Variant report

Variant	nsv520322
Chromosome Location	chr1:179944901-180071987
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	chr1:180023732-180023861	K562	blood:	n/a	n/a
2	ARID3A	chr1:180027943-180027952	K562	blood:	n/a	n/a
3	ARID3A	chr1:180022917-180023445	K562	blood:	n/a	n/a
4	ARID3A	chr1:180026837-180027685	K562	blood:	n/a	n/a
5	ATF1	chr1:179986755-179986766	K562	blood:	n/a	n/a
6	ATF1	chr1:180022859-180023490	K562	blood:	n/a	n/a
7	ATF1	chr1:180068146-180068158	K562	blood:	n/a	n/a
8	ATF2	chr1:179972174-179972960	GM12878	blood:	n/a	n/a
9	ATF3	chr1:179960014-179960325	K562	blood:	n/a	n/a
10	ATF3	chr1:180023152-180023468	K562	blood:	n/a	n/a
11	BACH1	chr1:180027050-180027297	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr1:180026917-180027441	K562	blood:	n/a	n/a
13	BATF	chr1:179965258-179965498	GM12878	blood:	n/a	n/a
14	BATF	chr1:179972484-179972723	GM12878	blood:	n/a	n/a
15	BCLAF1	chr1:179972185-179972836	GM12878	blood:	n/a	n/a
16	BRCA1	chr1:180067388-180068197	Hela-S3	cervix:	n/a	chr1:180067957-180067964
17	CCNT2	chr1:180039551-180039603	K562	blood:	n/a	n/a
18	CCNT2	chr1:180023071-180023396	K562	blood:	n/a	n/a
19	CEBPB	chr1:179997108-179997690	IMR90	lung:	n/a	chr1:179997478-179997491 chr1:179997493-179997504 chr1:179997492-179997503 chr1:179997478-179997489 chr1:179997492-179997503
20	CEBPB	chr1:179960000-179960373	K562	blood:	n/a	chr1:179960185-179960198 chr1:179960185-179960196
21	CEBPB	chr1:179960081-179960203	HepG2	liver:	n/a	chr1:179960185-179960198 chr1:179960185-179960196
22	CEBPB	chr1:180056279-180056563	HepG2	liver:	n/a	chr1:180056431-180056442
23	CEBPB	chr1:180023140-180023488	Hela-S3	cervix:	n/a	chr1:180023303-180023316 chr1:180023303-180023316 chr1:180023304-180023315
24	CEBPB	chr1:179959404-179959701	K562	blood:	n/a	chr1:179959546-179959557 chr1:179959544-179959561 chr1:179959545-179959556 chr1:179959545-179959558
25	CEBPB	chr1:180023114-180023449	K562	blood:	n/a	chr1:180023303-180023316 chr1:180023303-180023316 chr1:180023304-180023315
26	CEBPB	chr1:179960008-179960351	IMR90	lung:	n/a	chr1:179960185-179960198 chr1:179960185-179960196
27	CEBPB	chr1:180028988-180029094	HepG2	liver:	n/a	chr1:180029030-180029041
28	CEBPB	chr1:179992386-179992548	HepG2	liver:	n/a	chr1:179992470-179992483 chr1:179992471-179992482
29	CEBPB	chr1:180067704-180068041	MCF-7	breast:	n/a	chr1:180067796-180067805 chr1:180067794-180067807 chr1:180067794-180067807 chr1:180067796-180067805 chr1:180067796-180067805
30	CEBPB	chr1:179997168-179997603	HepG2	liver:	n/a	chr1:179997478-179997491 chr1:179997493-179997504 chr1:179997492-179997503 chr1:179997478-179997489 chr1:179997492-179997503
31	CEBPB	chr1:180067533-180067970	K562	blood:	n/a	chr1:180067796-180067805 chr1:180067794-180067807 chr1:180067794-180067807 chr1:180067796-180067805 chr1:180067796-180067805
32	CEBPB	chr1:180050541-180050778	A549	lung:	n/a	chr1:180050695-180050706
33	CEBPB	chr1:180067561-180068002	A549	lung:	n/a	chr1:180067796-180067805 chr1:180067794-180067807 chr1:180067794-180067807 chr1:180067796-180067805 chr1:180067796-180067805
34	CEBPB	chr1:179971964-179972296	IMR90	lung:	n/a	n/a
35	CEBPB	chr1:180028937-180029135	K562	blood:	n/a	chr1:180029030-180029041
36	CEBPB	chr1:180028940-180029169	A549	lung:	n/a	chr1:180029030-180029041
37	CEBPB	chr1:179960111-179960258	K562	blood:	n/a	chr1:179960185-179960198 chr1:179960185-179960196
38	CEBPB	chr1:179961390-179961503	HepG2	liver:	n/a	chr1:179961453-179961464
39	CEBPB	chr1:180056300-180056560	A549	lung:	n/a	chr1:180056431-180056442
40	CEBPB	chr1:180054895-180055030	K562	blood:	n/a	n/a
41	CEBPB	chr1:180050563-180050733	HepG2	liver:	n/a	chr1:180050695-180050706
42	CEBPB	chr1:180025022-180025218	K562	blood:	n/a	n/a
43	CEBPB	chr1:180067636-180067924	MCF-7	breast:	n/a	chr1:180067796-180067805 chr1:180067794-180067807 chr1:180067794-180067807 chr1:180067796-180067805 chr1:180067796-180067805
44	CEBPB	chr1:179960021-179960338	Hela-S3	cervix:	n/a	chr1:179960185-179960198 chr1:179960185-179960196
