Variant report

Variant	nsv889510
Chromosome Location	chr7:153050837-153413046
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1596)
CpG islands
(count:734)
Chromatin interactive
region (count:265)
LncRNA
region (count:22)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1596 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:153104655-153106258	K562	blood:	n/a	n/a
2	ARID3A	chr7:153130385-153130583	K562	blood:	n/a	n/a
3	ARID3A	chr7:153110322-153112174	K562	blood:	n/a	n/a
4	ARID3A	chr7:153078807-153079063	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:153109739-153110062	K562	blood:	n/a	n/a
6	ARID3A	chr7:153103307-153103458	K562	blood:	n/a	n/a
7	ARID3A	chr7:153108540-153108589	K562	blood:	n/a	n/a
8	ARID3A	chr7:153143735-153143934	K562	blood:	n/a	n/a
9	ARID3A	chr7:153082623-153082873	K562	blood:	n/a	n/a
10	ARID3A	chr7:153109096-153109296	K562	blood:	n/a	n/a
11	ARID3A	chr7:153103753-153104234	K562	blood:	n/a	n/a
12	ATF1	chr7:153154941-153155221	K562	blood:	n/a	n/a
13	ATF1	chr7:153130251-153130554	K562	blood:	n/a	n/a
14	ATF1	chr7:153104526-153104952	K562	blood:	n/a	n/a
15	ATF1	chr7:153119688-153120319	K562	blood:	n/a	n/a
16	ATF1	chr7:153074161-153074244	K562	blood:	n/a	n/a
17	ATF1	chr7:153110923-153111307	K562	blood:	n/a	n/a
18	ATF1	chr7:153112718-153113068	K562	blood:	n/a	n/a
19	ATF1	chr7:153308996-153309145	K562	blood:	n/a	n/a
20	ATF3	chr7:153119989-153120275	K562	blood:	n/a	n/a
21	BACH1	chr7:153097892-153097911	K562	blood:	n/a	n/a
22	BACH1	chr7:153133123-153133319	K562	blood:	n/a	n/a
23	BACH1	chr7:153203925-153204059	K562	blood:	n/a	n/a
24	BACH1	chr7:153055076-153055079	K562	blood:	n/a	n/a
25	BACH1	chr7:153110739-153112141	K562	blood:	n/a	n/a
26	BACH1	chr7:153099558-153099965	K562	blood:	n/a	n/a
27	BACH1	chr7:153113244-153113564	K562	blood:	n/a	n/a
28	BACH1	chr7:153109751-153110110	K562	blood:	n/a	n/a
29	BACH1	chr7:153108498-153108636	K562	blood:	n/a	n/a
30	BACH1	chr7:153100843-153101026	K562	blood:	n/a	n/a
31	BACH1	chr7:153200611-153200865	H1-hESC	embryonic stem cell:	n/a	n/a
32	BACH1	chr7:153111122-153111267	H1-hESC	embryonic stem cell:	n/a	n/a
33	BACH1	chr7:153244736-153244872	K562	blood:	n/a	n/a
34	BATF	chr7:153337705-153337995	GM12878	blood:	n/a	n/a
35	BATF	chr7:153337727-153337979	GM12878	blood:	n/a	n/a
36	BCL3	chr7:153109499-153110250	K562	blood:	n/a	n/a
37	BCL3	chr7:153105524-153106503	K562	blood:	n/a	n/a
38	BCL3	chr7:153101811-153102227	K562	blood:	n/a	n/a
39	BCL3	chr7:153104489-153105071	K562	blood:	n/a	n/a
40	BCL3	chr7:153103242-153103537	K562	blood:	n/a	n/a
41	BCLAF1	chr7:153110402-153111174	K562	blood:	n/a	n/a
42	BCLAF1	chr7:153105443-153107677	K562	blood:	n/a	n/a
43	BCLAF1	chr7:153107687-153111130	K562	blood:	n/a	n/a
44	BCLAF1	chr7:153104261-153105189	K562	blood:	n/a	n/a
45	BHLHE40	chr7:153082587-153083004	K562	blood:	n/a	n/a
46	BHLHE40	chr7:153122488-153122545	K562	blood:	n/a	n/a
47	BHLHE40	chr7:153108552-153108560	K562	blood:	n/a	n/a
48	BHLHE40	chr7:153103811-153104266	K562	blood:	n/a	n/a
49	BHLHE40	chr7:153110425-153112117	K562	blood:	n/a	n/a
50	BHLHE40	chr7:153078637-153079395	K562	blood:	n/a	n/a

