Variant report

Variant	nsv539211
Chromosome Location	chr7:152954795-153379878
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1729)
CpG islands
(count:794)
Chromatin interactive
region (count:301)
LncRNA
region (count:21)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1729 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:153109739-153110062	K562	blood:	n/a	n/a
2	ARID3A	chr7:153110322-153112174	K562	blood:	n/a	n/a
3	ARID3A	chr7:153108540-153108589	K562	blood:	n/a	n/a
4	ARID3A	chr7:153103307-153103458	K562	blood:	n/a	n/a
5	ARID3A	chr7:153143735-153143934	K562	blood:	n/a	n/a
6	ARID3A	chr7:153103753-153104234	K562	blood:	n/a	n/a
7	ARID3A	chr7:153130385-153130583	K562	blood:	n/a	n/a
8	ARID3A	chr7:153104655-153106258	K562	blood:	n/a	n/a
9	ARID3A	chr7:153109096-153109296	K562	blood:	n/a	n/a
10	ARID3A	chr7:153078807-153079063	HepG2	liver:	n/a	n/a
11	ARID3A	chr7:153043449-153043453	K562	blood:	n/a	n/a
12	ARID3A	chr7:153082623-153082873	K562	blood:	n/a	n/a
13	ATF1	chr7:153154941-153155221	K562	blood:	n/a	n/a
14	ATF1	chr7:153034781-153034828	K562	blood:	n/a	n/a
15	ATF1	chr7:153104526-153104952	K562	blood:	n/a	n/a
16	ATF1	chr7:153112718-153113068	K562	blood:	n/a	n/a
17	ATF1	chr7:153130251-153130554	K562	blood:	n/a	n/a
18	ATF1	chr7:153308996-153309145	K562	blood:	n/a	n/a
19	ATF1	chr7:153119688-153120319	K562	blood:	n/a	n/a
20	ATF1	chr7:153074161-153074244	K562	blood:	n/a	n/a
21	ATF1	chr7:153110923-153111307	K562	blood:	n/a	n/a
22	ATF3	chr7:153119989-153120275	K562	blood:	n/a	n/a
23	BACH1	chr7:153110739-153112141	K562	blood:	n/a	n/a
24	BACH1	chr7:153097892-153097911	K562	blood:	n/a	n/a
25	BACH1	chr7:153031945-153032120	K562	blood:	n/a	n/a
26	BACH1	chr7:153108498-153108636	K562	blood:	n/a	n/a
27	BACH1	chr7:153244736-153244872	K562	blood:	n/a	n/a
28	BACH1	chr7:152998916-152998999	K562	blood:	n/a	n/a
29	BACH1	chr7:153200611-153200865	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr7:153100843-153101026	K562	blood:	n/a	n/a
31	BACH1	chr7:153099558-153099965	K562	blood:	n/a	n/a
32	BACH1	chr7:153111122-153111267	H1-hESC	embryonic stem cell:	n/a	n/a
33	BACH1	chr7:153203925-153204059	K562	blood:	n/a	n/a
34	BACH1	chr7:153113244-153113564	K562	blood:	n/a	n/a
35	BACH1	chr7:153055076-153055079	K562	blood:	n/a	n/a
36	BACH1	chr7:153109751-153110110	K562	blood:	n/a	n/a
37	BACH1	chr7:153133123-153133319	K562	blood:	n/a	n/a
38	BATF	chr7:153337727-153337979	GM12878	blood:	n/a	n/a
39	BATF	chr7:153337705-153337995	GM12878	blood:	n/a	n/a
40	BCL3	chr7:153109499-153110250	K562	blood:	n/a	n/a
41	BCL3	chr7:153105524-153106503	K562	blood:	n/a	n/a
42	BCL3	chr7:153101811-153102227	K562	blood:	n/a	n/a
43	BCL3	chr7:153103242-153103537	K562	blood:	n/a	n/a
44	BCL3	chr7:153104489-153105071	K562	blood:	n/a	n/a
45	BCLAF1	chr7:153107687-153111130	K562	blood:	n/a	n/a
46	BCLAF1	chr7:153104261-153105189	K562	blood:	n/a	n/a
47	BCLAF1	chr7:153105443-153107677	K562	blood:	n/a	n/a
48	BCLAF1	chr7:153110402-153111174	K562	blood:	n/a	n/a
49	BHLHE40	chr7:153108552-153108560	K562	blood:	n/a	n/a
50	BHLHE40	chr7:153109125-153109401	K562	blood:	n/a	n/a

