Variant report

Variant	nsv1034277
Chromosome Location	chr7:152932263-153526276
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2009)
CpG islands
(count:1284)
Chromatin interactive
region (count:324)
LncRNA
region (count:23)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2009 , 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	chr7:153109096-153109296	K562	blood:	n/a	n/a
2	ARID3A	chr7:153110322-153112174	K562	blood:	n/a	n/a
3	ARID3A	chr7:153078807-153079063	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:153103307-153103458	K562	blood:	n/a	n/a
5	ARID3A	chr7:153109739-153110062	K562	blood:	n/a	n/a
6	ARID3A	chr7:153143735-153143934	K562	blood:	n/a	n/a
7	ARID3A	chr7:153082623-153082873	K562	blood:	n/a	n/a
8	ARID3A	chr7:153104655-153106258	K562	blood:	n/a	n/a
9	ARID3A	chr7:153103753-153104234	K562	blood:	n/a	n/a
10	ARID3A	chr7:153108540-153108589	K562	blood:	n/a	n/a
11	ARID3A	chr7:153130385-153130583	K562	blood:	n/a	n/a
12	ARID3A	chr7:153043449-153043453	K562	blood:	n/a	n/a
13	ATF1	chr7:153154941-153155221	K562	blood:	n/a	n/a
14	ATF1	chr7:153110923-153111307	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	chr7:153308996-153309145	K562	blood:	n/a	n/a
18	ATF1	chr7:153130251-153130554	K562	blood:	n/a	n/a
19	ATF1	chr7:153034781-153034828	K562	blood:	n/a	n/a
20	ATF1	chr7:153119688-153120319	K562	blood:	n/a	n/a
21	ATF1	chr7:153074161-153074244	K562	blood:	n/a	n/a
22	ATF3	chr7:153119989-153120275	K562	blood:	n/a	n/a
23	BACH1	chr7:153133123-153133319	K562	blood:	n/a	n/a
24	BACH1	chr7:153097892-153097911	K562	blood:	n/a	n/a
25	BACH1	chr7:153113244-153113564	K562	blood:	n/a	n/a
26	BACH1	chr7:153110739-153112141	K562	blood:	n/a	n/a
27	BACH1	chr7:153244736-153244872	K562	blood:	n/a	n/a
28	BACH1	chr7:153203925-153204059	K562	blood:	n/a	n/a
29	BACH1	chr7:153055076-153055079	K562	blood:	n/a	n/a
30	BACH1	chr7:153099558-153099965	K562	blood:	n/a	n/a
31	BACH1	chr7:153109751-153110110	K562	blood:	n/a	n/a
32	BACH1	chr7:153031945-153032120	K562	blood:	n/a	n/a
33	BACH1	chr7:153111122-153111267	H1-hESC	embryonic stem cell:	n/a	n/a
34	BACH1	chr7:153200611-153200865	H1-hESC	embryonic stem cell:	n/a	n/a
35	BACH1	chr7:153108498-153108636	K562	blood:	n/a	n/a
36	BACH1	chr7:153463065-153463215	K562	blood:	n/a	n/a
37	BACH1	chr7:152998916-152998999	K562	blood:	n/a	n/a
38	BACH1	chr7:153100843-153101026	K562	blood:	n/a	n/a
39	BATF	chr7:153474050-153474399	GM12878	blood:	n/a	chr7:153474228-153474239
40	BATF	chr7:153337705-153337995	GM12878	blood:	n/a	n/a
41	BATF	chr7:153337727-153337979	GM12878	blood:	n/a	n/a
42	BCL11A	chr7:153474048-153474497	GM12878	blood:	n/a	n/a
43	BCL3	chr7:153101811-153102227	K562	blood:	n/a	n/a
44	BCL3	chr7:153505225-153505579	GM12878	blood:	n/a	n/a
45	BCL3	chr7:153104489-153105071	K562	blood:	n/a	n/a
46	BCL3	chr7:153103242-153103537	K562	blood:	n/a	n/a
47	BCL3	chr7:153109499-153110250	K562	blood:	n/a	n/a
48	BCL3	chr7:153505233-153505545	GM12878	blood:	n/a	n/a
49	BCL3	chr7:153105524-153106503	K562	blood:	n/a	n/a
50	BCLAF1	chr7:153107687-153111130	K562	blood:	n/a	n/a

