Variant report

Variant	nsv889726
Chromosome Location	chr8:1768004-1798128
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:803)
CpG islands
(count:3607)
Chromatin interactive
region (count:32)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:803 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:1778106-1778154	K562	blood:	n/a	n/a
2	ATF3	chr8:1771788-1772056	K562	blood:	n/a	chr8:1771884-1771893 chr8:1771940-1771960 chr8:1771940-1771949
3	ATF3	chr8:1771806-1772022	H1-hESC	embryonic stem cell:	n/a	chr8:1771884-1771893 chr8:1771940-1771960 chr8:1771940-1771949
4	BACH1	chr8:1789055-1789249	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr8:1777522-1777722	K562	blood:	n/a	n/a
6	BACH1	chr8:1772500-1772545	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr8:1786794-1788094	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr8:1771322-1772099	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr8:1777228-1777861	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr8:1792557-1792581	K562	blood:	n/a	n/a
11	BHLHE40	chr8:1771793-1772093	K562	blood:	n/a	n/a
12	BHLHE40	chr8:1777502-1777862	K562	blood:	n/a	n/a
13	BHLHE40	chr8:1771338-1771455	K562	blood:	n/a	n/a
14	BRCA1	chr8:1771884-1772159	Hela-S3	cervix:	n/a	n/a
15	BRCA1	chr8:1792391-1792629	GM12878	blood:	n/a	n/a
16	BRCA1	chr8:1792449-1792452	HepG2	liver:	n/a	n/a
17	CBX3	chr8:1792450-1792695	K562	blood:	n/a	n/a
18	CBX3	chr8:1771711-1772165	K562	blood:	n/a	n/a
19	CBX3	chr8:1771260-1771580	K562	blood:	n/a	n/a
20	CCNT2	chr8:1794192-1794427	K562	blood:	n/a	n/a
21	CCNT2	chr8:1777538-1777751	K562	blood:	n/a	n/a
22	CCNT2	chr8:1771724-1772142	K562	blood:	n/a	chr8:1771784-1771793
23	CEBPB	chr8:1791838-1791972	HepG2	liver:	n/a	chr8:1791884-1791895
24	CEBPB	chr8:1768611-1768802	HepG2	liver:	n/a	n/a
25	CEBPB	chr8:1768456-1768774	K562	blood:	n/a	n/a
26	CEBPB	chr8:1771812-1772111	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr8:1771263-1771598	Hela-S3	cervix:	n/a	n/a
28	CHD2	chr8:1771333-1772203	H1-hESC	embryonic stem cell:	n/a	chr8:1771616-1771626 chr8:1771785-1771795
29	CHD2	chr8:1771333-1772575	Hela-S3	cervix:	n/a	chr8:1772438-1772448 chr8:1772508-1772518 chr8:1771616-1771626 chr8:1771785-1771795 chr8:1772352-1772362
30	CHD2	chr8:1792600-1792732	HepG2	liver:	n/a	n/a
31	CHD2	chr8:1771658-1772195	K562	blood:	n/a	chr8:1771785-1771795
32	CHD2	chr8:1789068-1789300	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD2	chr8:1792554-1792562	Hela-S3	cervix:	n/a	n/a
34	CREB1	chr8:1771286-1771573	A549	lung:	n/a	n/a
35	CREB1	chr8:1771668-1772168	A549	lung:	n/a	n/a
36	CREB1	chr8:1771616-1772282	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTBP2	chr8:1771575-1772007	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr8:1777620-1777770	HBMEC	blood vessel:	n/a	n/a
39	CTCF	chr8:1785820-1785970	SK-N-SH_RA	brain:	n/a	chr8:1785903-1785916 chr8:1785900-1785918
40	CTCF	chr8:1785818-1785960	MCF-7	breast:	n/a	chr8:1785903-1785916 chr8:1785900-1785918
41	CTCF	chr8:1789143-1789246	HepG2	liver:	n/a	n/a
42	CTCF	chr8:1789080-1789230	WERI-Rb-1	eye:	n/a	n/a
43	CTCF	chr8:1785845-1785954	MCF-7	breast:	n/a	chr8:1785903-1785916 chr8:1785900-1785918
44	CTCF	chr8:1789100-1789250	HepG2	liver:	n/a	n/a
45	CTCF	chr8:1785920-1786070	NB4	blood:	n/a	n/a
46	CTCF	chr8:1780945-1781039	Pancreas_OC	pancreas:	n/a	n/a
47	CTCF	chr8:1771620-1771770	AG04449	skin:	n/a	n/a
48	CTCF	chr8:1777660-1777810	AoAF	blood vessel:	n/a	n/a
49	CTCF	chr8:1795860-1796010	HMF	breast:	n/a	n/a
50	CTCF	chr8:1795740-1795890	AG09319	gingival:	n/a	n/a

