Variant report

Variant	nsv871290
Chromosome Location	chr1:10684098-10777260
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1752)
CpG islands
(count:8002)
Chromatin interactive
region (count:152)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1752 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:10739738-10739938	K562	blood:	n/a	n/a
2	ARID3A	chr1:10746020-10747010	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:10739699-10740090	HepG2	liver:	n/a	n/a
4	ATF1	chr1:10706410-10706754	K562	blood:	n/a	n/a
5	ATF2	chr1:10739666-10740097	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr1:10739634-10740012	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF3	chr1:10706374-10706728	K562	blood:	n/a	n/a
8	ATF3	chr1:10711894-10712078	K562	blood:	n/a	n/a
9	ATF3	chr1:10706380-10706785	K562	blood:	n/a	n/a
10	BACH1	chr1:10710049-10710152	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr1:10692955-10692981	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr1:10754909-10755258	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr1:10753920-10754204	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr1:10709033-10709307	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr1:10699434-10699676	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr1:10764501-10765022	H1-hESC	embryonic stem cell:	n/a	n/a
17	BATF	chr1:10751717-10752059	GM12878	blood:	n/a	chr1:10751881-10751889
18	BATF	chr1:10753514-10753789	GM12878	blood:	n/a	n/a
19	BATF	chr1:10751781-10752012	GM12878	blood:	n/a	chr1:10751881-10751889
20	BCL3	chr1:10722400-10722952	GM12878	blood:	n/a	n/a
21	BCL3	chr1:10711172-10711384	GM12878	blood:	n/a	n/a
22	BCL3	chr1:10722391-10722933	GM12878	blood:	n/a	n/a
23	BCL3	chr1:10711104-10711370	GM12878	blood:	n/a	n/a
24	BHLHE40	chr1:10750610-10750752	K562	blood:	n/a	n/a
25	BHLHE40	chr1:10701393-10701600	HepG2	liver:	n/a	n/a
26	BHLHE40	chr1:10764023-10764249	K562	blood:	n/a	n/a
27	BHLHE40	chr1:10764322-10764864	HepG2	liver:	n/a	n/a
28	BHLHE40	chr1:10722323-10722716	K562	blood:	n/a	n/a
29	BHLHE40	chr1:10706431-10706689	K562	blood:	n/a	n/a
30	BHLHE40	chr1:10745752-10746071	K562	blood:	n/a	chr1:10745933-10745942 chr1:10745934-10745943 chr1:10746013-10746029 chr1:10745934-10745943 chr1:10745935-10745944
31	BHLHE40	chr1:10704722-10704778	K562	blood:	n/a	n/a
32	BHLHE40	chr1:10745723-10746597	HepG2	liver:	n/a	chr1:10745933-10745942 chr1:10745934-10745943 chr1:10746013-10746029 chr1:10745934-10745943 chr1:10745935-10745944
33	BHLHE40	chr1:10752599-10752766	K562	blood:	n/a	n/a
34	BHLHE40	chr1:10739818-10739897	K562	blood:	n/a	n/a
35	BRCA1	chr1:10752620-10752670	HepG2	liver:	n/a	n/a
36	BRCA1	chr1:10753973-10754071	HepG2	liver:	n/a	chr1:10754024-10754033
37	BRCA1	chr1:10753893-10754093	Hela-S3	cervix:	n/a	chr1:10754024-10754033
38	BRCA1	chr1:10764695-10764882	H1-hESC	embryonic stem cell:	n/a	n/a
39	BRCA1	chr1:10737875-10737890	HepG2	liver:	n/a	n/a
40	CBX3	chr1:10750531-10750928	K562	blood:	n/a	n/a
41	CBX3	chr1:10706366-10706742	K562	blood:	n/a	n/a
42	CBX3	chr1:10739625-10740024	K562	blood:	n/a	n/a
43	CBX3	chr1:10750592-10750877	K562	blood:	n/a	n/a
44	CCNT2	chr1:10753915-10755167	K562	blood:	n/a	n/a
45	CCNT2	chr1:10689929-10690119	K562	blood:	n/a	n/a
46	CEBPB	chr1:10739707-10739926	K562	blood:	n/a	n/a
47	CEBPB	chr1:10695625-10695985	IMR90	lung:	n/a	n/a
48	CEBPB	chr1:10764723-10764853	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr1:10746636-10747091	HepG2	liver:	n/a	chr1:10746910-10746923
50	CEBPB	chr1:10739750-10739932	K562	blood:	n/a	n/a