(count:1284 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:153287752-153287802	ProgFib	skin:	n/a
2	chr7:153108726-153108776	HIPEpiC	eye:	n/a
3	chr7:153109375-153109425	GM12878	blood:	n/a
4	chr7:153287752-153287802	ProgFib	skin:	n/a
5	chr7:153108726-153108776	HIPEpiC	eye:	n/a
6	chr7:153109375-153109425	GM12878	blood:	n/a
7	chr7:153446256-153446306	HCM	heart:	n/a
8	chr7:153442389-153442439	PrEC	prostate:	n/a
9	chr7:153109375-153109425	PANC-1	pancreas:	n/a
10	chr7:153108684-153108734	NHBE	bronchial:	n/a
11	chr7:153109538-153109588	K562	blood:	n/a
12	chr7:153109538-153109588	Jurkat	blood:	n/a
13	chr7:153287591-153287641	HRE	kidney:	n/a
14	chr7:153446810-153446860	AG10803	skin:	n/a
15	chr7:153287529-153287579	HMEC	breast:	n/a
16	chr7:153446256-153446306	PrEC	prostate:	n/a
17	chr7:153109538-153109588	HPAEpiC	pulmonary alveolar:	n/a
18	chr7:153446106-153446156	HCM	heart:	n/a
19	chr7:153108684-153108734	GM19239	blood:	n/a
20	chr7:153446726-153446776	HEK293	kidney:	embryo
21	chr7:153287752-153287802	HIPEpiC	eye:	n/a
22	chr7:153287591-153287641	MCF10A-Er-Src	breast:	n/a
23	chr7:153108642-153108692	PrEC	prostate:	n/a
24	chr7:153442389-153442439	GM12892	blood:	n/a
25	chr7:153109538-153109588	HRCEpiC	kidney:	n/a
26	chr7:153110492-153110542	MCF10A-Er-Src	breast:	n/a
27	chr7:153449200-153449250	GM12891	blood:	n/a
28	chr7:153449200-153449250	NH-A	brain:	n/a
29	chr7:153108642-153108692	SK-N-SH_RA	brain:	n/a
30	chr7:153110762-153110812	HIPEpiC	eye:	n/a
31	chr7:153110762-153110812	HL-60	blood:	n/a
32	chr7:153287529-153287579	AG04449	skin:	fetal
33	chr7:153446810-153446860	AG09319	gingival:	n/a
34	chr7:153446726-153446776	AG09309	skin:	n/a
35	chr7:153110492-153110542	HIPEpiC	eye:	n/a
36	chr7:153445197-153445247	HepG2	liver:	n/a
37	chr7:153287752-153287802	HepG2	liver:	n/a
38	chr7:153012895-153012945	K562	blood:	n/a
39	chr7:153109538-153109588	GM12891	blood:	n/a
40	chr7:153446726-153446776	HIPEpiC	eye:	n/a
41	chr7:153287752-153287802	HEK293	kidney:	embryo
42	chr7:153445197-153445247	HRPEpiC	eye:	n/a
43	chr7:153442389-153442439	AG04450	lung:	fetal
44	chr7:153446726-153446776	SK-N-MC	brain:	n/a
45	chr7:153287529-153287579	BE2_C	brain:	n/a
46	chr7:153110994-153111044	ProgFib	skin:	n/a
47	chr7:153078797-153078847	NH-A	brain:	n/a
48	chr7:153110762-153110812	ECC-1	luminal epithelium:	n/a
49	chr7:153446726-153446776	AG04449	skin:	fetal
50	chr7:153110994-153111044	Jurkat	blood:	n/a

