Variant report

Variant	nsv889742
Chromosome Location	chr8:1918352-1955142
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:692)
CpG islands
(count:2385)
Chromatin interactive
region (count:15)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:692 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr8:1921474-1922031	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr8:1949444-1949648	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	chr8:1942047-1942399	HepG2	liver:	n/a	chr8:1942226-1942239 chr8:1942226-1942237 chr8:1942226-1942239
6	CEBPB	chr8:1942036-1942796	IMR90	lung:	n/a	chr8:1942226-1942239 chr8:1942226-1942237 chr8:1942226-1942239
7	CEBPB	chr8:1942047-1942403	A549	lung:	n/a	chr8:1942226-1942239 chr8:1942226-1942237 chr8:1942226-1942239
8	CEBPB	chr8:1931727-1931927	HepG2	liver:	n/a	n/a
9	CEBPB	chr8:1941969-1942515	A549	lung:	n/a	chr8:1942226-1942239 chr8:1942226-1942237 chr8:1942226-1942239
10	CEBPB	chr8:1942051-1942407	K562	blood:	n/a	chr8:1942226-1942239 chr8:1942226-1942237 chr8:1942226-1942239
11	CEBPB	chr8:1927713-1927808	HepG2	liver:	n/a	chr8:1927745-1927756
12	CEBPB	chr8:1942182-1942295	Hela-S3	cervix:	n/a	chr8:1942226-1942239 chr8:1942226-1942237 chr8:1942226-1942239
13	CEBPB	chr8:1942103-1942376	H1-hESC	embryonic stem cell:	n/a	chr8:1942226-1942239 chr8:1942226-1942237 chr8:1942226-1942239
14	CHD1	chr8:1950968-1950973	H1-hESC	embryonic stem cell:	n/a	n/a
15	CHD2	chr8:1949818-1950108	H1-hESC	embryonic stem cell:	n/a	n/a
16	CREB1	chr8:1949613-1950373	A549	lung:	n/a	n/a
17	CTBP2	chr8:1949754-1951026	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTCF	chr8:1926203-1926451	MCF-7	breast:	n/a	n/a
19	CTCF	chr8:1949340-1949490	HA-sp	spinal cord:	n/a	n/a
20	CTCF	chr8:1950000-1950150	BE2_C	brain:	n/a	n/a
21	CTCF	chr8:1948634-1948744	MCF-7	breast:	n/a	chr8:1948693-1948711
22	CTCF	chr8:1921280-1921430	HBMEC	blood vessel:	n/a	chr8:1921313-1921322
23	CTCF	chr8:1949280-1949430	HUVEC	blood vessel:	n/a	chr8:1949305-1949313
24	CTCF	chr8:1950226-1950229	Pancreas_OC	pancreas:	n/a	n/a
25	CTCF	chr8:1926220-1926370	Hela-S3	cervix:	n/a	n/a
26	CTCF	chr8:1927000-1927150	GM12875	blood:	n/a	n/a
27	CTCF	chr8:1926300-1926450	HMF	breast:	n/a	n/a
28	CTCF	chr8:1933408-1933646	K562	blood:	n/a	chr8:1933520-1933536
29	CTCF	chr8:1926244-1926493	K562	blood:	n/a	n/a
30	CTCF	chr8:1950040-1950190	Caco-2	colon:	n/a	n/a
31	CTCF	chr8:1953520-1953670	HRPEpiC	eye:	n/a	n/a
32	CTCF	chr8:1949528-1949616	NHEK	skin:	n/a	n/a
33	CTCF	chr8:1949220-1949370	HCM	heart:	n/a	chr8:1949305-1949313
34	CTCF	chr8:1926229-1926434	HUVEC	blood vessel:	n/a	n/a
35	CTCF	chr8:1942320-1942470	SAEC	small airway:	n/a	n/a
36	CTCF	chr8:1949440-1949590	AG09309	skin:	n/a	n/a
37	CTCF	chr8:1926240-1926390	HCM	heart:	n/a	n/a
38	CTCF	chr8:1950020-1950170	NHEK	skin:	n/a	n/a
39	CTCF	chr8:1921220-1921370	HRPEpiC	eye:	n/a	chr8:1921313-1921322
40	CTCF	chr8:1933460-1933610	BE2_C	brain:	n/a	chr8:1933520-1933536
41	CTCF	chr8:1921300-1921450	HepG2	liver:	n/a	chr8:1921313-1921322
42	CTCF	chr8:1949420-1949570	Caco-2	colon:	n/a	n/a
43	CTCF	chr8:1926200-1926350	HRE	kidney:	n/a	n/a
44	CTCF	chr8:1946340-1946490	WERI-Rb-1	eye:	n/a	n/a
45	CTCF	chr8:1926240-1926390	HCT-116	colon:	n/a	n/a
46	CTCF	chr8:1950014-1950121	Spleen_OC	spleen:	n/a	n/a
47	CTCF	chr8:1950040-1950190	HEK293	kidney:	n/a	n/a
48	CTCF	chr8:1921360-1921510	RPTEC	kidney:	n/a	n/a
49	CTCF	chr8:1948540-1948690	HPF	lung:	n/a	n/a
50	CTCF	chr8:1926223-1926437	MCF-7	breast:	n/a	n/a

