Variant report

Variant	nsv826809
Chromosome Location	chr1:223536032-223538665
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:142)
CpG islands
(count:673)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:142 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr1:223538550-223538750	K562	blood:	n/a	n/a
2	BACH1	chr1:223537063-223537589	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr1:223537905-223538237	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr1:223538485-223538731	K562	blood:	n/a	n/a
5	BHLHE40	chr1:223536627-223536677	K562	blood:	n/a	n/a
6	CBX3	chr1:223537298-223537571	K562	blood:	n/a	n/a
7	CCNT2	chr1:223537418-223538160	K562	blood:	n/a	n/a
8	CEBPB	chr1:223538560-223538655	H1-hESC	embryonic stem cell:	n/a	n/a
9	CHD2	chr1:223537326-223537511	GM12878	blood:	n/a	n/a
10	CHD2	chr1:223537333-223537528	H1-hESC	embryonic stem cell:	n/a	n/a
11	CHD2	chr1:223538089-223538289	H1-hESC	embryonic stem cell:	n/a	n/a
12	CHD2	chr1:223536406-223536658	H1-hESC	embryonic stem cell:	n/a	n/a
13	CREB1	chr1:223537234-223537736	H1-hESC	embryonic stem cell:	n/a	n/a
14	CREB1	chr1:223537176-223537594	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTBP2	chr1:223536947-223537533	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTBP2	chr1:223537772-223538667	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr1:223537436-223537506	Gliobla	brain:	n/a	n/a
18	CTCF	chr1:223537416-223537562	MCF-7	breast:	n/a	n/a
19	CTCF	chr1:223537426-223537531	Spleen_OC	spleen:	n/a	n/a
20	CTCF	chr1:223536640-223536790	AG10803	skin:	n/a	n/a
21	CTCF	chr1:223537408-223537607	GM12878	blood:	n/a	n/a
22	CTCF	chr1:223537405-223537613	K562	blood:	n/a	n/a
23	CTCF	chr1:223537360-223537510	AG09319	gingival:	n/a	n/a
24	CTCF	chr1:223537262-223537638	K562	blood:	n/a	n/a
25	CTCF	chr1:223537437-223537516	Fibrobl	skin:	n/a	n/a
26	CTCF	chr1:223537300-223537450	HRE	kidney:	n/a	n/a
27	CTCF	chr1:223537465-223537515	Pancreas_OC	pancreas:	n/a	n/a
28	CTCF	chr1:223537449-223537535	MCF-7	breast:	n/a	n/a
29	CTCF	chr1:223537380-223537530	GM12873	blood:	n/a	n/a
30	CTCF	chr1:223537438-223537584	LNCaP	prostate:	n/a	n/a
31	CTCF	chr1:223537457-223537496	NHEK	skin:	n/a	n/a
32	CTCF	chr1:223537463-223537578	LNCaP	prostate:	n/a	n/a
33	CTCF	chr1:223537369-223537538	K562	blood:	n/a	n/a
34	CTCF	chr1:223537380-223537530	Caco-2	colon:	n/a	n/a
35	CTCF	chr1:223537440-223537590	GM12871	blood:	n/a	n/a
36	CTCF	chr1:223537432-223537560	MCF-7	breast:	n/a	n/a
37	CTCF	chr1:223536640-223536790	GM12869	blood:	n/a	n/a
38	CTCF	chr1:223537416-223537603	K562	blood:	n/a	n/a
39	E2F6	chr1:223537371-223537640	K562	blood:	n/a	chr1:223537564-223537574 chr1:223537543-223537552
40	E2F6	chr1:223537700-223538243	K562	blood:	n/a	chr1:223538169-223538176 chr1:223538169-223538176 chr1:223538169-223538176
41	E2F6	chr1:223537730-223538027	A549	lung:	n/a	n/a
42	E2F6	chr1:223537658-223538020	A549	lung:	n/a	n/a
43	E2F6	chr1:223537703-223538550	H1-hESC	embryonic stem cell:	n/a	chr1:223538169-223538176 chr1:223538169-223538176 chr1:223538169-223538176 chr1:223538386-223538395 chr1:223538386-223538398 chr1:223538394-223538403
44	E2F6	chr1:223537699-223538417	H1-hESC	embryonic stem cell:	n/a	chr1:223538169-223538176 chr1:223538169-223538176 chr1:223538169-223538176 chr1:223538386-223538395 chr1:223538386-223538398 chr1:223538394-223538403
45	E2F6	chr1:223537688-223537961	K562	blood:	n/a	n/a
46	EBF1	chr1:223536500-223536806	GM12878	blood:	n/a	chr1:223536683-223536694
47	EBF1	chr1:223536525-223536744	GM12878	blood:	n/a	chr1:223536683-223536694
48	EBF1	chr1:223538089-223538391	GM12878	blood:	n/a	chr1:223538218-223538228 chr1:223538217-223538230 chr1:223538217-223538228 chr1:223538219-223538228 chr1:223538219-223538228
49	EGR1	chr1:223537372-223537773	K562	blood:	n/a	chr1:223537544-223537557
50	EGR1	chr1:223537361-223537691	K562	blood:	n/a	chr1:223537544-223537557

(count:673 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:223538627-223538677	SK-N-SH	brain:	n/a
2	chr1:223537199-223537249	ovcar-3	ovarian:	n/a
3	chr1:223538627-223538677	SK-N-SH	brain:	n/a
4	chr1:223537199-223537249	ovcar-3	ovarian:	n/a
5	chr1:223537435-223537485	H1-hESC	embryonic stem cell:	embryo
6	chr1:223536296-223536346	ECC-1	luminal epithelium:	n/a
7	chr1:223538359-223538409	HUVEC	blood vessel:	n/a
