Variant report

Variant	nsv889730
Chromosome Location	chr8:1821516-1883352
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:794)
CpG islands
(count:4581)
Chromatin interactive
region (count:32)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:794 , 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	ARID3A	chr8:1840485-1840774	K562	blood:	n/a	n/a
2	ATF1	chr8:1870725-1870958	K562	blood:	n/a	n/a
3	ATF2	chr8:1845619-1845955	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr8:1845258-1845710	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr8:1843208-1843523	GM12878	blood:	n/a	chr8:1843399-1843410
6	BHLHE40	chr8:1840626-1841001	K562	blood:	n/a	n/a
7	BHLHE40	chr8:1880551-1880723	K562	blood:	n/a	n/a
8	BHLHE40	chr8:1878968-1878979	K562	blood:	n/a	n/a
9	BHLHE40	chr8:1870659-1870932	K562	blood:	n/a	n/a
10	BHLHE40	chr8:1840627-1840944	GM12878	blood:	n/a	n/a
11	BHLHE40	chr8:1872763-1873004	K562	blood:	n/a	n/a
12	BHLHE40	chr8:1840631-1840990	HepG2	liver:	n/a	n/a
13	BRCA1	chr8:1840792-1840848	HepG2	liver:	n/a	n/a
14	CEBPB	chr8:1823550-1823699	K562	blood:	n/a	chr8:1823629-1823642
15	CEBPB	chr8:1869161-1869280	A549	lung:	n/a	n/a
16	CEBPB	chr8:1843162-1843456	A549	lung:	n/a	chr8:1843289-1843300
17	CEBPB	chr8:1843200-1843355	HepG2	liver:	n/a	chr8:1843289-1843300
18	CEBPB	chr8:1843116-1843481	HepG2	liver:	n/a	chr8:1843289-1843300
19	CEBPB	chr8:1840538-1840820	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr8:1843055-1843495	A549	lung:	n/a	chr8:1843070-1843083 chr8:1843289-1843300 chr8:1843070-1843081
21	CEBPB	chr8:1843136-1843472	Hela-S3	cervix:	n/a	chr8:1843289-1843300
22	CEBPB	chr8:1870616-1871016	K562	blood:	n/a	n/a
23	CEBPB	chr8:1843168-1843469	K562	blood:	n/a	chr8:1843289-1843300
24	CEBPB	chr8:1840650-1840906	K562	blood:	n/a	n/a
25	CEBPB	chr8:1820939-1821614	ECC-1	luminal epithelium:	n/a	n/a
26	CEBPB	chr8:1843202-1843426	MCF-7	breast:	n/a	chr8:1843289-1843300
27	CEBPB	chr8:1843045-1843547	IMR90	lung:	n/a	chr8:1843070-1843083 chr8:1843289-1843300 chr8:1843070-1843081
28	CEBPB	chr8:1832398-1832601	HepG2	liver:	n/a	chr8:1832512-1832523
29	CEBPB	chr8:1843168-1843414	H1-hESC	embryonic stem cell:	n/a	chr8:1843289-1843300
30	CTCF	chr8:1840673-1840871	Fibrobl	skin:	n/a	chr8:1840715-1840733 chr8:1840717-1840738
31	CTCF	chr8:1840631-1840829	SK-N-SH_RA	brain:	n/a	chr8:1840715-1840733 chr8:1840717-1840738
32	CTCF	chr8:1840300-1840450	GM12871	blood:	n/a	n/a
33	CTCF	chr8:1862560-1862710	HBMEC	blood vessel:	n/a	n/a
34	CTCF	chr8:1845500-1845650	Caco-2	colon:	n/a	n/a
35	CTCF	chr8:1845540-1845690	HCM	heart:	n/a	n/a
36	CTCF	chr8:1840680-1840830	HEEpiC	esophagus:	n/a	chr8:1840715-1840733 chr8:1840717-1840738
37	CTCF	chr8:1840638-1840917	GM19238	blood:	n/a	chr8:1840715-1840733 chr8:1840717-1840738
38	CTCF	chr8:1840577-1840870	HUVEC	blood vessel:	n/a	chr8:1840715-1840733 chr8:1840717-1840738
39	CTCF	chr8:1840523-1840933	GM12878	blood:	n/a	chr8:1840715-1840733 chr8:1840717-1840738
40	CTCF	chr8:1845700-1845850	HPF	lung:	n/a	n/a
41	CTCF	chr8:1880537-1880593	MCF-7	breast:	n/a	n/a
42	CTCF	chr8:1840607-1840846	GM10266	blood:	n/a	chr8:1840715-1840733 chr8:1840717-1840738
43	CTCF	chr8:1840660-1840810	AG09319	gingival:	n/a	chr8:1840715-1840733 chr8:1840717-1840738
44	CTCF	chr8:1828460-1828610	HPF	lung:	n/a	n/a
45	CTCF	chr8:1845600-1845750	HRE	kidney:	n/a	n/a
46	CTCF	chr8:1840620-1840770	HCT-116	colon:	n/a	chr8:1840715-1840733 chr8:1840717-1840738
47	CTCF	chr8:1840600-1840750	BJ	skin:	n/a	chr8:1840715-1840733 chr8:1840717-1840738
48	CTCF	chr8:1845382-1845940	K562	blood:	n/a	n/a
49	CTCF	chr8:1840640-1840790	HL-60	blood:	n/a	chr8:1840715-1840733 chr8:1840717-1840738
50	CTCF	chr8:1840630-1840841	A549	lung:	n/a	chr8:1840715-1840733 chr8:1840717-1840738