(count:2385 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:1922372-1922422	HNPCEpiC	eye:	n/a
2	chr8:1940523-1940573	SK-N-SH	brain:	n/a
3	chr8:1935720-1935770	AG09319	gingival:	n/a
4	chr8:1949342-1949392	NH-A	brain:	n/a
5	chr8:1951383-1951433	PrEC	prostate:	n/a
6	chr8:1949246-1949296	HRE	kidney:	n/a
7	chr8:1922372-1922422	HNPCEpiC	eye:	n/a
8	chr8:1940523-1940573	SK-N-SH	brain:	n/a
9	chr8:1935720-1935770	AG09319	gingival:	n/a
10	chr8:1949342-1949392	NH-A	brain:	n/a
11	chr8:1951383-1951433	PrEC	prostate:	n/a
12	chr8:1949246-1949296	HRE	kidney:	n/a
13	chr8:1925480-1925530	MCF10A-Er-Src	breast:	n/a
14	chr8:1935720-1935770	MCF10A-Er-Src	breast:	n/a
15	chr8:1955069-1955119	Hepatocyte	liver:	n/a
16	chr8:1923052-1923102	HCPEpiC	choroid plexus:	n/a
17	chr8:1950120-1950170	NH-A	brain:	n/a
18	chr8:1921165-1921215	IMR90	lung:	fetal
19	chr8:1950112-1950162	IMR90	lung:	fetal
20	chr8:1937676-1937726	BE2_C	brain:	n/a
21	chr8:1954777-1954827	HCPEpiC	choroid plexus:	n/a
22	chr8:1948874-1948924	NHBE	bronchial:	n/a
23	chr8:1922810-1922860	SK-N-SH	brain:	n/a
24	chr8:1921410-1921460	BE2_C	brain:	n/a
25	chr8:1955069-1955119	AG09319	gingival:	n/a
26	chr8:1923115-1923165	ECC-1	luminal epithelium:	n/a
27	chr8:1923052-1923102	AG10803	skin:	n/a
28	chr8:1921906-1921956	SK-N-MC	brain:	n/a
29	chr8:1955069-1955119	GM06990	blood:	n/a
30	chr8:1924394-1924444	HRE	kidney:	n/a
31	chr8:1925480-1925530	HRE	kidney:	n/a
32	chr8:1949342-1949392	HCF	heart:	n/a
33	chr8:1940523-1940573	Hepatocyte	liver:	n/a
34	chr8:1921906-1921956	HCT-116	colon:	n/a
35	chr8:1921328-1921378	AG09309	skin:	n/a
36	chr8:1954777-1954827	Hepatocyte	liver:	n/a
37	chr8:1937676-1937726	SKMC	muscle:	n/a
38	chr8:1940413-1940463	MCF-7	breast:	n/a
39	chr8:1923052-1923102	HL-60	blood:	n/a
40	chr8:1950965-1951015	GM12878	blood:	n/a
41	chr8:1919236-1919286	RPTEC	kidney:	n/a
42	chr8:1947038-1947088	IMR90	lung:	fetal
43	chr8:1921328-1921378	NT2-D1	testis:	n/a
44	chr8:1940523-1940573	HEK293	kidney:	embryo
45	chr8:1920950-1921000	MCF10A-Er-Src	breast:	n/a
46	chr8:1922165-1922215	IMR90	lung:	fetal
47	chr8:1938554-1938604	GM19239	blood:	n/a
48	chr8:1938554-1938604	NHDF-neo	bronchial:	n/a
49	chr8:1951383-1951433	HEEpiC	esophagus:	n/a
50	chr8:1938530-1938580	HAEpiC	amniotic membrane:	n/a

