Variant report

Variant	nsv824473
Chromosome Location	chr8:1914305-1965389
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:789)
CpG islands
(count:3484)
Chromatin interactive
region (count:20)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:789 , 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	chr8:1949877-1951075	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr8:1949444-1949648	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	chr8:1942103-1942376	H1-hESC	embryonic stem cell:	n/a	chr8:1942226-1942239 chr8:1942226-1942237 chr8:1942226-1942239
8	CEBPB	chr8:1927713-1927808	HepG2	liver:	n/a	chr8:1927745-1927756
9	CEBPB	chr8:1914751-1915120	IMR90	lung:	n/a	chr8:1914929-1914940 chr8:1914954-1914966 chr8:1914924-1914941 chr8:1914929-1914940
10	CEBPB	chr8:1942047-1942403	A549	lung:	n/a	chr8:1942226-1942239 chr8:1942226-1942237 chr8:1942226-1942239
11	CEBPB	chr8:1942051-1942407	K562	blood:	n/a	chr8:1942226-1942239 chr8:1942226-1942237 chr8:1942226-1942239
12	CEBPB	chr8:1914793-1914975	K562	blood:	n/a	chr8:1914929-1914940 chr8:1914954-1914966 chr8:1914924-1914941 chr8:1914929-1914940
13	CEBPB	chr8:1941969-1942515	A549	lung:	n/a	chr8:1942226-1942239 chr8:1942226-1942237 chr8:1942226-1942239
14	CEBPB	chr8:1931727-1931927	HepG2	liver:	n/a	n/a
15	CEBPB	chr8:1942047-1942399	HepG2	liver:	n/a	chr8:1942226-1942239 chr8:1942226-1942237 chr8:1942226-1942239
16	CEBPB	chr8:1917911-1918068	A549	lung:	n/a	n/a
17	CEBPB	chr8:1942182-1942295	Hela-S3	cervix:	n/a	chr8:1942226-1942239 chr8:1942226-1942237 chr8:1942226-1942239
18	CEBPB	chr8:1917870-1918070	K562	blood:	n/a	n/a
19	CEBPB	chr8:1942036-1942796	IMR90	lung:	n/a	chr8:1942226-1942239 chr8:1942226-1942237 chr8:1942226-1942239
20	CEBPB	chr8:1917852-1918103	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr8:1960032-1960245	IMR90	lung:	n/a	n/a
22	CHD1	chr8:1950968-1950973	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD2	chr8:1949818-1950108	H1-hESC	embryonic stem cell:	n/a	n/a
24	CREB1	chr8:1949613-1950373	A549	lung:	n/a	n/a
25	CREB1	chr8:1916164-1916330	A549	lung:	n/a	chr8:1916249-1916262
26	CREB1	chr8:1916103-1916317	A549	lung:	n/a	chr8:1916249-1916262
27	CTBP2	chr8:1949754-1951026	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr8:1950094-1950181	NHEK	skin:	n/a	n/a
29	CTCF	chr8:1950032-1950142	LNCaP	prostate:	n/a	n/a
30	CTCF	chr8:1958520-1958670	GM06990	blood:	n/a	n/a
31	CTCF	chr8:1924040-1924190	AG09319	gingival:	n/a	chr8:1924088-1924096
32	CTCF	chr8:1949400-1949550	RPTEC	kidney:	n/a	n/a
33	CTCF	chr8:1926200-1926350	BE2_C	brain:	n/a	n/a
34	CTCF	chr8:1948600-1948750	SK-N-SH_RA	brain:	n/a	chr8:1948693-1948711
35	CTCF	chr8:1921200-1921350	HPF	lung:	n/a	chr8:1921313-1921322
36	CTCF	chr8:1949380-1949530	AG04450	lung:	n/a	n/a
37	CTCF	chr8:1950030-1950198	A549	lung:	n/a	n/a
38	CTCF	chr8:1933531-1933538	Pancreas_OC	pancreas:	n/a	n/a
39	CTCF	chr8:1949533-1949595	MCF-7	breast:	n/a	n/a
40	CTCF	chr8:1949700-1949850	AG04449	skin:	n/a	n/a
41	CTCF	chr8:1926300-1926450	HAc	cerebellar:	n/a	n/a
42	CTCF	chr8:1948500-1948650	BE2_C	brain:	n/a	n/a
43	CTCF	chr8:1949500-1949650	HFF-Myc	foreskin:	n/a	n/a
44	CTCF	chr8:1926056-1926745	SK-N-SH	brain:	n/a	chr8:1926607-1926620
45	CTCF	chr8:1950000-1950150	RPTEC	kidney:	n/a	n/a
46	CTCF	chr8:1949280-1949430	BJ	skin:	n/a	chr8:1949305-1949313
47	CTCF	chr8:1926300-1926450	HCFaa	heart:	n/a	n/a
48	CTCF	chr8:1959340-1959490	A549	lung:	n/a	n/a
49	CTCF	chr8:1926300-1926450	HMF	breast:	n/a	n/a
50	CTCF	chr8:1926223-1926437	MCF-7	breast:	n/a	n/a