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:153110994-153111044	SK-N-MC	brain:	n/a
2	chr7:153110994-153111044	SK-N-MC	brain:	n/a
3	chr7:153287591-153287641	GM12878	blood:	n/a
4	chr7:153287752-153287802	HCM	heart:	n/a
5	chr7:153287752-153287802	HRCEpiC	kidney:	n/a
6	chr7:153109375-153109425	NT2-D1	testis:	n/a
7	chr7:153078797-153078847	NHDF-neo	bronchial:	n/a
8	chr7:153109538-153109588	ProgFib	skin:	n/a
9	chr7:153110994-153111044	GM12891	blood:	n/a
10	chr7:153108642-153108692	CMK	blood:	n/a
11	chr7:153287752-153287802	HCPEpiC	choroid plexus:	n/a
12	chr7:153108642-153108692	HNPCEpiC	eye:	n/a
13	chr7:153108684-153108734	ProgFib	skin:	n/a
14	chr7:153110994-153111044	HEK293	kidney:	embryo
15	chr7:153110762-153110812	PANC-1	pancreas:	n/a
16	chr7:153108726-153108776	HUVEC	blood vessel:	n/a
17	chr7:153012895-153012945	AG04450	lung:	fetal
18	chr7:153287752-153287802	CMK	blood:	n/a
19	chr7:153287752-153287802	HL-60	blood:	n/a
20	chr7:153078797-153078847	AG09319	gingival:	n/a
21	chr7:153287752-153287802	Jurkat	blood:	n/a
22	chr7:153287529-153287579	HEEpiC	esophagus:	n/a
23	chr7:153109538-153109588	Hela-S3	cervix:	n/a
24	chr7:153078797-153078847	HL-60	blood:	n/a
25	chr7:153108726-153108776	CMK	blood:	n/a
26	chr7:153287752-153287802	BJ	skin:	n/a
27	chr7:153110994-153111044	RPTEC	kidney:	n/a
28	chr7:153287529-153287579	NH-A	brain:	n/a
29	chr7:153110994-153111044	NT2-D1	testis:	n/a
30	chr7:153109538-153109588	HUVEC	blood vessel:	n/a
31	chr7:153108726-153108776	HCPEpiC	choroid plexus:	n/a
32	chr7:153110994-153111044	SAEC	small airway:	n/a
33	chr7:153012895-153012945	BJ	skin:	n/a
34	chr7:153110762-153110812	AG09319	gingival:	n/a
35	chr7:153108642-153108692	HEK293	kidney:	embryo
36	chr7:153108642-153108692	SAEC	small airway:	n/a
37	chr7:153109375-153109425	SK-N-SH_RA	brain:	n/a
38	chr7:153109538-153109588	LNCaP	prostate:	n/a
39	chr7:153109538-153109588	HCPEpiC	choroid plexus:	n/a
40	chr7:153110762-153110812	HCM	heart:	n/a
41	chr7:153108684-153108734	MCF10A-Er-Src	breast:	n/a
42	chr7:153287529-153287579	A549	lung:	n/a
43	chr7:153108642-153108692	Hepatocyte	liver:	n/a
44	chr7:153108726-153108776	HCT-116	colon:	n/a
45	chr7:153110994-153111044	NH-A	brain:	n/a
46	chr7:153110492-153110542	GM06990	blood:	n/a
47	chr7:153108684-153108734	SK-N-SH_RA	brain:	n/a
48	chr7:153012895-153012945	RPTEC	kidney:	n/a
49	chr7:153287591-153287641	NHDF-neo	bronchial:	n/a
50	chr7:153078797-153078847	GM19239	blood:	n/a