(count:4581 , 50 per page) page: 1 2 3 4 5 6 7 ... 92

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:1848407-1848457	NT2-D1	testis:	n/a
2	chr8:1876686-1876736	GM12878	blood:	n/a
3	chr8:1828573-1828623	AG10803	skin:	n/a
4	chr8:1831484-1831534	AG09319	gingival:	n/a
5	chr8:1822186-1822236	HRCEpiC	kidney:	n/a
6	chr8:1831484-1831534	GM06990	blood:	n/a
7	chr8:1848407-1848457	NT2-D1	testis:	n/a
8	chr8:1876686-1876736	GM12878	blood:	n/a
9	chr8:1828573-1828623	AG10803	skin:	n/a
10	chr8:1831484-1831534	AG09319	gingival:	n/a
11	chr8:1822186-1822236	HRCEpiC	kidney:	n/a
12	chr8:1831484-1831534	GM06990	blood:	n/a
13	chr8:1848614-1848664	HRE	kidney:	n/a
14	chr8:1829637-1829687	ECC-1	luminal epithelium:	n/a
15	chr8:1876715-1876765	HMEC	breast:	n/a
16	chr8:1831484-1831534	BJ	skin:	n/a
17	chr8:1830749-1830799	NHBE	bronchial:	n/a
18	chr8:1862499-1862549	AG09309	skin:	n/a
19	chr8:1822568-1822618	HCM	heart:	n/a
20	chr8:1879639-1879689	HCPEpiC	choroid plexus:	n/a
21	chr8:1842659-1842709	AoSMC	blood vessel:	n/a
22	chr8:1857241-1857291	NB4	blood:	n/a
23	chr8:1821603-1821653	NH-A	brain:	n/a
24	chr8:1857688-1857738	AG04449	skin:	fetal
25	chr8:1845444-1845494	U87	brain:	n/a
26	chr8:1847999-1848049	AG04450	lung:	fetal
27	chr8:1876715-1876765	A549	lung:	n/a
28	chr8:1861136-1861186	RPTEC	kidney:	n/a
29	chr8:1826088-1826138	AoSMC	blood vessel:	n/a
30	chr8:1854795-1854845	HCF	heart:	n/a
31	chr8:1851026-1851076	MCF-7	breast:	n/a
32	chr8:1830065-1830115	GM12878	blood:	n/a
33	chr8:1847999-1848049	Jurkat	blood:	n/a
34	chr8:1864422-1864472	HAEpiC	amniotic membrane:	n/a
35	chr8:1845444-1845494	NHBE	bronchial:	n/a
36	chr8:1857177-1857227	HCT-116	colon:	n/a
37	chr8:1830352-1830402	NB4	blood:	n/a
38	chr8:1853599-1853649	ProgFib	skin:	n/a
39	chr8:1822568-1822618	Hepatocyte	liver:	n/a
40	chr8:1861064-1861114	HPAEpiC	pulmonary alveolar:	n/a
41	chr8:1870798-1870848	LNCaP	prostate:	n/a
42	chr8:1848407-1848457	AG04450	lung:	fetal
43	chr8:1830965-1831015	HMEC	breast:	n/a
44	chr8:1848741-1848791	AG10803	skin:	n/a
45	chr8:1848040-1848090	Jurkat	blood:	n/a
46	chr8:1878323-1878373	BE2_C	brain:	n/a
47	chr8:1822186-1822236	HAEpiC	amniotic membrane:	n/a
48	chr8:1870798-1870848	Hela-S3	cervix:	n/a
49	chr8:1857839-1857889	RPTEC	kidney:	n/a
50	chr8:1879091-1879141	PANC-1	pancreas:	n/a

