Variant report

Variant	nsv824474
Chromosome Location	chr8:1915145-1960212
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:781)
CpG islands
(count:2991)
Chromatin interactive
region (count:19)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:781 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr8:1960110-1960275	K562	blood:	n/a	n/a
2	BACH1	chr8:1921474-1922031	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr8:1949444-1949648	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr8:1949877-1951075	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr8:1959469-1959507	K562	blood:	n/a	n/a
6	CCNT2	chr8:1921657-1922031	K562	blood:	n/a	n/a
7	CEBPB	chr8:1941969-1942515	A549	lung:	n/a	chr8:1942226-1942239 chr8:1942226-1942237 chr8:1942226-1942239
8	CEBPB	chr8:1917911-1918068	A549	lung:	n/a	n/a
9	CEBPB	chr8:1942182-1942295	Hela-S3	cervix:	n/a	chr8:1942226-1942239 chr8:1942226-1942237 chr8:1942226-1942239
10	CEBPB	chr8:1942103-1942376	H1-hESC	embryonic stem cell:	n/a	chr8:1942226-1942239 chr8:1942226-1942237 chr8:1942226-1942239
11	CEBPB	chr8:1942047-1942399	HepG2	liver:	n/a	chr8:1942226-1942239 chr8:1942226-1942237 chr8:1942226-1942239
12	CEBPB	chr8:1931727-1931927	HepG2	liver:	n/a	n/a
13	CEBPB	chr8:1917870-1918070	K562	blood:	n/a	n/a
14	CEBPB	chr8:1942047-1942403	A549	lung:	n/a	chr8:1942226-1942239 chr8:1942226-1942237 chr8:1942226-1942239
15	CEBPB	chr8:1960032-1960245	IMR90	lung:	n/a	n/a
16	CEBPB	chr8:1927713-1927808	HepG2	liver:	n/a	chr8:1927745-1927756
17	CEBPB	chr8:1942036-1942796	IMR90	lung:	n/a	chr8:1942226-1942239 chr8:1942226-1942237 chr8:1942226-1942239
18	CEBPB	chr8:1942051-1942407	K562	blood:	n/a	chr8:1942226-1942239 chr8:1942226-1942237 chr8:1942226-1942239
19	CEBPB	chr8:1917852-1918103	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD1	chr8:1950968-1950973	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD2	chr8:1949818-1950108	H1-hESC	embryonic stem cell:	n/a	n/a
22	CREB1	chr8:1916103-1916317	A549	lung:	n/a	chr8:1916249-1916262
23	CREB1	chr8:1949613-1950373	A549	lung:	n/a	n/a
24	CREB1	chr8:1916164-1916330	A549	lung:	n/a	chr8:1916249-1916262
25	CTBP2	chr8:1949754-1951026	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr8:1921240-1921390	HMF	breast:	n/a	chr8:1921313-1921322
27	CTCF	chr8:1921260-1921410	HCM	heart:	n/a	chr8:1921313-1921322
28	CTCF	chr8:1942320-1942470	HRE	kidney:	n/a	n/a
29	CTCF	chr8:1950029-1950225	Pancreas_OC	pancreas:	n/a	n/a
30	CTCF	chr8:1959520-1959670	GM12864	blood:	n/a	chr8:1959529-1959547 chr8:1959532-1959545 chr8:1959532-1959540
31	CTCF	chr8:1926060-1926210	HFF	foreskin:	n/a	n/a
32	CTCF	chr8:1950040-1950190	AG09319	gingival:	n/a	n/a
33	CTCF	chr8:1926203-1926451	MCF-7	breast:	n/a	n/a
34	CTCF	chr8:1933340-1933638	K562	blood:	n/a	chr8:1933520-1933536
35	CTCF	chr8:1927000-1927150	GM12875	blood:	n/a	n/a
36	CTCF	chr8:1949520-1949670	HAc	cerebellar:	n/a	n/a
37	CTCF	chr8:1959480-1959630	BJ	skin:	n/a	chr8:1959529-1959547 chr8:1959532-1959545 chr8:1959532-1959540
38	CTCF	chr8:1921220-1921370	AG09319	gingival:	n/a	chr8:1921313-1921322
39	CTCF	chr8:1926220-1926370	A549	lung:	n/a	n/a
40	CTCF	chr8:1942340-1942490	HBMEC	blood vessel:	n/a	n/a
41	CTCF	chr8:1948606-1948773	A549	lung:	n/a	chr8:1948693-1948711
42	CTCF	chr8:1949420-1949570	AG09309	skin:	n/a	n/a
43	CTCF	chr8:1949500-1949650	NHLF	lung:	n/a	n/a
44	CTCF	chr8:1949914-1949923	NHEK	skin:	n/a	n/a
45	CTCF	chr8:1950000-1950150	HPF	lung:	n/a	n/a
46	CTCF	chr8:1948589-1948736	MCF-7	breast:	n/a	chr8:1948693-1948711
47	CTCF	chr8:1924080-1924230	AG09319	gingival:	n/a	chr8:1924088-1924096
48	CTCF	chr8:1948800-1948950	A549	lung:	n/a	n/a
49	CTCF	chr8:1942300-1942450	HRE	kidney:	n/a	n/a
50	CTCF	chr8:1926180-1926330	HMF	breast:	n/a	n/a