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

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

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

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

No data

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

Extended variants
information (count: 2210 )
Associated
traits (count: 117 )

Variant overlapped rSNPs/rCNVs (count:2210 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6558568	chr8:1918352-1918353	Weak transcription Enhancers	TF binding region	3 gene(s)	Overlapped CNVs	mRNA abundance
2	rs148455737	chr8:1918354-1918355	Weak transcription Enhancers	TF binding region	3 gene(s)	Overlapped CNVs	n/a
3	rs186943513	chr8:1918380-1918381	Weak transcription Enhancers	TF binding region	3 gene(s)	Overlapped CNVs	n/a
4	rs192090114	chr8:1918402-1918403	Weak transcription Enhancers Flanking Active TSS	TF binding region	3 gene(s)	Overlapped CNVs	n/a
5	rs375093749	chr8:1918419-1918420	Weak transcription Enhancers Flanking Active TSS	TF binding region	3 gene(s)	Overlapped CNVs	n/a
6	rs543892991	chr8:1918455-1918456	Weak transcription Enhancers Flanking Active TSS	TF binding region	3 gene(s)	Overlapped CNVs	n/a
7	rs572011713	chr8:1918478-1918479	Weak transcription Enhancers Flanking Active TSS	TF binding region	3 gene(s)	Overlapped CNVs	n/a
8	rs575633695	chr8:1918495-1918496	Weak transcription Enhancers Flanking Active TSS	TF binding region	3 gene(s)	Overlapped CNVs	n/a
9	rs183887070	chr8:1918498-1918499	Weak transcription Enhancers Flanking Active TSS	TF binding region	3 gene(s)	Overlapped CNVs	n/a
10	rs530868000	chr8:1918503-1918504	Weak transcription Enhancers Flanking Active TSS	TF binding region	3 gene(s)	Overlapped CNVs	n/a
11	rs545831361	chr8:1918558-1918559	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs187599662	chr8:1918587-1918588	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs191164667	chr8:1918636-1918637	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs542568639	chr8:1918650-1918651	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs562264636	chr8:1918651-1918652	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs142035158	chr8:1918660-1918661	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs182579743	chr8:1918690-1918691	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs570406996	chr8:1918696-1918697	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs187146830	chr8:1918697-1918698	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs546156180	chr8:1918703-1918704	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs372266632	chr8:1918738-1918739	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs28672250	chr8:1918765-1918766	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs566163403	chr8:1918793-1918794	Weak transcription Enhancers Flanking Active TSS	TF binding region	3 gene(s)	Overlapped CNVs	n/a
24	rs191590707	chr8:1918815-1918816	Weak transcription Enhancers Flanking Active TSS	TF binding region	3 gene(s)	Overlapped CNVs	n/a
25	rs146344069	chr8:1918847-1918848	Weak transcription Enhancers Flanking Active TSS	TF binding region	3 gene(s)	Overlapped CNVs	n/a
26	rs569021544	chr8:1918848-1918849	Weak transcription Enhancers Flanking Active TSS	TF binding region	3 gene(s)	Overlapped CNVs	n/a