(count:32 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:1877543..1880354-chr8:1915068..1917833,2	K562	blood:
2	chr8:1848105..1850497-chr8:1856585..1858723,2	K562	blood:
3	chr8:1842826..1843459-chr8:1992468..1993115,2	K562	blood:
4	chr8:1876158..1879042-chr8:1903928..1907345,3	K562	blood:
5	chr8:1880957..1882903-chr8:1922237..1924079,2	MCF-7	breast:
6	chr8:1862307..1864338-chr8:1926078..1927839,2	K562	blood:
7	chr8:1839446..1841757-chr8:1844731..1847507,2	MCF-7	breast:
8	chr8:1840317..1841126-chr8:2027343..2028221,2	MCF-7	breast:
9	chr8:1839996..1842403-chr8:1970017..1972283,2	K562	blood:
10	chr8:1849167..1851254-chr8:1973705..1975822,2	MCF-7	breast:
11	chr8:1821991..1823766-chr8:1824351..1826161,2	K562	blood:
12	chr8:1843830..1846046-chr8:1856723..1858500,2	MCF-7	breast:
13	chr8:1821991..1823766-chr8:1824351..1826161,2	K562	blood:
14	chr8:1839446..1841757-chr8:1844731..1847507,2	MCF-7	breast:
15	chr8:1856064..1857841-chr8:1860067..1862495,2	K562	blood:
16	chr8:1809191..1811307-chr8:1819741..1822402,2	K562	blood:
17	chr8:1856064..1857841-chr8:1860067..1862495,2	K562	blood:
18	chr8:1846010..1848656-chr8:1851814..1854261,2	K562	blood:
19	chr8:1821259..1823766-chr8:1824661..1826790,2	K562	blood:
20	chr8:1843830..1846046-chr8:1856723..1858500,2	MCF-7	breast:
21	chr8:1821259..1823766-chr8:1824661..1826790,2	K562	blood:
22	chr8:1845253..1846025-chr8:1978398..1979174,5	MCF-7	breast:
23	chr8:1848233..1850462-chr8:1857880..1860759,2	MCF-7	breast:
24	chr8:1848233..1850462-chr8:1857880..1860759,2	MCF-7	breast:
25	chr8:1876812..1880065-chr8:1886346..1889205,3	K562	blood:
26	chr8:1839403..1841214-chr8:1971479..1972941,9	K562	blood:
27	chr8:1845361..1846326-chr8:1971978..1972609,2	MCF-7	breast:
28	chr8:1848105..1850497-chr8:1856585..1858723,2	K562	blood:
29	chr8:1840277..1841232-chr8:1978419..1979386,5	K562	blood:
30	chr8:1845240..1845932-chr8:1971897..1973021,5	MCF-7	breast:
31	chr8:1840257..1840999-chr8:1978353..1979355,3	MCF-7	breast:
32	chr8:1840240..1841043-chr8:1971863..1972750,4	MCF-7	breast:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CLN8-4	chr8:1823317-1823827	NONHSAT124690
2	lnc-CLN8-4	chr8:1822679-1823139	NONHSAT124690