(count:3607 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:1789288-1789338	GM12891	blood:	n/a
2	chr8:1794627-1794677	ECC-1	luminal epithelium:	n/a
3	chr8:1777766-1777816	AG10803	skin:	n/a
4	chr8:1772352-1772402	HCPEpiC	choroid plexus:	n/a
5	chr8:1786207-1786257	IMR90	lung:	fetal
6	chr8:1786207-1786257	LNCaP	prostate:	n/a
7	chr8:1773758-1773808	HCM	heart:	n/a
8	chr8:1779625-1779675	HCT-116	colon:	n/a
9	chr8:1789288-1789338	GM12891	blood:	n/a
10	chr8:1794627-1794677	ECC-1	luminal epithelium:	n/a
11	chr8:1777766-1777816	AG10803	skin:	n/a
12	chr8:1772352-1772402	HCPEpiC	choroid plexus:	n/a
13	chr8:1786207-1786257	IMR90	lung:	fetal
14	chr8:1786207-1786257	LNCaP	prostate:	n/a
15	chr8:1773758-1773808	HCM	heart:	n/a
16	chr8:1779625-1779675	HCT-116	colon:	n/a
17	chr8:1792160-1792210	HAEpiC	amniotic membrane:	n/a
18	chr8:1797886-1797936	Hepatocyte	liver:	n/a
19	chr8:1771541-1771591	PrEC	prostate:	n/a
20	chr8:1786207-1786257	Caco-2	colon:	n/a
21	chr8:1796506-1796556	H1-hESC	embryonic stem cell:	embryo
22	chr8:1779056-1779106	SK-N-SH	brain:	n/a
23	chr8:1772080-1772130	GM06990	blood:	n/a
24	chr8:1794627-1794677	HAEpiC	amniotic membrane:	n/a
25	chr8:1796568-1796618	AG10803	skin:	n/a
26	chr8:1777766-1777816	AG09309	skin:	n/a
27	chr8:1782850-1782900	GM06990	blood:	n/a
28	chr8:1792160-1792210	HL-60	blood:	n/a
29	chr8:1788325-1788375	NHBE	bronchial:	n/a
30	chr8:1785833-1785883	ProgFib	skin:	n/a
31	chr8:1786072-1786122	Jurkat	blood:	n/a
32	chr8:1779625-1779675	AG10803	skin:	n/a
33	chr8:1797886-1797936	SKMC	muscle:	n/a
34	chr8:1777766-1777816	HRE	kidney:	n/a
35	chr8:1771973-1772023	LNCaP	prostate:	n/a
36	chr8:1797917-1797967	T-47D	breast:	n/a
37	chr8:1789267-1789317	HEK293	kidney:	embryo
38	chr8:1790905-1790955	AG09319	gingival:	n/a
39	chr8:1776347-1776397	Hela-S3	cervix:	n/a
40	chr8:1789169-1789219	T-47D	breast:	n/a
41	chr8:1779117-1779167	NH-A	brain:	n/a
42	chr8:1783980-1784030	AG04449	skin:	fetal
43	chr8:1772352-1772402	SK-N-SH	brain:	n/a
44	chr8:1788325-1788375	AG04449	skin:	fetal
45	chr8:1796568-1796618	HNPCEpiC	eye:	n/a
46	chr8:1790793-1790843	MCF-7	breast:	n/a
47	chr8:1789537-1789587	A549	lung:	n/a
