Variant report

Variant	nsv532218
Chromosome Location	chr7:122360779-122934247
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3302)
CpG islands
(count:2199)
Chromatin interactive
region (count:164)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3302 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:122525653-122525930	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:122443416-122443772	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:122527046-122527681	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:122526484-122526694	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:122467950-122468098	HepG2	liver:	n/a	n/a
6	ARID3A	chr7:122523982-122524287	HepG2	liver:	n/a	n/a
7	ARID3A	chr7:122397065-122397362	HepG2	liver:	n/a	n/a
8	ARID3A	chr7:122794371-122794672	HepG2	liver:	n/a	n/a
9	ARID3A	chr7:122431984-122432331	HepG2	liver:	n/a	n/a
10	ARID3A	chr7:122488996-122489769	HepG2	liver:	n/a	n/a
11	ARID3A	chr7:122831360-122831634	HepG2	liver:	n/a	n/a
12	ATF1	chr7:122854532-122854595	K562	blood:	n/a	n/a
13	ATF1	chr7:122641820-122641853	K562	blood:	n/a	n/a
14	ATF1	chr7:122794273-122794661	K562	blood:	n/a	n/a
15	ATF2	chr7:122794171-122794733	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr7:122830143-122830769	GM12878	blood:	n/a	n/a
17	ATF2	chr7:122794188-122794655	GM12878	blood:	n/a	n/a
18	ATF2	chr7:122794208-122794716	GM12878	blood:	n/a	n/a
19	ATF2	chr7:122794224-122794703	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF2	chr7:122829987-122830921	GM12878	blood:	n/a	n/a
21	ATF3	chr7:122925096-122925470	H1-hESC	embryonic stem cell:	n/a	n/a
22	ATF3	chr7:122794194-122794569	K562	blood:	n/a	n/a
23	BACH1	chr7:122410986-122410996	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr7:122526369-122527153	H1-hESC	embryonic stem cell:	n/a	n/a
25	BATF	chr7:122694975-122695283	GM12878	blood:	n/a	n/a
26	BATF	chr7:122830203-122830589	GM12878	blood:	n/a	n/a
27	BATF	chr7:122387086-122387293	GM12878	blood:	n/a	n/a
28	BATF	chr7:122832135-122832453	GM12878	blood:	n/a	n/a
29	BATF	chr7:122387043-122387275	GM12878	blood:	n/a	n/a
30	BATF	chr7:122365495-122365692	GM12878	blood:	n/a	n/a
31	BATF	chr7:122715926-122716183	GM12878	blood:	n/a	n/a
32	BCL11A	chr7:122386912-122387429	GM12878	blood:	n/a	n/a
33	BCL11A	chr7:122830207-122830527	GM12878	blood:	n/a	n/a
34	BCL11A	chr7:122386981-122387296	GM12878	blood:	n/a	n/a
35	BCL11A	chr7:122407461-122407732	H1-hESC	embryonic stem cell:	n/a	n/a
36	BCL11A	chr7:122407372-122407682	H1-hESC	embryonic stem cell:	n/a	n/a
37	BCL3	chr7:122680639-122680893	GM12878	blood:	n/a	n/a
38	BCLAF1	chr7:122830191-122830909	GM12878	blood:	n/a	n/a
39	BHLHE40	chr7:122799350-122799527	GM12878	blood:	n/a	n/a
40	BHLHE40	chr7:122582848-122583160	HepG2	liver:	n/a	n/a
41	BHLHE40	chr7:122361311-122361406	HepG2	liver:	n/a	n/a
42	BHLHE40	chr7:122542972-122542982	GM12878	blood:	n/a	n/a
43	BHLHE40	chr7:122710767-122711008	GM12878	blood:	n/a	n/a
44	BHLHE40	chr7:122804175-122804176	GM12878	blood:	n/a	n/a
45	BHLHE40	chr7:122387024-122387362	GM12878	blood:	n/a	n/a
46	BHLHE40	chr7:122409003-122409090	GM12878	blood:	n/a	n/a
47	BHLHE40	chr7:122526507-122526841	GM12878	blood:	n/a	chr7:122526577-122526593 chr7:122526691-122526707
48	BHLHE40	chr7:122527388-122527560	K562	blood:	n/a	n/a
49	BHLHE40	chr7:122526388-122527567	HepG2	liver:	n/a	chr7:122526436-122526452 chr7:122526444-122526460 chr7:122526577-122526593 chr7:122526691-122526707 chr7:122526477-122526493
50	BHLHE40	chr7:122542886-122543077	K562	blood:	n/a	n/a

(count:2199 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:122526826-122526876	SKMC	muscle:	n/a
2	chr7:122443513-122443563	A549	lung:	n/a
3	chr7:122635522-122635572	SK-N-SH_RA	brain:	n/a
4	chr7:122526826-122526876	SKMC	muscle:	n/a
5	chr7:122443513-122443563	A549	lung:	n/a
6	chr7:122635522-122635572	SK-N-SH_RA	brain:	n/a
7	chr7:122527499-122527549	HCM	heart:	n/a
8	chr7:122525949-122525999	LNCaP	prostate:	n/a
9	chr7:122526824-122526874	HCPEpiC	choroid plexus:	n/a
10	chr7:122526763-122526813	HPAEpiC	pulmonary alveolar:	n/a