(count:8002 , 50 per page) page: 1 2 3 4 5 6 7 ... 161

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:10725332-10725382	ProgFib	skin:	n/a
2	chr1:10711457-10711507	MCF-7	breast:	n/a
3	chr1:10718221-10718271	LNCaP	prostate:	n/a
4	chr1:10732872-10732922	NH-A	brain:	n/a
5	chr1:10764512-10764562	HepG2	liver:	n/a
6	chr1:10769910-10769960	ECC-1	luminal epithelium:	n/a
7	chr1:10747107-10747157	PFSK-1	brain:	n/a
8	chr1:10733858-10733908	HRCEpiC	kidney:	n/a
9	chr1:10757436-10757486	HRPEpiC	eye:	n/a
10	chr1:10732519-10732569	PrEC	prostate:	n/a
11	chr1:10732558-10732608	HAEpiC	amniotic membrane:	n/a
12	chr1:10725332-10725382	ProgFib	skin:	n/a
13	chr1:10711457-10711507	MCF-7	breast:	n/a
14	chr1:10718221-10718271	LNCaP	prostate:	n/a
15	chr1:10732872-10732922	NH-A	brain:	n/a
16	chr1:10764512-10764562	HepG2	liver:	n/a
17	chr1:10769910-10769960	ECC-1	luminal epithelium:	n/a
18	chr1:10747107-10747157	PFSK-1	brain:	n/a
19	chr1:10733858-10733908	HRCEpiC	kidney:	n/a
20	chr1:10757436-10757486	HRPEpiC	eye:	n/a
21	chr1:10732519-10732569	PrEC	prostate:	n/a
22	chr1:10732558-10732608	HAEpiC	amniotic membrane:	n/a
23	chr1:10708003-10708053	HRCEpiC	kidney:	n/a
24	chr1:10726728-10726778	HUVEC	blood vessel:	n/a
25	chr1:10732356-10732406	HCF	heart:	n/a
26	chr1:10725218-10725268	MCF-7	breast:	n/a
27	chr1:10697703-10697753	HAEpiC	amniotic membrane:	n/a
28	chr1:10720368-10720418	Jurkat	blood:	n/a
29	chr1:10719619-10719669	HRE	kidney:	n/a
30	chr1:10712421-10712471	NH-A	brain:	n/a
31	chr1:10725218-10725268	AG04449	skin:	fetal
32	chr1:10684392-10684442	SK-N-SH	brain:	n/a
33	chr1:10738569-10738619	HIPEpiC	eye:	n/a
34	chr1:10757892-10757942	ECC-1	luminal epithelium:	n/a
35	chr1:10719929-10719979	HUVEC	blood vessel:	n/a
36	chr1:10732558-10732608	HIPEpiC	eye:	n/a
37	chr1:10715885-10715935	HEK293	kidney:	embryo
38	chr1:10761983-10762033	GM12891	blood:	n/a
39	chr1:10761983-10762033	HUVEC	blood vessel:	n/a
40	chr1:10733858-10733908	HL-60	blood:	n/a
41	chr1:10715690-10715740	AG10803	skin:	n/a
42	chr1:10750680-10750730	BE2_C	brain:	n/a
43	chr1:10690588-10690638	AoSMC	blood vessel:	n/a
44	chr1:10704886-10704936	AG04449	skin:	fetal
45	chr1:10732872-10732922	CMK	blood:	n/a
46	chr1:10706484-10706534	HCM	heart:	n/a
47	chr1:10764273-10764323	HCPEpiC	choroid plexus:	n/a
48	chr1:10733477-10733527	SKMC	muscle:	n/a
49	chr1:10719619-10719669	HEK293	kidney:	embryo
50	chr1:10725218-10725268	PrEC	prostate:	n/a

