Variant report

Variant	nsv900563
Chromosome Location	chr13:76093935-76169347
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1819)
CpG islands
(count:1833)
Chromatin interactive
region (count:53)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1819 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:76104571-76105292	HepG2	liver:	n/a	n/a
2	ARID3A	chr13:76119103-76119402	HepG2	liver:	n/a	n/a
3	ARID3A	chr13:76123347-76124671	HepG2	liver:	n/a	n/a
4	ARID3A	chr13:76111847-76112381	HepG2	liver:	n/a	n/a
5	ARID3A	chr13:76123487-76124101	K562	blood:	n/a	n/a
6	ARID3A	chr13:76140888-76140979	K562	blood:	n/a	n/a
7	ARID3A	chr13:76140823-76141209	HepG2	liver:	n/a	n/a
8	ARID3A	chr13:76111988-76112275	K562	blood:	n/a	n/a
9	ATF1	chr13:76115164-76115846	K562	blood:	n/a	n/a
10	ATF2	chr13:76123176-76123915	GM12878	blood:	n/a	n/a
11	ATF2	chr13:76161743-76162267	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr13:76111559-76112389	GM12878	blood:	n/a	n/a
13	ATF2	chr13:76112008-76112514	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr13:76123258-76124165	GM12878	blood:	n/a	n/a
15	ATF2	chr13:76161744-76162155	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF3	chr13:76124408-76124734	K562	blood:	n/a	n/a
17	BACH1	chr13:76123150-76123218	K562	blood:	n/a	n/a
18	BACH1	chr13:76123391-76124432	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr13:76130079-76130395	K562	blood:	n/a	n/a
20	BACH1	chr13:76111716-76112543	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr13:76152548-76152550	K562	blood:	n/a	n/a
22	BACH1	chr13:76123468-76123932	K562	blood:	n/a	n/a
23	BATF	chr13:76153723-76153987	GM12878	blood:	n/a	n/a
24	BATF	chr13:76153753-76153938	GM12878	blood:	n/a	n/a
25	BATF	chr13:76123360-76123696	GM12878	blood:	n/a	n/a
26	BCL3	chr13:76112015-76112538	A549	lung:	n/a	n/a
27	BCLAF1	chr13:76123288-76124229	GM12878	blood:	n/a	n/a
28	BCLAF1	chr13:76123254-76124297	GM12878	blood:	n/a	n/a
29	BCLAF1	chr13:76111591-76112186	GM12878	blood:	n/a	n/a
30	BHLHE40	chr13:76111626-76112484	HepG2	liver:	n/a	n/a
31	BHLHE40	chr13:76130055-76130270	K562	blood:	n/a	n/a
32	BHLHE40	chr13:76123284-76124344	HepG2	liver:	n/a	n/a
33	BHLHE40	chr13:76123174-76124311	GM12878	blood:	n/a	n/a
34	BHLHE40	chr13:76123495-76124021	A549	lung:	n/a	n/a
35	BHLHE40	chr13:76111942-76112433	A549	lung:	n/a	n/a
36	BHLHE40	chr13:76111845-76112497	K562	blood:	n/a	n/a
37	BHLHE40	chr13:76111540-76112825	GM12878	blood:	n/a	n/a
38	BHLHE40	chr13:76123316-76124079	K562	blood:	n/a	n/a
39	BRCA1	chr13:76123436-76123895	H1-hESC	embryonic stem cell:	n/a	n/a
40	BRCA1	chr13:76111808-76112292	GM12878	blood:	n/a	n/a
41	BRCA1	chr13:76111576-76112481	Hela-S3	cervix:	n/a	n/a
42	BRCA1	chr13:76123410-76124147	GM12878	blood:	n/a	n/a
43	BRCA1	chr13:76111988-76112550	H1-hESC	embryonic stem cell:	n/a	n/a
44	BRCA1	chr13:76123474-76123899	HepG2	liver:	n/a	n/a
45	BRCA1	chr13:76123401-76123970	Hela-S3	cervix:	n/a	n/a
46	BRCA1	chr13:76153639-76153677	Hela-S3	cervix:	n/a	n/a
47	BRCA1	chr13:76111647-76112440	HepG2	liver:	n/a	n/a
48	CBX3	chr13:76159288-76159637	K562	blood:	n/a	n/a
49	CBX3	chr13:76123316-76123877	K562	blood:	n/a	n/a
50	CBX3	chr13:76123404-76123686	K562	blood:	n/a	n/a

(count:1833 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:76123534-76123584	CMK	blood:	n/a
2	chr13:76112973-76113023	GM19239	blood:	n/a
3	chr13:76123895-76123945	HUVEC	blood vessel:	n/a
4	chr13:76123534-76123584	CMK	blood:	n/a
5	chr13:76112973-76113023	GM19239	blood:	n/a
6	chr13:76123895-76123945	HUVEC	blood vessel:	n/a
7	chr13:76112980-76113030	HRPEpiC	eye:	n/a
8	chr13:76112973-76113023	HCT-116	colon:	n/a
9	chr13:76115526-76115576	ECC-1	luminal epithelium:	n/a
10	chr13:76113014-76113064	HRPEpiC	eye:	n/a
11	chr13:76115526-76115576	H1-hESC	embryonic stem cell:	embryo
12	chr13:76123534-76123584	HCM	heart:	n/a
13	chr13:76123853-76123903	HCM	heart:	n/a
14	chr13:76112232-76112282	U87	brain:	n/a
15	chr13:76112274-76112324	HCT-116	colon:	n/a
