Variant report

Variant	nsv824455
Chromosome Location	chr8:1767334-1772637
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr8:1771788-1772056	K562	blood:	n/a	chr8:1771884-1771893 chr8:1771940-1771960 chr8:1771940-1771949
2	ATF3	chr8:1771806-1772022	H1-hESC	embryonic stem cell:	n/a	chr8:1771884-1771893 chr8:1771940-1771960 chr8:1771940-1771949
3	BACH1	chr8:1772500-1772545	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr8:1771322-1772099	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr8:1771793-1772093	K562	blood:	n/a	n/a
6	BHLHE40	chr8:1771338-1771455	K562	blood:	n/a	n/a
7	BRCA1	chr8:1771884-1772159	Hela-S3	cervix:	n/a	n/a
8	CBX3	chr8:1771711-1772165	K562	blood:	n/a	n/a
9	CBX3	chr8:1771260-1771580	K562	blood:	n/a	n/a
10	CCNT2	chr8:1771724-1772142	K562	blood:	n/a	chr8:1771784-1771793
11	CEBPB	chr8:1771812-1772111	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr8:1771263-1771598	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr8:1768456-1768774	K562	blood:	n/a	n/a
14	CEBPB	chr8:1768611-1768802	HepG2	liver:	n/a	n/a
15	CHD2	chr8:1771658-1772195	K562	blood:	n/a	chr8:1771785-1771795
16	CHD2	chr8:1771333-1772203	H1-hESC	embryonic stem cell:	n/a	chr8:1771616-1771626 chr8:1771785-1771795
17	CHD2	chr8:1771333-1772575	Hela-S3	cervix:	n/a	chr8:1772438-1772448 chr8:1772508-1772518 chr8:1771616-1771626 chr8:1771785-1771795 chr8:1772352-1772362
18	CREB1	chr8:1771668-1772168	A549	lung:	n/a	n/a
19	CREB1	chr8:1771616-1772282	H1-hESC	embryonic stem cell:	n/a	n/a
20	CREB1	chr8:1771286-1771573	A549	lung:	n/a	n/a
21	CTBP2	chr8:1771575-1772007	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr8:1771918-1771995	Kidney_OC	kidney:	n/a	chr8:1771932-1771945
23	CTCF	chr8:1768054-1768088	Lung_OC	lung:	n/a	n/a
24	CTCF	chr8:1770431-1770602	K562	blood:	n/a	n/a
25	CTCF	chr8:1770420-1770570	A549	lung:	n/a	n/a
26	CTCF	chr8:1771620-1771770	AG04449	skin:	n/a	n/a
27	CTCF	chr8:1770271-1770602	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr8:1770380-1770530	HCPEpiC	choroid plexus:	n/a	n/a
29	CTCF	chr8:1771901-1771988	K562	blood:	n/a	chr8:1771932-1771945
30	CTCF	chr8:1770362-1770555	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr8:1770277-1770558	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr8:1770400-1770550	Caco-2	colon:	n/a	n/a
33	E2F1	chr8:1771341-1772235	Hela-S3	cervix:	n/a	chr8:1771938-1771947 chr8:1771867-1771879 chr8:1771784-1771796 chr8:1771886-1771895 chr8:1771784-1771793 chr8:1771974-1771985
34	E2F4	chr8:1771170-1772176	MCF10A-Er-Src	breast:	n/a	chr8:1771938-1771947 chr8:1771867-1771879 chr8:1771784-1771796 chr8:1771886-1771895 chr8:1771784-1771793
35	E2F6	chr8:1771152-1772281	H1-hESC	embryonic stem cell:	n/a	chr8:1771938-1771947 chr8:1771867-1771879 chr8:1771784-1771796 chr8:1771886-1771895 chr8:1771784-1771793
