Variant report

Variant	nsv1026331
Chromosome Location	chr8:10955941-11046394
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	ATF2	chr8:10981506-10982207	GM12878	blood:	n/a	n/a
2	ATF2	chr8:10981488-10982324	GM12878	blood:	n/a	n/a
3	BACH1	chr8:11026563-11026651	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr8:11020411-11020492	K562	blood:	n/a	n/a
5	BACH1	chr8:10962868-10963169	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr8:11034754-11035025	GM12878	blood:	n/a	chr8:11034880-11034891
7	BATF	chr8:11018551-11018700	GM12878	blood:	n/a	n/a
8	BCL3	chr8:11027876-11028173	GM12878	blood:	n/a	n/a
9	BCLAF1	chr8:10981539-10982080	GM12878	blood:	n/a	n/a
10	BHLHE40	chr8:11016374-11016667	GM12878	blood:	n/a	n/a
11	BHLHE40	chr8:10981392-10982182	GM12878	blood:	n/a	n/a
12	CEBPB	chr8:11006147-11006536	A549	lung:	n/a	chr8:11006326-11006337
13	CEBPB	chr8:11028014-11028243	IMR90	lung:	n/a	chr8:11028140-11028151
14	CEBPB	chr8:11028120-11028158	H1-hESC	embryonic stem cell:	n/a	chr8:11028140-11028151
15	CEBPB	chr8:11006185-11006505	K562	blood:	n/a	chr8:11006326-11006337
16	CEBPB	chr8:10969442-10969756	IMR90	lung:	n/a	chr8:10969592-10969603 chr8:10969594-10969603 chr8:10969592-10969605 chr8:10969594-10969605
17	CEBPB	chr8:10969507-10969750	HepG2	liver:	n/a	chr8:10969592-10969603 chr8:10969594-10969603 chr8:10969592-10969605 chr8:10969594-10969605
18	CEBPB	chr8:10984322-10984480	HepG2	liver:	n/a	chr8:10984400-10984411
19	CEBPB	chr8:11006150-11006516	IMR90	lung:	n/a	chr8:11006326-11006337
20	CEBPB	chr8:11027061-11027382	IMR90	lung:	n/a	chr8:11027223-11027234
21	CEBPB	chr8:11027975-11028266	HepG2	liver:	n/a	chr8:11028140-11028151
22	CEBPB	chr8:11045483-11046128	IMR90	lung:	n/a	n/a
23	CEBPB	chr8:11006152-11006488	H1-hESC	embryonic stem cell:	n/a	chr8:11006326-11006337
24	CEBPB	chr8:11006166-11006493	HepG2	liver:	n/a	chr8:11006326-11006337
25	CEBPB	chr8:11027123-11027301	A549	lung:	n/a	chr8:11027223-11027234
26	CEBPB	chr8:10969452-10969699	K562	blood:	n/a	chr8:10969592-10969603 chr8:10969594-10969603 chr8:10969592-10969605 chr8:10969594-10969605
27	CEBPB	chr8:11027105-11027329	K562	blood:	n/a	chr8:11027223-11027234
28	CEBPB	chr8:11027148-11027316	HepG2	liver:	n/a	chr8:11027223-11027234
29	CEBPB	chr8:11006179-11006486	Hela-S3	cervix:	n/a	chr8:11006326-11006337
30	CEBPB	chr8:10986551-10986831	IMR90	lung:	n/a	n/a
31	CHD1	chr8:10981485-10982120	GM12878	blood:	n/a	n/a
32	CHD2	chr8:10981673-10981992	GM12878	blood:	n/a	n/a
33	CTCF	chr8:10962812-10963078	H1-hESC	embryonic stem cell:	n/a	chr8:10962907-10962920 chr8:10962905-10962923
34	CTCF	chr8:10996860-10997010	GM12872	blood:	n/a	chr8:10996901-10996909 chr8:10996892-10996905
35	CTCF	chr8:10996820-10996970	SK-N-SH_RA	brain:	n/a	chr8:10996901-10996909 chr8:10996892-10996905
36	CTCF	chr8:10996820-10996970	HAc	cerebellar:	n/a	chr8:10996901-10996909 chr8:10996892-10996905
37	CTCF	chr8:10971467-10971489	GM19239	blood:	n/a	n/a
38	CTCF	chr8:10962850-10963009	H1-hESC	embryonic stem cell:	n/a	chr8:10962907-10962920 chr8:10962905-10962923
39	CTCF	chr8:10996645-10997299	SK-N-SH	brain:	n/a	chr8:10996901-10996909 chr8:10997049-10997057 chr8:10996892-10996905
40	CTCF	chr8:10965980-10966130	BE2_C	brain:	n/a	chr8:10966022-10966040
41	CTCF	chr8:11032643-11032712	GM13976	blood:	n/a	n/a
42	CTCF	chr8:10962840-10962990	HBMEC	blood vessel:	n/a	chr8:10962907-10962920 chr8:10962905-10962923
43	CTCF	chr8:10996716-10996997	H1-hESC	embryonic stem cell:	n/a	chr8:10996901-10996909 chr8:10996892-10996905
44	CTCF	chr8:10996840-10996990	GM12871	blood:	n/a	chr8:10996901-10996909 chr8:10996892-10996905
45	CTCF	chr8:10962800-10962950	HFF-Myc	foreskin:	n/a	chr8:10962907-10962920 chr8:10962905-10962923
46	CTCF	chr8:10962820-10962970	SK-N-SH_RA	brain:	n/a	chr8:10962907-10962920 chr8:10962905-10962923
47	CTCF	chr8:10996845-10996957	SK-N-SH_RA	brain:	n/a	chr8:10996901-10996909 chr8:10996892-10996905
48	CTCF	chr8:10962887-10962969	MCF-7	breast:	n/a	chr8:10962907-10962920 chr8:10962905-10962923
49	CTCF	chr8:10962980-10963130	HRE	kidney:	n/a	n/a
