Variant report

Variant	nsv828030
Chromosome Location	chr1:10677562-10795161
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2020)
CpG islands
(count:8672)
Chromatin interactive
region (count:190)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2020 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:10746020-10747010	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:10777365-10777652	K562	blood:	n/a	n/a
3	ARID3A	chr1:10739738-10739938	K562	blood:	n/a	n/a
4	ARID3A	chr1:10739699-10740090	HepG2	liver:	n/a	n/a
5	ARID3A	chr1:10791060-10791514	HepG2	liver:	n/a	n/a
6	ATF1	chr1:10777412-10777648	K562	blood:	n/a	n/a
7	ATF1	chr1:10706410-10706754	K562	blood:	n/a	n/a
8	ATF2	chr1:10739666-10740097	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr1:10739634-10740012	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF3	chr1:10706374-10706728	K562	blood:	n/a	n/a
11	ATF3	chr1:10795000-10795326	K562	blood:	n/a	n/a
12	ATF3	chr1:10711894-10712078	K562	blood:	n/a	n/a
13	ATF3	chr1:10706380-10706785	K562	blood:	n/a	n/a
14	BACH1	chr1:10699434-10699676	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr1:10788799-10788909	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr1:10764501-10765022	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr1:10692955-10692981	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr1:10754909-10755258	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr1:10710049-10710152	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr1:10753920-10754204	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr1:10709033-10709307	H1-hESC	embryonic stem cell:	n/a	n/a
22	BATF	chr1:10751717-10752059	GM12878	blood:	n/a	chr1:10751881-10751889
23	BATF	chr1:10753514-10753789	GM12878	blood:	n/a	n/a
24	BATF	chr1:10751781-10752012	GM12878	blood:	n/a	chr1:10751881-10751889
25	BCL3	chr1:10711172-10711384	GM12878	blood:	n/a	n/a
26	BCL3	chr1:10722391-10722933	GM12878	blood:	n/a	n/a
27	BCL3	chr1:10711104-10711370	GM12878	blood:	n/a	n/a
28	BCL3	chr1:10722400-10722952	GM12878	blood:	n/a	n/a
29	BHLHE40	chr1:10739818-10739897	K562	blood:	n/a	n/a
30	BHLHE40	chr1:10750610-10750752	K562	blood:	n/a	n/a
31	BHLHE40	chr1:10793966-10794468	GM12878	blood:	n/a	n/a
32	BHLHE40	chr1:10704722-10704778	K562	blood:	n/a	n/a
33	BHLHE40	chr1:10701393-10701600	HepG2	liver:	n/a	n/a
34	BHLHE40	chr1:10752599-10752766	K562	blood:	n/a	n/a
35	BHLHE40	chr1:10706431-10706689	K562	blood:	n/a	n/a
36	BHLHE40	chr1:10745752-10746071	K562	blood:	n/a	chr1:10745933-10745942 chr1:10745934-10745943 chr1:10746013-10746029 chr1:10745934-10745943 chr1:10745935-10745944
37	BHLHE40	chr1:10722323-10722716	K562	blood:	n/a	n/a
38	BHLHE40	chr1:10745723-10746597	HepG2	liver:	n/a	chr1:10745933-10745942 chr1:10745934-10745943 chr1:10746013-10746029 chr1:10745934-10745943 chr1:10745935-10745944
39	BHLHE40	chr1:10764322-10764864	HepG2	liver:	n/a	n/a
40	BHLHE40	chr1:10764023-10764249	K562	blood:	n/a	n/a
41	BRCA1	chr1:10753973-10754071	HepG2	liver:	n/a	chr1:10754024-10754033
42	BRCA1	chr1:10752620-10752670	HepG2	liver:	n/a	n/a
43	BRCA1	chr1:10737875-10737890	HepG2	liver:	n/a	n/a
44	BRCA1	chr1:10764695-10764882	H1-hESC	embryonic stem cell:	n/a	n/a
45	BRCA1	chr1:10753893-10754093	Hela-S3	cervix:	n/a	chr1:10754024-10754033
46	CBX3	chr1:10750592-10750877	K562	blood:	n/a	n/a
47	CBX3	chr1:10706366-10706742	K562	blood:	n/a	n/a
48	CBX3	chr1:10750531-10750928	K562	blood:	n/a	n/a
49	CBX3	chr1:10739625-10740024	K562	blood:	n/a	n/a
50	CCNT2	chr1:10777414-10777638	K562	blood:	n/a	n/a