No data

Variant related genes	Relation type
ARHGEF10	TF binding region
ARHGEF10	CpG island
ENSG00000270988	chromatin interactions
ENSG00000104728	chromatin interactions
ENSG00000253764	chromatin interactions

Extended variants
information (count: 4115 )
Associated
traits (count: 119 )

Variant overlapped rSNPs/rCNVs (count:4115 , 50 per page) page: 1 2 3 4 5 6 7 ... 83

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12545104	chr8:1821516-1821517	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs73180724	chr8:1821520-1821521	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs529700175	chr8:1821524-1821525	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs549481317	chr8:1821546-1821547	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs67137760	chr8:1821566-1821567	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs73180726	chr8:1821590-1821591	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs55670556	chr8:1821599-1821600	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs11776715	chr8:1821617-1821618	Strong transcription Weak transcription Enhancers ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
9	rs76896388	chr8:1821619-1821620	Strong transcription Weak transcription Enhancers ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
10	rs372891585	chr8:1821622-1821623	Strong transcription Weak transcription Enhancers ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
11	rs60604047	chr8:1821629-1821630	Strong transcription Weak transcription Enhancers ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
12	rs113515498	chr8:1821633-1821634	Strong transcription Weak transcription Enhancers ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
13	rs56765961	chr8:1821635-1821636	Strong transcription Weak transcription Enhancers ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
14	rs71518097	chr8:1821637-1821638	Strong transcription Weak transcription Enhancers ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
15	rs59911764	chr8:1821644-1821645	Strong transcription Weak transcription Enhancers ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
16	rs60958354	chr8:1821646-1821647	Strong transcription Weak transcription Enhancers ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
17	rs554986560	chr8:1821650-1821651	Strong transcription Weak transcription Enhancers ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
18	rs565957453	chr8:1821654-1821655	Strong transcription Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs56137975	chr8:1821662-1821663	Strong transcription Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs377097769	chr8:1821664-1821665	Strong transcription Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs534655544	chr8:1821665-1821666	Strong transcription Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs57516302	chr8:1821674-1821675	Strong transcription Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs148062074	chr8:1821676-1821677	Strong transcription Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs36048880	chr8:1821677-1821678	Strong transcription Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs55640435	chr8:1821685-1821686	Strong transcription Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs57897495	chr8:1821686-1821687	Strong transcription Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs58822054	chr8:1821687-1821688	Strong transcription Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs370330780	chr8:1821697-1821698	Strong transcription Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs56117805	chr8:1821705-1821706	Strong transcription Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs75848606	chr8:1821715-1821716	Strong transcription Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs71518098	chr8:1821721-1821722	Strong transcription Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs11783429	chr8:1821724-1821725	Strong transcription Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs199543124	chr8:1821731-1821732	Strong transcription Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs35192870	chr8:1821732-1821733	Strong transcription Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs397945567	chr8:1821733-1821734	Strong transcription Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs201127548	chr8:1821750-1821751	Strong transcription Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs71518188	chr8:1821759-1821760	Strong transcription Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs11776750	chr8:1821765-1821766	Strong transcription Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs72448951	chr8:1821768-1821769	Strong transcription Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs59507011	chr8:1821771-1821772	Strong transcription Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs57248615	chr8:1821774-1821775	Strong transcription Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs148855911	chr8:1821776-1821777	Strong transcription Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs556715987	chr8:1821780-1821781	Strong transcription Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs61706797	chr8:1821793-1821794	Strong transcription Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs11780302	chr8:1821804-1821805	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs11776771	chr8:1821810-1821811	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs113371479	chr8:1821813-1821814	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs62477526	chr8:1821819-1821820	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs57790959	chr8:1821820-1821821	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs376294200	chr8:1821822-1821823	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:119)