50	CTCF	chr8:10977243-10977296	GM10266	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:10966224-10966274	AG04449	skin:	fetal
2	chr8:10982332-10982382	SK-N-SH_RA	brain:	n/a
3	chr8:10982332-10982382	MCF-7	breast:	n/a
4	chr8:10966224-10966274	AG04449	skin:	fetal
5	chr8:10982332-10982382	SK-N-SH_RA	brain:	n/a
6	chr8:10982332-10982382	MCF-7	breast:	n/a
7	chr8:10966251-10966301	Jurkat	blood:	n/a
8	chr8:10965533-10965583	HCT-116	colon:	n/a
9	chr8:11021173-11021223	GM06990	blood:	n/a
10	chr8:11044280-11044330	H1-hESC	embryonic stem cell:	embryo
11	chr8:10966192-10966242	AG10803	skin:	n/a
12	chr8:11044280-11044330	GM12891	blood:	n/a
13	chr8:10982332-10982382	HCT-116	colon:	n/a
14	chr8:10965430-10965480	HRE	kidney:	n/a
15	chr8:10966192-10966242	RPTEC	kidney:	n/a
16	chr8:10982332-10982382	HL-60	blood:	n/a
17	chr8:10987869-10987919	GM12878	blood:	n/a
18	chr8:10982332-10982382	Hepatocyte	liver:	n/a
19	chr8:11044280-11044330	AG04449	skin:	fetal
20	chr8:11021173-11021223	AG09319	gingival:	n/a
21	chr8:10988117-10988167	Hepatocyte	liver:	n/a
22	chr8:10982668-10982718	HPAEpiC	pulmonary alveolar:	n/a
23	chr8:10966251-10966301	HRPEpiC	eye:	n/a
24	chr8:10987869-10987919	NHBE	bronchial:	n/a
25	chr8:10966192-10966242	MCF-7	breast:	n/a
26	chr8:10987869-10987919	A549	lung:	n/a
27	chr8:11021173-11021223	PANC-1	pancreas:	n/a
28	chr8:10982836-10982886	HEEpiC	esophagus:	n/a
29	chr8:10987869-10987919	SK-N-SH_RA	brain:	n/a
30	chr8:11021173-11021223	PFSK-1	brain:	n/a
31	chr8:10982332-10982382	HCPEpiC	choroid plexus:	n/a
32	chr8:10988117-10988167	AG10803	skin:	n/a
33	chr8:10966224-10966274	GM06990	blood:	n/a
34	chr8:10966251-10966301	T-47D	breast:	n/a
35	chr8:10982836-10982886	ProgFib	skin:	n/a
36	chr8:11044280-11044330	AG04450	lung:	fetal
37	chr8:10966224-10966274	ovcar-3	ovarian:	n/a
38	chr8:10988117-10988167	HPAEpiC	pulmonary alveolar:	n/a
39	chr8:11044280-11044330	AoSMC	blood vessel:	n/a
40	chr8:10982668-10982718	SKMC	muscle:	n/a
41	chr8:10965533-10965583	PANC-1	pancreas:	n/a
42	chr8:11021173-11021223	BJ	skin:	n/a
43	chr8:10982836-10982886	U87	brain:	n/a
44	chr8:10966251-10966301	NHBE	bronchial:	n/a
45	chr8:10996424-10996474	HPAEpiC	pulmonary alveolar:	n/a
46	chr8:10966251-10966301	A549	lung:	n/a
47	chr8:10982332-10982382	CMK	blood:	n/a
48	chr8:10966192-10966242	HCT-116	colon:	n/a
49	chr8:11044280-11044330	BJ	skin:	n/a
50	chr8:10965430-10965480	K562	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:10989309..10991277-chr8:11000364..11001975,2	MCF-7	breast:
2	chr8:11011361..11013679-chr8:11086642..11088741,2	MCF-7	breast:
3	chr5:138973431..138974207-chr8:10970599..10971381,2	MCF-7	breast:
4	chr8:11020358..11021978-chr8:11037750..11039962,2	MCF-7	breast:
5	chr8:11032511..11035428-chr8:11039956..11042400,2	K562	blood:
6	chr8:11042275..11044106-chr8:11054861..11057806,2	MCF-7	breast:
7	chr8:10890969..10893547-chr8:10959450..10962216,2	K562	blood:
8	chr8:11042678..11045323-chr8:11057984..11059952,2	MCF-7	breast:
9	chr8:10987323..10988888-chr8:10996311..10998461,2	MCF-7	breast:
10	chr8:10953851..10956299-chr8:10959068..10961747,2	MCF-7	breast:
11	chr8:11040791..11043774-chr8:11044879..11047578,2	K562	blood:
12	chr8:11020358..11021978-chr8:11037750..11039962,2	MCF-7	breast:
13	chr8:11040791..11043774-chr8:11044879..11047578,2	K562	blood:
14	chr8:10953851..10956299-chr8:10959068..10961747,2	MCF-7	breast:
15	chr8:10989309..10991277-chr8:11000364..11001975,2	MCF-7	breast:
16	chr8:10953495..10955337-chr8:10955774..10957347,2	K562	blood:

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

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
ENSG00000231965	chromatin interactions
ENSG00000207600	chromatin interactions
ENSG00000215346	chromatin interactions
ENSG00000171044	chromatin interactions
ZFYVE20	miRNA target sites
KIF5C	miRNA target sites

Extended variants
information (count: 5112 )
Associated
traits (count: 138 )

Variant overlapped rSNPs/rCNVs (count:5112 , 50 per page) page: 1 2 3 4 5 6 7 ... 103

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567101330	chr8:10955962-10955963	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