(count:8672 , 50 per page) page: 1 2 3 4 5 6 7 ... 174

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:10723174-10723224	NHDF-neo	bronchial:	n/a
2	chr1:10758995-10759045	NT2-D1	testis:	n/a
3	chr1:10757954-10758004	K562	blood:	n/a
4	chr1:10725237-10725287	SK-N-SH	brain:	n/a
5	chr1:10732900-10732950	ProgFib	skin:	n/a
6	chr1:10690011-10690061	BJ	skin:	n/a
7	chr1:10711044-10711094	NHBE	bronchial:	n/a
8	chr1:10753832-10753882	AG04450	lung:	fetal
9	chr1:10731250-10731300	ovcar-3	ovarian:	n/a
10	chr1:10692435-10692485	Jurkat	blood:	n/a
11	chr1:10723174-10723224	NHDF-neo	bronchial:	n/a
12	chr1:10758995-10759045	NT2-D1	testis:	n/a
13	chr1:10757954-10758004	K562	blood:	n/a
14	chr1:10725237-10725287	SK-N-SH	brain:	n/a
15	chr1:10732900-10732950	ProgFib	skin:	n/a
16	chr1:10690011-10690061	BJ	skin:	n/a
17	chr1:10711044-10711094	NHBE	bronchial:	n/a
18	chr1:10753832-10753882	AG04450	lung:	fetal
19	chr1:10731250-10731300	ovcar-3	ovarian:	n/a
20	chr1:10692435-10692485	Jurkat	blood:	n/a
21	chr1:10719929-10719979	HNPCEpiC	eye:	n/a
22	chr1:10733511-10733561	SK-N-SH_RA	brain:	n/a
23	chr1:10690011-10690061	HCM	heart:	n/a
24	chr1:10758237-10758287	IMR90	lung:	fetal
25	chr1:10747107-10747157	HPAEpiC	pulmonary alveolar:	n/a
26	chr1:10788801-10788851	SKMC	muscle:	n/a
27	chr1:10709343-10709393	Hepatocyte	liver:	n/a
28	chr1:10692435-10692485	NT2-D1	testis:	n/a
29	chr1:10726728-10726778	HEK293	kidney:	embryo
30	chr1:10710134-10710184	HEK293	kidney:	embryo
31	chr1:10698313-10698363	U87	brain:	n/a
32	chr1:10730684-10730734	BJ	skin:	n/a
33	chr1:10687618-10687668	HNPCEpiC	eye:	n/a
34	chr1:10705035-10705085	GM06990	blood:	n/a
35	chr1:10732519-10732569	HEEpiC	esophagus:	n/a
36	chr1:10714619-10714669	SKMC	muscle:	n/a
37	chr1:10753832-10753882	HNPCEpiC	eye:	n/a
38	chr1:10755322-10755372	HCPEpiC	choroid plexus:	n/a
39	chr1:10733511-10733561	GM12878	blood:	n/a
40	chr1:10705842-10705892	Hela-S3	cervix:	n/a
41	chr1:10745727-10745777	NB4	blood:	n/a
42	chr1:10690588-10690638	GM12878	blood:	n/a
43	chr1:10702137-10702187	AoSMC	blood vessel:	n/a
44	chr1:10720269-10720319	HMEC	breast:	n/a
45	chr1:10705842-10705892	HEK293	kidney:	embryo
46	chr1:10711044-10711094	NB4	blood:	n/a
47	chr1:10738569-10738619	A549	lung:	n/a
48	chr1:10720993-10721043	HEK293	kidney:	embryo
49	chr1:10794229-10794279	Jurkat	blood:	n/a
50	chr1:10757954-10758004	HCF	heart:	n/a