45	CEBPB	chr1:179959414-179959699	HepG2	liver:	n/a	chr1:179959546-179959557 chr1:179959544-179959561 chr1:179959545-179959556 chr1:179959545-179959558
46	CEBPB	chr1:180023086-180023473	K562	blood:	n/a	chr1:180023303-180023316 chr1:180023303-180023316 chr1:180023304-180023315
47	CEBPB	chr1:180067631-180067930	HepG2	liver:	n/a	chr1:180067796-180067805 chr1:180067794-180067807 chr1:180067794-180067807 chr1:180067796-180067805 chr1:180067796-180067805
48	CEBPB	chr1:179960021-179960349	H1-hESC	embryonic stem cell:	n/a	chr1:179960185-179960198 chr1:179960185-179960196
49	CEBPB	chr1:179958955-179959052	HepG2	liver:	n/a	chr1:179959002-179959015 chr1:179959002-179959015 chr1:179959002-179959013
50	CEBPB	chr1:180023128-180023461	HepG2	liver:	n/a	chr1:180023303-180023316 chr1:180023303-180023316 chr1:180023304-180023315

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:180012272-180012322	HRCEpiC	kidney:	n/a
2	chr1:180012272-180012322	HRCEpiC	kidney:	n/a
3	chr1:180069210-180069260	LNCaP	prostate:	n/a
4	chr1:179997704-179997754	ProgFib	skin:	n/a
5	chr1:180069210-180069260	GM06990	blood:	n/a
6	chr1:179945973-179946023	H1-hESC	embryonic stem cell:	embryo
7	chr1:180069210-180069260	AG10803	skin:	n/a
8	chr1:180069210-180069260	Caco-2	colon:	n/a
9	chr1:179997704-179997754	PFSK-1	brain:	n/a
10	chr1:180069210-180069260	ovcar-3	ovarian:	n/a
11	chr1:180069210-180069260	NT2-D1	testis:	n/a
12	chr1:179945973-179946023	U87	brain:	n/a
13	chr1:179945973-179946023	HUVEC	blood vessel:	n/a
14	chr1:179945973-179946023	ProgFib	skin:	n/a
15	chr1:179997704-179997754	NT2-D1	testis:	n/a
16	chr1:179997704-179997754	HNPCEpiC	eye:	n/a
17	chr1:180012272-180012322	HRE	kidney:	n/a
18	chr1:179945973-179946023	HepG2	liver:	n/a
19	chr1:180069210-180069260	HRCEpiC	kidney:	n/a
20	chr1:179997704-179997754	SAEC	small airway:	n/a
21	chr1:180012272-180012322	HCF	heart:	n/a
22	chr1:180069210-180069260	PrEC	prostate:	n/a
23	chr1:180012272-180012322	CMK	blood:	n/a
24	chr1:179997704-179997754	Hepatocyte	liver:	n/a
25	chr1:180012272-180012322	HIPEpiC	eye:	n/a
26	chr1:179945973-179946023	SK-N-SH_RA	brain:	n/a
27	chr1:180069210-180069260	Hela-S3	cervix:	n/a
28	chr1:179945973-179946023	NH-A	brain:	n/a
29	chr1:180012272-180012322	HPAEpiC	pulmonary alveolar:	n/a
30	chr1:179945973-179946023	AG04449	skin:	fetal
31	chr1:179945973-179946023	GM12878	blood:	n/a
32	chr1:179997704-179997754	GM12878	blood:	n/a
33	chr1:180012272-180012322	HRPEpiC	eye:	n/a
34	chr1:180012272-180012322	AG10803	skin:	n/a
35	chr1:180069210-180069260	HRE	kidney:	n/a
36	chr1:179997704-179997754	MCF-7	breast:	n/a
37	chr1:179945973-179946023	AG09319	gingival:	n/a
38	chr1:179945973-179946023	T-47D	breast:	n/a
39	chr1:179997704-179997754	AG09319	gingival:	n/a
40	chr1:180069210-180069260	U87	brain:	n/a
41	chr1:179997704-179997754	GM19239	blood:	n/a
42	chr1:180069210-180069260	NH-A	brain:	n/a
43	chr1:179997704-179997754	AG10803	skin:	n/a
44	chr1:179945973-179946023	HNPCEpiC	eye:	n/a
45	chr1:179945973-179946023	PANC-1	pancreas:	n/a
46	chr1:179945973-179946023	CMK	blood:	n/a
47	chr1:180069210-180069260	ProgFib	skin:	n/a
48	chr1:179945973-179946023	Jurkat	blood:	n/a
49	chr1:180069210-180069260	IMR90	lung:	fetal
50	chr1:180069210-180069260	RPTEC	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:180067070..180070022-chr1:180093157..180094949,2	K562	blood:
2	chr1:179997127..180001716-chr1:180009044..180014069,5	MCF-7	breast:
3	chr1:179998094..180000667-chr1:180001189..180004534,3	MCF-7	breast:
4	chr1:179845220..179846816-chr1:179967799..179969791,2	MCF-7	breast:
5	chr1:180007479..180009332-chr1:180027865..180030769,2	K562	blood:
6	chr1:180044342..180046715-chr1:180123815..180125802,2	MCF-7	breast:
7	chr1:179922843..179924821-chr1:179984883..179987398,2	K562	blood:
8	chr1:179998094..180000667-chr1:180001189..180004534,3	MCF-7	breast:
9	chr1:180067800..180070199-chr1:180137539..180139968,2	MCF-7	breast:
10	chr1:180048120..180049622-chr1:180134453..180137364,2	MCF-7	breast:
11	chr1:179980682..179985119-chr1:179997024..179999746,4	MCF-7	breast:
12	chr1:179980840..179982638-chr1:180011899..180013783,2	K562	blood:
13	chr1:179922873..179925365-chr1:180021771..180024501,3	K562	blood:
14	chr1:179944177..179947056-chr1:179949748..179951797,3	K562	blood:
15	chr1:180053078..180054589-chr1:180146712..180148638,2	MCF-7	breast:
16	chr1:179851196..179853828-chr1:180057356..180059281,2	K562	blood:
17	chr1:179939932..179942929-chr1:179944050..179946455,4	K562	blood:
18	chr1:179850167..179851805-chr1:180029319..180031564,2	MCF-7	breast:
19	chr1:179998356..180000949-chr1:180019994..180021642,2	K562	blood:
20	chr1:179994934..179997849-chr1:180033158..180035390,2	MCF-7	breast:
21	chr1:179849763..179851404-chr1:180027993..180029985,2	K562	blood:
22	chr1:180004347..180006390-chr1:180011468..180013460,2	K562	blood:
23	chr1:179928179..179930214-chr1:179950625..179952274,2	MCF-7	breast:
24	chr1:179846821..179849157-chr1:179951247..179953699,2	MCF-7	breast:
25	chr1:180060871..180062560-chr1:180065238..180067423,2	K562	blood:
26	chr1:179999019..180000801-chr1:180002803..180004316,2	K562	blood:
27	chr1:180003860..180005800-chr1:180007847..180009537,2	MCF-7	breast:
28	chr1:180029884..180031484-chr1:180035395..180037562,2	MCF-7	breast:
29	chr1:180067842..180070098-chr1:180124230..180125960,2	MCF-7	breast:
30	chr1:180010589..180013566-chr1:180015108..180016921,2	K562	blood:
31	chr1:179852071..179854287-chr1:179987673..179989356,2	MCF-7	breast:
32	chr1:180012630..180014181-chr1:180020336..180022043,2	K562	blood:
33	chr1:179973630..179975308-chr1:179977263..179979537,2	MCF-7	breast:
34	chr1:180009796..180012302-chr1:180015081..180016602,2	MCF-7	breast:
35	chr1:179965716..179968520-chr1:179975367..179977989,2	MCF-7	breast:
36	chr1:179949372..179951758-chr1:179955024..179957989,3	K562	blood:
37	chr1:179947029..179952263-chr1:179955680..179959791,6	MCF-7	breast:
38	chr1:179952573..179954792-chr1:179964056..179965874,2	K562	blood:
39	chr1:179965148..179965648-chr8:43093862..43094700,2	MCF-7	breast:
40	chr1:179850786..179852448-chr1:180017093..180019020,2	MCF-7	breast:
41	chr1:180007479..180009332-chr1:180027865..180030769,2	K562	blood:
42	chr1:179851841..179853644-chr1:180059839..180062411,2	K562	blood:
43	chr1:179921867..179924634-chr1:180042656..180044466,2	MCF-7	breast:
44	chr1:180009514..180012969-chr1:180025548..180028168,4	MCF-7	breast:
45	chr1:179924257..179926025-chr1:179973260..179975368,2	K562	blood:
46	chr1:179969658..179972086-chr1:179982002..179983576,2	K562	blood:
47	chr1:179928118..179930055-chr1:179946472..179948702,2	K562	blood:
48	chr1:179995799..179998188-chr1:180047230..180050117,2	MCF-7	breast:
49	chr1:180039217..180042128-chr1:180125172..180126963,2	K562	blood:
50	chr1:180047479..180049656-chr1:180049971..180052341,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TOR1AIP2-6	chr1:179969573-179969943	NONHSAT008237

Variant related genes	Relation type
ENSG00000223450	TF binding region
CEP350	TF binding region
ENSG00000223450	CpG island
CEP350	CpG island
ENSG00000169905	chromatin interactions
ENSG00000260360	chromatin interactions
ENSG00000272906	chromatin interactions
ENSG00000116260	chromatin interactions
ENSG00000121454	chromatin interactions
ENSG00000135837	chromatin interactions
ENSG00000223450	chromatin interactions
ENSG00000258664	chromatin interactions
ENSG00000143337	chromatin interactions

Extended variants
information (count: 4520 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:4520 , 50 per page) page: 1 2 3 4 5 6 7 ... 91

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2501621	chr1:179944901-179944902	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs2501620	chr1:179944928-179944929	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs530286145	chr1:179944945-179944946	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs550085209	chr1:179945017-179945018	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs185913790	chr1:179945050-179945051	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs115392554	chr1:179945130-179945131	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs189182110	chr1:179945132-179945133	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs375489285	