Variant report

Variant	nsv1034393
Chromosome Location	chr9:12278703-12798236
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3826)
CpG islands
(count:490)
Chromatin interactive
region (count:92)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3826 , 50 per page) page: 1 2 3 4 5 6 7 ... 77

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:12775950-12776944	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:12784048-12785110	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:12702242-12702514	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:12794096-12794882	HepG2	liver:	n/a	n/a
5	ARID3A	chr9:12328968-12329168	HepG2	liver:	n/a	n/a
6	ARID3A	chr9:12719466-12719806	HepG2	liver:	n/a	n/a
7	ATF2	chr9:12735567-12735964	GM12878	blood:	n/a	n/a
8	ATF2	chr9:12735544-12735972	GM12878	blood:	n/a	n/a
9	ATF3	chr9:12776028-12776603	A549	lung:	n/a	n/a
10	ATF3	chr9:12784324-12785046	A549	lung:	n/a	n/a
11	ATF3	chr9:12784352-12784992	A549	lung:	n/a	n/a
12	ATF3	chr9:12708586-12708908	HCT-116	colon:	n/a	n/a
13	BACH1	chr9:12567176-12567212	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr9:12465730-12465736	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr9:12292536-12292567	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr9:12784537-12784775	K562	blood:	n/a	n/a
17	BACH1	chr9:12784589-12784652	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr9:12653013-12653212	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr9:12469180-12469392	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr9:12604207-12604421	H1-hESC	embryonic stem cell:	n/a	chr9:12604278-12604292
21	BACH1	chr9:12497880-12498136	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr9:12775963-12776675	H1-hESC	embryonic stem cell:	n/a	n/a
23	BATF	chr9:12329455-12329670	GM12878	blood:	n/a	n/a
24	BATF	chr9:12784487-12784808	GM12878	blood:	n/a	chr9:12784627-12784638
25	BATF	chr9:12784440-12784836	GM12878	blood:	n/a	chr9:12784627-12784638
26	BCL11A	chr9:12784486-12784786	GM12878	blood:	n/a	n/a
27	BCL3	chr9:12775944-12776770	A549	lung:	n/a	chr9:12776114-12776127
28	BCL3	chr9:12774751-12775592	A549	lung:	n/a	chr9:12775208-12775217
29	BCL3	chr9:12775887-12777064	A549	lung:	n/a	chr9:12776114-12776127
30	BCL3	chr9:12784221-12785015	A549	lung:	n/a	n/a
31	BCL3	chr9:12794096-12794785	A549	lung:	n/a	n/a
32	BCL3	chr9:12784331-12785068	A549	lung:	n/a	n/a
33	BCLAF1	chr9:12329426-12329668	GM12878	blood:	n/a	n/a
34	BHLHE40	chr9:12775478-12776767	HepG2	liver:	n/a	chr9:12775512-12775528 chr9:12776042-12776058
35	BHLHE40	chr9:12784559-12784788	GM12878	blood:	n/a	n/a
36	BHLHE40	chr9:12776015-12776514	GM12878	blood:	n/a	chr9:12776042-12776058
37	BHLHE40	chr9:12771808-12772164	A549	lung:	n/a	n/a
38	BHLHE40	chr9:12328884-12329725	HepG2	liver:	n/a	n/a
39	BHLHE40	chr9:12784391-12784791	K562	blood:	n/a	n/a
40	BHLHE40	chr9:12776058-12776346	HepG2	liver:	n/a	n/a
