Variant report

Variant	nsv1011293
Chromosome Location	chr1:86270649-86416972
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	ATF1	chr1:86360393-86360593	K562	blood:	n/a	n/a
2	ATF3	chr1:86315734-86316283	A549	lung:	n/a	chr1:86316105-86316119
3	ATF3	chr1:86315774-86316365	A549	lung:	n/a	chr1:86316105-86316119
4	BATF	chr1:86303953-86304139	GM12878	blood:	n/a	n/a
5	BCL3	chr1:86315776-86316328	A549	lung:	n/a	chr1:86315956-86315965 chr1:86316104-86316113 chr1:86316105-86316114
6	BCL3	chr1:86315690-86316374	A549	lung:	n/a	chr1:86315956-86315965 chr1:86316104-86316113 chr1:86316105-86316114
7	BCLAF1	chr1:86303894-86304316	GM12878	blood:	n/a	n/a
8	CBX3	chr1:86315792-86316447	HCT-116	colon:	n/a	n/a
9	CEBPB	chr1:86312504-86312622	H1-hESC	embryonic stem cell:	n/a	chr1:86312596-86312609 chr1:86312596-86312609 chr1:86312597-86312608 chr1:86312596-86312607
10	CEBPB	chr1:86315823-86316264	A549	lung:	n/a	chr1:86316001-86316014
11	CEBPB	chr1:86312443-86312728	IMR90	lung:	n/a	chr1:86312596-86312609 chr1:86312596-86312609 chr1:86312597-86312608 chr1:86312596-86312607
12	CEBPB	chr1:86406628-86406944	IMR90	lung:	n/a	chr1:86406773-86406784
13	CEBPB	chr1:86315836-86316751	IMR90	lung:	n/a	chr1:86316566-86316577 chr1:86316566-86316575 chr1:86316561-86316578 chr1:86316564-86316575 chr1:86316001-86316014
14	CEBPB	chr1:86288103-86288794	HCT-116	colon:	n/a	n/a
15	CEBPB	chr1:86409262-86409608	HepG2	liver:	n/a	chr1:86409470-86409481
16	CEBPB	chr1:86288238-86288706	HCT-116	colon:	n/a	n/a
17	CEBPB	chr1:86408363-86408477	H1-hESC	embryonic stem cell:	n/a	chr1:86408448-86408459
18	CEBPB	chr1:86315733-86316302	A549	lung:	n/a	chr1:86316001-86316014
19	CEBPB	chr1:86312488-86312731	A549	lung:	n/a	chr1:86312596-86312609 chr1:86312596-86312609 chr1:86312597-86312608 chr1:86312596-86312607
20	CEBPB	chr1:86408298-86408605	A549	lung:	n/a	chr1:86408448-86408459
21	CEBPB	chr1:86354701-86354883	A549	lung:	n/a	n/a
22	CEBPB	chr1:86330737-86331190	A549	lung:	n/a	chr1:86330998-86331009 chr1:86330996-86331009 chr1:86330977-86330988 chr1:86330996-86331007 chr1:86330998-86331009 chr1:86330996-86331009
23	CEBPB	chr1:86330822-86331164	IMR90	lung:	n/a	chr1:86330998-86331009 chr1:86330996-86331009 chr1:86330977-86330988 chr1:86330996-86331007 chr1:86330998-86331009 chr1:86330996-86331009
24	CEBPB	chr1:86312491-86312877	MCF-7	breast:	n/a	chr1:86312596-86312609 chr1:86312596-86312609 chr1:86312597-86312608 chr1:86312596-86312607
25	CEBPB	chr1:86312201-86312861	A549	lung:	n/a	chr1:86312596-86312609 chr1:86312596-86312609 chr1:86312597-86312608 chr1:86312596-86312607
26	CEBPB	chr1:86330862-86331150	H1-hESC	embryonic stem cell:	n/a	chr1:86330998-86331009 chr1:86330996-86331009 chr1:86330977-86330988 chr1:86330996-86331007 chr1:86330998-86331009 chr1:86330996-86331009
27	CEBPB	chr1:86316412-86316684	HepG2	liver:	n/a	chr1:86316566-86316577 chr1:86316566-86316575 chr1:86316561-86316578 chr1:86316564-86316575
28	CEBPB	chr1:86330880-86331152	ECC-1	luminal epithelium:	n/a	chr1:86330998-86331009 chr1:86330996-86331009 chr1:86330977-86330988 chr1:86330996-86331007 chr1:86330998-86331009 chr1:86330996-86331009
29	CEBPB	chr1:86315667-86316620	HCT-116	colon:	n/a	chr1:86316566-86316577 chr1:86316566-86316575 chr1:86316561-86316578 chr1:86316564-86316575 chr1:86316001-86316014
30	CEBPB	chr1:86408293-86408587	HepG2	liver:	n/a	chr1:86408448-86408459
31	CEBPB	chr1:86312158-86312748	A549	lung:	n/a	chr1:86312596-86312609 chr1:86312596-86312609 chr1:86312597-86312608 chr1:86312596-86312607
32	CEBPB	chr1:86315865-86316679	A549	lung:	n/a	chr1:86316566-86316577 chr1:86316566-86316575 chr1:86316561-86316578 chr1:86316564-86316575 chr1:86316001-86316014
