Variant report

Variant	nsv1033520
Chromosome Location	chr7:122366544-122992937
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3432)
CpG islands
(count:2260)
Chromatin interactive
region (count:174)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3432 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

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	chr7:122794371-122794672	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:122443416-122443772	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:122431984-122432331	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:122397065-122397362	HepG2	liver:	n/a	n/a
6	ARID3A	chr7:122526484-122526694	HepG2	liver:	n/a	n/a
7	ARID3A	chr7:122831360-122831634	HepG2	liver:	n/a	n/a
8	ARID3A	chr7:122488996-122489769	HepG2	liver:	n/a	n/a
9	ARID3A	chr7:122527046-122527681	HepG2	liver:	n/a	n/a
10	ARID3A	chr7:122523982-122524287	HepG2	liver:	n/a	n/a
11	ARID3A	chr7:122467950-122468098	HepG2	liver:	n/a	n/a
12	ATF1	chr7:122641820-122641853	K562	blood:	n/a	n/a
13	ATF1	chr7:122854532-122854595	K562	blood:	n/a	n/a
14	ATF1	chr7:122794273-122794661	K562	blood:	n/a	n/a
15	ATF2	chr7:122829987-122830921	GM12878	blood:	n/a	n/a
16	ATF2	chr7:122794224-122794703	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr7:122794171-122794733	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF2	chr7:122794208-122794716	GM12878	blood:	n/a	n/a
19	ATF2	chr7:122794188-122794655	GM12878	blood:	n/a	n/a
20	ATF2	chr7:122830143-122830769	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	chr7:122526369-122527153	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr7:122410986-122410996	H1-hESC	embryonic stem cell:	n/a	n/a
25	BATF	chr7:122830203-122830589	GM12878	blood:	n/a	n/a
26	BATF	chr7:122954973-122955249	GM12878	blood:	n/a	n/a
27	BATF	chr7:122694975-122695283	GM12878	blood:	n/a	n/a
28	BATF	chr7:122387043-122387275	GM12878	blood:	n/a	n/a
29	BATF	chr7:122955021-122955264	GM12878	blood:	n/a	n/a
30	BATF	chr7:122387086-122387293	GM12878	blood:	n/a	n/a
31	BATF	chr7:122832135-122832453	GM12878	blood:	n/a	n/a
32	BATF	chr7:122715926-122716183	GM12878	blood:	n/a	n/a
33	BCL11A	chr7:122830207-122830527	GM12878	blood:	n/a	n/a
34	BCL11A	chr7:122386912-122387429	GM12878	blood:	n/a	n/a
35	BCL11A	chr7:122407372-122407682	H1-hESC	embryonic stem cell:	n/a	n/a
36	BCL11A	chr7:122407461-122407732	H1-hESC	embryonic stem cell:	n/a	n/a
37	BCL11A	chr7:122386981-122387296	GM12878	blood:	n/a	n/a
38	BCL3	chr7:122680639-122680893	GM12878	blood:	n/a	n/a
39	BCLAF1	chr7:122830191-122830909	GM12878	blood:	n/a	n/a
40	BHLHE40	chr7:122542886-122543077	K562	blood:	n/a	n/a
41	BHLHE40	chr7:122387024-122387362	GM12878	blood:	n/a	n/a
42	BHLHE40	chr7:122799350-122799527	GM12878	blood:	n/a	n/a
43	BHLHE40	chr7:122409003-122409090	GM12878	blood:	n/a	n/a
44	BHLHE40	chr7:122804175-122804176	GM12878	blood:	n/a	n/a
45	BHLHE40	chr7:122582848-122583160	HepG2	liver:	n/a	n/a
46	BHLHE40	chr7:122710767-122711008	GM12878	blood:	n/a	n/a
47	BHLHE40	chr7:122527388-122527560	K562	blood:	n/a	n/a
48	BHLHE40	chr7:122526507-122526841	GM12878	blood:	n/a	chr7:122526577-122526593 chr7:122526691-122526707
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	chr7:122542972-122542982	GM12878	blood:	n/a	n/a