(count:734 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:153110994-153111044	A549	lung:	n/a
2	chr7:153287752-153287802	AG10803	skin:	n/a
3	chr7:153110994-153111044	A549	lung:	n/a
4	chr7:153287752-153287802	AG10803	skin:	n/a
5	chr7:153109538-153109588	HPAEpiC	pulmonary alveolar:	n/a
6	chr7:153110762-153110812	PrEC	prostate:	n/a
7	chr7:153109375-153109425	HRCEpiC	kidney:	n/a
8	chr7:153108642-153108692	LNCaP	prostate:	n/a
9	chr7:153108684-153108734	T-47D	breast:	n/a
10	chr7:153287752-153287802	HL-60	blood:	n/a
11	chr7:153287752-153287802	SK-N-SH_RA	brain:	n/a
12	chr7:153109538-153109588	MCF10A-Er-Src	breast:	n/a
13	chr7:153287752-153287802	HUVEC	blood vessel:	n/a
14	chr7:153287591-153287641	NHDF-neo	bronchial:	n/a
15	chr7:153108642-153108692	AG09309	skin:	n/a
16	chr7:153109538-153109588	AG04449	skin:	fetal
17	chr7:153108684-153108734	HEK293	kidney:	embryo
18	chr7:153109538-153109588	K562	blood:	n/a
19	chr7:153287591-153287641	NT2-D1	testis:	n/a
20	chr7:153110492-153110542	HRCEpiC	kidney:	n/a
21	chr7:153108726-153108776	PrEC	prostate:	n/a
22	chr7:153110762-153110812	HCF	heart:	n/a
23	chr7:153108642-153108692	AG10803	skin:	n/a
24	chr7:153110492-153110542	HL-60	blood:	n/a
25	chr7:153287752-153287802	A549	lung:	n/a
26	chr7:153078797-153078847	MCF10A-Er-Src	breast:	n/a
27	chr7:153109375-153109425	HRPEpiC	eye:	n/a
28	chr7:153110762-153110812	HRE	kidney:	n/a
29	chr7:153109375-153109425	RPTEC	kidney:	n/a
30	chr7:153110994-153111044	HPAEpiC	pulmonary alveolar:	n/a
31	chr7:153108684-153108734	H1-hESC	embryonic stem cell:	embryo
32	chr7:153110492-153110542	MCF-7	breast:	n/a
33	chr7:153287529-153287579	HCF	heart:	n/a
34	chr7:153108642-153108692	U87	brain:	n/a
35	chr7:153287752-153287802	NHBE	bronchial:	n/a
36	chr7:153108642-153108692	H1-hESC	embryonic stem cell:	embryo
37	chr7:153108684-153108734	AG09309	skin:	n/a
38	chr7:153287529-153287579	SAEC	small airway:	n/a
39	chr7:153108726-153108776	HMEC	breast:	n/a
40	chr7:153287591-153287641	AG09309	skin:	n/a
41	chr7:153287752-153287802	AG09319	gingival:	n/a
42	chr7:153287529-153287579	IMR90	lung:	fetal
43	chr7:153109375-153109425	HCPEpiC	choroid plexus:	n/a
44	chr7:153109538-153109588	HCPEpiC	choroid plexus:	n/a
45	chr7:153109375-153109425	HEK293	kidney:	embryo
46	chr7:153108684-153108734	ProgFib	skin:	n/a
47	chr7:153108642-153108692	HepG2	liver:	n/a
48	chr7:153109375-153109425	Hepatocyte	liver:	n/a
49	chr7:153110762-153110812	GM12892	blood:	n/a
50	chr7:153287529-153287579	Hela-S3	cervix:	n/a

