Variant report

Variant	nsv1004063
Chromosome Location	chr1:10675978-10780682
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1783)
CpG islands
(count:8425)
Chromatin interactive
region (count:166)
LncRNA
region (count:17)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1783 , 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	chr1:10739699-10740090	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:10746020-10747010	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:10777365-10777652	K562	blood:	n/a	n/a
4	ARID3A	chr1:10739738-10739938	K562	blood:	n/a	n/a
5	ATF1	chr1:10706410-10706754	K562	blood:	n/a	n/a
6	ATF1	chr1:10777412-10777648	K562	blood:	n/a	n/a
7	ATF2	chr1:10739666-10740097	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr1:10739634-10740012	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF3	chr1:10706380-10706785	K562	blood:	n/a	n/a
10	ATF3	chr1:10706374-10706728	K562	blood:	n/a	n/a
11	ATF3	chr1:10711894-10712078	K562	blood:	n/a	n/a
12	BACH1	chr1:10692955-10692981	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr1:10764501-10765022	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr1:10753920-10754204	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr1:10754909-10755258	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr1:10710049-10710152	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr1:10699434-10699676	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr1:10709033-10709307	H1-hESC	embryonic stem cell:	n/a	n/a
19	BATF	chr1:10751717-10752059	GM12878	blood:	n/a	chr1:10751881-10751889
20	BATF	chr1:10751781-10752012	GM12878	blood:	n/a	chr1:10751881-10751889
21	BATF	chr1:10753514-10753789	GM12878	blood:	n/a	n/a
22	BCL3	chr1:10722400-10722952	GM12878	blood:	n/a	n/a
23	BCL3	chr1:10722391-10722933	GM12878	blood:	n/a	n/a
24	BCL3	chr1:10711172-10711384	GM12878	blood:	n/a	n/a
25	BCL3	chr1:10711104-10711370	GM12878	blood:	n/a	n/a
26	BHLHE40	chr1:10752599-10752766	K562	blood:	n/a	n/a
27	BHLHE40	chr1:10701393-10701600	HepG2	liver:	n/a	n/a
28	BHLHE40	chr1:10722323-10722716	K562	blood:	n/a	n/a
29	BHLHE40	chr1:10764023-10764249	K562	blood:	n/a	n/a
30	BHLHE40	chr1:10750610-10750752	K562	blood:	n/a	n/a
31	BHLHE40	chr1:10739818-10739897	K562	blood:	n/a	n/a
32	BHLHE40	chr1:10764322-10764864	HepG2	liver:	n/a	n/a
33	BHLHE40	chr1:10745752-10746071	K562	blood:	n/a	chr1:10745933-10745942 chr1:10745934-10745943 chr1:10746013-10746029 chr1:10745934-10745943 chr1:10745935-10745944
34	BHLHE40	chr1:10745723-10746597	HepG2	liver:	n/a	chr1:10745933-10745942 chr1:10745934-10745943 chr1:10746013-10746029 chr1:10745934-10745943 chr1:10745935-10745944
35	BHLHE40	chr1:10706431-10706689	K562	blood:	n/a	n/a
36	BHLHE40	chr1:10704722-10704778	K562	blood:	n/a	n/a
37	BRCA1	chr1:10752620-10752670	HepG2	liver:	n/a	n/a
38	BRCA1	chr1:10753973-10754071	HepG2	liver:	n/a	chr1:10754024-10754033
39	BRCA1	chr1:10737875-10737890	HepG2	liver:	n/a	n/a
40	BRCA1	chr1:10764695-10764882	H1-hESC	embryonic stem cell:	n/a	n/a
41	BRCA1	chr1:10753893-10754093	Hela-S3	cervix:	n/a	chr1:10754024-10754033
42	CBX3	chr1:10750531-10750928	K562	blood:	n/a	n/a
43	CBX3	chr1:10739625-10740024	K562	blood:	n/a	n/a
44	CBX3	chr1:10750592-10750877	K562	blood:	n/a	n/a
45	CBX3	chr1:10706366-10706742	K562	blood:	n/a	n/a
46	CCNT2	chr1:10777414-10777638	K562	blood:	n/a	n/a
47	CCNT2	chr1:10689929-10690119	K562	blood:	n/a	n/a
48	CCNT2	chr1:10753915-10755167	K562	blood:	n/a	n/a
49	CEBPB	chr1:10695688-10695932	HepG2	liver:	n/a	n/a
50	CEBPB	chr1:10754305-10754339	Hela-S3	cervix:	n/a	n/a