(count:2260 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:122526824-122526874	A549	lung:	n/a
2	chr7:122526826-122526876	MCF-7	breast:	n/a
3	chr7:122526033-122526083	IMR90	lung:	fetal
4	chr7:122526824-122526874	A549	lung:	n/a
5	chr7:122526826-122526876	MCF-7	breast:	n/a
6	chr7:122526033-122526083	IMR90	lung:	fetal
7	chr7:122635522-122635572	Caco-2	colon:	n/a
8	chr7:122636635-122636685	HCF	heart:	n/a
9	chr7:122388911-122388961	HCT-116	colon:	n/a
10	chr7:122529707-122529757	AoSMC	blood vessel:	n/a
11	chr7:122526824-122526874	GM19239	blood:	n/a
12	chr7:122553875-122553925	HUVEC	blood vessel:	n/a
13	chr7:122443513-122443563	HMEC	breast:	n/a
14	chr7:122488330-122488380	PANC-1	pancreas:	n/a
15	chr7:122384836-122384886	MCF10A-Er-Src	breast:	n/a
16	chr7:122388911-122388961	HUVEC	blood vessel:	n/a
17	chr7:122525974-122526024	HEK293	kidney:	embryo
18	chr7:122925263-122925313	HCF	heart:	n/a
19	chr7:122526572-122526622	HL-60	blood:	n/a
20	chr7:122388911-122388961	BE2_C	brain:	n/a
21	chr7:122953117-122953167	Hepatocyte	liver:	n/a
22	chr7:122527351-122527401	HUVEC	blood vessel:	n/a
23	chr7:122526836-122526886	SKMC	muscle:	n/a
24	chr7:122526826-122526876	GM19239	blood:	n/a
25	chr7:122794551-122794601	IMR90	lung:	fetal
26	chr7:122527472-122527522	BE2_C	brain:	n/a
27	chr7:122526408-122526458	ovcar-3	ovarian:	n/a
28	chr7:122526824-122526874	HCM	heart:	n/a
29	chr7:122526033-122526083	SAEC	small airway:	n/a
30	chr7:122794551-122794601	HIPEpiC	eye:	n/a
31	chr7:122953117-122953167	HNPCEpiC	eye:	n/a
32	chr7:122553915-122553965	SK-N-SH_RA	brain:	n/a
33	chr7:122527437-122527487	H1-hESC	embryonic stem cell:	embryo
34	chr7:122839955-122840005	RPTEC	kidney:	n/a
35	chr7:122388911-122388961	AG04449	skin:	fetal
36	chr7:122526836-122526886	HEEpiC	esophagus:	n/a
37	chr7:122553915-122553965	AG09319	gingival:	n/a
38	chr7:122526940-122526990	PANC-1	pancreas:	n/a
39	chr7:122526824-122526874	HRE	kidney:	n/a
40	chr7:122953117-122953167	Hela-S3	cervix:	n/a
41	chr7:122526408-122526458	HRPEpiC	eye:	n/a
42	chr7:122529707-122529757	AG09309	skin:	n/a
43	chr7:122587034-122587084	HUVEC	blood vessel:	n/a
44	chr7:122526826-122526876	Hepatocyte	liver:	n/a
45	chr7:122388911-122388961	ProgFib	skin:	n/a
46	chr7:122524465-122524515	SKMC	muscle:	n/a
47	chr7:122526836-122526886	ECC-1	luminal epithelium:	n/a
48	chr7:122388911-122388961	HCM	heart:	n/a
49	chr7:122388911-122388961	K562	blood:	n/a
50	chr7:122525974-122526024	Caco-2	colon:	n/a