41	BHLHE40	chr9:12612186-12612202	GM12878	blood:	n/a	n/a
42	BHLHE40	chr9:12784373-12785060	HepG2	liver:	n/a	n/a
43	BHLHE40	chr9:12328995-12329158	K562	blood:	n/a	n/a
44	BHLHE40	chr9:12414650-12414651	HepG2	liver:	n/a	n/a
45	BHLHE40	chr9:12776329-12776638	K562	blood:	n/a	n/a
46	BHLHE40	chr9:12329021-12329257	GM12878	blood:	n/a	n/a
47	BRCA1	chr9:12776076-12776725	HepG2	liver:	n/a	n/a
48	BRCA1	chr9:12776070-12777883	Hela-S3	cervix:	n/a	n/a
49	BRCA1	chr9:12368889-12368916	GM12878	blood:	n/a	n/a
50	BRCA1	chr9:12784182-12784865	Hela-S3	cervix:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:12775750-12775800	SAEC	small airway:	n/a
2	chr9:12775700-12775750	AG09309	skin:	n/a
3	chr9:12775750-12775800	SAEC	small airway:	n/a
4	chr9:12775700-12775750	AG09309	skin:	n/a
5	chr9:12693326-12693376	BE2_C	brain:	n/a
6	chr9:12693694-12693744	BJ	skin:	n/a
7	chr9:12704964-12705014	SKMC	muscle:	n/a
8	chr9:12704964-12705014	ECC-1	luminal epithelium:	n/a
9	chr9:12693326-12693376	HCPEpiC	choroid plexus:	n/a
10	chr9:12693694-12693744	GM12878	blood:	n/a
11	chr9:12693694-12693744	SK-N-MC	brain:	n/a
12	chr9:12693326-12693376	HCM	heart:	n/a
13	chr9:12704964-12705014	GM19239	blood:	n/a
14	chr9:12774985-12775035	GM06990	blood:	n/a
15	chr9:12775750-12775800	IMR90	lung:	fetal
16	chr9:12775700-12775750	NHBE	bronchial:	n/a
17	chr9:12776218-12776268	HPAEpiC	pulmonary alveolar:	n/a
18	chr9:12775750-12775800	NT2-D1	testis:	n/a
19	chr9:12774985-12775035	SKMC	muscle:	n/a
20	chr9:12774985-12775035	PFSK-1	brain:	n/a
21	chr9:12693694-12693744	CMK	blood:	n/a
22	chr9:12693326-12693376	HUVEC	blood vessel:	n/a
23	chr9:12693326-12693376	ovcar-3	ovarian:	n/a
24	chr9:12774985-12775035	A549	lung:	n/a
25	chr9:12775750-12775800	HEEpiC	esophagus:	n/a
26	chr9:12704964-12705014	GM12892	blood:	n/a
27	chr9:12774985-12775035	HCPEpiC	choroid plexus:	n/a
28	chr9:12774985-12775035	SK-N-SH_RA	brain:	n/a
29	chr9:12693694-12693744	Hela-S3	cervix:	n/a
30	chr9:12774985-12775035	HEK293	kidney:	embryo
31	chr9:12776218-12776268	SKMC	muscle:	n/a
32	chr9:12775700-12775750	AG09319	gingival:	n/a
33	chr9:12776218-12776268	HCF	heart:	n/a
34	chr9:12704964-12705014	HIPEpiC	eye:	n/a
35	chr9:12704964-12705014	PANC-1	pancreas:	n/a
36	chr9:12775700-12775750	NT2-D1	testis:	n/a
37	chr9:12704964-12705014	GM12878	blood:	n/a
38	chr9:12704964-12705014	SAEC	small airway:	n/a
39	chr9:12776046-12776096	AoSMC	blood vessel:	n/a
40	chr9:12704964-12705014	SK-N-MC	brain:	n/a
41	chr9:12776046-12776096	PANC-1	pancreas:	n/a
42	chr9:12776046-12776096	HCF	heart:	n/a
43	chr9:12775700-12775750	GM12892	blood:	n/a
44	chr9:12775750-12775800	A549	lung:	n/a
45	chr9:12693694-12693744	A549	lung:	n/a
46	chr9:12775700-12775750	LNCaP	prostate:	n/a
47	chr9:12704964-12705014	BJ	skin:	n/a
48	chr9:12774985-12775035	BJ	skin:	n/a
49	chr9:12693694-12693744	GM12891	blood:	n/a
50	chr9:12775750-12775800	U87	brain:	n/a