(count:8425 , 50 per page) page: 1 2 3 4 5 6 7 ... 169

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:10684339-10684389	HNPCEpiC	eye:	n/a
2	chr1:10694312-10694362	CMK	blood:	n/a
3	chr1:10698313-10698363	BJ	skin:	n/a
4	chr1:10752632-10752682	GM12878	blood:	n/a
5	chr1:10705842-10705892	SAEC	small airway:	n/a
6	chr1:10752632-10752682	SK-N-MC	brain:	n/a
7	chr1:10732063-10732113	NB4	blood:	n/a
8	chr1:10684339-10684389	HNPCEpiC	eye:	n/a
9	chr1:10694312-10694362	CMK	blood:	n/a
10	chr1:10698313-10698363	BJ	skin:	n/a
11	chr1:10752632-10752682	GM12878	blood:	n/a
12	chr1:10705842-10705892	SAEC	small airway:	n/a
13	chr1:10752632-10752682	SK-N-MC	brain:	n/a
14	chr1:10732063-10732113	NB4	blood:	n/a
15	chr1:10700647-10700697	HNPCEpiC	eye:	n/a
16	chr1:10715885-10715935	SAEC	small airway:	n/a
17	chr1:10690564-10690614	GM06990	blood:	n/a
18	chr1:10757892-10757942	NHBE	bronchial:	n/a
19	chr1:10698719-10698769	SK-N-SH	brain:	n/a
20	chr1:10764273-10764323	HCPEpiC	choroid plexus:	n/a
21	chr1:10726728-10726778	PANC-1	pancreas:	n/a
22	chr1:10696066-10696116	GM12891	blood:	n/a
23	chr1:10711044-10711094	MCF10A-Er-Src	breast:	n/a
24	chr1:10764273-10764323	NT2-D1	testis:	n/a
25	chr1:10732872-10732922	GM12878	blood:	n/a
26	chr1:10699604-10699654	Hepatocyte	liver:	n/a
27	chr1:10755322-10755372	K562	blood:	n/a
28	chr1:10743216-10743266	K562	blood:	n/a
29	chr1:10766044-10766094	IMR90	lung:	fetal
30	chr1:10694312-10694362	SK-N-MC	brain:	n/a
31	chr1:10739980-10740030	AG09319	gingival:	n/a
32	chr1:10764896-10764946	T-47D	breast:	n/a
33	chr1:10757892-10757942	Jurkat	blood:	n/a
34	chr1:10683577-10683627	GM19239	blood:	n/a
35	chr1:10732912-10732962	LNCaP	prostate:	n/a
36	chr1:10690564-10690614	PANC-1	pancreas:	n/a
37	chr1:10715885-10715935	Hepatocyte	liver:	n/a
38	chr1:10699831-10699881	HL-60	blood:	n/a
39	chr1:10676576-10676626	GM06990	blood:	n/a
40	chr1:10700647-10700697	Hepatocyte	liver:	n/a
41	chr1:10705842-10705892	SK-N-SH_RA	brain:	n/a
42	chr1:10758995-10759045	HEEpiC	esophagus:	n/a
43	chr1:10719929-10719979	NT2-D1	testis:	n/a
44	chr1:10699604-10699654	NT2-D1	testis:	n/a
45	chr1:10684392-10684442	GM12891	blood:	n/a
46	chr1:10732333-10732383	Jurkat	blood:	n/a
47	chr1:10720368-10720418	ECC-1	luminal epithelium:	n/a
48	chr1:10717077-10717127	T-47D	breast:	n/a
49	chr1:10707934-10707984	HAEpiC	amniotic membrane:	n/a
50	chr1:10732912-10732962	GM19239	blood:	n/a