11	chr7:122495315-122495365	HEEpiC	esophagus:	n/a
12	chr7:122525949-122525999	HL-60	blood:	n/a
13	chr7:122525949-122525999	AG09319	gingival:	n/a
14	chr7:122529707-122529757	MCF-7	breast:	n/a
15	chr7:122529707-122529757	HRPEpiC	eye:	n/a
16	chr7:122527522-122527572	HEK293	kidney:	embryo
17	chr7:122495315-122495365	NHDF-neo	bronchial:	n/a
18	chr7:122636635-122636685	NT2-D1	testis:	n/a
19	chr7:122526033-122526083	U87	brain:	n/a
20	chr7:122635522-122635572	SAEC	small airway:	n/a
21	chr7:122384836-122384886	GM06990	blood:	n/a
22	chr7:122526836-122526886	HCM	heart:	n/a
23	chr7:122526940-122526990	AG09319	gingival:	n/a
24	chr7:122443513-122443563	GM19239	blood:	n/a
25	chr7:122388911-122388961	HepG2	liver:	n/a
26	chr7:122526408-122526458	PrEC	prostate:	n/a
27	chr7:122495315-122495365	PFSK-1	brain:	n/a
28	chr7:122526572-122526622	NHBE	bronchial:	n/a
29	chr7:122553915-122553965	RPTEC	kidney:	n/a
30	chr7:122900147-122900197	T-47D	breast:	n/a
31	chr7:122635522-122635572	Hela-S3	cervix:	n/a
32	chr7:122525949-122525999	Hepatocyte	liver:	n/a
33	chr7:122526824-122526874	SK-N-MC	brain:	n/a
34	chr7:122526940-122526990	NT2-D1	testis:	n/a
35	chr7:122526836-122526886	NHDF-neo	bronchial:	n/a
36	chr7:122553915-122553965	NT2-D1	testis:	n/a
37	chr7:122635522-122635572	ProgFib	skin:	n/a
38	chr7:122525974-122526024	HAEpiC	amniotic membrane:	n/a
39	chr7:122840109-122840159	SK-N-SH_RA	brain:	n/a
40	chr7:122525974-122526024	SAEC	small airway:	n/a
41	chr7:122636106-122636156	CMK	blood:	n/a
42	chr7:122636106-122636156	HMEC	breast:	n/a
43	chr7:122840109-122840159	GM19239	blood:	n/a
44	chr7:122635522-122635572	K562	blood:	n/a
45	chr7:122636635-122636685	Hepatocyte	liver:	n/a
46	chr7:122526763-122526813	T-47D	breast:	n/a
47	chr7:122526940-122526990	Hepatocyte	liver:	n/a
48	chr7:122587034-122587084	Hela-S3	cervix:	n/a
49	chr7:122527437-122527487	MCF-7	breast:	n/a
50	chr7:122524465-122524515	HCPEpiC	choroid plexus:	n/a

(count:164 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr7:122831362..122833476-chr7:122921040..122923721,2	MCF-7	breast:
2	chr7:122749840..122752839-chr7:122755099..122756855,2	K562	blood:
3	chr7:122471973..122475729-chr7:122484629..122488935,3	MCF-7	breast:
4	chr7:122482166..122484643-chr7:122531331..122532997,2	MCF-7	breast:
5	chr7:122829890..122831991-chr7:122835864..122837812,2	MCF-7	breast:
6	chr7:122443038..122444017-chr7:122710508..122711379,2	MCF-7	breast:
7	chr7:122922049..122923946-chr7:123011655..123013916,2	MCF-7	breast:
8	chr7:122597821..122600156-chr7:122601223..122603863,2	K562	blood:
9	chr7:122645062..122647735-chr7:122648443..122650987,2	K562	blood:
10	chr7:122710491..122711428-chr7:122770859..122771842,5	MCF-7	breast:
11	chr17:57920427..57922384-chr7:122390814..122393151,2	MCF-7	breast:
12	chr7:122382528..122384037-chr7:122398742..122400591,2	K562	blood:
13	chr7:122465847..122467550-chr7:122468926..122470489,2	MCF-7	breast:
14	chr7:122384641..122386460-chr7:122390684..122392862,2	K562	blood:
15	chr6:39197015..39197718-chr7:122735976..122736762,2	MCF-7	breast:
16	chr7:122833161..122834794-chr7:122835471..122837860,2	MCF-7	breast:
17	chr7:122697734..122699274-chr7:122700681..122702675,2	K562	blood:
18	chr7:122521246..122525169-chr7:122525278..122528321,3	MCF-7	breast:
19	chr7:122443209..122443881-chr7:122793957..122794553,2	MCF-7	breast:
20	chr7:122833161..122834794-chr7:122835471..122837860,2	MCF-7	breast:
21	chr14:94300599..94301313-chr7:122638050..122638667,2	MCF-7	breast:
22	chr7:122782662..122784626-chr7:122790468..122792424,2	MCF-7	breast:
23	chr7:122659402..122661138-chr7:122672194..122673932,2	K562	blood:
24	chr7:122789422..122791875-chr7:122803775..122805608,2	K562	blood:
25	chr7:122691550..122694011-chr7:122697023..122699631,2	MCF-7	breast:
26	chr20:52194928..52195546-chr7:122848642..122849152,2	MCF-7	breast:
27	chr7:122469925..122472134-chr7:122472549..122474182,2	MCF-7	breast:
28	chr7:122710606..122711512-chr7:122794280..122795375,4	MCF-7	breast:
29	chr7:122427597..122429988-chr7:122525727..122527279,2	MCF-7	breast:
30	chr7:122483143..122485209-chr7:122487221..122489725,2	MCF-7	breast:
31	chr7:122870849..122871836-chr7:123007323..123008263,3	MCF-7	breast:
32	chr7:122465847..122467550-chr7:122468926..122470489,2	MCF-7	breast:
33	chr7:122484005..122486884-chr7:122524580..122527500,2	MCF-7	breast:
34	chr7:122450452..122452718-chr7:122483355..122485678,2	MCF-7	breast:
35	chr7:122484843..122489106-chr7:122489595..122492470,4	MCF-7	breast:
36	chr7:122542099..122544437-chr7:122545966..122548062,2	K562	blood:
37	chr7:122471973..122475729-chr7:122484629..122488935,3	MCF-7	breast:
38	chr7:122792145..122793696-chr7:122798762..122801174,2	K562	blood:
39	chr10:134134492..134135246-chr7:122429520..122430067,2	MCF-7	breast:
40	chr7:122446373..122448694-chr7:122464114..122466557,2	MCF-7	breast:
41	chr7:122697734..122699274-chr7:122700681..122702675,2	K562	blood:
42	chr7:122544561..122547077-chr7:122568138..122570128,2	K562	blood:
43	chr20:45901177..45901824-chr7:122709196..122709916,2	MCF-7	breast:
44	chr7:122502243..122503856-chr7:122522076..122524661,2	MCF-7	breast:
45	chr7:122443541..122445086-chr7:122446749..122448778,2	K562	blood:
46	chr7:122708056..122711001-chr7:122717308..122719180,2	K562	blood:
47	chr7:122789422..122791875-chr7:122803775..122805608,2	K562	blood:
48	chr7:122710491..122711428-chr7:122770859..122771842,5	MCF-7	breast:
49	chr7:122556884..122558896-chr7:122561512..122564135,2	K562	blood:
50	chr7:122834027..122836988-chr7:122837135..122840063,2	K562	blood:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC13A1-1	chr7:122743580-122743643	XLOC_006586
2	lnc-SLC13A1-1	chr7:122709303-122709567	ENSG00000226680
3	lnc-SLC13A1-1	chr7:122710065-122710169	ENSG00000226680
4	lnc-SLC13A1-1	chr7:122709303-122709567	XLOC_006586
5	lnc-SLC13A1-1	chr7:122710065-122710169	XLOC_006586
6	lnc-SLC13A1-1	chr7:122742515-122742585	ENSG00000226680
7	lnc-SLC13A1-1	chr7:122711179-122711253	XLOC_006586
8	lnc-SLC13A1-2	chr7:122870174-122870795	NONHSAT123040
9	lnc-SLC13A1-1	chr7:122743580-122743643	ENSG00000226680

No data

Variant related genes	Relation type
LYPLA1P1	TF binding region
ENSG00000227573	TF binding region
ENSG00000226680	TF binding region
CADPS2	TF binding region
TAS2R16	TF binding region
SLC13A1	TF binding region
LYPLA1P1	CpG island
ENSG00000227573	CpG island
ENSG00000226680	CpG island
CADPS2	CpG island
TAS2R16	CpG island
SLC13A1	CpG island
ENSG00000236383	chromatin interactions
ENSG00000133805	chromatin interactions
ENSG00000081803	chromatin interactions
ENSG00000164626	chromatin interactions
ENSG00000227573	chromatin interactions
ENSG00000223595	chromatin interactions
ENSG00000081800	chromatin interactions
USP15	miRNA target sites
USF2	miRNA target sites
USP24	miRNA target sites

Extended variants
information (count: 15591 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:15591 , 50 per page) page: 1 2 3 4 5 6 7 ... 312

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs35325666	chr7:122360779-122360780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs527883990	chr7:122360782-122360783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs67549880	chr7:122360815-122360816	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs536378331	chr7:122360821-122360822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs552780437	chr7:122360839-122360840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs75144481	chr7:122360848-122360849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs567939480	chr7:122360930-122360931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs375827339	chr7:122360967-122360968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs34300133	chr7:122360975-122360976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs575573714	chr7:122360977-122360978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs372841268	chr7:122360981-122360982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs372159687	chr7:122360988-122360989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs10268190	chr7:122361000-122361001	