Variant report

Variant	nsv1025426
Chromosome Location	chr8:10942929-11037903
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	ARID3A	chr8:10950023-10950231	HepG2	liver:	n/a	n/a
2	ATF2	chr8:10981506-10982207	GM12878	blood:	n/a	n/a
3	ATF2	chr8:10981488-10982324	GM12878	blood:	n/a	n/a
4	BACH1	chr8:11026563-11026651	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr8:10962868-10963169	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr8:11020411-11020492	K562	blood:	n/a	n/a
7	BACH1	chr8:10949902-10950437	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr8:11034754-11035025	GM12878	blood:	n/a	chr8:11034880-11034891
9	BATF	chr8:11018551-11018700	GM12878	blood:	n/a	n/a
10	BCL3	chr8:11027876-11028173	GM12878	blood:	n/a	n/a
11	BCL3	chr8:10955674-10955884	GM12878	blood:	n/a	n/a
12	BCL3	chr8:10955629-10955850	GM12878	blood:	n/a	n/a
13	BCLAF1	chr8:10981539-10982080	GM12878	blood:	n/a	n/a
14	BHLHE40	chr8:11016374-11016667	GM12878	blood:	n/a	n/a
15	BHLHE40	chr8:10981392-10982182	GM12878	blood:	n/a	n/a
16	BHLHE40	chr8:10949920-10950325	GM12878	blood:	n/a	n/a
17	BHLHE40	chr8:10949925-10950310	HepG2	liver:	n/a	n/a
18	BHLHE40	chr8:10949941-10950287	K562	blood:	n/a	n/a
19	BHLHE40	chr8:10948427-10948708	GM12878	blood:	n/a	n/a
20	BHLHE40	chr8:10949968-10950240	HepG2	liver:	n/a	n/a
21	CEBPB	chr8:10984322-10984480	HepG2	liver:	n/a	chr8:10984400-10984411
22	CEBPB	chr8:11027105-11027329	K562	blood:	n/a	chr8:11027223-11027234
23	CEBPB	chr8:11006179-11006486	Hela-S3	cervix:	n/a	chr8:11006326-11006337
24	CEBPB	chr8:11006147-11006536	A549	lung:	n/a	chr8:11006326-11006337
25	CEBPB	chr8:11027061-11027382	IMR90	lung:	n/a	chr8:11027223-11027234
26	CEBPB	chr8:10948624-10948638	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr8:10969452-10969699	K562	blood:	n/a	chr8:10969592-10969603 chr8:10969594-10969603 chr8:10969592-10969605 chr8:10969594-10969605
28	CEBPB	chr8:11027975-11028266	HepG2	liver:	n/a	chr8:11028140-11028151
29	CEBPB	chr8:11006185-11006505	K562	blood:	n/a	chr8:11006326-11006337
30	CEBPB	chr8:10969507-10969750	HepG2	liver:	n/a	chr8:10969592-10969603 chr8:10969594-10969603 chr8:10969592-10969605 chr8:10969594-10969605
31	CEBPB	chr8:11027123-11027301	A549	lung:	n/a	chr8:11027223-11027234
32	CEBPB	chr8:11027148-11027316	HepG2	liver:	n/a	chr8:11027223-11027234
33	CEBPB	chr8:11028120-11028158	H1-hESC	embryonic stem cell:	n/a	chr8:11028140-11028151
34	CEBPB	chr8:11006152-11006488	H1-hESC	embryonic stem cell:	n/a	chr8:11006326-11006337
35	CEBPB	chr8:11028014-11028243	IMR90	lung:	n/a	chr8:11028140-11028151
36	CEBPB	chr8:10949928-10950160	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr8:11006166-11006493	HepG2	liver:	n/a	chr8:11006326-11006337
38	CEBPB	chr8:10986551-10986831	IMR90	lung:	n/a	n/a
39	CEBPB	chr8:10969442-10969756	IMR90	lung:	n/a	chr8:10969592-10969603 chr8:10969594-10969603 chr8:10969592-10969605 chr8:10969594-10969605
40	CEBPB	chr8:11006150-11006516	IMR90	lung:	n/a	chr8:11006326-11006337
41	CHD1	chr8:10981485-10982120	GM12878	blood:	n/a	n/a
42	CHD2	chr8:10949955-10950286	H1-hESC	embryonic stem cell:	n/a	n/a
43	CHD2	chr8:10981673-10981992	GM12878	blood:	n/a	n/a
44	CTCF	chr8:10996788-10997008	H1-hESC	embryonic stem cell:	n/a	chr8:10996901-10996909 chr8:10996892-10996905
45	CTCF	chr8:10962850-10963009	H1-hESC	embryonic stem cell:	n/a	chr8:10962907-10962920 chr8:10962905-10962923
46	CTCF	chr8:10948500-10948650	GM12872	blood:	n/a	chr8:10948584-10948602 chr8:10948586-10948607 chr8:10948585-10948601 chr8:10948587-10948595 chr8:10948587-10948600
47	CTCF	chr8:10948480-10948697	LNCaP	prostate:	n/a	chr8:10948584-10948602 chr8:10948586-10948607 chr8:10948585-10948601 chr8:10948587-10948595 chr8:10948587-10948600