(count:152 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr1:10689613..10692712-chr1:10692856..10694997,3	K562	blood:
2	chr1:10752290..10752910-chr1:10811240..10811848,2	MCF-7	breast:
3	chr1:10715834..10717814-chr1:10789112..10791954,2	K562	blood:
4	chr1:10750672..10753941-chr1:10753970..10757109,4	K562	blood:
5	chr1:10703574..10707168-chr1:10709558..10711927,3	MCF-7	breast:
6	chr1:10770692..10771316-chr1:10810904..10811625,4	MCF-7	breast:
7	chr1:10754753..10757262-chr1:10761899..10764106,2	MCF-7	breast:
8	chr1:10762987..10765112-chr1:10783613..10786344,2	MCF-7	breast:
9	chr1:10772697..10775308-chr1:10780608..10782302,2	MCF-7	breast:
10	chr1:10682455..10684022-chr1:10686446..10688809,2	K562	blood:
11	chr1:10753473..10759637-chr1:10760137..10763540,7	K562	blood:
12	chr1:10689613..10692712-chr1:10692856..10694997,3	K562	blood:
13	chr1:10679310..10682289-chr1:10684036..10687827,3	K562	blood:
14	chr1:10725635..10727609-chr1:10737981..10739512,2	K562	blood:
15	chr1:10677648..10679513-chr1:10690006..10691964,2	K562	blood:
16	chr1:10736438..10738952-chr1:10740834..10743683,3	K562	blood:
17	chr1:10735100..10736602-chr1:10738947..10741483,2	MCF-7	breast:
18	chr1:10741683..10743188-chr1:10744761..10747734,2	MCF-7	breast:
19	chr1:10738414..10740371-chr1:10749837..10752208,2	MCF-7	breast:
20	chr1:10765025..10766775-chr1:10767958..10770170,2	MCF-7	breast:
21	chr1:10731829..10734631-chr1:10737455..10739630,2	K562	blood:
22	chr1:10752106..10752658-chr1:10848551..10849222,2	MCF-7	breast:
23	chr1:10689513..10692457-chr1:10716597..10719078,2	K562	blood:
24	chr1:10576524..10577112-chr1:10770683..10771299,3	MCF-7	breast:
25	chr1:10712754..10714859-chr1:10715847..10719174,3	MCF-7	breast:
26	chr1:10770352..10771145-chr1:10784796..10785695,2	MCF-7	breast:
27	chr1:10738788..10740418-chr1:10744263..10746556,2	MCF-7	breast:
28	chr1:10717765..10719511-chr1:10863932..10866703,2	K562	blood:
29	chr1:10657337..10659085-chr1:10685902..10688707,2	MCF-7	breast:
30	chr1:10685500..10687497-chr1:10695365..10698289,2	K562	blood:
31	chr1:10708228..10710600-chr1:10848696..10851530,2	K562	blood:
32	chr1:10732310..10734082-chr1:10748973..10751556,2	K562	blood:
33	chr1:10735100..10736602-chr1:10738947..10741483,2	MCF-7	breast:
34	chr1:10651098..10652692-chr1:10684306..10686452,2	MCF-7	breast:
35	chr1:10744408..10746422-chr1:10754548..10756295,2	MCF-7	breast:
36	chr1:10685500..10687497-chr1:10695365..10698289,2	K562	blood:
37	chr1:10758262..10760519-chr1:10763379..10765606,2	MCF-7	breast:
38	chr1:10777259..10780263-chr1:10782530..10785488,3	K562	blood:
39	chr1:10672111..10674098-chr1:10684480..10687476,2	K562	blood:
40	chr1:10744408..10746422-chr1:10754548..10756295,2	MCF-7	breast:
41	chr1:10723769..10726210-chr1:10728292..10729827,2	MCF-7	breast:
42	chr1:10742297..10745036-chr1:10749705..10751341,3	MCF-7	breast:
43	chr1:10709257..10711552-chr1:10722180..10724225,2	K562	blood:
44	chr1:10752434..10753364-chr1:11001891..11002517,2	MCF-7	breast:
45	chr1:10767210..10770062-chr1:10773957..10776729,2	K562	blood:
46	chr1:10573337..10575488-chr1:10723481..10725688,2	K562	blood:
47	chr1:10759222..10762054-chr13:20579251..20582130,2	MCF-7	breast:
48	chr1:10708501..10711105-chr1:10716325..10718436,2	K562	blood:
49	chr1:10708501..10711105-chr1:10716325..10718436,2	K562	blood:
50	chr1:10712004..10714801-chr1:10852157..10855382,3	MCF-7	breast:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DFFA-4	chr1:10698772-10698820	NONHSAT000866
2	lnc-DFFA-8	chr1:10758720-10758975	uc_7_-
3	lnc-DFFA-4	chr1:10697178-10697465	NONHSAT000866
4	lnc-DFFA-6	chr1:10710998-10711157	NONHSAT000867
5	lnc-DFFA-7	chr1:10717708-10718008	uc_6_-
6	lnc-DFFA-5	chr1:10703938-10704151	uc_5_-
7	lnc-DFFA-9	chr1:10764253-10764619	NONHSAT000868
8	lnc-DFFA-9	chr1:10765549-10765632	NONHSAT000868
9	lnc-PEX14-6	chr1:10717708-10718008	uc_6_+
10	lnc-PEX14-4	chr1:10703938-10704151	uc_5_+
11	lnc-PEX14-8	chr1:10774405-10774620	uc_8_+
12	lnc-PEX14-7	chr1:10758720-10758975	uc_7_+
13	lnc-C1orf127-2	chr1:10774405-10774620	uc_8_-
14	lnc-DFFA-6	chr1:10710541-10710812	NONHSAT000867

