	Enhancers	HSMM	muscle
17	chr8:1914800-1921000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr8:1914800-1921200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr8:1915200-1916400	Weak transcription	Fetal Brain Female	brain
20	chr8:1915200-1916400	Weak transcription	Right Atrium	heart
21	chr8:1915200-1916600	Enhancers	Fetal Brain Male	brain
22	chr8:1915200-1916800	Enhancers	Muscle Satellite Cultured Cells	--
23	chr8:1915200-1918000	Weak transcription	Colonic Mucosa	Colon
24	chr8:1915200-1918000	Weak transcription	Rectal Mucosa Donor 31	rectum
25	chr8:1915200-1919000	Weak transcription	Fetal Lung	lung
26	chr8:1915200-1919000	Weak transcription	Pancreas	Pancrea
27	chr8:1915200-1919000	Weak transcription	Spleen	Spleen
28	chr8:1915400-1918000	Weak transcription	Duodenum Mucosa	Duodenum
29	chr8:1915800-1916400	Flanking Active TSS	A549	lung
30	chr8:1915800-1916600	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
31	chr8:1916000-1916600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr8:1916200-1916600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
33	chr8:1916200-1916800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr8:1916200-1916800	Enhancers	HUES6 Cell Line	embryonic stem cell
35	chr8:1916200-1916800	Enhancers	Fetal Heart	heart
36	chr8:1916400-1916600	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
37	chr8:1916400-1916600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr8:1916400-1916600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr8:1916400-1916600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr8:1916400-1916600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
41	chr8:1916400-1916600	Bivalent Enhancer	Fetal Stomach	stomach
42	chr8:1916400-1916600	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
43	chr8:1916400-1916600	Bivalent Enhancer	HUVEC	blood vessel
44	chr8:1916400-1916800	Enhancers	Fetal Brain Female	brain
45	chr8:1916400-1916800	Active TSS	A549	lung
46	chr8:1916600-1918400	Weak transcription	Fetal Brain Male	brain
47	chr8:1916600-1919000	Weak transcription	Fetal Muscle Leg	muscle
48	chr8:1916600-1920800	Weak transcription	HSMMtube	muscle
49	chr8:1916600-1921200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr8:1916800-1918200	Weak transcription	Fetal Brain Female	brain

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