48	CTCF	chr8:10948479-10948690	A549	lung:	n/a	chr8:10948584-10948602 chr8:10948586-10948607 chr8:10948585-10948601 chr8:10948587-10948595 chr8:10948587-10948600
49	CTCF	chr8:10962820-10962970	HEK293	kidney:	n/a	chr8:10962907-10962920 chr8:10962905-10962923
50	CTCF	chr8:10948478-10948703	A549	lung:	n/a	chr8:10948584-10948602 chr8:10948586-10948607 chr8:10948585-10948601 chr8:10948587-10948595 chr8:10948587-10948600

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:10965533-10965583	SKMC	muscle:	n/a
2	chr8:10988117-10988167	Hepatocyte	liver:	n/a
3	chr8:10966192-10966242	HCF	heart:	n/a
4	chr8:10996424-10996474	PANC-1	pancreas:	n/a
5	chr8:10965533-10965583	SKMC	muscle:	n/a
6	chr8:10988117-10988167	Hepatocyte	liver:	n/a
7	chr8:10966192-10966242	HCF	heart:	n/a
8	chr8:10996424-10996474	PANC-1	pancreas:	n/a
9	chr8:10982836-10982886	HRE	kidney:	n/a
10	chr8:10982668-10982718	GM12892	blood:	n/a
11	chr8:10965533-10965583	HRCEpiC	kidney:	n/a
12	chr8:10987869-10987919	ovcar-3	ovarian:	n/a
13	chr8:10982836-10982886	HEK293	kidney:	embryo
14	chr8:10965430-10965480	HUVEC	blood vessel:	n/a
15	chr8:10996424-10996474	PrEC	prostate:	n/a
16	chr8:10966251-10966301	HCT-116	colon:	n/a
17	chr8:10987869-10987919	BE2_C	brain:	n/a
18	chr8:10987869-10987919	SK-N-MC	brain:	n/a
19	chr8:10955796-10955846	NHDF-neo	bronchial:	n/a
20	chr8:10966192-10966242	T-47D	breast:	n/a
21	chr8:10966192-10966242	BE2_C	brain:	n/a
22	chr8:10955796-10955846	HCPEpiC	choroid plexus:	n/a
23	chr8:10987869-10987919	GM06990	blood:	n/a
24	chr8:10996424-10996474	SK-N-SH	brain:	n/a
25	chr8:10966251-10966301	PrEC	prostate:	n/a
26	chr8:10987869-10987919	LNCaP	prostate:	n/a
27	chr8:10966224-10966274	HIPEpiC	eye:	n/a
28	chr8:11021173-11021223	HCM	heart:	n/a
29	chr8:10966251-10966301	HRCEpiC	kidney:	n/a
30	chr8:10982668-10982718	PFSK-1	brain:	n/a
31	chr8:10955796-10955846	MCF10A-Er-Src	breast:	n/a
32	chr8:10965430-10965480	T-47D	breast:	n/a
33	chr8:10996424-10996474	BJ	skin:	n/a
34	chr8:10996424-10996474	SAEC	small airway:	n/a
35	chr8:10987869-10987919	GM12891	blood:	n/a
36	chr8:10982836-10982886	BJ	skin:	n/a
37	chr8:10988117-10988167	SK-N-SH_RA	brain:	n/a
38	chr8:11021173-11021223	SKMC	muscle:	n/a
39	chr8:10996424-10996474	HepG2	liver:	n/a
40	chr8:10966192-10966242	HEK293	kidney:	embryo
41	chr8:10965533-10965583	MCF-7	breast:	n/a
42	chr8:10982332-10982382	GM06990	blood:	n/a
43	chr8:10996424-10996474	GM12892	blood:	n/a
44	chr8:10966224-10966274	HMEC	breast:	n/a
45	chr8:10988117-10988167	LNCaP	prostate:	n/a
46	chr8:10988117-10988167	GM06990	blood:	n/a
47	chr8:10982668-10982718	MCF-7	breast:	n/a
48	chr8:10987869-10987919	U87	brain:	n/a
49	chr8:10966224-10966274	PrEC	prostate:	n/a
50	chr8:10965430-10965480	Caco-2	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:10953851..10956299-chr8:10959068..10961747,2	MCF-7	breast:
2	chr8:10989309..10991277-chr8:11000364..11001975,2	MCF-7	breast:
3	chr8:11011361..11013679-chr8:11086642..11088741,2	MCF-7	breast:
4	chr8:10987323..10988888-chr8:10996311..10998461,2	MCF-7	breast:
5	chr8:10953495..10955337-chr8:10955774..10957347,2	K562	blood:
6	chr8:10953495..10955337-chr8:10955774..10957347,2	K562	blood:
7	chr5:138973431..138974207-chr8:10970599..10971381,2	MCF-7	breast:
8	chr8:10948105..10949056-chr8:11136741..11137629,5	MCF-7	breast:
9	chr8:11020358..11021978-chr8:11037750..11039962,2	MCF-7	breast:
10	chr8:10953851..10956299-chr8:10959068..10961747,2	MCF-7	breast:
11	chr8:11020358..11021978-chr8:11037750..11039962,2	MCF-7	breast:
12	chr8:10890969..10893547-chr8:10959450..10962216,2	K562	blood:
13	chr8:10989309..10991277-chr8:11000364..11001975,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AF131215.3.1-2	chr8:10984315-10984600	NONHSAT125039
2	lnc-AF131215.3.1-2	chr8:10986134-10987275	NONHSAT125039
3	lnc-AF131215.4.1-3	chr8:11023544-11024685	ucscGeneNc_uc010lrw_1
4	lnc-AF131215.3.1-1	chr8:10980891-10982327	NONHSAT125036
5	lnc-AF131215.2.1-1	chr8:10962201-10964214	ENSG00000269918.1
6	lnc-AF131215.3.1-1	chr8:10983271-10983574	ENSG00000254936.3
7	lnc-AF131215.4.1-1	chr8:10994408-10996117	ENSG00000254556.1
8	lnc-AF131215.2.1-1	chr8:10965298-10967236	ENSG00000255310.2
9	lnc-AF131215.3.1-1	chr8:10980891-10982327	ENSG00000254936.3
10	lnc-AF131215.3.1-1	chr8:10983268-10983574	ENSG00000254936.3
11	lnc-AF131215.2.1-1	chr8:10964720-10967428	ENSG00000255310.1
12	lnc-MTMR9-1	chr8:10983268-10983574	ENSG00000247665
13	lnc-AF131215.4.1-3	chr8:11021724-11022010	ucscGeneNc_uc010lrw_1
14	lnc-AF131215.4.1-2	chr8:11018301-11019737	ucscGeneNc_uc010lrv_1
15	lnc-AF131215.2.1-1	chr8:10965064-10965184	NONHSAT125034
16	lnc-MTMR9-1	chr8:10980891-10982326	ENSG00000247665
17	lnc-AF131215.2.1-1	chr8:10962658-10964223	NONHSAT125034
18	lnc-AF131215.3.1-1	chr8:10980891-10982327	ENSG00000254936.3

Variant related genes	Relation type
ENSG00000269918	TF binding region
ENSG00000254936	TF binding region
ENSG00000231965	TF binding region
ENSG00000255310	TF binding region
ENSG00000215346	TF binding region
ENSG00000254556	TF binding region
ENSG00000269918	CpG island
ENSG00000254936	CpG island
ENSG00000231965	CpG island
ENSG00000255310	CpG island
ENSG00000215346	CpG island
ENSG00000254556	CpG island
ENSG00000215346	chromatin interactions
ENSG00000207600	chromatin interactions
ZFYVE20	miRNA target sites
KIF5C	miRNA target sites

Extended variants
information (count: 5323 )
Associated
traits (count: 138 )

Variant overlapped rSNPs/rCNVs (count:5323 , 50 per page) page: 1 2 3 4 5 6 7 ... 107

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17152841	chr8:10942929-10942930	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs114677581	chr8:10942941-10942942	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs142775403	chr8:10942949-10942950	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs562334978	chr8:10942962-10942963	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs532995888	chr8:10942973-10942974	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs140010745	chr8:10942979-10942980	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs190969661	chr8:10942984-10942985	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs182009328	chr8:10943000-10943001	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs534110305	chr8:10943010-10943011	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs186432332	chr8:10943014-10943015	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs190802660	chr8:10943044-10943045	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs149193430	chr8:10943074-10943075	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs556734275	chr8:10943090-10943091	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs78148452	chr8:10943095-10943096	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs550840064	chr8:10943098-10943099	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs529076740	chr8:10943111-10943112	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs182891856	chr8:10943197-10943198	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs572614134	chr8:10943210-10943211	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs543309826	chr8:10943221-10943222	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs548932971	chr8:10943232-10943233	