(count:166 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr1:10728805..10730887-chr1:10732213..10735865,3	MCF-7	breast:
2	chr1:10769186..10770686-chr1:10780232..10782829,2	K562	blood:
3	chr1:10672897..10674878-chr1:10677717..10679649,2	K562	blood:
4	chr1:10754244..10754954-chr1:32645198..32646026,2	NB4	blood:
5	chr1:10749491..10752032-chr1:10752294..10754052,2	K562	blood:
6	chr1:10752107..10753101-chr1:10848408..10849120,2	MCF-7	breast:
7	chr1:10750672..10753941-chr1:10753970..10757109,4	K562	blood:
8	chr1:10746278..10748730-chr1:10764916..10766801,2	K562	blood:
9	chr1:10765025..10766775-chr1:10767958..10770170,2	MCF-7	breast:
10	chr1:10755955..10758112-chr1:10760865..10764378,3	K562	blood:
11	chr1:10694140..10696229-chr1:10885047..10887221,2	MCF-7	breast:
12	chr1:10703132..10705545-chr1:10711056..10713011,2	K562	blood:
13	chr1:10722706..10724721-chr1:10733970..10736738,2	MCF-7	breast:
14	chr1:10689513..10692457-chr1:10716597..10719078,2	K562	blood:
15	chr1:10735100..10736602-chr1:10738947..10741483,2	MCF-7	breast:
16	chr1:10738789..10740392-chr1:10741913..10744233,2	MCF-7	breast:
17	chr1:10732310..10734082-chr1:10748973..10751556,2	K562	blood:
18	chr1:10757865..10759730-chr1:10835841..10837432,3	MCF-7	breast:
19	chr1:10777259..10780263-chr1:10782530..10785488,3	K562	blood:
20	chr1:10739997..10741906-chr1:10786836..10789661,2	MCF-7	breast:
21	chr1:10725435..10726303-chr1:10810964..10811494,2	MCF-7	breast:
22	chr1:10708501..10711105-chr1:10716325..10718436,2	K562	blood:
23	chr1:10746225..10747873-chr1:10749821..10751374,2	K562	blood:
24	chr1:10567723..10570074-chr1:10684964..10687923,2	K562	blood:
25	chr1:10750259..10753196-chr1:10853460..10855878,3	MCF-7	breast:
26	chr1:10682455..10684022-chr1:10686446..10688809,2	K562	blood:
27	chr1:10672111..10674098-chr1:10684480..10687476,2	K562	blood:
28	chr1:10673034..10676148-chr1:10680222..10683024,3	K562	blood:
29	chr1:10766203..10768945-chr1:10775376..10776882,2	MCF-7	breast:
30	chr1:10679310..10682289-chr1:10684036..10687827,3	K562	blood:
31	chr1:10738788..10740418-chr1:10744263..10746556,2	MCF-7	breast:
32	chr1:10712754..10714859-chr1:10715847..10719174,3	MCF-7	breast:
33	chr1:10689613..10692712-chr1:10692856..10694997,3	K562	blood:
34	chr1:10717765..10719511-chr1:10863932..10866703,2	K562	blood:
35	chr1:10762987..10765112-chr1:10783613..10786344,2	MCF-7	breast:
36	chr1:10573337..10575488-chr1:10723481..10725688,2	K562	blood:
37	chr1:10677648..10679513-chr1:10690006..10691964,2	K562	blood:
38	chr1:10754807..10756455-chr1:10925799..10928452,2	MCF-7	breast:
39	chr1:10672064..10673833-chr1:10681009..10682512,2	MCF-7	breast:
40	chr1:10738789..10740392-chr1:10741913..10744233,2	MCF-7	breast:
41	chr1:10574200..10574765-chr1:10689892..10690713,2	MCF-7	breast:
42	chr1:10715958..10718705-chr1:10751486..10753340,2	K562	blood:
43	chr1:10772697..10775308-chr1:10780608..10782302,2	MCF-7	breast:
44	chr1:10678742..10684022-chr1:10686327..10690416,7	K562	blood:
45	chr1:10711257..10713486-chr1:10721428..10724018,2	MCF-7	breast:
46	chr1:10712004..10714801-chr1:10852157..10855382,3	MCF-7	breast:
47	chr1:10708228..10710600-chr1:10848696..10851530,2	K562	blood:
48	chr1:10752376..10753024-chr1:10896001..10896596,2	MCF-7	breast:
49	chr1:10703574..10707168-chr1:10709558..10711927,3	MCF-7	breast:
50	chr1:10730915..10733198-chr1:10740298..10742012,2	K562	blood:

(count:17 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-APITD1-6	chr1:10676893-10677170	NONHSAT000865
2	lnc-DFFA-6	chr1:10710541-10710812	NONHSAT000867
3	lnc-PEX14-4	chr1:10703938-10704151	uc_5_+
4	lnc-CASZ1-1	chr1:10680836-10681194	uc_4_-
5	lnc-C1orf127-2	chr1:10774405-10774620	uc_8_-
6	lnc-DFFA-6	chr1:10710998-10711157	NONHSAT000867
7	lnc-PEX14-8	chr1:10774405-10774620	uc_8_+
8	lnc-DFFA-7	chr1:10717708-10718008	uc_6_-
9	lnc-DFFA-9	chr1:10764253-10764619	NONHSAT000868
10	lnc-DFFA-4	chr1:10697178-10697465	NONHSAT000866
11	lnc-DFFA-5	chr1:10703938-10704151	uc_5_-
12	lnc-DFFA-9	chr1:10765549-10765632	NONHSAT000868
13	lnc-APITD1-7	chr1:10680836-10681194	uc_4_+
14	lnc-DFFA-8	chr1:10758720-10758975	uc_7_-
15	lnc-DFFA-4	chr1:10698772-10698820	NONHSAT000866
16	lnc-PEX14-6	chr1:10717708-10718008	uc_6_+
17	lnc-PEX14-7	chr1:10758720-10758975	uc_7_+

No data

Variant related genes	Relation type
CASZ1	TF binding region
RN7SL614P	TF binding region
ENSG00000272078	TF binding region
CASZ1	CpG island
RN7SL614P	CpG island
ENSG00000272078	CpG island
ENSG00000084652	chromatin interactions
ENSG00000121741	chromatin interactions
ENSG00000271989	chromatin interactions
ENSG00000108298	chromatin interactions
ENSG00000130940	chromatin interactions
ENSG00000243267	chromatin interactions
ENSG00000272078	chromatin interactions
ENSG00000175279	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000251503	chromatin interactions

Extended variants
information (count: 4630 )
Associated
traits (count: 115 )

Variant overlapped rSNPs/rCNVs (count:4630 , 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	rs539402833	chr1:10676014-10676015	Enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
2	rs534991132	chr1:10676031-10676032	Enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs564406182	chr1:10676042-10676043	Enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs558141254	chr1:10676126-10676127	Enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs111862278	chr1:10676136-10676137	Enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs553207437	chr1:10676147-10676148	Enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs540349641	chr1:10676205-10676206	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs555467019	chr1:10676229-10676230	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs71583887	chr1:10676294-10676295	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	CpG island	1 gene(s)	Overlapped CNVs	n/a
10	rs537248982	chr1:10676309-10676310	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	CpG island	1 gene(s)	Overlapped CNVs	n/a
11	rs544433647	chr1:10676318-10676319	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	CpG island	1 gene(s)	Overlapped CNVs	n/a
12	rs530118654	chr1:10676370-10676371	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs578133733	chr1:10676401-10676402	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs144881455	chr1:10676423-10676424	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs149041325	chr1:10676477-10676478	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs544645943	chr1:10676489-10676490	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs373069593	chr1:10676557-10676558	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs550818762	chr1:10676575-10676576	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs142214332	chr1:10676576-10676577	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	CpG island	1 gene(s)	Overlapped CNVs	n/a
20	rs151233698	chr1:10676577-10676578	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	CpG island	1 gene(s)	Overlapped CNVs	n/a
21	rs529462863	chr1:10676583-10676584	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	CpG island	1 gene(s)	Overlapped CNVs	n/a
22	rs183077450	chr1:10676641-10676642	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs141283285	chr1:10676697-10676698	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs146988279	chr1:10676723-10676724	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs540140848	chr1:10676734-10676735	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs551458008	chr1:10676745-10676746	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs566503915	chr1:10676773-10676774	Weak transcription Enhancers Strong transcription Genic enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
28	rs546536008	chr1:10676777-10676778	Weak transcription Enhancers Strong transcription Genic enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
29	rs188485184	chr1:10676778-10676779	Weak transcription Enhancers Strong transcription Genic enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
30	rs567851332	chr1:10676785-10676786	Weak transcription Enhancers Strong transcription Genic enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
31	rs284239	chr1:10676800-10676801	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs78571926	chr1:10676803-10676804	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs141627405	chr1:10676833-10676834	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs577835467	chr1:10676846-10676847	Weak transcription Strong transcription Genic enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
35	rs545270429	chr1:10676893-10676894	Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
36	rs191359551	chr1:10676901-10676902	Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
37	rs572061569	chr1:10676933-10676934	Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
38	rs542692337	chr1:10676962-10676963	Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
39	rs150438408	chr1:10676971-10676972	Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
40	rs183226001	chr1:10676978-10676979	Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
41	rs550860809	chr1:10676986-10676987	Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
42	rs116276966	chr1:10676991-10676992	Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
43	rs533388554	chr1:10677020-10677021	Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
44	rs138142928	chr1:10677051-10677052	Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
45	rs187707002	chr1:10677057-10677058	Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
46	rs191185264	chr1:10677062-10677063	Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
47	rs183522024	chr1:10677208-10677209	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs374441517	chr1:10677210-10677211	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs187816767	chr1:10677328-10677329	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs6693692	chr1:10677349-10677350	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:3949 , 50 per page) page: 1 2 3 4 5 6 7 ... 79