(count:92 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr9:12771458..12774120-chr9:12775878..12777874,2	K562	blood:
2	chr9:12631997..12633907-chr9:12634270..12637039,2	MCF-7	breast:
3	chr19:32895532..32897847-chr9:12774427..12776236,2	MCF-7	breast:
4	chr9:12729225..12731478-chr9:12790178..12792905,2	MCF-7	breast:
5	chr9:12791617..12793320-chr9:12793855..12796172,2	MCF-7	breast:
6	chr9:12796888..12798629-chr9:12811320..12813907,2	MCF-7	breast:
7	chr9:12786137..12788108-chr9:12801967..12804015,2	MCF-7	breast:
8	chr9:12716514..12718700-chr9:12776478..12778096,2	MCF-7	breast:
9	chr9:12788711..12790306-chr9:12792707..12794507,2	K562	blood:
10	chr9:12615022..12617476-chr9:12617492..12619010,2	MCF-7	breast:
11	chr9:12783262..12785196-chr9:12857512..12860310,2	MCF-7	breast:
12	chr9:12716514..12718700-chr9:12776478..12778096,2	MCF-7	breast:
13	chr9:12607055..12609983-chr9:12671838..12674027,2	K562	blood:
14	chr9:12775994..12778011-chr9:12786037..12787743,2	K562	blood:
15	chr9:12715023..12717622-chr9:12718396..12720573,2	MCF-7	breast:
16	chr9:12775994..12778011-chr9:12786037..12787743,2	K562	blood:
17	chr9:12779288..12781566-chr9:12835012..12836710,2	MCF-7	breast:
18	chr9:12554435..12555308-chr9:12639713..12640600,2	MCF-7	breast:
19	chr9:12748565..12752577-chr9:12774636..12778893,4	MCF-7	breast:
20	chr9:12773974..12784053-chr9:12813051..12820453,19	MCF-7	breast:
21	chr9:12788809..12790728-chr9:12792217..12794767,4	MCF-7	breast:
22	chr9:12789292..12791495-chr9:12794969..12797067,2	MCF-7	breast:
23	chr9:12794502..12796197-chr9:13084693..13086368,2	MCF-7	breast:
24	chr9:12723429..12724424-chr9:12884471..12885741,6	MCF-7	breast:
25	chr9:12736141..12737643-chr9:12774520..12776197,2	MCF-7	breast:
26	chr9:12722041..12725292-chr9:12774361..12778280,6	MCF-7	breast:
27	chr9:12495478..12497603-chr9:12499554..12502350,2	MCF-7	breast:
28	chr9:12771458..12774120-chr9:12775878..12777874,2	K562	blood:
29	chr9:12708111..12711033-chr9:13076014..13078647,2	MCF-7	breast:
30	chr9:12729225..12731478-chr9:12790178..12792905,2	MCF-7	breast:
31	chr9:12784573..12785102-chr9:12794160..12794796,2	MCF-7	breast:
32	chr9:12784767..12786871-chr9:12796425..12798748,2	MCF-7	breast:
33	chr9:12789292..12791495-chr9:12794969..12797067,2	MCF-7	breast:
34	chr9:12719485..12720037-chr9:12987933..12988498,2	MCF-7	breast:
35	chr1:186649939..186650766-chr9:12429991..12430491,2	Hela-S3	cervix:
36	chr9:12774105..12776446-chr9:12796570..12799387,2	MCF-7	breast:
37	chr9:12723856..12726602-chr9:12884690..12886916,2	MCF-7	breast:
38	chr9:12776937..12779598-chr9:12883479..12885184,2	MCF-7	breast:
39	chr9:12723685..12724314-chr9:12988034..12988919,3	MCF-7	breast:
40	chr9:12615022..12617476-chr9:12617492..12619010,2	MCF-7	breast:
41	chr9:12788711..12790306-chr9:12792707..12794507,2	K562	blood:
42	chr9:12788809..12790728-chr9:12792217..12794767,4	MCF-7	breast:
43	chr9:12773433..12781932-chr9:12782481..12798090,47	MCF-7	breast:
44	chr9:12733476..12735004-chr9:12774992..12776567,2	MCF-7	breast:
45	chr9:12794075..12796517-chr9:12813544..12816073,2	MCF-7	breast:
46	chr9:12607055..12609983-chr9:12671838..12674027,2	K562	blood:
47	chr9:12776384..12777092-chr9:12988313..12988856,2	MCF-7	breast:
48	chr9:12784767..12786871-chr9:12796425..12798748,2	MCF-7	breast:
49	chr9:12737180..12738894-chr9:12739213..12741322,2	MCF-7	breast:
50	chr9:12526692..12528486-chr9:12531576..12533111,2	MCF-7	breast:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C9orf150-2	chr9:12759301-12759537	l_3734_chr9:12728518-12759537_heart
2	lnc-C9orf150-1	chr9:12768922-12770158	XLOC_007283
3	lnc-MPDZ-8	chr9:12764762-12765054	NONHSAT130228
4	lnc-C9orf150-2	chr9:12728519-12728662	l_3734_chr9:12728518-12759537_heart
5	lnc-C9orf150-4	chr9:12693912-12694487	NONHSAT130224
6	lnc-MPDZ-1	chr9:12700100-12700626	ENSG00000235448.1
7	lnc-MPDZ-1	chr9:12790619-12790764	ENSG00000235448.1
8	lnc-MPDZ-1	chr9:12759551-12759623	ENSG00000235448.1
9	lnc-C9orf150-2	chr9:12758922-12759300	l_3734_chr9:12728518-12759537_heart
10	lnc-C9orf150-4	chr9:12693309-12693478	NONHSAT130224
11	lnc-C9orf150-1	chr9:12738519-12738662	XLOC_007283
12	lnc-TYRP1-4	chr9:12287320-12288238	NONHSAT130222

