Variant report

Variant	nsv534945
Chromosome Location	chr1:46248667-46493959
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2525)
CpG islands
(count:976)
Chromatin interactive
region (count:199)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2525 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:46444549-46445261	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:46420318-46420492	K562	blood:	n/a	n/a
3	ARID3A	chr1:46275452-46275617	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:46358025-46358337	HepG2	liver:	n/a	n/a
5	ARID3A	chr1:46334608-46334873	HepG2	liver:	n/a	n/a
6	ARID3A	chr1:46347288-46347573	HepG2	liver:	n/a	n/a
7	ARID3A	chr1:46440638-46440907	HepG2	liver:	n/a	n/a
8	ARID3A	chr1:46396414-46396789	K562	blood:	n/a	n/a
9	ARID3A	chr1:46350455-46350607	K562	blood:	n/a	n/a
10	ARID3A	chr1:46336921-46338303	HepG2	liver:	n/a	n/a
11	ARID3A	chr1:46268405-46269160	K562	blood:	n/a	n/a
12	ARID3A	chr1:46288374-46288666	HepG2	liver:	n/a	n/a
13	ARID3A	chr1:46379137-46379290	K562	blood:	n/a	n/a
14	ARID3A	chr1:46268499-46269278	HepG2	liver:	n/a	n/a
15	ARID3A	chr1:46350498-46350690	HepG2	liver:	n/a	n/a
16	ATF1	chr1:46395037-46395359	K562	blood:	n/a	n/a
17	ATF1	chr1:46379051-46379278	K562	blood:	n/a	n/a
18	ATF1	chr1:46390439-46390744	K562	blood:	n/a	n/a
19	ATF1	chr1:46252905-46252920	K562	blood:	n/a	n/a
20	ATF1	chr1:46309326-46309534	K562	blood:	n/a	n/a
21	ATF1	chr1:46268403-46269065	K562	blood:	n/a	n/a
22	ATF2	chr1:46378895-46379457	GM12878	blood:	n/a	n/a
23	ATF2	chr1:46268428-46268979	H1-hESC	embryonic stem cell:	n/a	n/a
24	ATF2	chr1:46268444-46268793	H1-hESC	embryonic stem cell:	n/a	n/a
25	ATF2	chr1:46306272-46306830	GM12878	blood:	n/a	n/a
26	ATF2	chr1:46268462-46268881	GM12878	blood:	n/a	n/a
27	ATF2	chr1:46268393-46268945	GM12878	blood:	n/a	n/a
28	ATF3	chr1:46268962-46269408	K562	blood:	n/a	n/a
29	ATF3	chr1:46337783-46338146	A549	lung:	n/a	n/a
30	ATF3	chr1:46268279-46268864	K562	blood:	n/a	n/a
31	BACH1	chr1:46391484-46391522	H1-hESC	embryonic stem cell:	n/a	n/a
32	BACH1	chr1:46420211-46420568	H1-hESC	embryonic stem cell:	n/a	chr1:46420379-46420393
33	BACH1	chr1:46421636-46421646	K562	blood:	n/a	n/a
34	BACH1	chr1:46461003-46461251	H1-hESC	embryonic stem cell:	n/a	n/a
35	BACH1	chr1:46269216-46269229	H1-hESC	embryonic stem cell:	n/a	n/a
36	BACH1	chr1:46420274-46420543	K562	blood:	n/a	chr1:46420379-46420393
37	BACH1	chr1:46269744-46269925	H1-hESC	embryonic stem cell:	n/a	n/a
38	BATF	chr1:46268407-46268721	GM12878	blood:	n/a	chr1:46268569-46268579 chr1:46268635-46268648 chr1:46268568-46268579
39	BATF	chr1:46302487-46302754	GM12878	blood:	n/a	n/a
40	BATF	chr1:46379122-46379421	GM12878	blood:	n/a	n/a
41	BATF	chr1:46308522-46308841	GM12878	blood:	n/a	n/a
42	BATF	chr1:46308483-46308772	GM12878	blood:	n/a	n/a
43	BATF	chr1:46306368-46306703	GM12878	blood:	n/a	n/a
44	BCLAF1	chr1:46302137-46302794	GM12878	blood:	n/a	n/a
45	BHLHE40	chr1:46379117-46379265	K562	blood:	n/a	n/a
46	BHLHE40	chr1:46329931-46330173	K562	blood:	n/a	n/a
47	BHLHE40	chr1:46337766-46338131	HepG2	liver:	n/a	n/a
48	BHLHE40	chr1:46396498-46396641	K562	blood:	n/a	n/a
49	BHLHE40	chr1:46268379-46269420	K562	blood:	n/a	chr1:46269294-46269310 chr1:46269102-46269118
50	BHLHE40	chr1:46268856-46269477	GM12878	blood:	n/a	chr1:46269294-46269310 chr1:46269102-46269118