(count:301 , 50 per page) page: 1 2 3 4 5 6 7

No.	Distal block	Cell Line	Cell type
1	chr7:153103693..153106480-chr7:153169343..153171365,2	K562	blood:
2	chr7:153168042..153171876-chr7:153172518..153177517,5	K562	blood:
3	chr7:153119320..153121928-chr7:153170985..153172845,2	K562	blood:
4	chr7:153078806..153081206-chr7:153081350..153083333,2	K562	blood:
5	chr7:153207860..153209582-chr7:153211240..153212900,2	K562	blood:
6	chr7:153099524..153101138-chr7:153168192..153169885,2	K562	blood:
7	chr7:153073552..153076060-chr7:153082257..153085199,2	K562	blood:
8	chr7:153099940..153103347-chr7:153340908..153343699,3	K562	blood:
9	chr7:153168042..153171876-chr7:153172518..153177517,5	K562	blood:
10	chr7:153016352..153018288-chr7:153019848..153021405,2	K562	blood:
11	chr7:153179767..153181427-chr7:153183794..153186407,2	K562	blood:
12	chr7:153103375..153106774-chr7:153173661..153176724,3	K562	blood:
13	chr7:153341235..153342881-chr7:153346431..153348736,2	K562	blood:
14	chr7:153099524..153101138-chr7:153168192..153169885,2	K562	blood:
15	chr7:153035622..153038068-chr7:153039274..153041067,2	K562	blood:
16	chr11:5956902..5959925-chr7:153104319..153108206,5	K562	blood:
17	chr7:153033553..153036164-chr7:153103737..153105487,2	K562	blood:
18	chr7:152595309..152597143-chr7:153102901..153104884,2	K562	blood:
19	chr7:152615135..152617990-chr7:153104764..153107812,3	K562	blood:
20	chr7:152892350..152895331-chr7:153094490..153096046,2	K562	blood:
21	chr7:153104012..153105714-chr7:153166504..153168791,2	K562	blood:
22	chr7:153092517..153095170-chr7:153147417..153149033,2	K562	blood:
23	chr7:153100820..153103410-chr7:153246584..153249087,2	K562	blood:
24	chr7:153033553..153036164-chr7:153103737..153105487,2	K562	blood:
25	chr7:153089054..153091644-chr7:153185631..153188291,2	K562	blood:
26	chr7:153374613..153377425-chr7:153379537..153382036,2	K562	blood:
27	chr7:153044433..153047709-chr7:153053514..153056497,3	K562	blood:
28	chr7:153244368..153246054-chr7:153249661..153252423,2	K562	blood:
29	chr7:152964213..152967180-chr7:152968454..152970923,2	K562	blood:
30	chr7:152994343..152995845-chr7:152998674..153000220,2	K562	blood:
31	chr7:153029560..153032040-chr7:153105014..153106931,2	K562	blood:
32	chr7:153168165..153169692-chr7:153180801..153182343,2	K562	blood:
33	chr7:153111734..153114146-chr7:153170231..153173109,2	K562	blood:
34	chr7:153353677..153355280-chr7:153357292..153359740,2	K562	blood:
35	chr7:153353780..153355410-chr7:153357076..153358792,2	K562	blood:
36	chr7:152886507..152888458-chr7:153102294..153104030,2	K562	blood:
37	chr7:153102748..153104810-chr7:153194160..153196266,2	K562	blood:
38	chr7:153055542..153057416-chr7:153103974..153105838,2	K562	blood:
39	chr7:153130431..153132961-chr7:153133375..153135450,3	K562	blood:
40	chr7:153052023..153054684-chr7:153104200..153106325,2	K562	blood:
41	chr7:152993926..152995856-chr7:152996006..152997666,2	K562	blood:
42	chr7:152947748..152949504-chr7:153104988..153107669,2	K562	blood:
43	chr7:153288321..153290780-chr7:153315466..153317152,2	K562	blood:
44	chr7:153103154..153105187-chr7:153228223..153229957,2	K562	blood:
45	chr17:41463652..41466237-chr7:152975981..152977481,2	K562	blood:
46	chr7:152890212..152890787-chr7:153078742..153079279,2	MCF-7	breast:
47	chr7:153294161..153296429-chr7:153302912..153305388,2	K562	blood:
48	chr7:153179767..153181427-chr7:153183794..153186407,2	K562	blood:
49	chr7:153100488..153103412-chr7:153303424..153305965,2	K562	blood:
50	chr7:153095496..153100083-chr7:153227240..153231404,4	K562	blood:

(count:21 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DPP6-2	chr7:153120526-153120601	XLOC_006298
2	lnc-XRCC2-1	chr7:153097005-153097631	ENSG00000234722.3
3	lnc-DPP6-3	chr7:153086676-153086815	XLOC_006297
4	lnc-XRCC2-2	chr7:153120803-153121101	XLOC_006657
5	lnc-DPP6-2	chr7:153119376-153119626	XLOC_006298
6	lnc-XRCC2-1	chr7:153104041-153104169	ENSG00000234722.3
7	lnc-XRCC2-1	chr7:153102577-153102683	ENSG00000234722.3
8	lnc-XRCC2-1	chr7:153102578-153102683	ENSG00000234722
9	lnc-DPP6-7	chr7:153146514-153146960	NONHSAT124301
10	lnc-XRCC2-1	chr7:153104041-153104171	ENSG00000234722
11	lnc-XRCC2-1	chr7:153097005-153097631	ENSG00000234722
12	lnc-XRCC2-3	chr7:153221094-153221300	XLOC_006658
13	lnc-XRCC2-1	chr7:153109178-153109319	ENSG00000234722
14	lnc-XRCC2-3	chr7:153220300-153220910	XLOC_006658
15	lnc-XRCC2-2	chr7:153125396-153125424	XLOC_006657
16	lnc-XRCC2-1	chr7:153110698-153111021	ENSG00000234722
17	lnc-DPP6-3	chr7:153092527-153092639	XLOC_006297
18	lnc-XRCC2-1	chr7:153109176-153109319	ENSG00000234722.3
19	lnc-DPP6-3	chr7:153093149-153093207	XLOC_006297
20	lnc-DPP6-3	chr7:153092498-153092703	XLOC_006297
21	lnc-XRCC2-1	chr7:153102577-153102683	ENSG00000234722

No data

Variant related genes	Relation type
ENSG00000233489	TF binding region
ENSG00000234722	TF binding region
ENSG00000233489	CpG island
ENSG00000234722	CpG island
ENSG00000170832	chromatin interactions
ENSG00000261455	chromatin interactions
ENSG00000171222	chromatin interactions
ENSG00000197774	chromatin interactions
ENSG00000132256	chromatin interactions
ENSG00000236198	chromatin interactions
ENSG00000233489	chromatin interactions
ENSG00000222281	chromatin interactions
ENSG00000234338	chromatin interactions
ENSG00000155380	chromatin interactions
ENSG00000234722	chromatin interactions
ENSG00000223700	chromatin interactions
ENSG00000141371	chromatin interactions
ENSG00000188825	chromatin interactions
CCT2	miRNA target sites
DHX57	miRNA target sites
LRRC1	miRNA target sites
APAF1	miRNA target sites

Extended variants
information (count: 8062 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:8062 , 50 per page) page: 1 2 3 4 5 6 7 ... 162