(count:265 , 50 per page) page: 1 2 3 4 5 6

No.	Distal block	Cell Line	Cell type
1	chr7:153204732..153207238-chr7:153212337..153214692,2	MCF-7	breast:
2	chr7:153110155..153112303-chr7:153247620..153250543,3	K562	blood:
3	chr7:153065822..153067507-chr7:153075563..153078240,2	K562	blood:
4	chr7:153102849..153104905-chr7:153187331..153188983,2	K562	blood:
5	chr7:153110683..153112303-chr7:153248370..153250543,2	K562	blood:
6	chr7:153361300..153363555-chr7:153366208..153367723,2	K562	blood:
7	chr7:153103413..153106356-chr7:153237101..153239788,2	K562	blood:
8	chr7:153103866..153106849-chr7:153334968..153337420,2	K562	blood:
9	chr7:153104137..153106481-chr7:153366224..153368570,2	K562	blood:
10	chr7:153052023..153054684-chr7:153104200..153106325,2	K562	blood:
11	chr7:153073552..153076060-chr7:153082257..153085199,2	K562	blood:
12	chr7:153102450..153104761-chr7:153532927..153535675,2	K562	blood:
13	chr7:153119320..153121928-chr7:153170985..153172845,2	K562	blood:
14	chr7:153033553..153036164-chr7:153103737..153105487,2	K562	blood:
15	chr7:153250299..153251916-chr7:153251980..153254318,2	K562	blood:
16	chr7:153104344..153107285-chr7:153206128..153208703,2	K562	blood:
17	chr7:152877954..152879856-chr7:153096882..153099868,2	K562	blood:
18	chr7:153104593..153107356-chr7:153151532..153153946,4	K562	blood:
19	chr7:153150343..153152572-chr7:153153820..153155844,2	K562	blood:
20	chr7:153353677..153355280-chr7:153357292..153359740,2	K562	blood:
21	chr7:153094563..153096914-chr7:153326913..153328518,2	K562	blood:
22	chr7:153100549..153102656-chr7:153210062..153212505,2	K562	blood:
23	chr7:153100549..153102656-chr7:153210062..153212505,2	K562	blood:
24	chr7:153104012..153105714-chr7:153166504..153168791,2	K562	blood:
25	chr7:153291103..153293422-chr7:153317816..153319821,2	K562	blood:
26	chr7:153037739..153042014-chr7:153077281..153081479,4	K562	blood:
27	chr7:153374613..153377425-chr7:153379537..153382036,2	K562	blood:
28	chr7:153091082..153093692-chr7:153327387..153329268,2	K562	blood:
29	chr7:153100488..153103412-chr7:153303424..153305965,2	K562	blood:
30	chr7:153103413..153106073-chr7:153238288..153241221,2	K562	blood:
31	chr7:64297147..64300763-chr7:153106859..153112373,8	K562	blood:
32	chr7:153103427..153106418-chr7:153612695..153615251,3	K562	blood:
33	chr7:153078444..153079476-chr7:153379433..153380748,5	MCF-7	breast:
34	chr7:153137391..153139228-chr7:153141759..153143841,2	K562	blood:
35	chr7:153021290..153023389-chr7:153093979..153096811,2	K562	blood:
36	chr7:152993644..152995828-chr7:153101841..153103974,2	K562	blood:
37	chr7:153346075..153348909-chr7:153353457..153355073,2	K562	blood:
38	chr7:153099524..153101138-chr7:153168192..153169885,2	K562	blood:
39	chr7:153054222..153056316-chr7:153099590..153102499,2	K562	blood:
40	chr7:153100664..153102886-chr7:154843246..154845747,2	K562	blood:
41	chr7:153144216..153146051-chr7:153150642..153152282,2	K562	blood:
42	chr7:153092517..153095170-chr7:153147417..153149033,2	K562	blood:
43	chr7:153105710..153107855-chr7:153165499..153167992,2	K562	blood:
44	chr7:153212579..153217619-chr7:153220846..153223669,4	K562	blood:
45	chr7:153100739..153103301-chr7:153343816..153346301,2	K562	blood:
46	chr7:153137391..153139228-chr7:153141759..153143841,2	K562	blood:
47	chr7:153101066..153103741-chr7:153151385..153153304,3	K562	blood:
48	chr7:153313143..153316198-chr7:153317253..153319908,4	K562	blood:
49	chr7:153207860..153209582-chr7:153211240..153212900,2	K562	blood:
50	chr7:153137391..153141168-chr7:153141506..153146066,7	K562	blood:

(count:22 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DPP6-3	chr7:153093149-153093207	XLOC_006297
2	lnc-DPP6-3	chr7:153086676-153086815	XLOC_006297
3	lnc-XRCC2-1	chr7:153104041-153104169	ENSG00000234722.3
4	lnc-DPP6-3	chr7:153092498-153092703	XLOC_006297
5	lnc-XRCC2-1	chr7:153109176-153109319	ENSG00000234722.3
6	lnc-XRCC2-1	chr7:153102578-153102683	ENSG00000234722
7	lnc-DPP6-2	chr7:153120526-153120601	XLOC_006298
8	lnc-XRCC2-1	chr7:153110698-153111021	ENSG00000234722
9	lnc-DPP6-7	chr7:153146514-153146960	NONHSAT124301
10	lnc-XRCC2-1	chr7:153109178-153109319	ENSG00000234722
11	lnc-XRCC2-1	chr7:153097005-153097631	ENSG00000234722
12	lnc-XRCC2-2	chr7:153125396-153125424	XLOC_006657
13	lnc-DPP6-3	chr7:153092527-153092639	XLOC_006297
14	lnc-XRCC2-3	chr7:153220300-153220910	XLOC_006658
15	lnc-XRCC2-1	chr7:153104041-153104171	ENSG00000234722
16	lnc-XRCC2-3	chr7:153221094-153221300	XLOC_006658
17	lnc-XRCC2-2	chr7:153120803-153121101	XLOC_006657
18	lnc-XRCC2-1	chr7:153102577-153102683	ENSG00000234722.3
19	lnc-XRCC2-4	chr7:153406738-153407404	XLOC_006659
20	lnc-XRCC2-1	chr7:153097005-153097631	ENSG00000234722.3
21	lnc-DPP6-2	chr7:153119376-153119626	XLOC_006298
22	lnc-XRCC2-1	chr7:153102577-153102683	ENSG00000234722

No data

Variant related genes	Relation type
ENSG00000234722	TF binding region
ENSG00000233489	TF binding region
ENSG00000234722	CpG island
ENSG00000233489	CpG island
ENSG00000197774	chromatin interactions
ENSG00000234722	chromatin interactions
ENSG00000234338	chromatin interactions
ENSG00000222281	chromatin interactions
ENSG00000155380	chromatin interactions
ENSG00000223700	chromatin interactions
ENSG00000132256	chromatin interactions
ENSG00000236198	chromatin interactions
ENSG00000233489	chromatin interactions
ENSG00000261455	chromatin interactions
ENSG00000171222	chromatin interactions
LRRC1	miRNA target sites
DHX57	miRNA target sites
CCT2	miRNA target sites
APAF1	miRNA target sites
CDKN1A	miRNA target sites

Extended variants
information (count: 7081 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:7081 , 50 per page) page: 1 2 3 4 5 6 7 ... 142

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs76456447	chr7:153060718-153060719	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs376829682	chr7:153060760-153060761	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs148800545	chr7:153060800-153060801	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs369434021	chr7:153060826-153060827	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs557202967	chr7:153060831-153060832	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs144778865	chr7:153060832-153060833	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs373122858	chr7:153060838-153060839	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs75485256	chr7:153060848-153060849	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs557571428	chr7:153060885-153060886	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs575291139	chr7:153060915-153060916	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs572959404	chr7:153061084-153061085	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs531916492	chr7:153061089-153061090	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs34253936	chr7:153061103-153061104	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs189777167	chr7:153061123-153061124	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs377576536	chr7:153061128-153061129	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs36021182	chr7:153061138-153061139	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs572447484	chr7:153061141-153061142	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs555447637	chr7:153061157-153061158	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs34653872	chr7:153061169-153061170	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs386411704	chr7:153061176-153061177	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs386411705	chr7:153061177-153061178	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs370597309	chr7:153061183-153061184	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs960839	chr7:153061216-153061217	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs5888508	chr7:153061258-153061259	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs78488236	chr7:153061259-153061260	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs544308053	chr7:153061305-153061306	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs563173244	chr7:153061310-153061311	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs578260354	chr7:153061348-153061349	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs34304278	chr7:153061379-153061380	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs573495617	chr7:153061412-153061413	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs960840	chr7:153061413-153061414	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs75867675	chr7:153061437-153061438	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs528914520	chr7:153061457-153061458	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs535368334	chr7:153067339-153067340	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs34217462	chr7:153067374-153067375	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs568729171	chr7:153067402-153067403	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs114213561	chr7:153067436-153067437	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs181837448	chr7:153067474-153067475	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs184496813	chr7:153067477-153067478	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs115380233	chr7:153067510-153067511	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs189021115	chr7:153067553-153067554	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs181582058	chr7:153067554-153067555	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs574360218	chr7:153067592-153067593	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs544937291	chr7:153067695-153067696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs551793161	chr7:153067697-153067698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs186326504	chr7:153067702-153067703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs1037005	chr7:153067709-153067710	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs117557667	chr7:153067809-153067810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs564197134	chr7:153067833-153067834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs528180488	chr7:153067921-153067922	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
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
Breast cancer	21509527	CNVD
small cell lung cancer	20016488	CNVD
Autism	20531469	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Chordoma	21215367	CNVD
Congenital anomalies of the kidney and urinary tract	20605837	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	21346763	CNVD
Non-syndromic sensorineural hearing loss	19212409	CNVD
Attention deficit hyperactivity disorder	19546859	CNVD