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
Tetralogy of Fallot	22912587	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Lung adenocarcinoma	21935476	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Glioma	20126413	CNVD

Chromatin state (count:2096 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:1774000-1845000	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr8:1802200-1845000	Weak transcription	Right Atrium	heart
3	chr8:1806000-1828800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr8:1806000-1844000	Strong transcription	HUES48 Cell Line	embryonic stem cell
5	chr8:1806200-1821800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr8:1806200-1821800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr8:1806400-1839800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
8	chr8:1808600-1848400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
9	chr8:1812000-1840400	Weak transcription	Fetal Brain Male	brain
10	chr8:1813000-1840800	Weak transcription	Rectal Mucosa Donor 31	rectum
11	chr8:1814000-1835200	Weak transcription	Fetal Intestine Large	intestine
12	chr8:1814400-1822200	Weak transcription	Skeletal Muscle Male	skeletal muscle
13	chr8:1814400-1834800	Weak transcription	Esophagus	oesophagus
14	chr8:1814600-1828200	Weak transcription	Brain Germinal Matrix	brain
15	chr8:1814600-1834000	Weak transcription	Spleen	Spleen
16	chr8:1814800-1824800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
17	chr8:1814800-1834000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr8:1815000-1824800	Weak transcription	Cortex derived primary cultured neurospheres	brain
19	chr8:1815000-1826000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr8:1815200-1824600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr8:1815200-1828000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr8:1815200-1829000	Weak transcription	Right Ventricle	heart
23	chr8:1815200-1835000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr8:1816200-1845000	Weak transcription	Hela-S3	cervix
25	chr8:1816400-1831000	Weak transcription	Fetal Heart	heart
26	chr8:1816800-1834000	Weak transcription	Rectal Mucosa Donor 29	rectum
27	chr8:1816800-1834800	Weak transcription	Colon Smooth Muscle	Colon
28	chr8:1817000-1821800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr8:1817000-1834600	Weak transcription	Duodenum Mucosa	Duodenum
30	chr8:1817000-1836600	Weak transcription	Fetal Kidney	kidney
31	chr8:1817000-1838000	Weak transcription	Rectal Smooth Muscle	rectum
32	chr8:1817200-1823400	Weak transcription	Brain Inferior Temporal Lobe	brain
33	chr8:1817400-1822800	Strong transcription	A549	lung
34	chr8:1818000-1823400	Weak transcription	Brain Substantia Nigra	brain
35	chr8:1818000-1824800	Weak transcription	NHEK	skin
36	chr8:1818200-1822000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr8:1818200-1829000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
38	chr8:1818400-1821600	Weak transcription	Aorta	Aorta
39	chr8:1818400-1824400	Weak transcription	Left Ventricle	heart
40	chr8:1818400-1824400	Weak transcription	Ovary	ovary
41	chr8:1818400-1826000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
42	chr8:1818400-1827800	Weak transcription	Brain Angular Gyrus	brain
43	chr8:1818400-1829800	Weak transcription	Placenta Amnion	Placenta Amnion
44	chr8:1818400-1831200	Weak transcription	Pancreas	Pancrea
45	chr8:1818400-1831400	Weak transcription	HSMMtube	muscle
46	chr8:1818600-1834600	Weak transcription	Fetal Intestine Small	intestine
47	chr8:1818800-1822600	Weak transcription	Brain Hippocampus Middle	brain
48	chr8:1818800-1824400	Weak transcription	HUVEC	blood vessel
49	chr8:1818800-1825800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr8:1818800-1833200	Weak transcription	NH-A	brain

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