48	chr8:1771541-1771591	HCM	heart:	n/a
49	chr8:1785833-1785883	HIPEpiC	eye:	n/a
50	chr8:1789288-1789338	ovcar-3	ovarian:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr8:1710415..1713375-chr8:1784468..1786850,2	MCF-7	breast:
2	chr8:1703592..1705221-chr8:1778659..1781628,2	MCF-7	breast:
3	chr8:1771136..1772958-chr8:1777807..1779958,2	K562	blood:
4	chr8:1792966..1795761-chr8:1797297..1800005,2	MCF-7	breast:
5	chr8:1790802..1792919-chr8:1794714..1797248,2	K562	blood:
6	chr8:1790802..1792919-chr8:1794714..1797248,2	K562	blood:
7	chr8:1778222..1780570-chr8:1782075..1784994,4	MCF-7	breast:
8	chr8:1692125..1694169-chr8:1767018..1769382,2	MCF-7	breast:
9	chr8:1711111..1712724-chr8:1772703..1775383,2	MCF-7	breast:
10	chr8:1792966..1795761-chr8:1797297..1800005,2	MCF-7	breast:
11	chr8:1770355..1772056-chr8:1783670..1785482,2	MCF-7	breast:
12	chr8:1770355..1772056-chr8:1783670..1785482,2	MCF-7	breast:
13	chr8:1768039..1769894-chr8:1773535..1776325,2	MCF-7	breast:
14	chr8:1754619..1756376-chr8:1765622..1768454,2	K562	blood:
15	chr8:1731431..1734296-chr8:1777100..1779564,2	MCF-7	breast:
16	chr8:1757521..1759166-chr8:1766213..1768564,2	K562	blood:
17	chr8:1770343..1774803-chr8:1776185..1779512,9	MCF-7	breast:
18	chr8:1709347..1712341-chr8:1770235..1771752,2	MCF-7	breast:
19	chr8:1791902..1794095-chr8:1800796..1802523,2	K562	blood:
20	chr8:1784051..1785744-chr8:1790168..1791878,2	MCF-7	breast:
21	chr8:1708451..1710291-chr8:1769924..1772142,2	K562	blood:
22	chr8:1769937..1771639-chr8:1774044..1776450,2	MCF-7	breast:
23	chr8:1710918..1712882-chr8:1766102..1768969,2	K562	blood:
24	chr8:1772602..1774106-chr8:1775619..1777566,2	K562	blood:
25	chr8:1791902..1793927-chr8:1800796..1802494,2	K562	blood:
26	chr8:1778222..1780570-chr8:1782075..1784994,4	MCF-7	breast:
27	chr8:1784051..1785744-chr8:1790168..1791878,2	MCF-7	breast:
28	chr8:1764550..1766629-chr8:1770415..1772487,2	K562	blood:
29	chr19:39574470..39577467-chr8:1791052..1792928,2	MCF-7	breast:
30	chr14:102430509..102431237-chr8:1771618..1772329,2	HCT-116	colon:
31	chr8:1772602..1774106-chr8:1775619..1777566,2	K562	blood:
32	chr8:1766697..1768556-chr8:1771343..1773099,2	MCF-7	breast:

No data

Variant related genes	Relation type
ARHGEF10	TF binding region
ARHGEF10	CpG island
ENSG00000104728	chromatin interactions
ENSG00000183760	chromatin interactions
ENSG00000182372	chromatin interactions
ENSG00000197102	chromatin interactions
ENSG00000253982	chromatin interactions
ENSG00000207826	chromatin interactions

Extended variants
information (count: 1942 )
Associated
traits (count: 118 )

Variant overlapped rSNPs/rCNVs (count:1942 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6558550	chr8:1768004-1768005	Weak transcription Enhancers	CpG island Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs141523684	chr8:1768010-1768011	Weak transcription Enhancers	CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs569827744	chr8:1768045-1768046	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs369943810	chr8:1768054-1768055	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs538958612	chr8:1768069-1768070	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs58927236	chr8:1768093-1768094	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs185461666	chr8:1768131-1768132	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs192053508	chr8:1768159-1768160	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs577746948	chr8:1768176-1768177	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs545131847	chr8:1768183-1768184	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs554315724	chr8:1768198-1768199	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs559814841	chr8:1768199-1768200	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs574223938	chr8:1768211-1768212	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs542654895	chr8:1768257-1768258	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs554790763	chr8:1768301-1768302	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs372608433	chr8:1768302-1768303	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs376481444	chr8:1768315-1768316	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs115536199	chr8:1768324-1768325	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs145243171	chr8:1768401-1768402	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs78396585	chr8:1768422-1768423	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs181501844	chr8:1768432-1768433	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs7002072	chr8:1768448-1768449	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs548579903	chr8:1768467-1768468	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs78157513	chr8:1768477-1768478	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs372922204	chr8:1768485-1768486	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs529823292	chr8:1768489-1768490	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs187415708	chr8:1768491-1768492	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs34915482	chr8:1768494-1768495	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs548397531	chr8:1768546-1768547	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs138064158	chr8:1768560-1768561	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs538526115	chr8:1768573-1768574	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs191879267	chr8:1768634-1768635	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs565838228	chr8:1768635-1768636	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs79927892	chr8:1768639-1768640	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs554853815	chr8:1768643-1768644	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs113040206	chr8:1768671-1768672	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs536789824	chr8:1768673-1768674	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs556252202	chr8:1768675-1768676	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs182355582	chr8:1768708-1768709	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs549794128	chr8:1768716-1768717	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs186934168	chr8:1768718-1768719	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs565247860	chr8:1768730-1768731	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs572448131	chr8:1768731-1768732	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs77269271	chr8:1768778-1768779	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs112964070	chr8:1768803-1768804	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs561179944	chr8:1768840-1768841	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs569465677	chr8:1768847-1768848	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs111831079	chr8:1768855-1768856	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs4474063	chr8:1768890-1768891	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs189751817	chr8:1768946-1768947	Weak transcription Enhancers	Chromatin interactive region	3 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
Tetralogy of Fallot	22912587	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Lung adenocarcinoma	21935476	CNVD

Chromatin state (count:1677 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:1762000-1771400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr8:1762800-1770200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr8:1763200-1771000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr8:1763400-1770400	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr8:1764000-1771000	Weak transcription	Brain Substantia Nigra	brain
6	chr8:1764200-1768600	Enhancers	Lung	lung
7	chr8:1765600-1768400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr8:1765600-1770200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
9	chr8:1765600-1770800	Weak transcription	Brain Cingulate Gyrus	brain
10	chr8:1765600-1771200	Weak transcription	Right Atrium	heart
11	chr8:1765800-1770200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr8:1765800-1770400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
13	chr8:1765800-1770400	Weak transcription	Brain Anterior Caudate	brain
14	chr8:1765800-1771000	Weak transcription	Brain Hippocampus Middle	brain
15	chr8:1765800-1771400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr8:1766000-1768200	Weak transcription	HUVEC	blood vessel
17	chr8:1766000-1771000	Weak transcription	Placenta Amnion	Placenta Amnion
18	chr8:1766200-1771200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr8:1766400-1770200	Weak transcription	H1 Cell Line	embryonic stem cell
20	chr8:1766400-1770600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
21	chr8:1766400-1771000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
22	chr8:1766400-1771400	Weak transcription	Left Ventricle	heart
23	chr8:1766400-1771400	Weak transcription	Pancreas	Pancrea
24	chr8:1766600-1768800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr8:1766600-1770200	Weak transcription	HUES48 Cell Line	embryonic stem cell
26	chr8:1766600-1770200	Weak transcription	HUES6 Cell Line	embryonic stem cell
27	chr8:1766600-1771600	Weak transcription	Spleen	Spleen
28	chr8:1766800-1771200	Weak transcription	NHEK	skin
29	chr8:1767400-1768800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr8:1767600-1768600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr8:1767800-1771600	Weak transcription	Gastric	stomach
32	chr8:1768200-1769000	Enhancers	HUVEC	blood vessel
33	chr8:1768200-1770200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
34	chr8:1768400-1768600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
35	chr8:1768400-1768800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr8:1768600-1771400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr8:1768600-1771600	Weak transcription	Lung	lung
38	chr8:1768800-1771000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr8:1768800-1771400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr8:1769000-1770800	Weak transcription	HUVEC	blood vessel
41	chr8:1769600-1771000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
42	chr8:1770200-1770400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr8:1770200-1770600	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr8:1770200-1770600	Enhancers	H1 Cell Line	embryonic stem cell
45	chr8:1770200-1770800	Enhancers	iPS-20b Cell Line	embryonic stem cell
46	chr8:1770200-1771000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr8:1770200-1771000	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr8:1770200-1771000	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr8:1770200-1771000	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr8:1770400-1770800	Enhancers	iPS-15b Cell Line	embryonic stem cell

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