16	chr13:76124267-76124317	T-47D	breast:	n/a
17	chr13:76112980-76113030	AG04450	lung:	fetal
18	chr13:76124424-76124474	GM19239	blood:	n/a
19	chr13:76112187-76112237	HMEC	breast:	n/a
20	chr13:76119663-76119713	AG04450	lung:	fetal
21	chr13:76123901-76123951	AG09309	skin:	n/a
22	chr13:76124267-76124317	A549	lung:	n/a
23	chr13:76115526-76115576	Hepatocyte	liver:	n/a
24	chr13:76123907-76123957	T-47D	breast:	n/a
25	chr13:76123478-76123528	SK-N-MC	brain:	n/a
26	chr13:76119663-76119713	PrEC	prostate:	n/a
27	chr13:76099592-76099642	IMR90	lung:	fetal
28	chr13:76124267-76124317	LNCaP	prostate:	n/a
29	chr13:76123478-76123528	HCF	heart:	n/a
30	chr13:76123853-76123903	HIPEpiC	eye:	n/a
31	chr13:76111785-76111835	NHDF-neo	bronchial:	n/a
32	chr13:76111980-76112030	GM12892	blood:	n/a
33	chr13:76111918-76111968	BE2_C	brain:	n/a
34	chr13:76123907-76123957	A549	lung:	n/a
35	chr13:76111107-76111157	SKMC	muscle:	n/a
36	chr13:76123853-76123903	RPTEC	kidney:	n/a
37	chr13:76123907-76123957	HL-60	blood:	n/a
38	chr13:76123781-76123831	Jurkat	blood:	n/a
39	chr13:76123904-76123954	HEEpiC	esophagus:	n/a
40	chr13:76119663-76119713	SK-N-MC	brain:	n/a
41	chr13:76128081-76128131	AoSMC	blood vessel:	n/a
42	chr13:76111918-76111968	HCM	heart:	n/a
43	chr13:76123895-76123945	GM19239	blood:	n/a
44	chr13:76111107-76111157	AG09319	gingival:	n/a
45	chr13:76113014-76113064	LNCaP	prostate:	n/a
46	chr13:76123895-76123945	HepG2	liver:	n/a
47	chr13:76111107-76111157	HMEC	breast:	n/a
48	chr13:76123086-76123136	ProgFib	skin:	n/a
49	chr13:76111918-76111968	HEEpiC	esophagus:	n/a
50	chr13:76111107-76111157	HPAEpiC	pulmonary alveolar:	n/a

(count:53 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr13:76122653..76127194-chr13:76130432..76132318,4	MCF-7	breast:
2	chr13:76111452..76114150-chr13:76122087..76125338,6	MCF-7	breast:
3	chr13:76152309..76155041-chr13:76158108..76159629,2	K562	blood:
4	chr13:76101020..76103303-chr13:76108939..76111291,2	K562	blood:
5	chr13:76111859..76112746-chr13:76123326..76123936,2	MCF-7	breast:
6	chr13:76160277..76161808-chr13:76162172..76164407,2	K562	blood:
7	chr13:76107791..76110428-chr13:76144234..76145882,2	K562	blood:
8	chr13:76055137..76056712-chr13:76122225..76124650,2	MCF-7	breast:
9	chr13:76055434..76058277-chr13:76123047..76126766,3	K562	blood:
10	chr13:76153049..76155664-chr13:76161169..76162949,2	K562	blood:
11	chr13:76124376..76126025-chr13:76132730..76134454,2	K562	blood:
12	chr13:76111404..76112078-chr17:26989037..26989702,2	Hela-S3	cervix:
13	chr13:76110734..76112526-chr13:76124795..76127675,2	K562	blood:
14	chr13:76109717..76113590-chr13:76122029..76126081,5	MCF-7	breast:
15	chr13:76109687..76114004-chr13:76118514..76122227,3	K562	blood:
16	chr13:76109717..76113590-chr13:76122029..76126081,5	MCF-7	breast:
17	chr13:76055248..76057886-chr13:76110224..76112780,4	MCF-7	breast:
18	chr13:76143405..76146053-chr13:76147700..76149492,2	K562	blood:
19	chr13:76111452..76114150-chr13:76122087..76125338,6	MCF-7	breast:
20	chr13:76111859..76112746-chr13:76123326..76123936,2	MCF-7	breast:
21	chr13:76123475..76126296-chr13:76136199..76138617,2	MCF-7	breast:
22	chr13:76124018..76125732-chr13:76125795..76127481,2	MCF-7	breast:
23	chr13:76141660..76144515-chr13:76144732..76146608,2	MCF-7	breast:
24	chr13:76056169..76056921-chr13:76123095..76123971,5	MCF-7	breast:
25	chr13:76124076..76125593-chr13:76162284..76165016,2	K562	blood:
26	chr13:76102775..76109881-chr13:76110381..76113047,9	MCF-7	breast:
27	chr13:76123621..76124364-chrX:134654253..134654910,2	NB4	blood:
28	chr13:76106394..76109955-chr13:76110419..76113939,6	MCF-7	breast:
29	chr13:76118168..76119687-chr13:76122527..76125250,2	MCF-7	breast:
30	chr13:76124076..76125593-chr13:76162284..76165016,2	K562	blood:
31	chr13:76111578..76112381-chrX:73511953..73512510,2	Hela-S3	cervix:
32	chr11:65339613..65340413-chr13:76111532..76112034,2	NB4	blood:
33	chr13:76115839..76118347-chr13:76129572..76131579,2	K562	blood:
34	chr13:76055919..76057695-chr13:76110507..76112437,2	MCF-7	breast:
35	chr13:76143405..76146053-chr13:76147700..76149492,2	K562	blood:
36	chr13:76101122..76104303-chr13:76108576..76110569,3	K562	blood:
37	chr13:75946802..75947592-chr13:76121701..76122528,2	MCF-7	breast:
38	chr13:76123894..76126209-chr13:76129145..76131618,3	K562	blood:
39	chr13:76160277..76161808-chr13:76162172..76164407,2	K562	blood:
40	chr13:76107791..76110428-chr13:76144234..76145882,2	K562	blood:
41	chr13:76123286..76125327-chr13:76160450..76162067,2	K562	blood:
42	chr13:76109113..76111805-chr13:76112674..76114626,2	K562	blood:
43	chr13:76101122..76104303-chr13:76108576..76110569,3	K562	blood:
44	chr13:76101020..76103303-chr13:76108939..76111291,2	K562	blood:
45	chr13:76115839..76118347-chr13:76129572..76131579,2	K562	blood:
46	chr13:76153049..76155664-chr13:76161169..76162949,2	K562	blood:
47	chr13:76109113..76111805-chr13:76112674..76114626,2	K562	blood:
48	chr13:76152309..76155041-chr13:76158108..76159629,2	K562	blood:
49	chr13:76124018..76125732-chr13:76125795..76127481,2	MCF-7	breast:
50	chr13:76124376..76126025-chr13:76132730..76134454,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TBC1D4-2	chr13:76104250-76104402	NONHSAT034360
2	lnc-LMO7-2	chr13:76140968-76140987	ENSG00000261553.1
3	lnc-COMMD6-4	chr13:76161358-76161715	l_873_chr13:76072523-76201534_testes
4	lnc-TBC1D4-2	chr13:76111635-76111811	NONHSAT034360
5	lnc-LMO7-2	chr13:76169051-76169126	ENSG00000261553.1
6	lnc-LMO7-2	chr13:76143596-76143643	ENSG00000261553.1
7	lnc-TBC1D4-2	chr13:76123459-76123575	NONHSAT034360
8	lnc-COMMD6-4	chr13:76140115-76140230	l_873_chr13:76072523-76201534_testes
9	lnc-LMO7-2	chr13:76141363-76141448	ENSG00000261553.1

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	COMMD6	hsa-miR-106b-5p	chr13:76100615-76100635

Variant related genes	Relation type
COMMD6	TF binding region
ENSG00000261553	TF binding region
UCHL3	TF binding region
COMMD6	CpG island
ENSG00000261553	CpG island
UCHL3	CpG island
ENSG00000225235	chromatin interactions
ENSG00000165359	chromatin interactions
ENSG00000132581	chromatin interactions
ENSG00000109111	chromatin interactions
ENSG00000232671	chromatin interactions
ENSG00000188243	chromatin interactions
ENSG00000176973	chromatin interactions
ENSG00000230590	chromatin interactions
ENSG00000118939	chromatin interactions
ENSG00000261553	chromatin interactions
ENSG00000143373	chromatin interactions
ENSG00000136111	chromatin interactions

Extended variants
information (count: 2824 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:2824 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6562904	chr13:76093935-76093936	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs567005859	chr13:76093942-76093943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs537564626	chr13:76093943-76093944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs67211435	chr13:76093948-76093949	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs571158576	chr13:76094010-76094011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs538884922	chr13:76094013-76094014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs553775048	chr13:76094027-76094028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs149552832	chr13:76094028-76094029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs536039876	chr13:76094045-76094046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs537051730	chr13:76094068-76094069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs144401473	chr13:76094090-76094091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs375024901	chr13:76094097-76094098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs574150441	chr13:76094189-76094190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs146191337	chr13:76094240-76094241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs202038809	chr13:76094243-76094244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs145131549	