8	chr1:223537435-223537485	ECC-1	luminal epithelium:	n/a
9	chr1:223538379-223538429	U87	brain:	n/a
10	chr1:223538601-223538651	AG09319	gingival:	n/a
11	chr1:223538174-223538224	LNCaP	prostate:	n/a
12	chr1:223538334-223538384	GM06990	blood:	n/a
13	chr1:223538623-223538673	SKMC	muscle:	n/a
14	chr1:223538379-223538429	H1-hESC	embryonic stem cell:	embryo
15	chr1:223537363-223537413	HCF	heart:	n/a
16	chr1:223537435-223537485	BE2_C	brain:	n/a
17	chr1:223538379-223538429	SKMC	muscle:	n/a
18	chr1:223538174-223538224	AoSMC	blood vessel:	n/a
19	chr1:223537199-223537249	ECC-1	luminal epithelium:	n/a
20	chr1:223538627-223538677	GM19239	blood:	n/a
21	chr1:223538379-223538429	HL-60	blood:	n/a
22	chr1:223538379-223538429	HRCEpiC	kidney:	n/a
23	chr1:223538359-223538409	AG04450	lung:	fetal
24	chr1:223538174-223538224	PANC-1	pancreas:	n/a
25	chr1:223537435-223537485	GM06990	blood:	n/a
26	chr1:223538627-223538677	HEK293	kidney:	embryo
27	chr1:223538359-223538409	Jurkat	blood:	n/a
28	chr1:223538601-223538651	IMR90	lung:	fetal
29	chr1:223537363-223537413	HRE	kidney:	n/a
30	chr1:223538601-223538651	CMK	blood:	n/a
31	chr1:223537363-223537413	Caco-2	colon:	n/a
32	chr1:223538334-223538384	HEK293	kidney:	embryo
33	chr1:223537363-223537413	MCF-7	breast:	n/a
34	chr1:223536296-223536346	AG09319	gingival:	n/a
35	chr1:223538174-223538224	HRPEpiC	eye:	n/a
36	chr1:223537435-223537485	NT2-D1	testis:	n/a
37	chr1:223538623-223538673	T-47D	breast:	n/a
38	chr1:223538601-223538651	NHBE	bronchial:	n/a
39	chr1:223538379-223538429	GM12878	blood:	n/a
40	chr1:223538174-223538224	AG04450	lung:	fetal
41	chr1:223537435-223537485	AG04449	skin:	fetal
42	chr1:223538174-223538224	ovcar-3	ovarian:	n/a
43	chr1:223538627-223538677	Hepatocyte	liver:	n/a
44	chr1:223537435-223537485	HRPEpiC	eye:	n/a
45	chr1:223538627-223538677	NHDF-neo	bronchial:	n/a
46	chr1:223536296-223536346	PrEC	prostate:	n/a
47	chr1:223538623-223538673	A549	lung:	n/a
48	chr1:223537435-223537485	AG09319	gingival:	n/a
49	chr1:223537199-223537249	K562	blood:	n/a
50	chr1:223538359-223538409	MCF10A-Er-Src	breast:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr1:223305860..223308306-chr1:223535536..223539484,5	MCF-7	breast:
2	chr1:223536301..223536801-chr22:50639192..50639860,2	HCT-116	colon:
3	chr1:223536038..223539069-chr1:223546089..223550790,4	MCF-7	breast:
4	chr1:223534957..223537393-chr1:223566287..223567830,2	MCF-7	breast:

No data

Variant related genes	Relation type
SUSD4	TF binding region
SUSD4	CpG island
ENSG00000187554	chromatin interactions
ENSG00000251789	chromatin interactions
ENSG00000178395	chromatin interactions
ENSG00000073169	chromatin interactions

Extended variants
information (count: 85 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:85 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs139062316	chr1:223536045-223536046	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Bivalent Enhancer Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs542452063	chr1:223536086-223536087	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Bivalent Enhancer Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs35119441	chr1:223536099-223536100	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Bivalent Enhancer Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs560782864	chr1:223536101-223536102	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Bivalent Enhancer Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs554083849	chr1:223536123-223536124	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Bivalent Enhancer Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs572400275	chr1:223536133-223536134	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Bivalent Enhancer Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs542639320	chr1:223536144-223536145	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Bivalent Enhancer Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs538109569	chr1:223536287-223536288	Bivalent/Poised TSS Enhancers Bivalent Enhancer Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs111732241	chr1:223536294-223536295	Bivalent/Poised TSS Enhancers Bivalent Enhancer Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs376390273	chr1:223536342-223536343	Bivalent/Poised TSS Enhancers Bivalent