No data

Variant related genes	Relation type
ENSG00000272078	TF binding region
CASZ1	TF binding region
ENSG00000272078	CpG island
CASZ1	CpG island
ENSG00000271989	chromatin interactions
ENSG00000108298	chromatin interactions
ENSG00000084652	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000130940	chromatin interactions
ENSG00000121741	chromatin interactions
ENSG00000175279	chromatin interactions
ENSG00000272078	chromatin interactions
ENSG00000251503	chromatin interactions

Extended variants
information (count: 4152 )
Associated
traits (count: 115 )

Variant overlapped rSNPs/rCNVs (count:4152 , 50 per page) page: 1 2 3 4 5 6 7 ... 84

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2242288	chr1:10684098-10684099	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs149722273	chr1:10684099-10684100	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs532566242	chr1:10684112-10684113	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs550976289	chr1:10684141-10684142	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs145230374	chr1:10684159-10684160	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs149170235	chr1:10684171-10684172	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs531768916	chr1:10684179-10684180	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs142364635	chr1:10684183-10684184	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs190115464	chr1:10684191-10684192	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs182497449	chr1:10684223-10684224	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs547621214	chr1:10684229-10684230	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs185207930	chr1:10684267-10684268	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs536174096	chr1:10684273-10684274	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs548489154	chr1:10684294-10684295	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs569534099	chr1:10684303-10684304	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs536689769	chr1:10684311-10684312	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs558226128	chr1:10684321-10684322	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs576532515	chr1:10684335-10684336	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs538814390	chr1:10684339-10684340	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs564462875	chr1:10684340-10684341	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs369045156	chr1:10684375-10684376	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs553967795	chr1:10684376-10684377	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs200684088	chr1:10684383-10684384	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs376837541	chr1:10684393-10684394	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs190952292	chr1:10684412-10684413	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs146781531	chr1:10684413-10684414	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs374000675	chr1:10684416-10684417	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs368473343	chr1:10684417-10684418	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs35046754	chr1:10684422-10684423	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs543843635	chr1:10684425-10684426	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs200019568	chr1:10684426-10684427	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs61752116	chr1:10684462-10684463	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs543130270	chr1:10684465-10684466	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs147210317	chr1:10684476-10684477	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs144362955	chr1:10684477-10684478	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs147706488	chr1:10684484-10684485	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs377059083	chr1:10684485-10684486	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs369625174	chr1:10684486-10684487	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs566024461	chr1:10684512-10684513	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs375718381	chr1:10684531-10684532	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs569277622	chr1:10684557-10684558	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs559258851	chr1:10684570-10684571	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs529932677	chr1:10684648-10684649	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs536745609	chr1:10684691-10684692	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs375541497	chr1:10684752-10684753	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs548176874	chr1:10684778-10684779	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs145893811	chr1:10684815-10684816	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs530377803	chr1:10684863-10684864	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs114621436	chr1:10684912-10684913	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs570184151	chr1:10684923-10684924	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:115)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Follicular lymphoma	18703704	CNVD
Lung cancer	22429812	CNVD
Epilepsy	22118685	CNVD
Schizophrenia	22118685	CNVD
Ovarian cancer	21720365	CNVD
Developmental delay	19490664	CNVD
Ewing''s sarcoma	21437220	CNVD
Prader-willi syndrome	18797701	CNVD
periventricular nodular heterotopia	20648244	CNVD