33	CEBPB	chr1:86330802-86331170	Hela-S3	cervix:	n/a	chr1:86330998-86331009 chr1:86330996-86331009 chr1:86330977-86330988 chr1:86330996-86331007 chr1:86330998-86331009 chr1:86330996-86331009
34	CEBPB	chr1:86312489-86312717	MCF-7	breast:	n/a	chr1:86312596-86312609 chr1:86312596-86312609 chr1:86312597-86312608 chr1:86312596-86312607
35	CEBPB	chr1:86330866-86331186	A549	lung:	n/a	chr1:86330998-86331009 chr1:86330996-86331009 chr1:86330977-86330988 chr1:86330996-86331007 chr1:86330998-86331009 chr1:86330996-86331009
36	CEBPB	chr1:86312164-86312478	MCF-7	breast:	n/a	n/a
37	CEBPB	chr1:86312217-86312800	Hela-S3	cervix:	n/a	chr1:86312596-86312609 chr1:86312596-86312609 chr1:86312597-86312608 chr1:86312596-86312607
38	CEBPB	chr1:86312169-86312410	A549	lung:	n/a	n/a
39	CEBPB	chr1:86409314-86409590	IMR90	lung:	n/a	chr1:86409470-86409481
40	CEBPB	chr1:86328150-86328521	IMR90	lung:	n/a	n/a
41	CEBPB	chr1:86330810-86331167	A549	lung:	n/a	chr1:86330998-86331009 chr1:86330996-86331009 chr1:86330977-86330988 chr1:86330996-86331007 chr1:86330998-86331009 chr1:86330996-86331009
42	CEBPB	chr1:86330870-86331147	K562	blood:	n/a	chr1:86330998-86331009 chr1:86330996-86331009 chr1:86330977-86330988 chr1:86330996-86331007 chr1:86330998-86331009 chr1:86330996-86331009
43	CEBPB	chr1:86312273-86312758	HepG2	liver:	n/a	chr1:86312596-86312609 chr1:86312596-86312609 chr1:86312597-86312608 chr1:86312596-86312607
44	CEBPB	chr1:86408356-86408556	IMR90	lung:	n/a	chr1:86408448-86408459
45	CEBPB	chr1:86330799-86331170	HepG2	liver:	n/a	chr1:86330998-86331009 chr1:86330996-86331009 chr1:86330977-86330988 chr1:86330996-86331007 chr1:86330998-86331009 chr1:86330996-86331009
46	CEBPB	chr1:86399690-86399971	IMR90	lung:	n/a	n/a
47	CHD2	chr1:86327651-86327685	GM12878	blood:	n/a	n/a
48	CTCF	chr1:86377520-86377670	BJ	skin:	n/a	n/a
49	CTCF	chr1:86316180-86316330	GM12878	blood:	n/a	n/a
50	CTCF	chr1:86350460-86350610	HUVEC	blood vessel:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:86283470-86283520	HNPCEpiC	eye:	n/a
2	chr1:86296346-86296396	ovcar-3	ovarian:	n/a
3	chr1:86283470-86283520	NHBE	bronchial:	n/a
4	chr1:86296346-86296396	HCPEpiC	choroid plexus:	n/a
5	chr1:86296346-86296396	NB4	blood:	n/a
6	chr1:86283470-86283520	HRPEpiC	eye:	n/a
7	chr1:86283470-86283520	NH-A	brain:	n/a
8	chr1:86296346-86296396	CMK	blood:	n/a
9	chr1:86283470-86283520	T-47D	breast:	n/a
10	chr1:86283470-86283520	HAEpiC	amniotic membrane:	n/a
11	chr1:86283470-86283520	HRE	kidney:	n/a
12	chr1:86296346-86296396	PANC-1	pancreas:	n/a
13	chr1:86296346-86296396	AG04449	skin:	fetal
14	chr1:86283470-86283520	BE2_C	brain:	n/a
15	chr1:86283470-86283520	SK-N-SH_RA	brain:	n/a
16	chr1:86283470-86283520	CMK	blood:	n/a
17	chr1:86296346-86296396	HepG2	liver:	n/a
18	chr1:86296346-86296396	ProgFib	skin:	n/a
19	chr1:86296346-86296396	HCM	heart:	n/a
20	chr1:86296346-86296396	Jurkat	blood:	n/a
21	chr1:86283470-86283520	HCT-116	colon:	n/a
22	chr1:86296346-86296396	H1-hESC	embryonic stem cell:	embryo
23	chr1:86283470-86283520	HMEC	breast:	n/a
24	chr1:86283470-86283520	HCF	heart:	n/a
25	chr1:86283470-86283520	ovcar-3	ovarian:	n/a
26	chr1:86283470-86283520	AG04450	lung:	fetal
27	chr1:86283470-86283520	HepG2	liver:	n/a
28	chr1:86283470-86283520	HCM	heart:	n/a
29	chr1:86296346-86296396	HUVEC	blood vessel:	n/a
30	chr1:86283470-86283520	BJ	skin:	n/a
31	chr1:86296346-86296396	BE2_C	brain:	n/a
32	chr1:86296346-86296396	AoSMC	blood vessel:	n/a
33	chr1:86283470-86283520	Hepatocyte	liver:	n/a
34	chr1:86283470-86283520	GM19239	blood:	n/a
35	chr1:86296346-86296396	HCT-116	colon:	n/a
36	chr1:86296346-86296396	MCF10A-Er-Src	breast:	n/a
37	chr1:86283470-86283520	PANC-1	pancreas:	n/a
38	chr1:86296346-86296396	AG04450	lung:	fetal
39	chr1:86296346-86296396	Hela-S3	cervix:	n/a
40	chr1:86283470-86283520	HRCEpiC	kidney:	n/a
41	chr1:86296346-86296396	HAEpiC	amniotic membrane:	n/a