Enhancer Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs185424189	chr1:223536363-223536364	Bivalent/Poised TSS Enhancers Bivalent Enhancer Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs543526963	chr1:223536476-223536477	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs574357752	chr1:223536484-223536485	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs562708669	chr1:223536487-223536488	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs532944814	chr1:223536532-223536533	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs551595145	chr1:223536577-223536578	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs75318848	chr1:223536607-223536608	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs368559778	chr1:223536614-223536615	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs376831634	chr1:223536629-223536630	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs143193274	chr1:223536657-223536658	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs143717734	chr1:223536690-223536691	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs371162328	chr1:223536702-223536703	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs143929528	chr1:223536703-223536704	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs568360954	chr1:223536705-223536706	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs549033740	chr1:223536770-223536771	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs567117963	chr1:223536779-223536780	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs374178534	chr1:223536782-223536783	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs537948291	chr1:223536789-223536790	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs555945479	chr1:223536890-223536891	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs571308829	chr1:223536913-223536914	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs369126563	chr1:223536924-223536925	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs553924270	chr1:223536959-223536960	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs572437182	chr1:223536978-223536979	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs533594120	chr1:223537074-223537075	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs542876489	chr1:223537082-223537083	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs373844571	chr1:223537095-223537096	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs576314026	chr1:223537106-223537107	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs189901488	chr1:223537147-223537148	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs565278063	chr1:223537239-223537240	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs577415171	chr1:223537256-223537257	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs545253227	chr1:223537260-223537261	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs374448635	chr1:223537286-223537287	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs555047214	chr1:223537337-223537338	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs368087997	chr1:223537362-223537363	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs527599910	chr1:223537379-223537380	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs1618537	chr1:223537385-223537386	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs560947393	chr1:223537435-223537436	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs373961200	chr1:223537442-223537443	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs531246907	chr1:223537447-223537448	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs549746416	chr1:223537482-223537483	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	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
Liposarcoma	21253554	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
Breast cancer	17603634	CNVD
Neuroblastoma	21899760	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
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	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
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Acute myeloid leukemia	17268525	CNVD
Lung cancer	16740712	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17053054	CNVD
Developmental delay	21147756	CNVD