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs573623060	chr8:10943234-10943235	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs543890314	chr8:10943241-10943242	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs562269713	chr8:10943252-10943253	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs532885352	chr8:10943270-10943271	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs2409691	chr8:10943276-10943277	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs560304356	chr8:10943283-10943284	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs527542702	chr8:10943293-10943294	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs549303058	chr8:10943307-10943308	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs567540256	chr8:10943323-10943324	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs35888233	chr8:10943337-10943338	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs531772487	chr8:10943338-10943339	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs187192666	chr8:10943345-10943346	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs148382326	chr8:10943368-10943369	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs539147759	chr8:10943369-10943370	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs531042427	chr8:10943391-10943392	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs141610444	chr8:10943409-10943410	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs145802426	chr8:10943438-10943439	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs7812573	chr8:10943449-10943450	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs2409692	chr8:10943455-10943456	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs2409693	chr8:10943468-10943469	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs543775694	chr8:10943489-10943490	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs191076996	chr8:10943542-10943543	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs555754518	chr8:10943546-10943547	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs577277386	chr8:10943556-10943557	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs547303339	chr8:10943570-10943571	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs138365092	chr8:10943643-10943644	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs567096174	chr8:10943658-10943659	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs71203369	chr8:10943659-10943660	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs11250116	chr8:10943660-10943661	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs187680067	chr8:10943662-10943663	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:138)

Disease	PMID	Source
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
Prostate cancer	16573809	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
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Autism	22495311	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Breast cancer	21990379	CNVD
Psoriasis	20403174	CNVD
Psoriasis	20663923	CNVD
Crohn''s disease	16909382	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Crohn''s disease	20877625	CNVD
Inflammatory disorder	20877625	CNVD
Cardiac defect	21933911	CNVD
Psoriasis	18059266	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Psoriasis	20877625	CNVD
Mental retardation	17847001	CNVD
Prostate cancer	17217626	CNVD
Schizophrenia	21399695	CNVD
Colorectal cancer	21128281	CNVD
Colorectal cancer	19455253	CNVD
Psoriasis	18848619	CNVD
Squamous cell cancer	19047905	CNVD
Colorectal cancer	17229543	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Developmental disorder	20461109	CNVD