36	E2F6	chr8:1771721-1772200	A549	lung:	n/a	chr8:1771938-1771947 chr8:1771867-1771879 chr8:1771784-1771796 chr8:1771886-1771895 chr8:1771784-1771793
37	E2F6	chr8:1771631-1772167	K562	blood:	n/a	chr8:1771938-1771947 chr8:1771867-1771879 chr8:1771784-1771796 chr8:1771886-1771895 chr8:1771784-1771793
38	E2F6	chr8:1771718-1772126	K562	blood:	n/a	chr8:1771938-1771947 chr8:1771867-1771879 chr8:1771784-1771796 chr8:1771886-1771895 chr8:1771784-1771793
39	E2F6	chr8:1771346-1772213	K562	blood:	n/a	chr8:1771938-1771947 chr8:1771867-1771879 chr8:1771784-1771796 chr8:1771886-1771895 chr8:1771784-1771793
40	E2F6	chr8:1772218-1772339	K562	blood:	n/a	n/a
41	E2F6	chr8:1771132-1772286	A549	lung:	n/a	chr8:1771938-1771947 chr8:1771867-1771879 chr8:1771784-1771796 chr8:1771886-1771895 chr8:1771784-1771793
42	E2F6	chr8:1771340-1771608	A549	lung:	n/a	n/a
43	E2F6	chr8:1771306-1772169	H1-hESC	embryonic stem cell:	n/a	chr8:1771938-1771947 chr8:1771867-1771879 chr8:1771784-1771796 chr8:1771886-1771895 chr8:1771784-1771793
44	E2F6	chr8:1771290-1771509	K562	blood:	n/a	n/a
45	EGR1	chr8:1771348-1772352	HCT-116	colon:	n/a	chr8:1771900-1771909 chr8:1771894-1771905 chr8:1771635-1771650 chr8:1771887-1771900 chr8:1771862-1771875 chr8:1771894-1771904 chr8:1771933-1771946 chr8:1771888-1771898 chr8:1771862-1771875 chr8:1771892-1771906 chr8:1771935-1771945 chr8:1771972-1771981
46	EGR1	chr8:1771560-1772210	ECC-1	luminal epithelium:	n/a	chr8:1771900-1771909 chr8:1771894-1771905 chr8:1771635-1771650 chr8:1771887-1771900 chr8:1771862-1771875 chr8:1771894-1771904 chr8:1771933-1771946 chr8:1771888-1771898 chr8:1771862-1771875 chr8:1771892-1771906 chr8:1771935-1771945 chr8:1771972-1771981
47	EGR1	chr8:1771481-1772103	H1-hESC	embryonic stem cell:	n/a	chr8:1771900-1771909 chr8:1771894-1771905 chr8:1771635-1771650 chr8:1771887-1771900 chr8:1771862-1771875 chr8:1771894-1771904 chr8:1771933-1771946 chr8:1771888-1771898 chr8:1771862-1771875 chr8:1771892-1771906 chr8:1771935-1771945 chr8:1771972-1771981
48	EGR1	chr8:1771637-1772136	K562	blood:	n/a	chr8:1771900-1771909 chr8:1771894-1771905 chr8:1771887-1771900 chr8:1771862-1771875 chr8:1771894-1771904 chr8:1771933-1771946 chr8:1771888-1771898 chr8:1771862-1771875 chr8:1771892-1771906 chr8:1771935-1771945 chr8:1771972-1771981
49	EGR1	chr8:1771632-1772161	MCF-7	breast:	n/a	chr8:1771900-1771909 chr8:1771894-1771905 chr8:1771635-1771650 chr8:1771887-1771900 chr8:1771862-1771875 chr8:1771894-1771904 chr8:1771933-1771946 chr8:1771888-1771898 chr8:1771862-1771875 chr8:1771892-1771906 chr8:1771935-1771945 chr8:1771972-1771981
50	EGR1	chr8:1771635-1772098	K562	blood:	n/a	chr8:1771900-1771909 chr8:1771894-1771905 chr8:1771635-1771650 chr8:1771887-1771900 chr8:1771862-1771875 chr8:1771894-1771904 chr8:1771933-1771946 chr8:1771888-1771898 chr8:1771862-1771875 chr8:1771892-1771906 chr8:1771935-1771945 chr8:1771972-1771981