(count:2991 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:1955069-1955119	GM12892	blood:	n/a
2	chr8:1958930-1958980	GM12878	blood:	n/a
3	chr8:1955069-1955119	GM12892	blood:	n/a
4	chr8:1958930-1958980	GM12878	blood:	n/a
5	chr8:1920950-1921000	T-47D	breast:	n/a
6	chr8:1925480-1925530	HUVEC	blood vessel:	n/a
7	chr8:1922810-1922860	T-47D	breast:	n/a
8	chr8:1933522-1933572	HUVEC	blood vessel:	n/a
9	chr8:1950120-1950170	HCM	heart:	n/a
10	chr8:1925480-1925530	BE2_C	brain:	n/a
11	chr8:1955069-1955119	HL-60	blood:	n/a
12	chr8:1937676-1937726	K562	blood:	n/a
13	chr8:1933651-1933701	HCM	heart:	n/a
14	chr8:1955323-1955373	IMR90	lung:	fetal
15	chr8:1933522-1933572	HCT-116	colon:	n/a
16	chr8:1916285-1916335	HRCEpiC	kidney:	n/a
17	chr8:1942462-1942512	NT2-D1	testis:	n/a
18	chr8:1923115-1923165	Jurkat	blood:	n/a
19	chr8:1921410-1921460	AG09319	gingival:	n/a
20	chr8:1922165-1922215	GM19239	blood:	n/a
21	chr8:1952319-1952369	NB4	blood:	n/a
22	chr8:1959442-1959492	HL-60	blood:	n/a
23	chr8:1951383-1951433	PrEC	prostate:	n/a
24	chr8:1937676-1937726	MCF-7	breast:	n/a
25	chr8:1950120-1950170	BJ	skin:	n/a
26	chr8:1955196-1955246	Caco-2	colon:	n/a
27	chr8:1921410-1921460	NB4	blood:	n/a
28	chr8:1921410-1921460	BJ	skin:	n/a
29	chr8:1923115-1923165	NB4	blood:	n/a
30	chr8:1957038-1957088	NHBE	bronchial:	n/a
31	chr8:1920950-1921000	H1-hESC	embryonic stem cell:	embryo
32	chr8:1937676-1937726	HRPEpiC	eye:	n/a
33	chr8:1955069-1955119	GM12891	blood:	n/a
34	chr8:1949329-1949379	MCF-7	breast:	n/a
35	chr8:1923115-1923165	Hela-S3	cervix:	n/a
36	chr8:1933651-1933701	MCF10A-Er-Src	breast:	n/a
37	chr8:1925480-1925530	A549	lung:	n/a
38	chr8:1921165-1921215	HIPEpiC	eye:	n/a
39	chr8:1923115-1923165	AG04450	lung:	fetal
40	chr8:1951383-1951433	ProgFib	skin:	n/a
41	chr8:1947038-1947088	Hela-S3	cervix:	n/a
42	chr8:1921906-1921956	SAEC	small airway:	n/a
43	chr8:1959121-1959171	PFSK-1	brain:	n/a
44	chr8:1921369-1921419	AG09309	skin:	n/a
45	chr8:1925480-1925530	IMR90	lung:	fetal
46	chr8:1923052-1923102	HAEpiC	amniotic membrane:	n/a
47	chr8:1916285-1916335	HAEpiC	amniotic membrane:	n/a
48	chr8:1919236-1919286	ProgFib	skin:	n/a
49	chr8:1921328-1921378	HL-60	blood:	n/a
50	chr8:1921906-1921956	PFSK-1	brain:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:1920180..1923138-chr8:1945737..1947399,2	MCF-7	breast:
2	chr8:1939104..1942044-chr8:1945221..1947708,2	MCF-7	breast:
3	chr8:1906659..1908488-chr8:1948019..1949630,2	MCF-7	breast:
4	chr8:1959134..1959995-chr8:1972066..1972791,2	MCF-7	breast:
5	chr8:1945649..1948332-chr8:1948376..1949994,2	MCF-7	breast:
6	chr1:8021103..8021603-chr8:1931796..1932353,2	HCT-116	colon:
7	chr8:1920801..1923588-chr8:1929639..1933248,3	MCF-7	breast:
8	chr8:1923575..1926096-chr8:1929371..1931428,2	K562	blood:
9	chr8:1947283..1948870-chr8:1955148..1956732,2	MCF-7	breast:
10	chr8:1920209..1923568-chr8:1948553..1950993,3	MCF-7	breast:
11	chr8:1945649..1948332-chr8:1948376..1949994,2	MCF-7	breast:
12	chr8:1862307..1864338-chr8:1926078..1927839,2	K562	blood:
13	chr8:1939104..1942044-chr8:1945221..1947708,2	MCF-7	breast:
14	chr17:8339151..8339685-chr8:1949081..1949841,2	Hela-S3	cervix:
15	chr8:1923575..1926096-chr8:1929371..1931428,2	K562	blood:
16	chr8:1953398..1956111-chr8:1957370..1959528,2	MCF-7	breast:
17	chr8:1947283..1948870-chr8:1955148..1956732,2	MCF-7	breast:
18	chr8:1953398..1956111-chr8:1957370..1959528,2	MCF-7	breast:
19	chr8:1877543..1880354-chr8:1915068..1917833,2	K562	blood:

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

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

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
ENSG00000176595	chromatin interactions
ENSG00000270988	chromatin interactions
ENSG00000166579	chromatin interactions
ENSG00000253764	chromatin interactions

Extended variants
information (count: 2798 )
Associated
traits (count: 117 )

Variant overlapped rSNPs/rCNVs (count:2798 , 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	rs562281966	chr8:1915164-1915165	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs531310286	chr8:1915180-1915181	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs551063559	chr8:1915199-1915200	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs564913236	chr8:1915241-1915242	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs527575807	chr8:1915252-1915253	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs373462821	chr8:1915297-1915298	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs547248392	chr8:1915331-1915332	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs189687747	chr8:1915365-1915366	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs386720728	chr8:1915393-1915394	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs7012265	chr8:1915394-1915395	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs550008393	chr8:1915401-1915402	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs184471230	chr8:1915418-1915419	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs538358239	chr8:1915434-1915435	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs6982208	chr8:1915441-1915442	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs549661123	chr8:1915448-1915449	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs188776172	chr8:1915470-1915471	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs554088180	chr8:1915473-1915474	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs369891579	chr8:1915480-1915481	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs111740502	chr8:1915505-1915506	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs542768167	chr8:1915506-1915507	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs62476269	chr8:1915546-1915547	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs576024564	chr8:1915552-1915553	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs552567881	chr8:1915556-1915557	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs181886363	chr8:1915564-1915565	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs527328844	chr8:1915579-1915580	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs540958558	chr8:1915627-1915628	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs561127913	chr8:1915639-1915640	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs566009709	chr8:1915643-1915644	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs186144453	chr8:1915666-1915667	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs549973696	chr8:1915673-1915674	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs535132951	chr8:1915675-1915676	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs74361486	chr8:1915712-1915713	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs531696115	chr8:1915738-1915739	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs551877164	chr8:1915739-1915740	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs143326466	chr8:1915751-1915752	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs534237946	chr8:1915758-1915759	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs563844785	chr8:1915765-1915766	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs553757503	chr8:1915774-1915775	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs567592848	chr8:1915783-1915784	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs536564807	chr8:1915797-1915798	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs556323988	chr8:1915817-1915818	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs576603898	chr8:1915818-1915819	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs544776280	chr8:1915835-1915836	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs558661968	chr8:1915843-1915844	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs572056963	chr8:1915856-1915857	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs540979591	chr8:1915913-1915914	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs560887396	chr8:1915946-1915947	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs529979998	chr8:1915950-1915951	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs151303937	chr8:1916002-1916003	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs543771064	chr8:1916016-1916017	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region	1 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:1794 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

