Variant report

Variant	nsv999743
Chromosome Location	chr1:86241246-86364846
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	chr1:86315774-86316365	A549	lung:	n/a	chr1:86316105-86316119
3	ATF3	chr1:86315734-86316283	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	chr1:86328150-86328521	IMR90	lung:	n/a	n/a
10	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
11	CEBPB	chr1:86265556-86265752	K562	blood:	n/a	chr1:86265616-86265627
12	CEBPB	chr1:86312491-86312877	MCF-7	breast:	n/a	chr1:86312596-86312609 chr1:86312596-86312609 chr1:86312597-86312608 chr1:86312596-86312607
13	CEBPB	chr1:86312201-86312861	A549	lung:	n/a	chr1:86312596-86312609 chr1:86312596-86312609 chr1:86312597-86312608 chr1:86312596-86312607
14	CEBPB	chr1:86288238-86288706	HCT-116	colon:	n/a	n/a
15	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
16	CEBPB	chr1:86312489-86312717	MCF-7	breast:	n/a	chr1:86312596-86312609 chr1:86312596-86312609 chr1:86312597-86312608 chr1:86312596-86312607
17	CEBPB	chr1:86312158-86312748	A549	lung:	n/a	chr1:86312596-86312609 chr1:86312596-86312609 chr1:86312597-86312608 chr1:86312596-86312607
18	CEBPB	chr1:86265444-86265801	HepG2	liver:	n/a	chr1:86265452-86265465 chr1:86265616-86265627
19	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
20	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
21	CEBPB	chr1:86265445-86265772	IMR90	lung:	n/a	chr1:86265452-86265465 chr1:86265616-86265627
22	CEBPB	chr1:86315865-86316679	A549	lung:	n/a	chr1:86316566-86316577 chr1:86316566-86316575 chr1:86316561-86316578 chr1:86316564-86316575 chr1:86316001-86316014
23	CEBPB	chr1:86312164-86312478	MCF-7	breast:	n/a	n/a
24	CEBPB	chr1:86312443-86312728	IMR90	lung:	n/a	chr1:86312596-86312609 chr1:86312596-86312609 chr1:86312597-86312608 chr1:86312596-86312607
25	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
26	CEBPB	chr1:86312273-86312758	HepG2	liver:	n/a	chr1:86312596-86312609 chr1:86312596-86312609 chr1:86312597-86312608 chr1:86312596-86312607
27	CEBPB	chr1:86312488-86312731	A549	lung:	n/a	chr1:86312596-86312609 chr1:86312596-86312609 chr1:86312597-86312608 chr1:86312596-86312607
28	CEBPB	chr1:86312504-86312622	H1-hESC	embryonic stem cell:	n/a	chr1:86312596-86312609 chr1:86312596-86312609 chr1:86312597-86312608 chr1:86312596-86312607
29	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
30	CEBPB	chr1:86265524-86265733	A549	lung:	n/a	chr1:86265616-86265627
31	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
32	CEBPB	chr1:86315733-86316302	A549	lung:	n/a	chr1:86316001-86316014
33	CEBPB	chr1:86288103-86288794	HCT-116	colon:	n/a	n/a
34	CEBPB	chr1:86312217-86312800	Hela-S3	cervix:	n/a	chr1:86312596-86312609 chr1:86312596-86312609 chr1:86312597-86312608 chr1:86312596-86312607
35	CEBPB	chr1:86315667-86316620	HCT-116	colon:	n/a	chr1:86316566-86316577 chr1:86316566-86316575 chr1:86316561-86316578 chr1:86316564-86316575 chr1:86316001-86316014
36	CEBPB	chr1:86354701-86354883	A549	lung:	n/a	n/a
37	CEBPB	chr1:86312169-86312410	A549	lung:	n/a	n/a
38	CEBPB	chr1:86316412-86316684	HepG2	liver:	n/a	chr1:86316566-86316577 chr1:86316566-86316575 chr1:86316561-86316578 chr1:86316564-86316575
39	CEBPB	chr1:86315836-86316751	IMR90	lung:	n/a	chr1:86316566-86316577 chr1:86316566-86316575 chr1:86316561-86316578 chr1:86316564-86316575 chr1:86316001-86316014
40	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
41	CEBPB	chr1:86315823-86316264	A549	lung:	n/a	chr1:86316001-86316014
42	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
43	CHD2	chr1:86327651-86327685	GM12878	blood:	n/a	n/a
44	CHD2	chr1:86259018-86259019	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTCF	chr1:86360420-86360570	SAEC	small airway:	n/a	chr1:86360532-86360545
46	CTCF	chr1:86289902-86289985	ProgFib	skin:	n/a	n/a
47	CTCF	chr1:86289860-86290010	RPTEC	kidney:	n/a	n/a
48	CTCF	chr1:86350237-86350703	IMR90	lung:	n/a	n/a
49	CTCF	chr1:86360460-86360610	HPF	lung:	n/a	chr1:86360532-86360545
50	CTCF	chr1:86360520-86360670	GM12864	blood:	n/a	chr1:86360532-86360545

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:86283470-86283520	HRPEpiC	eye:	n/a
2	chr1:86283470-86283520	NH-A	brain:	n/a
3	chr1:86283470-86283520	Hepatocyte	liver:	n/a