(count:190 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr1:10672111..10674098-chr1:10684480..10687476,2	K562	blood:
2	chr1:10746278..10748730-chr1:10764916..10766801,2	K562	blood:
3	chr1:10717594..10722225-chr1:10722686..10725044,4	K562	blood:
4	chr1:10682455..10684022-chr1:10686446..10688809,2	K562	blood:
5	chr1:10573337..10575488-chr1:10723481..10725688,2	K562	blood:
6	chr1:10772697..10775308-chr1:10780608..10782302,2	MCF-7	breast:
7	chr1:10755955..10758112-chr1:10760865..10764378,3	K562	blood:
8	chr1:10769186..10770686-chr1:10780232..10782829,2	K562	blood:
9	chr1:10774888..10776718-chr1:10783178..10785593,2	MCF-7	breast:
10	chr1:10739929..10741898-chr1:10854079..10856532,2	MCF-7	breast:
11	chr1:10685463..10687143-chr1:10735500..10738364,2	K562	blood:
12	chr1:10736438..10738952-chr1:10740834..10743683,3	K562	blood:
13	chr1:10756914..10759117-chr1:10783394..10785219,2	MCF-7	breast:
14	chr1:10679310..10682289-chr1:10684036..10687827,3	K562	blood:
15	chr1:10685463..10687143-chr1:10735500..10738364,2	K562	blood:
16	chr1:10769186..10770686-chr1:10780232..10782829,2	K562	blood:
17	chr1:10750259..10753196-chr1:10853460..10855878,3	MCF-7	breast:
18	chr1:10608473..10610056-chr1:10690153..10691726,2	MCF-7	breast:
19	chr1:10753843..10754435-chr17:37356222..37356754,2	Hela-S3	cervix:
20	chr1:10742297..10745036-chr1:10749705..10751341,3	MCF-7	breast:
21	chr1:10738788..10740418-chr1:10744263..10746556,2	MCF-7	breast:
22	chr1:10782189..10784150-chr1:10795398..10797015,2	K562	blood:
23	chr1:10777259..10780263-chr1:10782530..10785488,3	K562	blood:
24	chr1:10752709..10754408-chr1:10782360..10784898,3	MCF-7	breast:
25	chr1:10725435..10726303-chr1:10810964..10811494,2	MCF-7	breast:
26	chr1:10574993..10577268-chr1:10694934..10697136,2	MCF-7	breast:
27	chr1:10785675..10789087-chr1:10792936..10797329,5	K562	blood:
28	chr1:10689513..10692457-chr1:10716597..10719078,2	K562	blood:
29	chr1:10658291..10660875-chr1:10678955..10680939,2	MCF-7	breast:
30	chr1:10738789..10740392-chr1:10741913..10744233,2	MCF-7	breast:
31	chr1:10753473..10759637-chr1:10760137..10763540,7	K562	blood:
32	chr1:10758262..10760519-chr1:10763379..10765606,2	MCF-7	breast:
33	chr1:10715958..10718705-chr1:10751486..10753340,2	K562	blood:
34	chr1:10678742..10684022-chr1:10686327..10690416,7	K562	blood:
35	chr1:10781321..10784166-chr1:10789319..10791144,2	K562	blood:
36	chr1:10703574..10707168-chr1:10709558..10711927,3	MCF-7	breast:
37	chr1:10741683..10743188-chr1:10744761..10747734,2	MCF-7	breast:
38	chr1:10733440..10737843-chr1:10738072..10740756,3	K562	blood:
39	chr1:10703132..10705545-chr1:10711056..10713011,2	K562	blood:
40	chr1:10711257..10713486-chr1:10721428..10724018,2	MCF-7	breast:
41	chr1:10698341..10701476-chr1:10701646..10704585,3	MCF-7	breast:
42	chr1:10698140..10700728-chr1:10703080..10705863,3	K562	blood:
43	chr1:10756523..10758997-chr1:10766760..10768325,2	K562	blood:
44	chr1:10751847..10753495-chr1:10763556..10766439,2	K562	blood:
45	chr1:10746225..10747873-chr1:10749821..10751374,2	K562	blood:
46	chr1:10703132..10705545-chr1:10711056..10713011,2	K562	blood:
47	chr1:10739770..10741770-chr1:10741804..10744517,2	K562	blood:
48	chr1:10712754..10714859-chr1:10715847..10719174,3	MCF-7	breast:
49	chr1:10770692..10771316-chr1:10810904..10811625,4	MCF-7	breast:
50	chr1:10672897..10674878-chr1:10677717..10679649,2	K562	blood:

(count:16 , 50 per page) page: 1

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

No data

Variant related genes	Relation type
ENSG00000272078	TF binding region
CASZ1	TF binding region
ENSG00000272078	CpG island
CASZ1	CpG island
ENSG00000272078	chromatin interactions
ENSG00000116649	chromatin interactions
ENSG00000251503	chromatin interactions
ENSG00000108298	chromatin interactions
ENSG00000084652	chromatin interactions
ENSG00000271989	chromatin interactions
ENSG00000121741	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000175279	chromatin interactions
ENSG00000130940	chromatin interactions
ENSG00000243267	chromatin interactions

Extended variants
information (count: 5130 )
Associated
traits (count: 115 )

Variant overlapped rSNPs/rCNVs (count:5130 , 50 per page) page: 1 2 3 4 5 6 7 ... 103