chr13:76094244-76094245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs141160744	chr13:76094245-76094246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs544742693	chr13:76094322-76094323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs562827695	chr13:76094332-76094333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs184927524	chr13:76094341-76094342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs545430264	chr13:76094344-76094345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs140972762	chr13:76094369-76094370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs528021049	chr13:76094407-76094408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs534982410	chr13:76094474-76094475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs8002157	chr13:76094545-76094546	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs561167847	chr13:76094605-76094606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs565277524	chr13:76094610-76094611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs372563136	chr13:76094625-76094626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs571493926	chr13:76094660-76094661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs538823665	chr13:76094735-76094736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs549475155	chr13:76094753-76094754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs571361891	chr13:76094800-76094801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs538253710	chr13:76094824-76094825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs187386788	chr13:76094858-76094859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs560328450	chr13:76094874-76094875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs371845420	chr13:76094897-76094898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs144830020	chr13:76094919-76094920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs77466495	chr13:76094936-76094937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs147507543	chr13:76094969-76094970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs537281115	chr13:76095004-76095005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs556378556	chr13:76095019-76095020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs578067571	chr13:76095028-76095029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs545057644	chr13:76095101-76095102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs369782198	chr13:76095166-76095167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs577093415	chr13:76095167-76095168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs560548798	chr13:76095223-76095224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs373931106	chr13:76095224-76095225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs572622651	chr13:76095247-76095248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs116113824	chr13:76095264-76095265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs1080347	chr13:76095273-76095274	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:96)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Burkitt''s lymphoma	18698080	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	18632612	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	17053054	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21858162	CNVD
Metanephric adenoma	20802469	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Gastric cancer	17908304	CNVD
Breast cancer	17393978	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Colorectal cancer	16774939	CNVD
Adenoid cystic carcinoma	17372589	CNVD
abnormal development	18461090	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal cancer	21851588	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hirschsprung''s Disease	21712996	CNVD
Prostate cancer	21965145	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Intracranial aneurysm	16715129	CNVD