(count:976 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:46269788-46269838	Caco-2	colon:	n/a
2	chr1:46265164-46265214	GM19239	blood:	n/a
3	chr1:46269788-46269838	BJ	skin:	n/a
4	chr1:46265164-46265214	U87	brain:	n/a
5	chr1:46269397-46269447	PrEC	prostate:	n/a
6	chr1:46268207-46268257	HCPEpiC	choroid plexus:	n/a
7	chr1:46269305-46269355	H1-hESC	embryonic stem cell:	embryo
8	chr1:46391567-46391617	Jurkat	blood:	n/a
9	chr1:46269324-46269374	ProgFib	skin:	n/a
10	chr1:46391567-46391617	SAEC	small airway:	n/a
11	chr1:46269394-46269444	ovcar-3	ovarian:	n/a
12	chr1:46391567-46391617	AG09319	gingival:	n/a
13	chr1:46265164-46265214	GM12891	blood:	n/a
14	chr1:46268158-46268208	BJ	skin:	n/a
15	chr1:46269788-46269838	GM12878	blood:	n/a
16	chr1:46273758-46273808	NH-A	brain:	n/a
17	chr1:46265164-46265214	HCT-116	colon:	n/a
18	chr1:46485352-46485402	H1-hESC	embryonic stem cell:	embryo
19	chr1:46269394-46269444	NHDF-neo	bronchial:	n/a
20	chr1:46265164-46265214	HPAEpiC	pulmonary alveolar:	n/a
21	chr1:46269324-46269374	Hela-S3	cervix:	n/a
22	chr1:46269397-46269447	ProgFib	skin:	n/a
23	chr1:46268207-46268257	HCF	heart:	n/a
24	chr1:46378857-46378907	HepG2	liver:	n/a
25	chr1:46267883-46267933	HRPEpiC	eye:	n/a
26	chr1:46268158-46268208	AG04450	lung:	fetal
27	chr1:46269788-46269838	T-47D	breast:	n/a
28	chr1:46269394-46269444	MCF10A-Er-Src	breast:	n/a
29	chr1:46269394-46269444	ECC-1	luminal epithelium:	n/a
30	chr1:46269788-46269838	CMK	blood:	n/a
31	chr1:46269397-46269447	U87	brain:	n/a
32	chr1:46268207-46268257	ProgFib	skin:	n/a
33	chr1:46269788-46269838	NT2-D1	testis:	n/a
34	chr1:46268158-46268208	HPAEpiC	pulmonary alveolar:	n/a
35	chr1:46269788-46269838	GM12891	blood:	n/a
36	chr1:46485352-46485402	LNCaP	prostate:	n/a
37	chr1:46269788-46269838	U87	brain:	n/a
38	chr1:46269120-46269170	SKMC	muscle:	n/a
39	chr1:46378857-46378907	CMK	blood:	n/a
40	chr1:46269788-46269838	AG04449	skin:	fetal
41	chr1:46268979-46269029	HMEC	breast:	n/a
42	chr1:46273758-46273808	HepG2	liver:	n/a
43	chr1:46268207-46268257	HCT-116	colon:	n/a
44	chr1:46268207-46268257	ovcar-3	ovarian:	n/a
45	chr1:46420220-46420270	HEK293	kidney:	embryo
46	chr1:46269397-46269447	GM12891	blood:	n/a
47	chr1:46378857-46378907	SAEC	small airway:	n/a
48	chr1:46269324-46269374	ECC-1	luminal epithelium:	n/a
49	chr1:46391567-46391617	SK-N-MC	brain:	n/a
50	chr1:46485352-46485402	U87	brain:	n/a