(count:174 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr7:122948016..122949684-chr7:122953914..122955993,2	MCF-7	breast:
2	chr7:122847313..122848069-chr7:123007356..123008168,3	MCF-7	breast:
3	chr7:122527428..122528069-chr7:122694498..122695060,2	MCF-7	breast:
4	chr7:122471973..122475729-chr7:122484629..122488935,3	MCF-7	breast:
5	chr7:122764225..122765975-chr7:122771823..122774214,2	MCF-7	breast:
6	chr7:122685457..122687299-chr7:122693793..122695789,2	MCF-7	breast:
7	chr7:122822079..122826673-chr7:122828939..122831603,4	MCF-7	breast:
8	chr7:122764225..122765975-chr7:122771823..122774214,2	MCF-7	breast:
9	chr7:122449452..122451074-chr7:122524570..122526706,2	MCF-7	breast:
10	chr7:122443541..122445086-chr7:122446749..122448778,2	K562	blood:
11	chr7:122443509..122444465-chr7:122848624..122849606,2	MCF-7	breast:
12	chr7:122502243..122503856-chr7:122522076..122524661,2	MCF-7	breast:
13	chr7:122946336..122948933-chr7:123387387..123389739,2	K562	blood:
14	chr7:122922883..122925729-chr7:122928465..122930574,2	MCF-7	breast:
15	chr7:122645062..122647735-chr7:122648443..122650987,2	K562	blood:
16	chr7:122543710..122545744-chr7:122546916..122548861,2	MCF-7	breast:
17	chr7:122789422..122791875-chr7:122803775..122805608,2	K562	blood:
18	chr7:122487239..122489689-chr7:122524785..122526755,2	MCF-7	breast:
19	chr7:122443038..122444017-chr7:122710508..122711379,2	MCF-7	breast:
20	chr7:122473308..122475619-chr7:122484474..122486171,2	MCF-7	breast:
21	chr7:122443541..122445086-chr7:122446749..122448778,2	K562	blood:
22	chr7:122697734..122699274-chr7:122700681..122702675,2	K562	blood:
23	chr7:122836105..122838339-chr7:122842677..122844991,2	K562	blood:
24	chr20:52491297..52491798-chr7:122756625..122757125,2	MCF-7	breast:
25	chr7:122630874..122632395-chr7:122639111..122641768,2	K562	blood:
26	chr7:122923301..122926065-chr7:122941993..122944808,2	K562	blood:
27	chr14:24748707..24751147-chr7:122509604..122511809,2	MCF-7	breast:
28	chr7:122829890..122831991-chr7:122835864..122837812,2	MCF-7	breast:
29	chr7:122630874..122632395-chr7:122639111..122641768,2	K562	blood:
30	chr6:39197015..39197718-chr7:122735976..122736762,2	MCF-7	breast:
31	chr7:122427597..122429988-chr7:122525727..122527279,2	MCF-7	breast:
32	chr7:122645062..122647735-chr7:122648443..122650987,2	K562	blood:
33	chr7:122384641..122386460-chr7:122390684..122392862,2	K562	blood:
34	chr7:122753986..122756806-chr7:122794513..122796021,2	K562	blood:
35	chr7:122443209..122443881-chr7:122793957..122794553,2	MCF-7	breast:
36	chr14:94300599..94301313-chr7:122638050..122638667,2	MCF-7	breast:
37	chr7:122441614..122445923-chr7:122446621..122449236,4	MCF-7	breast:
38	chr7:122685457..122687299-chr7:122693793..122695789,2	MCF-7	breast:
39	chr7:122922883..122925729-chr7:122928465..122930574,2	MCF-7	breast:
40	chr7:122792145..122793696-chr7:122798762..122801174,2	K562	blood:
41	chr7:122382528..122384037-chr7:122398742..122400591,2	K562	blood:
42	chr7:122441614..122445923-chr7:122446621..122449236,4	MCF-7	breast:
43	chr7:122382528..122384037-chr7:122398742..122400591,2	K562	blood:
44	chr7:122894215..122897024-chr7:122899451..122901556,2	K562	blood:
45	chr7:122473493..122475814-chr7:122480570..122483503,2	MCF-7	breast:
46	chr7:122792145..122793696-chr7:122798762..122801174,2	K562	blood:
47	chr7:122916042..122917906-chr7:123194513..123196585,2	K562	blood:
48	chr7:122848186..122849079-chr7:123007484..123008258,3	MCF-7	breast:
49	chr7:122988435..122990035-chr7:122992718..122994529,2	K562	blood:
50	chr7:122836105..122838339-chr7:122842677..122844991,2	K562	blood:

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

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

No data

Variant related genes	Relation type
LYPLA1P1	TF binding region
ENSG00000227573	TF binding region
ENSG00000226680	TF binding region
TAS2R16	TF binding region
SLC13A1	TF binding region
CADPS2	TF binding region
LYPLA1P1	CpG island
ENSG00000227573	CpG island
ENSG00000226680	CpG island
TAS2R16	CpG island
SLC13A1	CpG island
CADPS2	CpG island
ENSG00000106299	chromatin interactions
ENSG00000133805	chromatin interactions
ENSG00000081800	chromatin interactions
ENSG00000164626	chromatin interactions
ENSG00000236383	chromatin interactions
ENSG00000223595	chromatin interactions
ENSG00000227573	chromatin interactions
ENSG00000272686	chromatin interactions
ENSG00000081803	chromatin interactions
USP24	miRNA target sites
USF2	miRNA target sites
USP15	miRNA target sites

Extended variants
information (count: 16293 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:16293 , 50 per page) page: 1 2 3 4 5 6 7 ... 326