chr1:179945167-179945168	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs566075056	chr1:179945193-179945194	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs541603262	chr1:179945204-179945205	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs147920890	chr1:179945237-179945238	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs554830598	chr1:179945273-179945274	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs574669429	chr1:179945306-179945307	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs202245315	chr1:179945364-179945365	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs34951847	chr1:179945366-179945367	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs397707847	chr1:179945374-179945375	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs71118425	chr1:179945375-179945376	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs17371084	chr1:179945390-179945391	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs536389903	chr1:179945400-179945401	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs181171920	chr1:179945410-179945411	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs141880049	chr1:179945417-179945418	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs559064111	chr1:179945435-179945436	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs376732829	chr1:179945437-179945438	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs147245474	chr1:179945486-179945487	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs71649184	chr1:179945490-179945491	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs541453531	chr1:179945547-179945548	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs561746687	chr1:179945552-179945553	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs75541635	chr1:179945599-179945600	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs80092332	chr1:179945621-179945622	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs570102728	chr1:179945705-179945706	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs532800588	chr1:179945721-179945722	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs550040347	chr1:179945726-179945727	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs143806800	chr1:179945733-179945734	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs564067982	chr1:179945741-179945742	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs572887692	chr1:179945743-179945744	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs111646475	chr1:179945767-179945768	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs559980758	chr1:179945786-179945787	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs568453793	chr1:179945793-179945794	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs2477119	chr1:179945838-179945839	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs140086032	chr1:179945846-179945847	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs185762844	chr1:179945852-179945853	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs543701906	chr1:179945858-179945859	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs558908267	chr1:179945936-179945937	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs554741092	chr1:179945996-179945997	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs77044199	chr1:179946021-179946022	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs150336271	chr1:179946196-179946197	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs190572765	chr1:179946215-179946216	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs541924998	chr1:179946239-179946240	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs12123201	chr1:179946276-179946277	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs79311522	chr1:179946277-179946278	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	16750200	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Rett syndrome	21593744	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Glioblastoma multiforme	17369134	CNVD