(count:199 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr1:46270679..46272758-chr1:46394759..46396446,2	K562	blood:
2	chr1:46294880..46298299-chr1:46298592..46300540,3	K562	blood:
3	chr1:46280079..46281713-chr1:46349138..46351196,2	K562	blood:
4	chr1:46360342..46362505-chr1:46373607..46378298,4	K562	blood:
5	chr1:46269300..46271660-chr1:46713127..46714994,2	K562	blood:
6	chr1:46441452..46444214-chr1:46444558..46446459,2	K562	blood:
7	chr1:46298641..46301041-chr1:46305694..46307488,2	K562	blood:
8	chr1:46493789..46494398-chr1:46502594..46503341,2	K562	blood:
9	chr1:46409703..46413152-chr1:46663099..46666504,3	K562	blood:
10	chr1:46490032..46491762-chr1:46646589..46649571,2	K562	blood:
11	chr1:46269243..46271272-chr1:46282626..46285190,2	K562	blood:
12	chr1:46149604..46155141-chr1:46267151..46271003,9	MCF-7	breast:
13	chr1:46214506..46217457-chr1:46320126..46323086,2	K562	blood:
14	chr1:46151182..46154055-chr1:46326132..46330387,5	K562	blood:
15	chr1:46321425..46323613-chr1:46327352..46330305,2	K562	blood:
16	chr1:46349975..46352089-chr1:46365133..46367847,2	K562	blood:
17	chr1:46488776..46491318-chr1:46492009..46494441,2	K562	blood:
18	chr1:46280205..46283034-chr1:46287288..46288792,2	K562	blood:
19	chr1:46345992..46348458-chr1:46350883..46353705,2	K562	blood:
20	chr1:46483034..46485890-chr1:46486254..46490637,7	K562	blood:
21	chr1:46278125..46279001-chr1:46347298..46347802,2	MCF-7	breast:
22	chr1:46460300..46463881-chr1:46464665..46468860,3	K562	blood:
23	chr1:46291760..46294499-chr1:46299751..46301295,2	K562	blood:
24	chr1:46438424..46439938-chr1:46443321..46445387,2	K562	blood:
25	chr1:46267846..46271685-chr1:46273024..46275916,3	MCF-7	breast:
26	chr1:46461020..46463343-chr1:46476267..46478373,2	K562	blood:
27	chr1:46437212..46439415-chr1:46449491..46452410,2	MCF-7	breast:
28	chr1:46457031..46460006-chr1:46461254..46463100,2	K562	blood:
29	chr1:46458380..46460334-chr1:46463131..46465257,2	K562	blood:
30	chr1:46048559..46050395-chr1:46327197..46329514,2	MCF-7	breast:
31	chr1:46280079..46281713-chr1:46349138..46351196,2	K562	blood:
32	chr1:46407006..46408992-chr1:46409790..46412710,2	K562	blood:
33	chr1:46258378..46261508-chr1:46262395..46264420,3	K562	blood:
34	chr1:46397000..46399613-chr1:46401523..46403700,2	K562	blood:
35	chr1:46418299..46420870-chr1:46424946..46427341,2	K562	blood:
36	chr1:46334925..46337529-chr1:46338611..46340794,2	K562	blood:
37	chr1:46327585..46329581-chr1:46331185..46333590,2	K562	blood:
38	chr1:46048521..46050568-chr1:46327605..46330996,3	K562	blood:
39	chr1:46470355..46473674-chr1:46477475..46480255,3	K562	blood:
40	chr1:46319707..46321501-chr1:46343782..46345819,2	K562	blood:
41	chr1:46270679..46272758-chr1:46394759..46396446,2	K562	blood:
42	chr1:46150825..46154977-chr1:46267620..46271634,6	MCF-7	breast:
43	chr1:46152331..46153862-chr1:46251195..46252754,2	K562	blood:
44	chr1:46464725..46466384-chr1:46509331..46511919,2	K562	blood:
45	chr1:46244095..46246858-chr1:46259918..46262871,2	K562	blood:
46	chr1:46467498..46470215-chr1:46486949..46488855,2	K562	blood:
47	chr1:46320115..46321797-chr1:46330424..46332965,2	K562	blood:
48	chr1:46477455..46479604-chr1:46504836..46506778,2	K562	blood:
49	chr1:46431686..46433580-chr1:46435940..46437552,2	MCF-7	breast:
50	chr1:46334716..46337442-chr1:46355883..46358850,3	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PIK3R3-5	chr1:46413745-46413888	NONHSAT002972
2	lnc-PIK3R3-1	chr1:46398107-46399249	ENSG00000248250
3	lnc-PIK3R3-1	chr1:46396865-46397420	ENSG00000248250
4	lnc-PIK3R3-5	chr1:46414487-46414737	NONHSAT002972