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	chr8:1907200-1916000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr8:1908600-1915600	Weak transcription	A549	lung
6	chr8:1909000-1919000	Weak transcription	Fetal Kidney	kidney
7	chr8:1910400-1915200	Bivalent Enhancer	Fetal Stomach	stomach
8	chr8:1911600-1919200	Weak transcription	Brain Germinal Matrix	brain
9	chr8:1912000-1920600	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr8:1912200-1918800	Weak transcription	Liver	Liver
11	chr8:1912200-1920800	Weak transcription	Brain Hippocampus Middle	brain
12	chr8:1912400-1915200	Enhancers	Fetal Lung	lung
13	chr8:1913200-1915200	Enhancers	Spleen	Spleen
14	chr8:1913400-1916200	Enhancers	Placenta	Placenta
15	chr8:1913600-1915600	Enhancers	Lung	lung
16	chr8:1913600-1916600	Enhancers	Fetal Muscle Leg	muscle
17	chr8:1913600-1921200	Weak transcription	Esophagus	oesophagus
18	chr8:1913800-1916600	Enhancers	HSMMtube	muscle
19	chr8:1914000-1915200	Enhancers	Pancreas	Pancrea
20	chr8:1914000-1915200	Enhancers	Rectal Mucosa Donor 31	rectum
21	chr8:1914200-1915200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr8:1914200-1915200	Enhancers	Adipose Nuclei	Adipose
23	chr8:1914400-1915200	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr8:1914400-1915200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
25	chr8:1914400-1916600	Enhancers	Psoas Muscle	Psoas
26	chr8:1914600-1915200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr8:1914600-1915200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr8:1914600-1915200	Enhancers	Skeletal Muscle Female	skeletal muscle
29	chr8:1914600-1915400	Weak transcription	Sigmoid Colon	Sigmoid Colon
30	chr8:1914600-1918200	Weak transcription	Small Intestine	intestine
31	chr8:1914600-1921200	Weak transcription	Left Ventricle	heart
32	chr8:1914800-1915200	Enhancers	Colonic Mucosa	Colon
33	chr8:1914800-1915200	Weak transcription	Fetal Brain Male	brain
34	chr8:1914800-1915200	Enhancers	Fetal Brain Female	brain
35	chr8:1914800-1915400	Enhancers	Duodenum Mucosa	Duodenum
36	chr8:1914800-1916400	Enhancers	Fetal Muscle Trunk	muscle
37	chr8:1914800-1916800	Enhancers	HSMM	muscle
38	chr8:1914800-1921000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr8:1914800-1921200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
40	chr8:1915000-1915200	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr8:1915000-1915200	Enhancers	Right Atrium	heart
42	chr8:1915200-1916200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr8:1915200-1916400	Weak transcription	Fetal Brain Female	brain
44	chr8:1915200-1916400	Weak transcription	Right Atrium	heart
45	chr8:1915200-1916600	Enhancers	Fetal Brain Male	brain
46	chr8:1915200-1916800	Enhancers	Muscle Satellite Cultured Cells	--
47	chr8:1915200-1918000	Weak transcription	Colonic Mucosa	Colon
48	chr8:1915200-1918000	Weak transcription	Rectal Mucosa Donor 31	rectum
49	chr8:1915200-1919000	Weak transcription	Fetal Lung	lung
50	chr8:1915200-1919000	Weak transcription	Pancreas	Pancrea

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