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs571270024	chr7:122366572-122366573	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs116004220	chr7:122366643-122366644	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs187898969	chr7:122366662-122366663	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs79456163	chr7:122366669-122366670	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs532135667	chr7:122366721-122366722	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs551300733	chr7:122366768-122366769	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs192575665	chr7:122366772-122366773	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs202140194	chr7:122366827-122366828	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs113911501	chr7:122366841-122366842	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs377296137	chr7:122366854-122366855	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs183153299	chr7:122366869-122366870	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs116314065	chr7:122366886-122366887	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs186657726	chr7:122366902-122366903	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs567976535	chr7:122366935-122366936	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs192549622	chr7:122366939-122366940	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs536264980	chr7:122366963-122366964	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs546614943	chr7:122366965-122366966	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs184930466	chr7:122367003-122367004	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs536591612	chr7:122367010-122367011	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs538794833	chr7:122367034-122367035	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs559005107	chr7:122367051-122367052	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs553252209	chr7:122367114-122367115	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs573158079	chr7:122367126-122367127	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs555318229	chr7:122367133-122367134	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs575158099	chr7:122367179-122367180	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs553499937	chr7:122367217-122367218	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs552658654	chr7:122367227-122367228	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs373901124	chr7:122367341-122367342	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs570484562	chr7:122367343-122367344	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs2159824	chr7:122367349-122367350	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs546874335	chr7:122367358-122367359	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs545628859	chr7:122367365-122367366	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs565252641	chr7:122367384-122367385	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs34758968	chr7:122367395-122367396	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs140039938	chr7:122367427-122367428	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs531418045	chr7:122367462-122367463	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs374277912	chr7:122367493-122367494	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs189829344	chr7:122367512-122367513	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs368667467	chr7:122367533-122367534	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs536148727	chr7:122367762-122367763	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs547278766	chr7:122367765-122367766	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs192956387	chr7:122367794-122367795	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs184472104	chr7:122367822-122367823	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs149823104	chr7:122367835-122367836	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs569300231	chr7:122367847-122367848	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs538463054	chr7:122367849-122367850	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs555230393	chr7:122367860-122367861	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs568654698	chr7:122367873-122367874	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs575676370	chr7:122367885-122367886	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs146375186	chr7:122367890-122367891	Weak transcription Enhancers	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:1820 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

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	chr7:122359800-122375000	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr7:122362400-122367000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr7:122365600-122376200	Weak transcription	Fetal Kidney	kidney
6	chr7:122366000-122384200	Weak transcription	Pancreas	Pancrea
7	chr7:122366200-122367400	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr7:122366400-122367800	Enhancers	Fetal Heart	heart
9	chr7:122367000-122367200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr7:122367200-122373600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr7:122367600-122368200	Enhancers	Stomach Mucosa	stomach
12	chr7:122368200-122378800	Weak transcription	Stomach Mucosa	stomach
13	chr7:122369200-122377400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr7:122370600-122371400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr7:122370600-122371800	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr7:122371200-122371800	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr7:122371800-122374800	Weak transcription	HUES64 Cell Line	embryonic stem cell
18	chr7:122371800-122374800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
19	chr7:122372000-122386600	Weak transcription	Ovary	ovary
20	chr7:122373000-122373600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
21	chr7:122373400-122373800	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
22	chr7:122373600-122373800	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
23	chr7:122373600-122374000	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
24	chr7:122373600-122374000	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr7:122373600-122374000	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
26	chr7:122373800-122375000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
27	chr7:122373800-122376200	Weak transcription	H1 Cell Line	embryonic stem cell
28	chr7:122374000-122375000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
29	chr7:122374000-122375000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
30	chr7:122374600-122377800	Weak transcription	Placenta Amnion	Placenta Amnion
31	chr7:122374800-122376200	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr7:122374800-122376600	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr7:122374800-122380000	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr7:122375000-122376000	Enhancers	iPS-20b Cell Line	embryonic stem cell
35	chr7:122375000-122376600	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr7:122375000-122379800	Enhancers	ES-I3 Cell Line	embryonic stem cell
37	chr7:122375000-122380000	Enhancers	HUES6 Cell Line	embryonic stem cell
38	chr7:122375200-122378400	Weak transcription	HepG2	liver
39	chr7:122376000-122377000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
40	chr7:122376000-122378400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
41	chr7:122376200-122376400	Enhancers	H9 Cell Line	embryonic stem cell
42	chr7:122376200-122376400	Enhancers	Fetal Kidney	kidney
43	chr7:122376200-122377000	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
44	chr7:122376200-122379600	Enhancers	H1 Cell Line	embryonic stem cell
45	chr7:122376400-122376800	Weak transcription	H9 Cell Line	embryonic stem cell
46	chr7:122376400-122379400	Weak transcription	Fetal Kidney	kidney
47	chr7:122376600-122377000	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
48	chr7:122376600-122377200	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
49	chr7:122376800-122377000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr7:122376800-122378200	Enhancers	H9 Cell Line	embryonic stem cell

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