No data

Variant related genes	Relation type
MAST2	TF binding region
TMA16P2	TF binding region
MAST2	CpG island
TMA16P2	CpG island
ENSG00000085999	chromatin interactions
ENSG00000159592	chromatin interactions
ENSG00000086015	chromatin interactions
ENSG00000122566	chromatin interactions
ENSG00000197429	chromatin interactions
ENSG00000085998	chromatin interactions
ENSG00000132780	chromatin interactions
ENSG00000151353	chromatin interactions
ENSG00000233296	chromatin interactions
ENSG00000122565	chromatin interactions
ENSG00000117472	chromatin interactions
ENSG00000110321	chromatin interactions
ENSG00000117448	chromatin interactions
ENSG00000159596	chromatin interactions
ENSG00000117450	chromatin interactions
ENSG00000232467	chromatin interactions

Extended variants
information (count: 8679 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:8679 , 50 per page) page: 1 2 3 4 5 6 7 ... 174

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs150325171	chr1:46249688-46249689	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs386366874	chr1:46249700-46249701	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs140523926	chr1:46249707-46249708	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs386366875	chr1:46249718-46249719	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs377543687	chr1:46249719-46249720	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs184738903	chr1:46249720-46249721	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs200819722	chr1:46249721-46249722	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs560320320	chr1:46249730-46249731	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs12239318	chr1:46249744-46249745	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs180870760	chr1:46250000-46250001	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs10789474	chr1:46250040-46250041	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs184452683	chr1:46250081-46250082	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs77112504	chr1:46250117-46250118	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs145868909	chr1:46250162-46250163	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs558095811	chr1:46250164-46250165	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs532785265	chr1:46250180-46250181	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs553348209	chr1:46250220-46250221	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs74227051	chr1:46250291-46250292	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs537004715	chr1:46250318-46250319	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs112198988	chr1:46250365-46250366	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs35160148	chr1:46250372-46250373	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs146736480	chr1:46250373-46250374	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs397814743	chr1:46250392-46250393	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs79208018	chr1:46250393-46250394	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs555076299	chr1:46250436-46250437	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs368523230	chr1:46250557-46250558	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs567328009	chr1:46250566-46250567	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs189777319	chr1:46250625-46250626	Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs4275489	chr1:46250646-46250647	Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs577406854	chr1:46250693-46250694	Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs371529734	chr1:46250734-46250735	Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs544853530	chr1:46250771-46250772	Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs12072999	chr1:46250793-46250794	Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs376597348	chr1:46250840-46250841	Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs181337237	chr1:46250842-46250843	Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs575183726	chr1:46250854-46250855	Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs6683500	chr1:46250873-46250874	Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs186863457	chr1:46250896-46250897	Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs371483841	chr1:46250911-46250912	Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs4607936	chr1:46250925-46250926	Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs367649771	chr1:46250942-46250943	Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs12074077	chr1:46250944-46250945	Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs532750003	chr1:46250962-46250963	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs551199670	chr1:46251107-46251108	Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs190660188	chr1:46251130-46251131	Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs530342685	chr1:46251145-46251146	Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs74227052	chr1:46251160-46251161	Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs34835041	chr1:46251198-46251199	Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs397861304	chr1:46251206-46251207	Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs181807917	chr1:46251238-46251239	Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:99)