Chromatin state (count:370 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:153067200-153067600	Enhancers	K562	blood
2	chr7:153067600-153082400	Weak transcription	K562	blood
3	chr7:153071000-153071200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr7:153071800-153072000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr7:153078000-153078800	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr7:153078200-153078800	Active TSS	Pancreatic Islets	Pancreatic Islet
7	chr7:153078400-153078600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr7:153078400-153078600	Enhancers	Brain Anterior Caudate	brain
9	chr7:153078400-153078600	Active TSS	Duodenum Smooth Muscle	Duodenum
10	chr7:153078400-153078600	Enhancers	Fetal Kidney	kidney
11	chr7:153078400-153078600	Enhancers	Fetal Stomach	stomach
12	chr7:153078400-153078800	Active TSS	ES-I3 Cell Line	embryonic stem cell
13	chr7:153078400-153078800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
14	chr7:153078400-153078800	Active TSS	HUES48 Cell Line	embryonic stem cell
15	chr7:153078400-153078800	Active TSS	HUES6 Cell Line	embryonic stem cell
16	chr7:153078400-153078800	Active TSS	iPS-20b Cell Line	embryonic stem cell
17	chr7:153078400-153078800	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
18	chr7:153078400-153078800	Enhancers	Brain Hippocampus Middle	brain
19	chr7:153078400-153079000	Enhancers	Breast Myoepithelial Primary Cells	Breast
20	chr7:153078400-153079000	Enhancers	Rectal Smooth Muscle	rectum
21	chr7:153078400-153079000	Active TSS	Stomach Smooth Muscle	stomach
22	chr7:153078400-153082000	Enhancers	Colon Smooth Muscle	Colon
23	chr7:153078600-153078800	Enhancers	H1 Cell Line	embryonic stem cell
24	chr7:153078600-153078800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr7:153078600-153078800	Flanking Active TSS	Brain Anterior Caudate	brain
26	chr7:153078600-153078800	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
27	chr7:153078600-153079000	Flanking Active TSS	Fetal Kidney	kidney
28	chr7:153078600-153079000	Enhancers	Fetal Muscle Trunk	muscle
29	chr7:153078600-153079800	Enhancers	Fetal Muscle Leg	muscle
30	chr7:153078600-153082000	Enhancers	Adipose Nuclei	Adipose
31	chr7:153078800-153079000	Active TSS	Brain Anterior Caudate	brain
32	chr7:153078800-153079600	Enhancers	Duodenum Smooth Muscle	Duodenum
33	chr7:153078800-153083200	Weak transcription	HUES48 Cell Line	embryonic stem cell
34	chr7:153079000-153079200	Enhancers	Fetal Kidney	kidney
35	chr7:153079000-153079200	Flanking Active TSS	Rectal Smooth Muscle	rectum
36	chr7:153079000-153079200	Flanking Active TSS	Stomach Smooth Muscle	stomach
37	chr7:153079200-153081800	Enhancers	Rectal Smooth Muscle	rectum
38	chr7:153079200-153083200	Enhancers	Stomach Smooth Muscle	stomach
39	chr7:153079600-153080800	Weak transcription	Duodenum Smooth Muscle	Duodenum
40	chr7:153080200-153081000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr7:153080600-153080800	Enhancers	Spleen	Spleen
42	chr7:153080800-153081600	Enhancers	Duodenum Smooth Muscle	Duodenum
43	chr7:153081600-153082600	Weak transcription	Duodenum Smooth Muscle	Duodenum
44	chr7:153081800-153082400	Weak transcription	Rectal Smooth Muscle	rectum
45	chr7:153082000-153086000	Weak transcription	Colon Smooth Muscle	Colon
46	chr7:153082400-153082600	Enhancers	Rectal Smooth Muscle	rectum
47	chr7:153082400-153083800	Enhancers	K562	blood
48	chr7:153082600-153082800	Enhancers	Duodenum Smooth Muscle	Duodenum
49	chr7:153083200-153083800	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chr7:153083200-153085800	Weak transcription	Stomach Smooth Muscle	stomach

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