27	rs537603462	chr8:1918853-1918854	Weak transcription Enhancers Flanking Active TSS	TF binding region	3 gene(s)	Overlapped CNVs	n/a
28	rs540665932	chr8:1918910-1918911	Weak transcription Enhancers Flanking Active TSS	TF binding region	3 gene(s)	Overlapped CNVs	n/a
29	rs554228867	chr8:1918911-1918912	Weak transcription Enhancers Flanking Active TSS	TF binding region	3 gene(s)	Overlapped CNVs	n/a
30	rs577237314	chr8:1918917-1918918	Weak transcription Enhancers Flanking Active TSS	TF binding region	3 gene(s)	Overlapped CNVs	n/a
31	rs539937692	chr8:1918919-1918920	Weak transcription Enhancers Flanking Active TSS	TF binding region	3 gene(s)	Overlapped CNVs	n/a
32	rs73184718	chr8:1918938-1918939	Weak transcription Enhancers Flanking Active TSS	TF binding region	3 gene(s)	Overlapped CNVs	n/a
33	rs543185049	chr8:1918947-1918948	Weak transcription Enhancers Flanking Active TSS	TF binding region	3 gene(s)	Overlapped CNVs	n/a
34	rs573322692	chr8:1918962-1918963	Weak transcription Enhancers Flanking Active TSS	TF binding region	3 gene(s)	Overlapped CNVs	n/a
35	rs185357084	chr8:1918971-1918972	Weak transcription Enhancers Flanking Active TSS	TF binding region	3 gene(s)	Overlapped CNVs	n/a
36	rs139499990	chr8:1918980-1918981	Weak transcription Enhancers Flanking Active TSS	TF binding region	3 gene(s)	Overlapped CNVs	n/a
37	rs575899925	chr8:1918992-1918993	Weak transcription Enhancers Flanking Active TSS	TF binding region	3 gene(s)	Overlapped CNVs	n/a
38	rs111521959	chr8:1918995-1918996	Weak transcription Enhancers Flanking Active TSS	TF binding region	3 gene(s)	Overlapped CNVs	n/a
39	rs564720706	chr8:1918999-1919000	Weak transcription Enhancers Flanking Active TSS	TF binding region	3 gene(s)	Overlapped CNVs	n/a
40	rs190206267	chr8:1919025-1919026	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region	3 gene(s)	Overlapped CNVs	n/a
41	rs1125177	chr8:1919047-1919048	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region	3 gene(s)	Overlapped CNVs	n/a
42	rs559712242	chr8:1919051-1919052	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region	3 gene(s)	Overlapped CNVs	n/a
43	rs11780256	chr8:1919068-1919069	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region	3 gene(s)	Overlapped CNVs	n/a
44	rs528894273	chr8:1919076-1919077	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region	3 gene(s)	Overlapped CNVs	n/a
45	rs375464326	chr8:1919083-1919084	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region	3 gene(s)	Overlapped CNVs	n/a
46	rs548575756	chr8:1919139-1919140	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region	3 gene(s)	Overlapped CNVs	n/a
47	rs151042089	chr8:1919148-1919149	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region	3 gene(s)	Overlapped CNVs	n/a
48	rs139950573	chr8:1919164-1919165	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region	3 gene(s)	Overlapped CNVs	n/a
49	rs149854706	chr8:1919183-1919184	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region	3 gene(s)	Overlapped CNVs	n/a
50	rs571453583	chr8:1919184-1919185	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region	3 gene(s)	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:1547 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:1905600-1921000	Weak transcription	Aorta	Aorta