4	chr1:86283470-86283520	IMR90	lung:	fetal
5	chr1:86296346-86296396	AG04450	lung:	fetal
6	chr1:86296346-86296396	PFSK-1	brain:	n/a
7	chr1:86296346-86296396	ovcar-3	ovarian:	n/a
8	chr1:86296346-86296396	HAEpiC	amniotic membrane:	n/a
9	chr1:86296346-86296396	MCF10A-Er-Src	breast:	n/a
10	chr1:86283470-86283520	GM19239	blood:	n/a
11	chr1:86296346-86296396	IMR90	lung:	fetal
12	chr1:86283470-86283520	PFSK-1	brain:	n/a
13	chr1:86283470-86283520	AG10803	skin:	n/a
14	chr1:86283470-86283520	HCM	heart:	n/a
15	chr1:86283470-86283520	AG04449	skin:	fetal
16	chr1:86296346-86296396	GM19239	blood:	n/a
17	chr1:86296346-86296396	HL-60	blood:	n/a
18	chr1:86283470-86283520	HAEpiC	amniotic membrane:	n/a
19	chr1:86296346-86296396	GM06990	blood:	n/a
20	chr1:86296346-86296396	HRPEpiC	eye:	n/a
21	chr1:86283470-86283520	GM12892	blood:	n/a
22	chr1:86283470-86283520	T-47D	breast:	n/a
23	chr1:86296346-86296396	T-47D	breast:	n/a
24	chr1:86296346-86296396	HRE	kidney:	n/a
25	chr1:86283470-86283520	AG09309	skin:	n/a
26	chr1:86283470-86283520	AG09319	gingival:	n/a
27	chr1:86283470-86283520	SKMC	muscle:	n/a
28	chr1:86296346-86296396	A549	lung:	n/a
29	chr1:86283470-86283520	HL-60	blood:	n/a
30	chr1:86296346-86296396	PANC-1	pancreas:	n/a
31	chr1:86296346-86296396	BE2_C	brain:	n/a
32	chr1:86283470-86283520	LNCaP	prostate:	n/a
33	chr1:86296346-86296396	AoSMC	blood vessel:	n/a
34	chr1:86283470-86283520	HUVEC	blood vessel:	n/a
35	chr1:86283470-86283520	HepG2	liver:	n/a
36	chr1:86283470-86283520	PrEC	prostate:	n/a
37	chr1:86296346-86296396	PrEC	prostate:	n/a
38	chr1:86283470-86283520	RPTEC	kidney:	n/a
39	chr1:86296346-86296396	U87	brain:	n/a
40	chr1:86296346-86296396	H1-hESC	embryonic stem cell:	embryo
41	chr1:86283470-86283520	SK-N-SH_RA	brain:	n/a
42	chr1:86296346-86296396	SK-N-SH_RA	brain:	n/a
43	chr1:86296346-86296396	GM12892	blood:	n/a
44	chr1:86283470-86283520	HCPEpiC	choroid plexus:	n/a
45	chr1:86296346-86296396	Jurkat	blood:	n/a
46	chr1:86296346-86296396	HCT-116	colon:	n/a
47	chr1:86283470-86283520	ProgFib	skin:	n/a
48	chr1:86296346-86296396	SAEC	small airway:	n/a
49	chr1:86296346-86296396	HCM	heart:	n/a
50	chr1:86296346-86296396	LNCaP	prostate:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:86078662..86080625-chr1:86320837..86323478,2	K562	blood:
2	chr1:86289855..86290389-chr1:86350572..86351446,2	MCF-7	breast:
3	chr1:86278878..86280687-chr1:86286928..86289556,2	K562	blood:
4	chr1:86263300..86265589-chr1:86281895..86284677,2	K562	blood:
5	chr1:86283869..86285851-chr1:86286499..86288640,2	MCF-7	breast:
6	chr1:86283944..86286909-chr1:86290122..86291813,2	MCF-7	breast:
7	chr1:86263300..86265589-chr1:86281895..86284677,2	K562	blood:
8	chr1:86289855..86290389-chr1:86350572..86351446,2	MCF-7	breast:
9	chr1:86278454..86281211-chr1:86282044..86284613,2	K562	blood:
10	chr1:86262773..86264767-chr1:86274959..86276756,2	MCF-7	breast:
11	chr1:86173609..86174719-chr1:86349901..86350977,5	MCF-7	breast:
12	chr1:86278454..86281211-chr1:86282044..86284613,2	K562	blood:
13	chr1:86173527..86174504-chr1:86315716..86316608,2	MCF-7	breast:
14	chr1:86282182..86284490-chr1:86287465..86289002,2	MCF-7	breast:
15	chr1:86360081..86361020-chr1:86483694..86484478,3	MCF-7	breast:
16	chr1:86278102..86279954-chr1:86282044..86284732,2	K562	blood:
17	chr1:86349495..86351039-chr1:86359014..86361069,2	MCF-7	breast:
18	chr1:86278102..86279954-chr1:86282044..86284732,2	K562	blood:
19	chr1:86211855..86213533-chr1:86285001..86287776,2	K562	blood:
20	chr1:86360058..86360590-chr1:86821594..86822114,2	MCF-7	breast:
21	chr1:86278878..86280687-chr1:86286928..86289556,2	K562	blood:
22	chr1:86046089..86048406-chr1:86314306..86316948,2	MCF-7	breast:
23	chr1:86282182..86284490-chr1:86287465..86289002,2	MCF-7	breast:
24	chr1:86283944..86286909-chr1:86290122..86291813,2	MCF-7	breast:
25	chr1:86262773..86264767-chr1:86274959..86276756,2	MCF-7	breast:
26	chr1:86225931..86227937-chr1:86257811..86259355,2	K562	blood:
27	chr1:85773662..85774295-chr1:86315658..86316288,2	MCF-7	breast:
28	chr1:86283869..86285851-chr1:86286499..86288640,2	MCF-7	breast:
29	chr1:86349495..86351039-chr1:86359014..86361069,2	MCF-7	breast:

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