Disease	PMID	Source
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21080181	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	17603634	CNVD
Soft tissue tumor	16732325	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	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
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
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
Chronic myeloid leukemia	21384125	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	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
Uveal melanoma	20484589	CNVD
Ovarian cancer	22174824	CNVD
Muscle-eye-brain disease	21572526	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	20680643	CNVD
Colorectal cancer	19287155	CNVD
small cell lung cancer	20016488	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Ovarian cancer	17875760	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ovarian cancer	21781307	CNVD
Barrett''s syndrome	19417022	CNVD

Chromatin state (count:5001 , 50 per page) page: 1 2 3 4 5 6 7 ... 101

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:46250000-46251000	Enhancers	Primary T helper cells PMA-I stimulated	--
2	chr1:46250200-46251200	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
3	chr1:46250200-46251200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
4	chr1:46250200-46251200	Enhancers	Primary T helper cells fromperipheralblood	blood
5	chr1:46250200-46251200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
6	chr1:46250400-46250600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr1:46250400-46251200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
8	chr1:46250400-46252400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
9	chr1:46250400-46252400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
10	chr1:46250600-46251200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
11	chr1:46250600-46251200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
12	chr1:46250600-46251200	Enhancers	Primary T killer memory cells from peripheral blood	blood
13	chr1:46250600-46252800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
14	chr1:46250800-46251200	Enhancers	Primary T helper naive cells from peripheral blood	blood
15	chr1:46251000-46251200	Enhancers	Primary T cells from cord blood	blood
16	chr1:46251000-46251600	Enhancers	Primary neutrophils fromperipheralblood	blood
17	chr1:46251000-46251600	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
18	chr1:46251000-46251600	Enhancers	GM12878-XiMat	blood
19	chr1:46251000-46251800	Enhancers	Dnd41	blood
20	chr1:46251000-46252000	Enhancers	Primary hematopoietic stem cells short term culture	blood
21	chr1:46251200-46251600	Enhancers	Primary B cells from peripheral blood	blood
22	chr1:46251200-46251600	Flanking Active TSS	Primary T cells from cord blood	blood
23	chr1:46251200-46251600	Flanking Active TSS	Primary T cells fromperipheralblood	blood
24	chr1:46251200-46251600	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
25	chr1:46251200-46251600	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
26	chr1:46251200-46251600	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
27	chr1:46251200-46251600	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
28	chr1:46251200-46251600	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
29	chr1:46251200-46251600	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
30	chr1:46251200-46251600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr1:46251200-46251600	Enhancers	Fetal Thymus	thymus
32	chr1:46251200-46251600	Enhancers	Thymus	Thymus
33	chr1:46251200-46251600	Enhancers	K562	blood
34	chr1:46251200-46251800	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
35	chr1:46251200-46251800	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
36	chr1:46251200-46251800	Enhancers	Monocytes-CD14+_RO01746	blood
37	chr1:46251200-46252400	Enhancers	Primary monocytes fromperipheralblood	blood
38	chr1:46251600-46252000	Active TSS	Primary T cells from cord blood	blood
39	chr1:46251600-46252000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
40	chr1:46251600-46252200	Enhancers	Primary T cells fromperipheralblood	blood
41	chr1:46251600-46252200	Enhancers	Primary T helper naive cells from peripheral blood	blood
42	chr1:46251600-46252400	Enhancers	Primary T helper cells PMA-I stimulated	--
43	chr1:46251600-46252400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
44	chr1:46251600-46252600	Enhancers	Primary T killer memory cells from peripheral blood	blood
45	chr1:46251600-46253000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
46	chr1:46251600-46253000	Enhancers	Primary T helper cells fromperipheralblood	blood
47	chr1:46251600-46253600	Weak transcription	Primary B cells from peripheral blood	blood
48	chr1:46251600-46253600	Weak transcription	GM12878-XiMat	blood
49	chr1:46251600-46253800	Weak transcription	K562	blood
50	chr1:46251800-46252000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood

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