Cancer	17440070	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21611746	CNVD
Breast cancer	16397240	CNVD
Mental retardation	17847001	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	23248035	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:3554 , 50 per page) page: 1 2 3 4 5 6 7 ... 72

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:179924800-179963600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr1:179925200-179946200	Weak transcription	Stomach Mucosa	stomach
3	chr1:179925400-179946000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr1:179926800-179961400	Weak transcription	A549	lung
5	chr1:179927000-179965600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
6	chr1:179934600-179945000	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr1:179936000-179946400	Weak transcription	NHLF	lung
8	chr1:179936200-179946000	Weak transcription	Fetal Lung	lung
9	chr1:179936200-179946000	Weak transcription	HepG2	liver
10	chr1:179936400-179955600	Weak transcription	Dnd41	blood
11	chr1:179936600-179958800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr1:179937800-179946200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr1:179938000-179983200	Weak transcription	Brain Germinal Matrix	brain
14	chr1:179938400-179948600	Weak transcription	Fetal Muscle Trunk	muscle
15	chr1:179938600-179945400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
16	chr1:179938600-179946000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr1:179938600-179946000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr1:179938600-179946000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr1:179938600-179946000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
20	chr1:179938600-179954600	Weak transcription	Fetal Thymus	thymus
21	chr1:179938600-179956400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
22	chr1:179938600-179956800	Weak transcription	Duodenum Mucosa	Duodenum
23	chr1:179938600-179956800	Weak transcription	Fetal Intestine Small	intestine
24	chr1:179938600-179956800	Weak transcription	Fetal Stomach	stomach
25	chr1:179938600-179957600	Weak transcription	Rectal Mucosa Donor 31	rectum
26	chr1:179938600-179959000	Weak transcription	Sigmoid Colon	Sigmoid Colon
27	chr1:179938600-179965800	Weak transcription	Esophagus	oesophagus
28	chr1:179938600-179975800	Weak transcription	Thymus	Thymus
29	chr1:179938600-179983200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr1:179938600-179984600	Weak transcription	Lung	lung
31	chr1:179938800-179953400	Weak transcription	Fetal Intestine Large	intestine
32	chr1:179938800-179959800	Weak transcription	Rectal Mucosa Donor 29	rectum
33	chr1:179939000-179945400	Weak transcription	Osteobl	bone
34	chr1:179939000-179946000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
35	chr1:179939000-179948800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr1:179939000-179954800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
37	chr1:179939000-179989000	Weak transcription	Gastric	stomach
38	chr1:179939200-179945800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr1:179939200-179946000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr1:179939600-179955600	Weak transcription	Primary hematopoietic stem cells	blood
41	chr1:179939800-179946000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
42	chr1:179939800-179946200	Weak transcription	Duodenum Smooth Muscle	Duodenum
43	chr1:179939800-179946200	Weak transcription	Pancreatic Islets	Pancreatic Islet
44	chr1:179939800-179948000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
45	chr1:179939800-179956800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr1:179939800-179959400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
47	chr1:179939800-179974800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
48	chr1:179940000-179945200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
49	chr1:179940000-179946000	Weak transcription	Liver	Liver
50	chr1:179940000-179953400	Weak transcription	Muscle Satellite Cultured Cells	--

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