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:10632600-10698000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
2	chr1:10644200-10683400	Weak transcription	K562	blood
3	chr1:10651600-10715800	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr1:10652400-10678400	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chr1:10653600-10688600	Weak transcription	Colon Smooth Muscle	Colon
6	chr1:10654800-10691600	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr1:10655800-10677200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
8	chr1:10656800-10687200	Weak transcription	Small Intestine	intestine
9	chr1:10657600-10683200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
10	chr1:10657800-10683600	Weak transcription	Primary monocytes fromperipheralblood	blood
11	chr1:10657800-10684200	Weak transcription	Colonic Mucosa	Colon
12	chr1:10658200-10694400	Weak transcription	Primary neutrophils fromperipheralblood	blood
13	chr1:10658400-10678200	Weak transcription	Ovary	ovary
14	chr1:10658400-10688600	Weak transcription	Fetal Lung	lung
15	chr1:10658400-10691600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr1:10658600-10678000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr1:10658800-10678400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr1:10659200-10687800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
19	chr1:10659400-10684400	Weak transcription	Dnd41	blood
20	chr1:10659600-10678400	Weak transcription	Placenta	Placenta
21	chr1:10659600-10683800	Weak transcription	Duodenum Smooth Muscle	Duodenum
22	chr1:10659800-10676200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr1:10659800-10690800	Weak transcription	Primary hematopoietic stem cells	blood
24	chr1:10660000-10682000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr1:10660000-10683600	Weak transcription	Rectal Mucosa Donor 31	rectum
26	chr1:10660000-10684200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr1:10660200-10684400	Weak transcription	NHLF	lung
28	chr1:10660200-10697600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
29	chr1:10660400-10679000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr1:10660400-10679000	Weak transcription	HMEC	breast
31	chr1:10660400-10683800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr1:10661800-10678200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr1:10661800-10678400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr1:10661800-10692000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr1:10662000-10676600	Weak transcription	Adipose Nuclei	Adipose
36	chr1:10662000-10678200	Weak transcription	Placenta Amnion	Placenta Amnion
37	chr1:10662000-10678400	Weak transcription	Duodenum Mucosa	Duodenum
38	chr1:10662000-10682600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
39	chr1:10662000-10683000	Weak transcription	Rectal Mucosa Donor 29	rectum
40	chr1:10662200-10694400	Weak transcription	HSMM	muscle
41	chr1:10662400-10678600	Weak transcription	Primary B cells from peripheral blood	blood
42	chr1:10662400-10694400	Weak transcription	Muscle Satellite Cultured Cells	--
43	chr1:10663000-10678800	Weak transcription	NHEK	skin
44	chr1:10663200-10677800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
45	chr1:10663200-10678200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr1:10663200-10678200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr1:10664400-10678200	Weak transcription	Monocytes-CD14+_RO01746	blood
48	chr1:10664400-10698000	Weak transcription	Primary B cells from cord blood	blood
49	chr1:10665800-10683000	Weak transcription	Aorta	Aorta
50	chr1:10666000-10677800	Weak transcription	Primary T helper cells PMA-I stimulated	--

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