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs563730646	chr7:122361007-122361008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs185308171	chr7:122361010-122361011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs377374156	chr7:122361014-122361015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs543148875	chr7:122361070-122361071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs112339629	chr7:122361122-122361123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs559420860	chr7:122361132-122361133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs7797250	chr7:122361213-122361214	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs551520855	chr7:122361219-122361220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs565254046	chr7:122361257-122361258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs531262524	chr7:122361294-122361295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs550973620	chr7:122361303-122361304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs369170034	chr7:122361321-122361322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs567292556	chr7:122361332-122361333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs373664903	chr7:122361340-122361341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs559558187	chr7:122361353-122361354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs535864394	chr7:122361387-122361388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs546721733	chr7:122361390-122361391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs549202299	chr7:122361407-122361408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs566532242	chr7:122361412-122361413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs567964033	chr7:122361419-122361420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs190669393	chr7:122361420-122361421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs181553440	chr7:122361437-122361438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs538175901	chr7:122361447-122361448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs187593299	chr7:122361470-122361471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs574025728	chr7:122361517-122361518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs191920856	chr7:122361565-122361566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs13223497	chr7:122361570-122361571	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs576742720	chr7:122361571-122361572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs183908930	chr7:122361574-122361575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs55926419	chr7:122361578-122361579	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs56353151	chr7:122361579-122361580	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs187664043	chr7:122361592-122361593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs541953901	chr7:122361613-122361614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs189651300	chr7:122361658-122361659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs529700756	chr7:122361659-122361660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs572130798	chr7:122361672-122361673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs182702182	chr7:122361691-122361692	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
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	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
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelodysplastic syndrome	21251322	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Biliary cancer	19435499	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	23792589	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Non-small cell lung cancer	19889201	CNVD
Acute myeloid leukemia	18000384	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Metastatic melanoma	18483359	CNVD
Autism	18414403	CNVD
Autism	19401682	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