1p36 deletion syndrome	22283845	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
Neuroblastoma	18923524	CNVD
Retinoblastoma	22278416	CNVD
Mental retardation	20152051	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Astrocytoma	17934521	CNVD
Glioblastoma	20031968	CNVD
Acute myeloid leukemia	18000384	CNVD
Glioblastoma multiforme	16951158	CNVD
Neuroblastoma	18574593	CNVD
Glioblastoma multiforme	17369134	CNVD
Autism	18414403	CNVD
Breast cancer	17001317	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Myoepithelioma	18604193	CNVD
Wilms tumour	19047088	CNVD
Breast cancer	16608533	CNVD
T-cell lymphomas	19863542	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Metanephric adenoma	20802469	CNVD
Soft tissue tumor	16732325	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Adenoid cystic carcinoma	18698036	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
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
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	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
small cell lung cancer	20016488	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic myeloid leukemia	21384125	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Neuroblastoma	18923191	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21138945	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Ovarian neoplasms	16753589	CNVD
Neuroblastoma	19287153	CNVD
Hepatocellular carcinoma	18929564	CNVD
Melanoma	17363583	CNVD
renal disease	17924346	CNVD
Uveal melanoma	20484589	CNVD
Multiple myeloma	16616336	CNVD
Glioblastoma multiforme	22286061	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	20808228	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:3640 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:10632600-10698000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
2	chr1:10651600-10715800	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr1:10653600-10688600	Weak transcription	Colon Smooth Muscle	Colon
4	chr1:10654800-10691600	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr1:10656800-10687200	Weak transcription	Small Intestine	intestine
6	chr1:10657800-10684200	Weak transcription	Colonic Mucosa	Colon
7	chr1:10658200-10694400	Weak transcription	Primary neutrophils fromperipheralblood	blood
8	chr1:10658400-10688600	Weak transcription	Fetal Lung	lung
9	chr1:10658400-10691600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr1:10659200-10687800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
11	chr1:10659400-10684400	Weak transcription	Dnd41	blood
12	chr1:10659800-10690800	Weak transcription	Primary hematopoietic stem cells	blood
13	chr1:10660000-10684200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr1:10660200-10684400	Weak transcription	NHLF	lung
15	chr1:10660200-10697600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
16	chr1:10661800-10692000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr1:10662200-10694400	Weak transcription	HSMM	muscle
18	chr1:10662400-10694400	Weak transcription	Muscle Satellite Cultured Cells	--
19	chr1:10664400-10698000	Weak transcription	Primary B cells from cord blood	blood
20	chr1:10669800-10686600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr1:10672600-10694800	Strong transcription	Fetal Intestine Small	intestine
22	chr1:10673000-10688400	Weak transcription	Fetal Heart	heart
23	chr1:10673200-10688800	Weak transcription	Psoas Muscle	Psoas
24	chr1:10673600-10688600	Weak transcription	Right Atrium	heart
25	chr1:10675600-10684600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr1:10675600-10690200	Weak transcription	GM12878-XiMat	blood
27	chr1:10676000-10691600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
28	chr1:10676200-10684200	Weak transcription	HUES48 Cell Line	embryonic stem cell
29	chr1:10676200-10684400	Weak transcription	HUES6 Cell Line	embryonic stem cell
30	chr1:10676200-10684400	Weak transcription	Brain Angular Gyrus	brain
31	chr1:10676200-10691600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
32	chr1:10676400-10690600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr1:10676400-10691800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
34	chr1:10676400-10691800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
35	chr1:10676600-10691800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr1:10676800-10691000	Weak transcription	H1 Cell Line	embryonic stem cell
37	chr1:10677000-10690000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr1:10678600-10686000	Strong transcription	Fetal Stomach	stomach
39	chr1:10679800-10684400	Weak transcription	HMEC	breast
40	chr1:10680000-10684200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr1:10680400-10685200	Strong transcription	Fetal Muscle Leg	muscle
42	chr1:10680400-10693800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
43	chr1:10680400-10694400	Weak transcription	HSMMtube	muscle
44	chr1:10680800-10685200	Strong transcription	Primary T helper cells fromperipheralblood	blood
45	chr1:10681000-10685600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
46	chr1:10681200-10697600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
47	chr1:10681600-10685600	Strong transcription	Adipose Nuclei	Adipose
48	chr1:10681600-10686600	Strong transcription	Duodenum Mucosa	Duodenum
49	chr1:10681600-10687200	Strong transcription	Spleen	Spleen
50	chr1:10681600-10691600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood

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