2	rs193282358	chr8:10955963-10955964	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs571785955	chr8:10955984-10955985	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs77012973	chr8:10956058-10956059	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs34070511	chr8:10956070-10956071	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs117927616	chr8:10956105-10956106	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs553936910	chr8:10956109-10956110	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs185497561	chr8:10956114-10956115	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs113163277	chr8:10956117-10956118	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs138394151	chr8:10956134-10956135	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs373727502	chr8:10956158-10956159	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs116227339	chr8:10956181-10956182	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs143936246	chr8:10956188-10956189	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs76384741	chr8:10956235-10956236	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs140869495	chr8:10956258-10956259	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs561977215	chr8:10956268-10956269	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs141532382	chr8:10956284-10956285	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs562001116	chr8:10956291-10956292	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs550948480	chr8:10956311-10956312	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs562781910	chr8:10956312-10956313	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs533448093	chr8:10956328-10956329	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs114715674	chr8:10956350-10956351	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs566991015	chr8:10956373-10956374	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs530150546	chr8:10956416-10956417	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs200577805	chr8:10956418-10956419	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs543685061	chr8:10956419-10956420	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs189097303	chr8:10956432-10956433	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs139428032	chr8:10956447-10956448	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs556909481	chr8:10956448-10956449	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs115513555	chr8:10956450-10956451	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs575664555	chr8:10956457-10956458	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs530729042	chr8:10956500-10956501	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs181547155	chr8:10956510-10956511	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs557396377	chr8:10956513-10956514	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs550331713	chr8:10956533-10956534	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs563944478	chr8:10956566-10956567	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs565282556	chr8:10956579-10956580	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs78111630	chr8:10956580-10956581	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs544618540	chr8:10956592-10956593	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs532431064	chr8:10956672-10956673	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs573868608	chr8:10956684-10956685	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs544213307	chr8:10956696-10956697	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs34891368	chr8:10956707-10956708	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
44	rs114886461	chr8:10956724-10956725	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs545437579	chr8:10956729-10956730	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs7004366	chr8:10956768-10956769	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs527791143	chr8:10956780-10956781	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs183993093	chr8:10956825-10956826	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs549554150	chr8:10956846-10956847	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs146679181	chr8:10956856-10956857	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:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:10950600-10965000	Weak transcription	Gastric	stomach