Glioblastoma multiforme	21922591	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21509527	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Acute monocytic leukemia	16498392	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Pancreatic cancer	17952125	CNVD
Chordoma	21215367	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1772 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:122359600-122376000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr7:122359600-122376200	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr7:122359800-122366200	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr7:122359800-122375000	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr7:122362400-122367000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr7:122364600-122365000	Enhancers	Fetal Kidney	kidney
7	chr7:122365000-122365400	Weak transcription	Fetal Kidney	kidney
8	chr7:122365400-122365600	Enhancers	Fetal Kidney	kidney
9	chr7:122365600-122366000	Enhancers	Pancreas	Pancrea
10	chr7:122365600-122366000	Enhancers	Right Atrium	heart
11	chr7:122365600-122376200	Weak transcription	Fetal Kidney	kidney
12	chr7:122366000-122384200	Weak transcription	Pancreas	Pancrea
13	chr7:122366200-122367400	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr7:122366400-122367800	Enhancers	Fetal Heart	heart
15	chr7:122367000-122367200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr7:122367200-122373600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr7:122367600-122368200	Enhancers	Stomach Mucosa	stomach
18	chr7:122368200-122378800	Weak transcription	Stomach Mucosa	stomach
19	chr7:122369200-122377400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr7:122370600-122371400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr7:122370600-122371800	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr7:122371200-122371800	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr7:122371800-122374800	Weak transcription	HUES64 Cell Line	embryonic stem cell
24	chr7:122371800-122374800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
25	chr7:122372000-122386600	Weak transcription	Ovary	ovary
26	chr7:122373000-122373600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
27	chr7:122373400-122373800	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
28	chr7:122373600-122373800	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
29	chr7:122373600-122374000	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
30	chr7:122373600-122374000	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr7:122373600-122374000	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
32	chr7:122373800-122375000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
33	chr7:122373800-122376200	Weak transcription	H1 Cell Line	embryonic stem cell
34	chr7:122374000-122375000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
35	chr7:122374000-122375000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
36	chr7:122374600-122377800	Weak transcription	Placenta Amnion	Placenta Amnion
37	chr7:122374800-122376200	Enhancers	HUES64 Cell Line	embryonic stem cell
38	chr7:122374800-122376600	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr7:122374800-122380000	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr7:122375000-122376000	Enhancers	iPS-20b Cell Line	embryonic stem cell
41	chr7:122375000-122376600	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr7:122375000-122379800	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr7:122375000-122380000	Enhancers	HUES6 Cell Line	embryonic stem cell
44	chr7:122375200-122378400	Weak transcription	HepG2	liver
45	chr7:122376000-122377000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
46	chr7:122376000-122378400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
47	chr7:122376200-122376400	Enhancers	H9 Cell Line	embryonic stem cell
48	chr7:122376200-122376400	Enhancers	Fetal Kidney	kidney
49	chr7:122376200-122377000	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
50	chr7:122376200-122379600	Enhancers	H1 Cell Line	embryonic stem cell

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