(count:324 , 50 per page) page: 1 2 3 4 5 6 7

No.	Distal block	Cell Line	Cell type
1	chr7:153291103..153293422-chr7:153317816..153319821,2	K562	blood:
2	chr7:153102748..153104810-chr7:153194160..153196266,2	K562	blood:
3	chr7:153244368..153246054-chr7:153249661..153252423,2	K562	blood:
4	chr7:153100820..153103410-chr7:153246584..153249087,2	K562	blood:
5	chr7:153100739..153103301-chr7:153343816..153346301,2	K562	blood:
6	chr7:153077622..153081135-chr7:153081678..153084143,4	K562	blood:
7	chr7:153103866..153106849-chr7:153334968..153337420,2	K562	blood:
8	chr7:152993926..152995856-chr7:152996006..152997666,2	K562	blood:
9	chr7:153103375..153106774-chr7:153173661..153176724,3	K562	blood:
10	chr7:153104483..153106622-chr7:154809652..154811276,2	K562	blood:
11	chr7:153095496..153100083-chr7:153227240..153231404,4	K562	blood:
12	chr2:84103331..84106345-chr7:153106704..153111137,6	K562	blood:
13	chr7:153099940..153103347-chr7:153340908..153343699,3	K562	blood:
14	chr7:153361300..153363555-chr7:153366208..153367723,2	K562	blood:
15	chr7:153054753..153057546-chr7:153057782..153059510,2	K562	blood:
16	chr17:58469104..58471678-chr7:153043936..153045780,2	MCF-7	breast:
17	chr7:153341235..153342881-chr7:153346431..153348736,2	K562	blood:
18	chr7:152948657..152952054-chr7:152952493..152957481,5	K562	blood:
19	chr7:153089054..153091644-chr7:153185631..153188291,2	K562	blood:
20	chr7:153104593..153107356-chr7:153151532..153153946,4	K562	blood:
21	chr7:153044919..153047709-chr7:153054180..153055947,2	K562	blood:
22	chr7:152938733..152940838-chr7:153103273..153105378,2	K562	blood:
23	chr7:153102721..153106606-chr7:153212905..153219163,7	K562	blood:
24	chr7:153054222..153056316-chr7:153099590..153102499,2	K562	blood:
25	chr7:153119320..153121928-chr7:153170985..153172845,2	K562	blood:
26	chr7:153111734..153114146-chr7:153170231..153173109,2	K562	blood:
27	chr7:153137391..153141168-chr7:153141506..153146066,7	K562	blood:
28	chr7:153366174..153368925-chr7:153372775..153374765,2	K562	blood:
29	chr7:153095496..153100083-chr7:153227240..153231404,4	K562	blood:
30	chr7:153298050..153299925-chr7:153304254..153305961,2	K562	blood:
31	chr7:153107803..153110775-chr7:153221727..153224014,2	K562	blood:
32	chr7:153103515..153106229-chr7:153225211..153227248,2	K562	blood:
33	chr7:153106993..153109091-chr7:153192344..153194750,2	K562	blood:
34	chr7:153103413..153106073-chr7:153238288..153241221,2	K562	blood:
35	chr7:153029560..153032040-chr7:153105014..153106931,2	K562	blood:
36	chr7:152595309..152597143-chr7:153102901..153104884,2	K562	blood:
37	chr7:153103154..153105187-chr7:153228223..153229957,2	K562	blood:
38	chr7:152592588..152594175-chr7:153102302..153103832,2	K562	blood:
39	chr7:153100739..153103301-chr7:153343816..153346301,2	K562	blood:
40	chr7:153055542..153057416-chr7:153103974..153105838,2	K562	blood:
41	chr7:153016352..153018288-chr7:153019848..153021405,2	K562	blood:
42	chr7:153102564..153104715-chr7:153192183..153194069,2	K562	blood:
43	chr7:153298050..153299925-chr7:153304254..153305961,2	K562	blood:
44	chr7:153102849..153104905-chr7:153187331..153188983,2	K562	blood:
45	chr7:153133971..153136584-chr7:153144727..153146368,2	K562	blood:
46	chr16:1825198..1826827-chr7:153150973..153152473,2	K562	blood:
47	chr7:153033175..153035096-chr7:153059959..153061462,2	K562	blood:
48	chr7:153374613..153377425-chr7:153379537..153382036,2	K562	blood:
49	chr7:153100664..153102886-chr7:154843246..154845747,2	K562	blood:
50	chr7:153244368..153246054-chr7:153249661..153252423,2	K562	blood:

(count:23 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-XRCC2-2	chr7:153120803-153121101	XLOC_006657
2	lnc-XRCC2-1	chr7:153102577-153102683	ENSG00000234722.3
3	lnc-XRCC2-3	chr7:153220300-153220910	XLOC_006658
4	lnc-XRCC2-4	chr7:153406738-153407404	XLOC_006659
5	lnc-XRCC2-1	chr7:153097005-153097631	ENSG00000234722
6	lnc-DPP6-3	chr7:153086676-153086815	XLOC_006297
7	lnc-XRCC2-1	chr7:153109176-153109319	ENSG00000234722.3
8	lnc-XRCC2-1	chr7:153097005-153097631	ENSG00000234722.3
9	lnc-XRCC2-1	chr7:153104041-153104169	ENSG00000234722.3
10	lnc-DPP6-7	chr7:153146514-153146960	NONHSAT124301
11	lnc-XRCC2-1	chr7:153102577-153102683	ENSG00000234722
12	lnc-XRCC2-2	chr7:153125396-153125424	XLOC_006657
13	lnc-XRCC2-1	chr7:153110698-153111021	ENSG00000234722
14	lnc-DPP6-3	chr7:153092527-153092639	XLOC_006297
15	lnc-XRCC2-3	chr7:153221094-153221300	XLOC_006658
16	lnc-DPP6-2	chr7:153120526-153120601	XLOC_006298
17	lnc-XRCC2-4	chr7:153413334-153413531	XLOC_006659
18	lnc-XRCC2-1	chr7:153109178-153109319	ENSG00000234722
19	lnc-DPP6-2	chr7:153119376-153119626	XLOC_006298
20	lnc-XRCC2-1	chr7:153102578-153102683	ENSG00000234722
21	lnc-DPP6-3	chr7:153092498-153092703	XLOC_006297
22	lnc-DPP6-3	chr7:153093149-153093207	XLOC_006297
23	lnc-XRCC2-1	chr7:153104041-153104171	ENSG00000234722

No data

Variant related genes	Relation type
ENSG00000233489	TF binding region
ENSG00000234722	TF binding region
ENSG00000233489	CpG island
ENSG00000234722	CpG island
ENSG00000223700	chromatin interactions
ENSG00000141371	chromatin interactions
ENSG00000236198	chromatin interactions
ENSG00000171222	chromatin interactions
ENSG00000234722	chromatin interactions
ENSG00000233489	chromatin interactions
ENSG00000155380	chromatin interactions
ENSG00000197774	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000234338	chromatin interactions
ENSG00000132256	chromatin interactions
ENSG00000222281	chromatin interactions
ENSG00000170832	chromatin interactions
ENSG00000261455	chromatin interactions
LRRC1	miRNA target sites
DHX57	miRNA target sites
CCT2	miRNA target sites
CDKN1A	miRNA target sites
APAF1	miRNA target sites

Extended variants
information (count: 9323 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:9323 , 50 per page) page: 1 2 3 4 5 6 7 ... 187

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2710242	chr7:152941413-152941414	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs184484709	chr7:152941427-152941428	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs188944612	chr7:152941428-152941429	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs547129633	chr7:152941444-152941445	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs568428100	chr7:152941446-152941447	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs565255232	chr7:152941470-152941471	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs543622584	chr7:152941476-152941477	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs377163906	chr7:152941486-152941487	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs35554507	chr7:152941515-152941516	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs569293533	chr7:152941563-152941564	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs374122225	chr7:152941568-152941569	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs367666484	chr7:152941583-152941584	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs577293020	chr7:152941584-152941585	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs537189417	chr7:152941590-152941591	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs118107273	chr7:152941597-152941598	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs182216535	chr7:152941617-152941618	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs117468394	chr7:152941654-152941655	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs79264340	chr7:152941659-152941660	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs574806420	chr7:152941694-152941695	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs542123942	chr7:152941728-152941729	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs563709297	chr7:152941749-152941750	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs187206796	chr7:152941754-152941755	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs546326515	chr7:152941756-152941757	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs564429005	chr7:152941769-152941770	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs528549256	chr7:152941780-152941781	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs190822318	chr7:152941799-152941800	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs568290477	chr7:152941841-152941842	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs529575237	chr7:152941852-152941853	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs577354950	chr7:152941877-152941878	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs550853345	chr7:152941885-152941886	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs569679880	chr7:152941886-152941887	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs374524455	chr7:152941902-152941903	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs180858496	chr7:152941956-152941957	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs146996069	chr7:152941993-152941994	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs570471485	chr7:152942040-152942041	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs185658672	chr7:152942077-152942078	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs553232661	chr7:152942086-152942087	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs574672869	chr7:152942116-152942117	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs542189174	chr7:152942136-152942137	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs557291916	chr7:152942147-152942148	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs137989202	chr7:152942152-152942153	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs545890767	chr7:152942182-152942183	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs564475717	chr7:152942201-152942202	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs528603337	chr7:152942202-152942203	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs540312263	chr7:152942206-152942207	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs373761901	chr7:152942218-152942219	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs190022048	chr7:152942223-152942224	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs529442601	chr7:152942316-152942317	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs143557972	chr7:152942317-152942318	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs569458459	chr7:152942329-152942330	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