Autism	14699429	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	20808228	CNVD
Fumarase deficiency	21572526	CNVD
Autism	17483303	CNVD
Kartagener syndrome	16639409	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Leukoplakia	24403051	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Glioblastoma multiforme	21138945	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:485 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:223528000-223536400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr1:223531200-223536400	Weak transcription	Psoas Muscle	Psoas
3	chr1:223533800-223536400	Weak transcription	Esophagus	oesophagus
4	chr1:223534600-223536400	Enhancers	Primary T helper cells fromperipheralblood	blood
5	chr1:223534800-223536400	Enhancers	Primary T helper cells PMA-I stimulated	--
6	chr1:223535000-223536400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
7	chr1:223535200-223536400	Weak transcription	Brain Substantia Nigra	brain
8	chr1:223535600-223536200	Flanking Bivalent TSS/Enh	Primary T cells from cord blood	blood
9	chr1:223535600-223536600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
10	chr1:223535800-223536200	Bivalent Enhancer	H9 Cell Line	embryonic stem cell
11	chr1:223535800-223536400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr1:223535800-223536400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
13	chr1:223535800-223536400	Active TSS	Brain Angular Gyrus	brain
14	chr1:223535800-223536400	Enhancers	Brain Cingulate Gyrus	brain
15	chr1:223535800-223536400	Enhancers	Fetal Heart	heart
16	chr1:223535800-223536400	Bivalent Enhancer	Fetal Thymus	thymus
17	chr1:223535800-223536400	Enhancers	Pancreas	Pancrea
18	chr1:223535800-223536600	Enhancers	Primary T killer memory cells from peripheral blood	blood
19	chr1:223535800-223538200	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
20	chr1:223535800-223538800	Active TSS	Brain Inferior Temporal Lobe	brain
21	chr1:223535800-223538800	Active TSS	Pancreatic Islets	Pancreatic Islet
22	chr1:223535800-223538800	Active TSS	Ovary	ovary
23	chr1:223535800-223539000	Active TSS	Brain Anterior Caudate	brain
24	chr1:223536000-223536200	Flanking Bivalent TSS/Enh	ES-I3 Cell Line	embryonic stem cell
25	chr1:223536000-223536200	Flanking Bivalent TSS/Enh	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr1:223536000-223536200	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
27	chr1:223536000-223536200	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
28	chr1:223536000-223536200	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
29	chr1:223536000-223536200	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
30	chr1:223536000-223536200	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
31	chr1:223536000-223536200	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
32	chr1:223536000-223536400	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr1:223536000-223536400	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr1:223536000-223536400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr1:223536000-223536400	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
36	chr1:223536000-223536400	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr1:223536000-223536400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
38	chr1:223536000-223536400	Bivalent Enhancer	Fetal Brain Female	brain
39	chr1:223536000-223536400	Bivalent/Poised TSS	Fetal Muscle Trunk	muscle
40	chr1:223536000-223536400	Enhancers	Left Ventricle	heart
41	chr1:223536000-223536400	Bivalent Enhancer	NH-A	brain
42	chr1:223536000-223536600	Enhancers	Primary T helper naive cells from peripheral blood	blood
43	chr1:223536000-223536600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
44	chr1:223536000-223536600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr1:223536000-223536600	Bivalent Enhancer	Fetal Lung	lung
46	chr1:223536000-223536800	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
47	chr1:223536000-223538200	Bivalent/Poised TSS	Brain Germinal Matrix	brain
48	chr1:223536000-223538400	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
49	chr1:223536000-223538600	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
50	chr1:223536000-223538600	Active TSS	Brain Hippocampus Middle	brain

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