Extended variants
information (count: 4604 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:4604 , 50 per page) page: 1 2 3 4 5 6 7 ... 93

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs374908126	chr1:86241316-86241317	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs200383865	chr1:86241379-86241380	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs528451622	chr1:86241399-86241400	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs550729519	chr1:86241400-86241401	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs184513433	chr1:86241402-86241403	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs370588081	chr1:86241432-86241433	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs374747073	chr1:86241438-86241439	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs368488549	chr1:86241439-86241440	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs573113208	chr1:86241462-86241463	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs571796429	chr1:86241464-86241465	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs114744777	chr1:86241486-86241487	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs550833348	chr1:86241615-86241616	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs34471406	chr1:86241616-86241617	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs567463385	chr1:86241658-86241659	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs189294036	chr1:86241664-86241665	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs181886478	chr1:86241712-86241713	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs75364489	chr1:86241713-86241714	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs538659776	chr1:86241802-86241803	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs140914635	chr1:86241819-86241820	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs377746545	chr1:86241824-86241825	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs575037715	chr1:86241829-86241830	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs144746246	chr1:86241874-86241875	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs557137946	chr1:86241892-86241893	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs144726088	chr1:86241972-86241973	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs542965738	chr1:86241991-86241992	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs199525388	chr1:86242003-86242004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs148512750	chr1:86242013-86242014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs115219807	chr1:86242017-86242018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs142770795	chr1:86242048-86242049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs544676679	chr1:86242060-86242061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs184594538	chr1:86242066-86242067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs61783134	chr1:86242080-86242081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs560943848	chr1:86242097-86242098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs151223342	chr1:86242114-86242115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs140373504	chr1:86242119-86242120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs114037202	chr1:86242161-86242162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs200005462	chr1:86242184-86242185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs201307502	chr1:86242185-86242186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs77302736	chr1:86242186-86242187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs67085584	chr1:86242187-86242188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs201802215	chr1:86242188-86242189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs10648395	chr1:86242189-86242190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs139064867	chr1:86242190-86242191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs201798124	chr1:86242196-86242197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs538548311	chr1:86242211-86242212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs551802833	chr1:86242290-86242291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs544191139	chr1:86242319-86242320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs568468960	chr1:86242333-86242334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs374384092	chr1:86242434-86242435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs189003852	chr1:86242487-86242488	Weak transcription	n/a	n/a	Overlapped CNVs	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:312 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:86222400-86246400	Weak transcription	Primary hematopoietic stem cells	blood