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs560881376	chr1:10677581-10677582	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs576026833	chr1:10677595-10677596	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs192335239	chr1:10677631-10677632	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs374076066	chr1:10677666-10677667	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs533559972	chr1:10677678-10677679	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs564863244	chr1:10677699-10677700	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs545240745	chr1:10677734-10677735	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs560365723	chr1:10677747-10677748	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs527995743	chr1:10677751-10677752	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs185357151	chr1:10677788-10677789	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs116852591	chr1:10677855-10677856	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs531646308	chr1:10677929-10677930	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs190204107	chr1:10677936-10677937	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs367996016	chr1:10677948-10677949	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs571697076	chr1:10677977-10677978	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs538791785	chr1:10677978-10677979	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs532054608	chr1:10677997-10677998	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs554020023	chr1:10678005-10678006	Weak transcription Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs550403222	chr1:10678032-10678033	Weak transcription Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs181419137	chr1:10678133-10678134	Weak transcription Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs142105861	chr1:10678256-10678257	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
22	rs554930632	chr1:10678262-10678263	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
23	rs575976548	chr1:10678271-10678272	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
24	rs543088303	chr1:10678292-10678293	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
25	rs558614865	chr1:10678294-10678295	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
26	rs371526494	chr1:10678295-10678296	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
27	rs146370382	chr1:10678336-10678337	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
28	rs368165737	chr1:10678337-10678338	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
29	rs536996984	chr1:10678346-10678347	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
30	rs527910883	chr1:10678351-10678352	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
31	rs529794233	chr1:10678356-10678357	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
32	rs76387807	chr1:10678357-10678358	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
33	rs201545377	chr1:10678373-10678374	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
34	rs531729105	chr1:10678380-10678381	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
35	rs112851814	chr1:10678381-10678382	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
36	rs375835870	chr1:10678382-10678383	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
37	rs200270470	chr1:10678392-10678393	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
38	rs199552789	chr1:10678393-10678394	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
39	rs367754543	chr1:10678417-10678418	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs137949667	chr1:10678438-10678439	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs12061667	chr1:10678439-10678440	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs148479162	chr1:10678450-10678451	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs536484568	chr1:10678455-10678456	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs184807866	chr1:10678465-10678466	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs372630614	chr1:10678471-10678472	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs284238	chr1:10678488-10678489	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs367548044	chr1:10678489-10678490	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs201704437	chr1:10678490-10678491	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs199913711	chr1:10678491-10678492	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs373204498	chr1:10678494-10678495	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	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:4315 , 50 per page) page: 1 2 3 4 5 6 7 ... 87

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	chr1:10656800-10687200	Weak transcription	Small Intestine	intestine
8	chr1:10657600-10683200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
9	chr1:10657800-10683600	Weak transcription	Primary monocytes fromperipheralblood	blood
10	chr1:10657800-10684200	Weak transcription	Colonic Mucosa	Colon
11	chr1:10658200-10694400	Weak transcription	Primary neutrophils fromperipheralblood	blood
12	chr1:10658400-10678200	Weak transcription	Ovary	ovary
13	chr1:10658400-10688600	Weak transcription	Fetal Lung	lung
14	chr1:10658400-10691600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr1:10658600-10678000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr1:10658800-10678400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr1:10659200-10687800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
18	chr1:10659400-10684400	Weak transcription	Dnd41	blood
19	chr1:10659600-10678400	Weak transcription	Placenta	Placenta
20	chr1:10659600-10683800	Weak transcription	Duodenum Smooth Muscle	Duodenum
21	chr1:10659800-10690800	Weak transcription	Primary hematopoietic stem cells	blood
22	chr1:10660000-10682000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr1:10660000-10683600	Weak transcription	Rectal Mucosa Donor 31	rectum
24	chr1:10660000-10684200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr1:10660200-10684400	Weak transcription	NHLF	lung
26	chr1:10660200-10697600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
27	chr1:10660400-10679000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr1:10660400-10679000	Weak transcription	HMEC	breast
29	chr1:10660400-10683800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr1:10661800-10678200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr1:10661800-10678400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr1:10661800-10692000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr1:10662000-10678200	Weak transcription	Placenta Amnion	Placenta Amnion
34	chr1:10662000-10678400	Weak transcription	Duodenum Mucosa	Duodenum
35	chr1:10662000-10682600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
36	chr1:10662000-10683000	Weak transcription	Rectal Mucosa Donor 29	rectum
37	chr1:10662200-10694400	Weak transcription	HSMM	muscle
38	chr1:10662400-10678600	Weak transcription	Primary B cells from peripheral blood	blood
39	chr1:10662400-10694400	Weak transcription	Muscle Satellite Cultured Cells	--
40	chr1:10663000-10678800	Weak transcription	NHEK	skin
41	chr1:10663200-10677800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
42	chr1:10663200-10678200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr1:10663200-10678200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr1:10664400-10678200	Weak transcription	Monocytes-CD14+_RO01746	blood
45	chr1:10664400-10698000	Weak transcription	Primary B cells from cord blood	blood
46	chr1:10665800-10683000	Weak transcription	Aorta	Aorta
47	chr1:10666000-10677800	Weak transcription	Primary T helper cells PMA-I stimulated	--
48	chr1:10666200-10677600	Weak transcription	Primary T helper cells fromperipheralblood	blood
49	chr1:10666600-10678400	Weak transcription	Stomach Smooth Muscle	stomach
50	chr1:10666600-10683600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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