(count:3484 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:1952319-1952369	T-47D	breast:	n/a
2	chr8:1940523-1940573	U87	brain:	n/a
3	chr8:1922810-1922860	NH-A	brain:	n/a
4	chr8:1921328-1921378	AG10803	skin:	n/a
5	chr8:1958930-1958980	IMR90	lung:	fetal
6	chr8:1922810-1922860	GM06990	blood:	n/a
7	chr8:1914991-1915041	GM12892	blood:	n/a
8	chr8:1952319-1952369	T-47D	breast:	n/a
9	chr8:1940523-1940573	U87	brain:	n/a
10	chr8:1922810-1922860	NH-A	brain:	n/a
11	chr8:1921328-1921378	AG10803	skin:	n/a
12	chr8:1958930-1958980	IMR90	lung:	fetal
13	chr8:1922810-1922860	GM06990	blood:	n/a
14	chr8:1914991-1915041	GM12892	blood:	n/a
15	chr8:1921328-1921378	HNPCEpiC	eye:	n/a
16	chr8:1921560-1921610	U87	brain:	n/a
17	chr8:1921906-1921956	NHBE	bronchial:	n/a
18	chr8:1955069-1955119	HCF	heart:	n/a
19	chr8:1957008-1957058	SK-N-MC	brain:	n/a
20	chr8:1959121-1959171	NT2-D1	testis:	n/a
21	chr8:1920950-1921000	GM12878	blood:	n/a
22	chr8:1935720-1935770	ovcar-3	ovarian:	n/a
23	chr8:1922165-1922215	HCM	heart:	n/a
24	chr8:1920950-1921000	Jurkat	blood:	n/a
25	chr8:1922372-1922422	HRCEpiC	kidney:	n/a
26	chr8:1938530-1938580	A549	lung:	n/a
27	chr8:1935720-1935770	GM12891	blood:	n/a
28	chr8:1938554-1938604	PFSK-1	brain:	n/a
29	chr8:1921165-1921215	Jurkat	blood:	n/a
30	chr8:1950112-1950162	HCPEpiC	choroid plexus:	n/a
31	chr8:1957008-1957058	U87	brain:	n/a
32	chr8:1949246-1949296	HepG2	liver:	n/a
33	chr8:1924394-1924444	SAEC	small airway:	n/a
34	chr8:1922165-1922215	HNPCEpiC	eye:	n/a
35	chr8:1921410-1921460	PANC-1	pancreas:	n/a
36	chr8:1924394-1924444	MCF10A-Er-Src	breast:	n/a
37	chr8:1914262-1914312	MCF-7	breast:	n/a
38	chr8:1922165-1922215	NHDF-neo	bronchial:	n/a
39	chr8:1960217-1960267	HCM	heart:	n/a
40	chr8:1933651-1933701	NHBE	bronchial:	n/a
41	chr8:1935720-1935770	BJ	skin:	n/a
42	chr8:1925480-1925530	PANC-1	pancreas:	n/a
43	chr8:1921410-1921460	GM12891	blood:	n/a
44	chr8:1914991-1915041	MCF-7	breast:	n/a
45	chr8:1950112-1950162	K562	blood:	n/a
46	chr8:1955069-1955119	K562	blood:	n/a
47	chr8:1949246-1949296	HCF	heart:	n/a
48	chr8:1958171-1958221	MCF-7	breast:	n/a
49	chr8:1923115-1923165	ProgFib	skin:	n/a
50	chr8:1950120-1950170	SK-N-MC	brain:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:1953398..1956111-chr8:1957370..1959528,2	MCF-7	breast:
2	chr8:1906659..1908488-chr8:1948019..1949630,2	MCF-7	breast:
3	chr1:8021103..8021603-chr8:1931796..1932353,2	HCT-116	colon:
4	chr8:1939104..1942044-chr8:1945221..1947708,2	MCF-7	breast:
5	chr8:1920209..1923568-chr8:1948553..1950993,3	MCF-7	breast:
6	chr8:1945649..1948332-chr8:1948376..1949994,2	MCF-7	breast:
7	chr8:1923575..1926096-chr8:1929371..1931428,2	K562	blood:
8	chr8:1920801..1923588-chr8:1929639..1933248,3	MCF-7	breast:
9	chr8:1939104..1942044-chr8:1945221..1947708,2	MCF-7	breast:
10	chr8:1953398..1956111-chr8:1957370..1959528,2	MCF-7	breast:
11	chr8:1947283..1948870-chr8:1955148..1956732,2	MCF-7	breast:
12	chr8:1911383..1914358-chr8:1918883..1921800,2	MCF-7	breast:
13	chr8:1959134..1959995-chr8:1972066..1972791,2	MCF-7	breast:
14	chr8:1862307..1864338-chr8:1926078..1927839,2	K562	blood:
15	chr8:1945649..1948332-chr8:1948376..1949994,2	MCF-7	breast:
16	chr8:1877543..1880354-chr8:1915068..1917833,2	K562	blood:
17	chr8:1920180..1923138-chr8:1945737..1947399,2	MCF-7	breast:
18	chr8:1947283..1948870-chr8:1955148..1956732,2	MCF-7	breast:
19	chr17:8339151..8339685-chr8:1949081..1949841,2	Hela-S3	cervix:
20	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	ENSG00000253696.1
2	lnc-KBTBD11-1	chr8:1920091-1920203	ENSG00000253696.1
3	lnc-CSMD1-7	chr8:1921314-1921511	ENSG00000253764.1
4	lnc-KBTBD11-1	chr8:1919296-1920689	NONHSAT124692
5	lnc-CSMD1-7	chr8:1922773-1922803	ENSG00000253764.1
6	lnc-CSMD1-7	chr8:1920987-1921202	ENSG00000253764.1
7	lnc-KBTBD11-1	chr8:1924065-1924644	ENSG00000253696.2
8	lnc-KBTBD11-1	chr8:1919563-1919684	ENSG00000253696.2
9	lnc-CSMD1-7	chr8:1921314-1921776	ENSG00000253764.1
10	lnc-KBTBD11-1	chr8:1919427-1919611	NONHSAT124693
11	lnc-ARHGEF10-1	chr8:1922984-1923480	ENSG00000270988.1
12	lnc-KBTBD11-1	chr8:1924065-1924610	ENSG00000253696.1
13	lnc-KBTBD11-1	chr8:1920091-1920203	ENSG00000253696.2
14	lnc-KBTBD11-1	chr8:1920091-1920518	NONHSAT124693
15	lnc-CSMD1-7	chr8:1920736-1920829	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
ENSG00000253696	chromatin interactions
ENSG00000253764	chromatin interactions
ENSG00000166579	chromatin interactions
ENSG00000176595	chromatin interactions
ENSG00000270988	chromatin interactions