2	chr8:10951000-10956600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr8:10954400-10959200	Weak transcription	Pancreas	Pancrea
4	chr8:10955200-10968000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr8:10955400-10956200	Enhancers	Fetal Heart	heart
6	chr8:10955600-10956000	Bivalent Enhancer	Fetal Brain Male	brain
7	chr8:10955800-10957200	Enhancers	Primary B cells from peripheral blood	blood
8	chr8:10956600-10956800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr8:10956600-10956800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
10	chr8:10956800-10957200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr8:10956800-10964800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
12	chr8:10957200-10957600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr8:10957200-10964800	Weak transcription	Primary B cells from peripheral blood	blood
14	chr8:10957600-10958600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
15	chr8:10957600-10958600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
16	chr8:10957800-10958600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
17	chr8:10957800-10958600	Enhancers	Primary T helper cells PMA-I stimulated	--
18	chr8:10958000-10958200	Enhancers	H9 Cell Line	embryonic stem cell
19	chr8:10958000-10958200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
20	chr8:10958000-10958200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
21	chr8:10958000-10958200	Bivalent Enhancer	Primary mononuclear cells fromperipheralblood	Blood
22	chr8:10958000-10958400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
23	chr8:10958000-10958600	Enhancers	Primary T helper cells fromperipheralblood	blood
24	chr8:10958000-10958600	Enhancers	Fetal Thymus	thymus
25	chr8:10958200-10958400	Enhancers	Primary T helper naive cells from peripheral blood	blood
26	chr8:10958200-10958600	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
27	chr8:10958200-10965000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
28	chr8:10958200-10967200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
29	chr8:10958200-10970200	Weak transcription	H9 Cell Line	embryonic stem cell
30	chr8:10958400-10965200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
31	chr8:10958400-10974800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
32	chr8:10958600-10964800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
33	chr8:10958600-10965000	Weak transcription	Primary T helper cells fromperipheralblood	blood
34	chr8:10958600-10971200	Weak transcription	Primary T helper cells PMA-I stimulated	--
35	chr8:10958600-10971200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
36	chr8:10958800-10967400	Weak transcription	Primary T cells fromperipheralblood	blood
37	chr8:10959200-10959600	Enhancers	Pancreas	Pancrea
38	chr8:10959600-10964800	Weak transcription	Pancreas	Pancrea
39	chr8:10960400-10963800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr8:10960400-10967000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr8:10960400-10968400	Weak transcription	Spleen	Spleen
42	chr8:10960800-10961800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr8:10960800-10965200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr8:10960800-10970800	Weak transcription	HSMM	muscle
45	chr8:10961200-10961800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr8:10961200-10964600	Weak transcription	Fetal Intestine Small	intestine
47	chr8:10961200-10964800	Weak transcription	Fetal Stomach	stomach
48	chr8:10961200-10975400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
49	chr8:10961600-10970600	Weak transcription	Fetal Intestine Large	intestine
50	chr8:10961800-10962800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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