42	chr1:86296346-86296396	GM06990	blood:	n/a
43	chr1:86296346-86296396	K562	blood:	n/a
44	chr1:86283470-86283520	LNCaP	prostate:	n/a
45	chr1:86283470-86283520	PFSK-1	brain:	n/a
46	chr1:86283470-86283520	MCF-7	breast:	n/a
47	chr1:86283470-86283520	SAEC	small airway:	n/a
48	chr1:86283470-86283520	AG10803	skin:	n/a
49	chr1:86283470-86283520	SK-N-SH	brain:	n/a
50	chr1:86296346-86296396	HRCEpiC	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:85773662..85774295-chr1:86315658..86316288,2	MCF-7	breast:
2	chr1:86263300..86265589-chr1:86281895..86284677,2	K562	blood:
3	chr1:86173609..86174719-chr1:86349901..86350977,5	MCF-7	breast:
4	chr1:86397392..86400390-chr9:100675486..100677661,2	K562	blood:
5	chr1:86211855..86213533-chr1:86285001..86287776,2	K562	blood:
6	chr1:86360081..86361020-chr1:86483694..86484478,3	MCF-7	breast:
7	chr1:86278102..86279954-chr1:86282044..86284732,2	K562	blood:
8	chr1:86282182..86284490-chr1:86287465..86289002,2	MCF-7	breast:
9	chr1:86283869..86285851-chr1:86286499..86288640,2	MCF-7	breast:
10	chr1:86289855..86290389-chr1:86350572..86351446,2	MCF-7	breast:
11	chr1:86373838..86377077-chr1:86378435..86381961,4	K562	blood:
12	chr1:86289855..86290389-chr1:86350572..86351446,2	MCF-7	breast:
13	chr1:86283944..86286909-chr1:86290122..86291813,2	MCF-7	breast:
14	chr1:86397300..86400343-chr9:100673063..100676674,4	K562	blood:
15	chr1:86262773..86264767-chr1:86274959..86276756,2	MCF-7	breast:
16	chr1:86349495..86351039-chr1:86359014..86361069,2	MCF-7	breast:
17	chr1:86278454..86281211-chr1:86282044..86284613,2	K562	blood:
18	chr1:86283869..86285851-chr1:86286499..86288640,2	MCF-7	breast:
19	chr1:86046089..86048406-chr1:86314306..86316948,2	MCF-7	breast:
20	chr1:86278878..86280687-chr1:86286928..86289556,2	K562	blood:
21	chr1:86278102..86279954-chr1:86282044..86284732,2	K562	blood:
22	chr1:86360058..86360590-chr1:86821594..86822114,2	MCF-7	breast:
23	chr1:86283944..86286909-chr1:86290122..86291813,2	MCF-7	breast:
24	chr1:86173527..86174504-chr1:86315716..86316608,2	MCF-7	breast:
25	chr1:86349495..86351039-chr1:86359014..86361069,2	MCF-7	breast:
26	chr1:86373838..86377077-chr1:86378435..86381961,4	K562	blood:
27	chr1:86278878..86280687-chr1:86286928..86289556,2	K562	blood:
28	chr1:86278454..86281211-chr1:86282044..86284613,2	K562	blood:
29	chr1:86282182..86284490-chr1:86287465..86289002,2	MCF-7	breast:
30	chr1:86078662..86080625-chr1:86320837..86323478,2	K562	blood:

Variant related genes	Relation type
RNA5SP51	TF binding region
RNA5SP51	CpG island
ENSG00000136932	chromatin interactions
ENSG00000117174	chromatin interactions
ENSG00000142871	chromatin interactions

Extended variants
information (count: 5293 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:5293 , 50 per page) page: 1 2 3 4 5 6 7 ... 106

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs74514926	chr1:86270649-86270650	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs543809595	chr1:86270724-86270725	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs558209398	chr1:86270728-86270729	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs191991144	chr1:86270729-86270730	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs540350624	chr1:86270762-86270763	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs6677315	chr1:86270803-86270804	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs183871199	chr1:86270819-86270820	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs551998900	chr1:86270895-86270896	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs571971411	chr1:86270911-86270912	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs375606389	chr1:86270950-86270951	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs546159686	