Extended variants
information (count: 3139 )
Associated
traits (count: 118 )

Variant overlapped rSNPs/rCNVs (count:3139 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs80225548	chr8:1914328-1914329	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs73671070	chr8:1914354-1914355	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs183136257	chr8:1914364-1914365	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs187510419	chr8:1914394-1914395	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs537767715	chr8:1914396-1914397	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs555681372	chr8:1914408-1914409	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs577793453	chr8:1914412-1914413	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs62476268	chr8:1914421-1914422	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs553234022	chr8:1914423-1914424	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs573299359	chr8:1914426-1914427	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs549730618	chr8:1914440-1914441	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs34246231	chr8:1914453-1914454	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs199569468	chr8:1914459-1914460	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs539069392	chr8:1914477-1914478	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs114021091	chr8:1914518-1914519	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs192666982	chr8:1914523-1914524	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs116337300	chr8:1914551-1914552	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs564681975	chr8:1914572-1914573	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs533408330	chr8:1914579-1914580	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs184761661	chr8:1914582-1914583	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs566403223	chr8:1914603-1914604	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs528958525	chr8:1914637-1914638	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs548542041	chr8:1914642-1914643	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs10085927	chr8:1914644-1914645	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs573907141	chr8:1914645-1914646	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs557793250	chr8:1914662-1914663	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs531518862	chr8:1914678-1914679	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs571414934	chr8:1914684-1914685	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs533709528	chr8:1914705-1914706	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs139562436	chr8:1914712-1914713	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs534882929	chr8:1914728-1914729	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs17830215	chr8:1914752-1914753	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs542358653	chr8:1914761-1914762	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs187886993	chr8:1914778-1914779	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs555783477	chr8:1914789-1914790	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs144493242	chr8:1914790-1914791	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs544919233	chr8:1914798-1914799	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs192220688	chr8:1914807-1914808	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs544135178	chr8:1914825-1914826	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs533686748	chr8:1914940-1914941	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs74510054	chr8:1914941-1914942	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs560759173	chr8:1914943-1914944	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs544414813	chr8:1914944-1914945	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs548700250	chr8:1914951-1914952	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs11136449	chr8:1914967-1914968	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs576107376	chr8:1914980-1914981	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs545030200	chr8:1914981-1914982	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs73184714	chr8:1914992-1914993	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs571407749	chr8:1914998-1914999	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
50	rs534118652	chr8:1915003-1915004	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:118)