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs148456489	chr7:152954800-152954801	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs566830963	chr7:152955829-152955830	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs115114753	chr7:152955834-152955835	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs187856791	chr7:152955835-152955836	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs574254009	chr7:152955852-152955853	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs544973837	chr7:152955859-152955860	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs538585629	chr7:152955920-152955921	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs556785371	chr7:152955932-152955933	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs578233256	chr7:152956016-152956017	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs545890937	chr7:152956029-152956030	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs564190288	chr7:152956058-152956059	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs192420011	chr7:152956074-152956075	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs185456684	chr7:152956086-152956087	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs10264070	chr7:152956196-152956197	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs547408861	chr7:152956285-152956286	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs550497716	chr7:152956291-152956292	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs527813929	chr7:152956332-152956333	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs149188546	chr7:152956384-152956385	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs374490871	chr7:152956402-152956403	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs551428360	chr7:152956422-152956423	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs187887303	chr7:152956425-152956426	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs565640742	chr7:152956428-152956429	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs368573885	chr7:152956429-152956430	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs549104399	chr7:152956455-152956456	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs146865763	chr7:152956456-152956457	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs538522725	chr7:152956461-152956462	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs192178277	chr7:152956472-152956473	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs578194909	chr7:152956553-152956554	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs539249912	chr7:152956559-152956560	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs185052335	chr7:152956576-152956577	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs549474197	chr7:152956591-152956592	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs572852046	chr7:152956605-152956606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs540365252	chr7:152956611-152956612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs544056830	chr7:152956640-152956641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs542439136	chr7:152956660-152956661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs573331990	chr7:152956661-152956662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs565555482	chr7:152956700-152956701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs139120104	chr7:152956719-152956720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs562458288	chr7:152956742-152956743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs188669989	chr7:152956765-152956766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs113244944	chr7:152956782-152956783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs112125300	chr7:152956805-152956806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs181691800	chr7:152956818-152956819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs201788365	chr7:152956826-152956827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs549490889	chr7:152956902-152956903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs567529971	chr7:152956949-152956950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs111618292	chr7:152956955-152956956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs184474383	chr7:152956982-152956983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs115845277	chr7:152957011-152957012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs550458609	chr7:152957016-152957017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Myelodysplastic syndrome	17634407	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	16864856	CNVD
Autism	20808228	CNVD
Ovarian cancer	21720365	CNVD
Lobular carcinoma	20920651	CNVD
Long-qt syndrome	20920651	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Sudden cardiac death	19188705	CNVD
renal disease	17924346	CNVD
Autism	22102821	CNVD
Myelofibrosis	22110671	CNVD
Nasopharyngeal cancer	20548289	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Chordoma	21215367	CNVD
Breast cancer	21509527	CNVD
Autism	20531469	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Congenital anomalies of the kidney and urinary tract	20605837	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	21346763	CNVD
Non-syndromic sensorineural hearing loss	19212409	CNVD
Attention deficit hyperactivity disorder	19546859	CNVD

Chromatin state (count:419 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:152952400-152954800	Enhancers	Primary hematopoietic stem cells short term culture	blood
2	chr7:152955800-152956200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr7:152955800-152956200	Enhancers	Brain Anterior Caudate	brain
4	chr7:152955800-152956200	Enhancers	Brain Cingulate Gyrus	brain
5	chr7:152955800-152956400	Enhancers	H1 Cell Line	embryonic stem cell
6	chr7:152955800-152956400	Enhancers	H9 Cell Line	embryonic stem cell
7	chr7:152955800-152956400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr7:152955800-152956400	Enhancers	Brain Substantia Nigra	brain
9	chr7:152955800-152956600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr7:152956000-152956400	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr7:152956000-152956400	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr7:152956000-152956400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr7:152956400-152961400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr7:152961400-152962000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
15	chr7:152961600-152961800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr7:152961800-152964600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr7:152962000-152962800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr7:152964600-152964800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr7:152986200-152986800	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr7:152986400-152987000	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr7:152986400-152987000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
22	chr7:152986800-152987000	Enhancers	Primary hematopoietic stem cells	blood
23	chr7:152986800-152987600	Enhancers	Primary hematopoietic stem cells short term culture	blood
24	chr7:152987000-152987200	Enhancers	HSMM	muscle
25	chr7:152987600-152987800	Enhancers	Primary hematopoietic stem cells	blood
26	chr7:152992800-152993000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr7:152993000-152994400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr7:152993600-152994800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr7:152994000-152994400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr7:152994200-152994600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr7:152994200-152995600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr7:152994400-152994800	Enhancers	Placenta	Placenta
33	chr7:152994400-152995600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr7:152995200-152996200	Enhancers	Fetal Kidney	kidney
35	chr7:152995600-152997600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr7:152997600-152999600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr7:152998000-152999200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr7:152998200-152998400	Enhancers	Fetal Kidney	kidney
39	chr7:152999000-152999400	Active TSS	Pancreatic Islets	Pancreatic Islet
40	chr7:152999400-152999600	Enhancers	Pancreatic Islets	Pancreatic Islet
41	chr7:153016400-153017400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr7:153017000-153017800	Enhancers	Colon Smooth Muscle	Colon
43	chr7:153017000-153018400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr7:153017400-153017800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr7:153017800-153018600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr7:153018000-153018200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
47	chr7:153018200-153019000	Enhancers	Spleen	Spleen
48	chr7:153018400-153020400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr7:153018600-153020200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr7:153019800-153020400	Enhancers	Breast Myoepithelial Primary Cells	Breast

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