chr1:86270957-86270958	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs71654724	chr1:86270967-86270968	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs138032556	chr1:86270972-86270973	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs554308896	chr1:86271079-86271080	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs149491072	chr1:86271089-86271090	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs313738	chr1:86271144-86271145	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs538493722	chr1:86271185-86271186	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs369435380	chr1:86271191-86271192	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs558285231	chr1:86271258-86271259	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs541974291	chr1:86271266-86271267	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs143942783	chr1:86271267-86271268	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs112308047	chr1:86271299-86271300	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs72728341	chr1:86271303-86271304	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs187592350	chr1:86271330-86271331	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs530549591	chr1:86271338-86271339	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs141498868	chr1:86271372-86271373	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs115053148	chr1:86271401-86271402	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs74532370	chr1:86271423-86271424	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs78868751	chr1:86271485-86271486	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs545625708	chr1:86271486-86271487	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs565443318	chr1:86271539-86271540	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs61783154	chr1:86271540-86271541	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs192020954	chr1:86271568-86271569	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs561409819	chr1:86271582-86271583	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs184483369	chr1:86271619-86271620	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs546675319	chr1:86271620-86271621	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs566628507	chr1:86271690-86271691	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs570155338	chr1:86271706-86271707	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs187287483	chr1:86271707-86271708	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs369190831	chr1:86271708-86271709	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs546984096	chr1:86271713-86271714	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs537628049	chr1:86271714-86271715	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs554887952	chr1:86271716-86271717	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs111786109	chr1:86271753-86271754	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs59669169	chr1:86271759-86271760	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs78422277	chr1:86271774-86271775	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs397980692	chr1:86271776-86271777	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs368089086	chr1:86271777-86271778	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs567123009	chr1:86271793-86271794	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs313739	chr1:86271817-86271818	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Colorectal cancer	16272173	CNVD
Medulloblastoma	21979893	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Breast cancer	17133270	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Multiple myeloma	17550852	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	16397240	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:355 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:86257200-86274000	Weak transcription	Fetal Lung	lung