2	chr1:86222400-86248200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
3	chr1:86222800-86254400	Weak transcription	Fetal Lung	lung
4	chr1:86239800-86253800	Weak transcription	GM12878-XiMat	blood
5	chr1:86240000-86242000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr1:86241200-86241600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr1:86241600-86246200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr1:86242000-86244600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr1:86244600-86251400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr1:86246200-86251000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr1:86246400-86249200	Strong transcription	Primary hematopoietic stem cells	blood
12	chr1:86248200-86251400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
13	chr1:86249200-86251000	Weak transcription	Primary hematopoietic stem cells	blood
14	chr1:86251000-86252000	Strong transcription	Primary hematopoietic stem cells	blood
15	chr1:86251000-86256400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr1:86251400-86254200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr1:86251400-86255200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
18	chr1:86252000-86256600	Weak transcription	Primary hematopoietic stem cells	blood
19	chr1:86254400-86254800	ZNF genes & repeats	Fetal Lung	lung
20	chr1:86254800-86256800	Weak transcription	Fetal Lung	lung
21	chr1:86255200-86257600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
22	chr1:86255800-86256000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr1:86256000-86257400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr1:86256400-86257200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr1:86256600-86257400	Strong transcription	Primary hematopoietic stem cells	blood
26	chr1:86256800-86257200	Strong transcription	Fetal Lung	lung
27	chr1:86257200-86263000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr1:86257200-86274000	Weak transcription	Fetal Lung	lung
29	chr1:86257400-86262800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr1:86257400-86266800	Weak transcription	Primary hematopoietic stem cells	blood
31	chr1:86257600-86263000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
32	chr1:86260800-86261800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr1:86261800-86264200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr1:86262400-86264800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr1:86262800-86268600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr1:86263000-86264600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr1:86263000-86264800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
38	chr1:86263400-86263800	Enhancers	Aorta	Aorta
39	chr1:86263400-86272200	Weak transcription	GM12878-XiMat	blood
40	chr1:86264200-86264800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr1:86264400-86265000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr1:86264600-86272600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr1:86264800-86265600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr1:86264800-86267600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
45	chr1:86265000-86265600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr1:86265600-86265800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr1:86265600-86266200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr1:86265800-86272400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr1:86266200-86267200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr1:86266200-86267600	Enhancers	NHDF-Ad	bronchial

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