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:1767962-1768012	SK-N-SH	brain:	n/a
2	chr8:1772393-1772443	LNCaP	prostate:	n/a
3	chr8:1772116-1772166	ProgFib	skin:	n/a
4	chr8:1767962-1768012	A549	lung:	n/a
5	chr8:1772393-1772443	NT2-D1	testis:	n/a
6	chr8:1772080-1772130	U87	brain:	n/a
7	chr8:1772080-1772130	T-47D	breast:	n/a
8	chr8:1771973-1772023	SK-N-MC	brain:	n/a
9	chr8:1772080-1772130	SAEC	small airway:	n/a
10	chr8:1772264-1772314	NHBE	bronchial:	n/a
11	chr8:1772116-1772166	PANC-1	pancreas:	n/a
12	chr8:1771541-1771591	PANC-1	pancreas:	n/a
13	chr8:1772116-1772166	SK-N-MC	brain:	n/a
14	chr8:1772352-1772402	HUVEC	blood vessel:	n/a
15	chr8:1772116-1772166	HRE	kidney:	n/a
16	chr8:1771973-1772023	SAEC	small airway:	n/a
17	chr8:1771541-1771591	HAEpiC	amniotic membrane:	n/a
18	chr8:1771541-1771591	HCPEpiC	choroid plexus:	n/a
19	chr8:1771973-1772023	T-47D	breast:	n/a
20	chr8:1771561-1771611	HPAEpiC	pulmonary alveolar:	n/a
21	chr8:1772352-1772402	HCM	heart:	n/a
22	chr8:1771973-1772023	RPTEC	kidney:	n/a
23	chr8:1771973-1772023	HCF	heart:	n/a
24	chr8:1772352-1772402	AG04450	lung:	fetal
25	chr8:1771561-1771611	NHBE	bronchial:	n/a
26	chr8:1772264-1772314	GM19239	blood:	n/a
27	chr8:1772080-1772130	GM19239	blood:	n/a
28	chr8:1771561-1771611	BJ	skin:	n/a
29	chr8:1772393-1772443	RPTEC	kidney:	n/a
30	chr8:1771541-1771591	AG10803	skin:	n/a
31	chr8:1767962-1768012	CMK	blood:	n/a
32	chr8:1767962-1768012	AG04449	skin:	fetal
33	chr8:1771561-1771611	Hela-S3	cervix:	n/a
34	chr8:1772264-1772314	HepG2	liver:	n/a
35	chr8:1772352-1772402	Caco-2	colon:	n/a
36	chr8:1772116-1772166	LNCaP	prostate:	n/a
37	chr8:1772264-1772314	GM12891	blood:	n/a
38	chr8:1772116-1772166	AoSMC	blood vessel:	n/a
39	chr8:1772264-1772314	ECC-1	luminal epithelium:	n/a
40	chr8:1771561-1771611	LNCaP	prostate:	n/a
41	chr8:1772264-1772314	BJ	skin:	n/a
42	chr8:1772264-1772314	K562	blood:	n/a
43	chr8:1771561-1771611	AG04450	lung:	fetal
44	chr8:1771541-1771591	AG09309	skin:	n/a
45	chr8:1771973-1772023	Caco-2	colon:	n/a
46	chr8:1767962-1768012	HMEC	breast:	n/a
47	chr8:1772352-1772402	HRCEpiC	kidney:	n/a
48	chr8:1772116-1772166	HRCEpiC	kidney:	n/a
49	chr8:1772264-1772314	SKMC	muscle:	n/a
50	chr8:1771541-1771591	HMEC	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:1764550..1766629-chr8:1770415..1772487,2	K562	blood:
2	chr8:1769937..1771639-chr8:1774044..1776450,2	MCF-7	breast:
3	chr8:1768039..1769894-chr8:1773535..1776325,2	MCF-7	breast:
4	chr8:1770355..1772056-chr8:1783670..1785482,2	MCF-7	breast:
5	chr14:102430509..102431237-chr8:1771618..1772329,2	HCT-116	colon:
6	chr8:1772602..1774106-chr8:1775619..1777566,2	K562	blood:
7	chr8:1708451..1710291-chr8:1769924..1772142,2	K562	blood:
8	chr8:1709347..1712341-chr8:1770235..1771752,2	MCF-7	breast:
9	chr8:1710918..1712882-chr8:1766102..1768969,2	K562	blood:
10	chr8:1757521..1759166-chr8:1766213..1768564,2	K562	blood:
11	chr8:1766697..1768556-chr8:1771343..1773099,2	MCF-7	breast:
12	chr8:1754619..1756376-chr8:1765622..1768454,2	K562	blood:
13	chr8:1710901..1715165-chr8:1763143..1767602,4	K562	blood:
14	chr8:1692125..1694169-chr8:1767018..1769382,2	MCF-7	breast:

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

Extended variants
information (count: 270 )
Associated
traits (count: 118 )

Variant overlapped rSNPs/rCNVs (count:270 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs80217526	chr8:1767334-1767335	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs551994002	chr8:1767370-1767371	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs144653615	chr8:1767401-1767402	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs533671121	chr8:1767409-1767410	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs368811901	chr8:1767411-1767412	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs553338045	chr8:1767429-1767430	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs192892768	chr8:1767446-1767447	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs372139006	chr8:1767496-1767497	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs368439305	chr8:1767497-1767498	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs536115396	chr8:1767571-1767572	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs551167826	chr8:1767603-1767604	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs138618595	chr8:1767607-1767608	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs77684828	chr8:1767615-1767616	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs7827288	chr8:1767633-1767634	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs185836206	chr8:1767637-1767638	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs190213667	chr8:1767652-1767653	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs180908237	chr8:1767687-1767688	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs112579422	chr8:1767720-1767721	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs558268246	chr8:1767723-1767724	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs578132301	chr8:1767731-1767732	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs540744541	chr8:1767753-1767754	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs560482716	chr8:1767757-1767758	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs78524408	chr8:1767801-1767802	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs534180450	chr8:1767850-1767851	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs543262597	chr8:1767851-1767852	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs61024005	chr8:1767879-1767880	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs532080594	chr8:1767887-1767888	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs183525098	chr8:1767892-1767893	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs571545185	chr8:1767896-1767897	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs78946839	chr8:1767897-1767898	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs533476065	chr8:1767902-1767903	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs188601405	chr8:1767955-1767956	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs6558550	chr8:1768004-1768005	Weak transcription Enhancers	CpG island Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs141523684	chr8:1768010-1768011	Weak transcription Enhancers	CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs569827744	chr8:1768045-1768046	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs369943810	chr8:1768054-1768055	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs538958612	chr8:1768069-1768070	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs58927236	chr8:1768093-1768094	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs185461666	chr8:1768131-1768132	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs192053508	chr8:1768159-1768160	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs577746948	chr8:1768176-1768177	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs545131847	chr8:1768183-1768184	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs554315724	chr8:1768198-1768199	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs559814841	chr8:1768199-1768200	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs574223938	chr8:1768211-1768212	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs542654895	chr8:1768257-1768258	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs554790763	chr8:1768301-1768302	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs372608433	chr8:1768302-1768303	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs376481444	chr8:1768315-1768316	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs115536199	chr8:1768324-1768325	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 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:338 , 50 per page) page: 1 2 3 4 5 6 7

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	chr8:1766600-1767600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr8:1766600-1768800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr8:1766600-1770200	Weak transcription	HUES48 Cell Line	embryonic stem cell
27	chr8:1766600-1770200	Weak transcription	HUES6 Cell Line	embryonic stem cell
28	chr8:1766600-1771600	Weak transcription	Spleen	Spleen
29	chr8:1766800-1767600	Weak transcription	Gastric	stomach
30	chr8:1766800-1771200	Weak transcription	NHEK	skin
31	chr8:1767400-1768800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr8:1767600-1767800	Enhancers	Gastric	stomach
33	chr8:1767600-1768000	Enhancers	NHDF-Ad	bronchial
34	chr8:1767600-1768600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr8:1767800-1768000	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr8:1767800-1771600	Weak transcription	Gastric	stomach
37	chr8:1768200-1769000	Enhancers	HUVEC	blood vessel
38	chr8:1768200-1770200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
39	chr8:1768400-1768600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
40	chr8:1768400-1768800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr8:1768600-1771400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr8:1768600-1771600	Weak transcription	Lung	lung
43	chr8:1768800-1771000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr8:1768800-1771400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr8:1769000-1770800	Weak transcription	HUVEC	blood vessel
46	chr8:1769600-1771000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
47	chr8:1770200-1770400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr8:1770200-1770600	Enhancers	ES-I3 Cell Line	embryonic stem cell
49	chr8:1770200-1770600	Enhancers	H1 Cell Line	embryonic stem cell
50	chr8:1770200-1770800	Enhancers	iPS-20b Cell Line	embryonic stem cell

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