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
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:1862 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

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	chr8:1906600-1914600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr8:1906600-1921000	Weak transcription	Right Ventricle	heart
5	chr8:1907000-1914400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr8:1907200-1916000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr8:1908600-1915000	Weak transcription	Right Atrium	heart
8	chr8:1908600-1915600	Weak transcription	A549	lung
9	chr8:1909000-1919000	Weak transcription	Fetal Kidney	kidney
10	chr8:1910400-1915200	Bivalent Enhancer	Fetal Stomach	stomach
11	chr8:1911600-1914400	Weak transcription	Gastric	stomach
12	chr8:1911600-1919200	Weak transcription	Brain Germinal Matrix	brain
13	chr8:1912000-1914400	Weak transcription	Psoas Muscle	Psoas
14	chr8:1912000-1914600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
15	chr8:1912000-1920600	Weak transcription	Cortex derived primary cultured neurospheres	brain
16	chr8:1912200-1914600	Weak transcription	Skeletal Muscle Female	skeletal muscle
17	chr8:1912200-1918800	Weak transcription	Liver	Liver
18	chr8:1912200-1920800	Weak transcription	Brain Hippocampus Middle	brain
19	chr8:1912400-1915200	Enhancers	Fetal Lung	lung
20	chr8:1912600-1914800	Weak transcription	Fetal Brain Female	brain
21	chr8:1913000-1914600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
22	chr8:1913200-1914600	Weak transcription	Fetal Brain Male	brain
23	chr8:1913200-1915200	Enhancers	Spleen	Spleen
24	chr8:1913400-1916200	Enhancers	Placenta	Placenta
25	chr8:1913600-1915600	Enhancers	Lung	lung
26	chr8:1913600-1916600	Enhancers	Fetal Muscle Leg	muscle
27	chr8:1913600-1921200	Weak transcription	Esophagus	oesophagus
28	chr8:1913800-1914600	Enhancers	Ovary	ovary
29	chr8:1913800-1914600	Enhancers	Rectal Mucosa Donor 29	rectum
30	chr8:1913800-1914600	Enhancers	Sigmoid Colon	Sigmoid Colon
31	chr8:1913800-1914800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr8:1913800-1914800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr8:1913800-1915000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr8:1913800-1916600	Enhancers	HSMMtube	muscle
35	chr8:1914000-1914400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr8:1914000-1914400	Enhancers	HSMM	muscle
37	chr8:1914000-1914600	Enhancers	NHLF	lung
38	chr8:1914000-1914800	Enhancers	Fetal Intestine Small	intestine
39	chr8:1914000-1915200	Enhancers	Pancreas	Pancrea
40	chr8:1914000-1915200	Enhancers	Rectal Mucosa Donor 31	rectum
41	chr8:1914200-1914400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr8:1914200-1914400	Enhancers	Muscle Satellite Cultured Cells	--
43	chr8:1914200-1914400	Enhancers	Colonic Mucosa	Colon
44	chr8:1914200-1914600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr8:1914200-1914600	Enhancers	Left Ventricle	heart
46	chr8:1914200-1914800	Flanking Active TSS	Duodenum Mucosa	Duodenum
47	chr8:1914200-1914800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
48	chr8:1914200-1914800	Enhancers	Fetal Intestine Large	intestine
49	chr8:1914200-1915000	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
50	chr8:1914200-1915000	Enhancers	Osteobl	bone

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