2	chr8:1906600-1921000	Weak transcription	Right Ventricle	heart
3	chr8:1909000-1919000	Weak transcription	Fetal Kidney	kidney
4	chr8:1911600-1919200	Weak transcription	Brain Germinal Matrix	brain
5	chr8:1912000-1920600	Weak transcription	Cortex derived primary cultured neurospheres	brain
6	chr8:1912200-1918800	Weak transcription	Liver	Liver
7	chr8:1912200-1920800	Weak transcription	Brain Hippocampus Middle	brain
8	chr8:1913600-1921200	Weak transcription	Esophagus	oesophagus
9	chr8:1914600-1921200	Weak transcription	Left Ventricle	heart
10	chr8:1914800-1921000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr8:1914800-1921200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr8:1915200-1919000	Weak transcription	Fetal Lung	lung
13	chr8:1915200-1919000	Weak transcription	Pancreas	Pancrea
14	chr8:1915200-1919000	Weak transcription	Spleen	Spleen
15	chr8:1916600-1918400	Weak transcription	Fetal Brain Male	brain
16	chr8:1916600-1919000	Weak transcription	Fetal Muscle Leg	muscle
17	chr8:1916600-1920800	Weak transcription	HSMMtube	muscle
18	chr8:1916600-1921200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr8:1916800-1920800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr8:1916800-1920800	Weak transcription	Muscle Satellite Cultured Cells	--
21	chr8:1916800-1920800	Weak transcription	Fetal Heart	heart
22	chr8:1916800-1921000	Weak transcription	HSMM	muscle
23	chr8:1917800-1918400	Enhancers	Rectal Mucosa Donor 29	rectum
24	chr8:1918000-1918600	Enhancers	Colonic Mucosa	Colon
25	chr8:1918000-1919000	Enhancers	Duodenum Mucosa	Duodenum
26	chr8:1918000-1919000	Enhancers	Rectal Mucosa Donor 31	rectum
27	chr8:1918200-1918600	Enhancers	Small Intestine	intestine
28	chr8:1918200-1919000	Enhancers	Fetal Brain Female	brain
29	chr8:1918400-1919200	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
30	chr8:1918400-1920000	Enhancers	Fetal Brain Male	brain
31	chr8:1918600-1919600	Weak transcription	Colonic Mucosa	Colon
32	chr8:1918600-1921000	Weak transcription	Small Intestine	intestine
33	chr8:1918800-1919800	Enhancers	Fetal Intestine Large	intestine
34	chr8:1918800-1921000	Enhancers	Liver	Liver
35	chr8:1919000-1919200	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
36	chr8:1919000-1919200	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon
37	chr8:1919000-1919400	Active TSS	Duodenum Mucosa	Duodenum
38	chr8:1919000-1919400	Enhancers	Fetal Kidney	kidney
39	chr8:1919000-1919600	Enhancers	Fetal Intestine Small	intestine
40	chr8:1919000-1919600	Enhancers	Pancreas	Pancrea
41	chr8:1919000-1920000	Flanking Active TSS	Fetal Brain Female	brain
42	chr8:1919000-1920000	Enhancers	Fetal Lung	lung
43	chr8:1919000-1921000	Enhancers	Fetal Muscle Leg	muscle
44	chr8:1919000-1921400	Enhancers	Spleen	Spleen
45	chr8:1919200-1919400	Enhancers	Brain Germinal Matrix	brain
46	chr8:1919200-1919400	Active TSS	Rectal Mucosa Donor 29	rectum
47	chr8:1919200-1919400	Enhancers	Rectal Mucosa Donor 31	rectum
48	chr8:1919200-1920000	Enhancers	Sigmoid Colon	Sigmoid Colon
49	chr8:1919400-1919600	Flanking Active TSS	Duodenum Mucosa	Duodenum
50	chr8:1919400-1919800	Flanking Active TSS	Fetal Kidney	kidney

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