2	chr1:86263400-86272200	Weak transcription	GM12878-XiMat	blood
3	chr1:86264600-86272600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr1:86265800-86272400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr1:86267400-86273400	Weak transcription	Primary hematopoietic stem cells	blood
6	chr1:86267600-86271800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr1:86269000-86274000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr1:86270200-86271000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
9	chr1:86271000-86274000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
10	chr1:86271800-86272800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr1:86272400-86272800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr1:86272400-86272800	Enhancers	Fetal Brain Female	brain
13	chr1:86272400-86272800	Enhancers	Stomach Mucosa	stomach
14	chr1:86272600-86274000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr1:86273400-86276000	ZNF genes & repeats	Primary hematopoietic stem cells	blood
16	chr1:86274000-86275200	ZNF genes & repeats	Fetal Lung	lung
17	chr1:86274000-86276400	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
18	chr1:86274000-86276400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr1:86274000-86277000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr1:86274200-86275400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr1:86275200-86282000	Weak transcription	Fetal Lung	lung
22	chr1:86276000-86278600	Strong transcription	Primary hematopoietic stem cells	blood
23	chr1:86276400-86280200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr1:86276400-86284200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
25	chr1:86277000-86279000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr1:86278600-86279600	Weak transcription	Primary hematopoietic stem cells	blood
27	chr1:86279000-86279400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr1:86279400-86279800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr1:86279600-86283600	Strong transcription	Primary hematopoietic stem cells	blood
30	chr1:86279800-86284600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr1:86280000-86296600	Weak transcription	GM12878-XiMat	blood
32	chr1:86280200-86281600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr1:86281000-86281800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr1:86281600-86284200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr1:86281800-86282000	Enhancers	Adipose Nuclei	Adipose
36	chr1:86281800-86282200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr1:86282000-86284000	Strong transcription	Fetal Lung	lung
38	chr1:86282200-86283400	Weak transcription	Adipose Nuclei	Adipose
39	chr1:86282200-86283600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr1:86282800-86284400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr1:86283400-86283800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
42	chr1:86283400-86284200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr1:86283400-86285000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr1:86283400-86285000	Enhancers	Adipose Nuclei	Adipose
45	chr1:86283600-86284000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr1:86283600-86284400	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr1:86283600-86284400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr1:86283600-86284600	Enhancers	Osteobl	bone
49	chr1:86283600-86284800	Enhancers	Muscle Satellite Cultured Cells	--
50	chr1:86283600-86284800	Enhancers	NHDF-Ad	bronchial

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