abnormal development	18461090	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioblastoma multiforme	21138945	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Gastric cancer	21811585	CNVD
Colorectal cancer	16774939	CNVD
Breast cancer	22522925	CNVD
Acute lymphoblastic leukemia	21390130	CNVD

Chromatin state (count:876 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:10925600-10944400	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr8:10935200-10943800	Weak transcription	Brain Anterior Caudate	brain
3	chr8:10940600-10943400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr8:10941600-10943000	Enhancers	Gastric	stomach
5	chr8:10942200-10944400	Enhancers	Fetal Heart	heart
6	chr8:10942400-10943000	Enhancers	Pancreas	Pancrea
7	chr8:10942400-10943400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr8:10942400-10943400	Enhancers	Breast Myoepithelial Primary Cells	Breast
9	chr8:10942600-10943000	Enhancers	H1 Cell Line	embryonic stem cell
10	chr8:10942600-10943200	Weak transcription	Spleen	Spleen
11	chr8:10942600-10943400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr8:10942800-10943400	Bivalent Enhancer	Fetal Brain Male	brain
13	chr8:10943000-10948400	Weak transcription	Gastric	stomach
14	chr8:10943400-10943600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr8:10943800-10944200	Enhancers	Brain Anterior Caudate	brain
16	chr8:10944400-10944600	Enhancers	Right Atrium	heart
17	chr8:10948400-10949600	Enhancers	Gastric	stomach
18	chr8:10948600-10949600	Enhancers	Duodenum Mucosa	Duodenum
19	chr8:10949000-10950200	Enhancers	Fetal Intestine Small	intestine
20	chr8:10949000-10950600	Enhancers	Pancreas	Pancrea
21	chr8:10949200-10951000	Enhancers	Stomach Mucosa	stomach
22	chr8:10949400-10950000	Enhancers	Liver	Liver
23	chr8:10949600-10950000	Flanking Active TSS	Duodenum Mucosa	Duodenum
24	chr8:10949600-10950000	Enhancers	Fetal Heart	heart
25	chr8:10949600-10950000	Weak transcription	Gastric	stomach
26	chr8:10949800-10950000	Enhancers	Fetal Muscle Leg	muscle
27	chr8:10949800-10950200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr8:10949800-10950200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr8:10949800-10950200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr8:10949800-10950200	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
31	chr8:10949800-10950200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr8:10949800-10950200	Active TSS	Duodenum Smooth Muscle	Duodenum
33	chr8:10950000-10950400	Active TSS	Duodenum Mucosa	Duodenum
34	chr8:10950000-10950600	Enhancers	Gastric	stomach
35	chr8:10950000-10955400	Weak transcription	Fetal Heart	heart
36	chr8:10950400-10950600	Weak transcription	Duodenum Mucosa	Duodenum
37	chr8:10950400-10951000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr8:10950600-10951000	Enhancers	Duodenum Mucosa	Duodenum
39	chr8:10950600-10954000	Weak transcription	Pancreas	Pancrea
40	chr8:10950600-10965000	Weak transcription	Gastric	stomach
41	chr8:10951000-10956600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr8:10952800-10953800	Enhancers	Fetal Brain Female	brain
43	chr8:10953000-10954400	Enhancers	Fetal Brain Male	brain
44	chr8:10954000-10954400	Enhancers	Pancreas	Pancrea
45	chr8:10954400-10959200	Weak transcription	Pancreas	Pancrea
46	chr8:10955200-10968000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr8:10955400-10956200	Enhancers	Fetal Heart	heart
48	chr8:10955600-10956000	Bivalent Enhancer	Fetal Brain Male	brain
49	chr8:10955800-10957200	Enhancers	Primary B cells from peripheral blood	blood
50	chr8:10956600-10956800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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