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
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Chordoma	21215367	CNVD
Breast cancer	21509527	CNVD
Autism	20531469	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
Attention deficit hyperactivity disorder	22138692	CNVD

Chromatin state (count:490 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:152941400-152943400	Enhancers	Placenta	Placenta
2	chr7:152942800-152943400	Enhancers	Skeletal Muscle Female	skeletal muscle
3	chr7:152943400-152943800	Weak transcription	Placenta	Placenta
4	chr7:152943800-152945200	Enhancers	Placenta	Placenta
5	chr7:152945200-152945600	Weak transcription	Placenta	Placenta
6	chr7:152945600-152945800	Enhancers	Placenta	Placenta
7	chr7:152945800-152948600	Weak transcription	Placenta	Placenta
8	chr7:152948600-152948800	Enhancers	Placenta	Placenta
9	chr7:152950200-152950400	Enhancers	Pancreas	Pancrea
10	chr7:152950400-152950600	Weak transcription	Pancreas	Pancrea
11	chr7:152952400-152954800	Enhancers	Primary hematopoietic stem cells short term culture	blood
12	chr7:152953200-152953600	Enhancers	Primary hematopoietic stem cells	blood
13	chr7:152955800-152956200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr7:152955800-152956200	Enhancers	Brain Anterior Caudate	brain
15	chr7:152955800-152956200	Enhancers	Brain Cingulate Gyrus	brain
16	chr7:152955800-152956400	Enhancers	H1 Cell Line	embryonic stem cell
17	chr7:152955800-152956400	Enhancers	H9 Cell Line	embryonic stem cell
18	chr7:152955800-152956400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr7:152955800-152956400	Enhancers	Brain Substantia Nigra	brain
20	chr7:152955800-152956600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr7:152956000-152956400	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr7:152956000-152956400	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr7:152956000-152956400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr7:152956400-152961400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr7:152961400-152962000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
26	chr7:152961600-152961800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr7:152961800-152964600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr7:152962000-152962800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr7:152964600-152964800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr7:152986200-152986800	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr7:152986400-152987000	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr7:152986400-152987000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
33	chr7:152986800-152987000	Enhancers	Primary hematopoietic stem cells	blood
34	chr7:152986800-152987600	Enhancers	Primary hematopoietic stem cells short term culture	blood
35	chr7:152987000-152987200	Enhancers	HSMM	muscle
36	chr7:152987600-152987800	Enhancers	Primary hematopoietic stem cells	blood
37	chr7:152992800-152993000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr7:152993000-152994400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr7:152993600-152994800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr7:152994000-152994400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr7:152994200-152994600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr7:152994200-152995600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr7:152994400-152994800	Enhancers	Placenta	Placenta
44	chr7:152994400-152995600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr7:152995200-152996200	Enhancers	Fetal Kidney	kidney
46	chr7:152995600-152997600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr7:152997600-152999600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr7:152998000-152999200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr7:152998200-152998400	Enhancers	Fetal Kidney	kidney
50	chr7:152999000-152999400	Active TSS	Pancreatic Islets	Pancreatic Islet

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