Non-small cell lung cancer	19010865	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	22341455	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2650 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:76082600-76095400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr13:76089000-76099400	Weak transcription	Monocytes-CD14+_RO01746	blood
3	chr13:76089000-76104800	Weak transcription	NHDF-Ad	bronchial
4	chr13:76089200-76099400	Weak transcription	Dnd41	blood
5	chr13:76093600-76109400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr13:76094400-76101800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr13:76095400-76095600	Enhancers	Gastric	stomach
8	chr13:76095400-76095800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr13:76095600-76109200	Weak transcription	Gastric	stomach
10	chr13:76095800-76111400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr13:76096000-76096200	Enhancers	Primary B cells from peripheral blood	blood
12	chr13:76096000-76099200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr13:76096000-76099400	Weak transcription	Fetal Thymus	thymus
14	chr13:76096000-76099600	Weak transcription	Primary monocytes fromperipheralblood	blood
15	chr13:76096200-76096400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
16	chr13:76096200-76099400	Weak transcription	Primary B cells from peripheral blood	blood
17	chr13:76096200-76099400	Weak transcription	Thymus	Thymus
18	chr13:76096400-76099200	Weak transcription	Primary T cells fromperipheralblood	blood
19	chr13:76096400-76099400	Weak transcription	Primary hematopoietic stem cells	blood
20	chr13:76096400-76099400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
21	chr13:76096400-76099600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
22	chr13:76096600-76099400	Weak transcription	Adipose Nuclei	Adipose
23	chr13:76096600-76099400	Weak transcription	Fetal Muscle Leg	muscle
24	chr13:76096600-76099400	Weak transcription	Sigmoid Colon	Sigmoid Colon
25	chr13:76096600-76099600	Weak transcription	HUES48 Cell Line	embryonic stem cell
26	chr13:76096600-76099600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr13:76096600-76101800	Weak transcription	HUES6 Cell Line	embryonic stem cell
28	chr13:76096600-76107400	Weak transcription	Fetal Intestine Small	intestine
29	chr13:76096600-76110400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chr13:76096600-76111400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr13:76096800-76104400	Weak transcription	Primary B cells from cord blood	blood
32	chr13:76097000-76099600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr13:76097000-76099800	Weak transcription	H1 Cell Line	embryonic stem cell
34	chr13:76097000-76111000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr13:76097000-76111600	Weak transcription	Spleen	Spleen
36	chr13:76097200-76099400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
37	chr13:76097200-76100000	Weak transcription	HUES64 Cell Line	embryonic stem cell
38	chr13:76097400-76099200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
39	chr13:76097400-76099400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
40	chr13:76097400-76099400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
41	chr13:76097400-76099400	Weak transcription	Duodenum Smooth Muscle	Duodenum
42	chr13:76097400-76099600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr13:76097400-76104800	Weak transcription	GM12878-XiMat	blood
44	chr13:76097400-76106200	Weak transcription	Brain Hippocampus Middle	brain
45	chr13:76097600-76099200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr13:76097600-76099400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr13:76097600-76099400	Weak transcription	Muscle Satellite Cultured Cells	--
48	chr13:76097600-76099400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr13:76097600-76099400	Weak transcription	Duodenum Mucosa	Duodenum
50	chr13:76097600-76099400	Weak transcription	Fetal Intestine Large	intestine

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