No data

Variant related genes	Relation type
RN7SL849P	TF binding region
ENSG00000231491	TF binding region
TYRP1	TF binding region
LURAP1L	TF binding region
RNU2-47P	TF binding region
RN7SL849P	CpG island
ENSG00000231491	CpG island
TYRP1	CpG island
LURAP1L	CpG island
RNU2-47P	CpG island
ENSG00000267213	chromatin interactions
ENSG00000223621	chromatin interactions
ENSG00000222658	chromatin interactions
ENSG00000153714	chromatin interactions
ENSG00000269093	chromatin interactions
ENSG00000107165	chromatin interactions
ENSG00000235448	chromatin interactions
ENSG00000178904	chromatin interactions
ENSG00000206737	chromatin interactions

Extended variants
information (count: 12982 )
Associated
traits (count: 111 )

Variant overlapped rSNPs/rCNVs (count:12982 , 50 per page) page: 1 2 3 4 5 6 7 ... 260

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561810495	chr9:12280832-12280833	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs551100652	chr9:12280846-12280847	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs373154665	chr9:12280857-12280858	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs530760921	chr9:12280859-12280860	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs188380940	chr9:12280860-12280861	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs567515936	chr9:12280863-12280864	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs575040320	chr9:12280915-12280916	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs55755763	chr9:12280916-12280917	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs377417129	chr9:12280928-12280929	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs180739227	chr9:12280969-12280970	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs192054772	chr9:12283008-12283009	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs576301954	chr9:12283092-12283093	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs540443185	chr9:12283096-12283097	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs144725105	chr9:12283102-12283103	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs368996735	chr9:12283118-12283119	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs373129434	chr9:12283127-12283128	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs117786830	chr9:12283214-12283215	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs35886835	chr9:12283258-12283259	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs375818790	chr9:12283261-12283262	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs546727762	chr9:12283271-12283272	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs11789892	chr9:12283297-12283298	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs184987009	chr9:12283298-12283299	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs552755485	chr9:12283324-12283325	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs551417886	chr9:12283330-12283331	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs369362420	chr9:12283340-12283341	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs371927709	chr9:12283350-12283351	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs373042358	chr9:12283360-12283361	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs78340009	chr9:12283390-12283391	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs189406352	chr9:12283413-12283414	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs180978774	chr9:12283416-12283417	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs531554155	chr9:12283417-12283418	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs537017283	chr9:12283494-12283495	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs568103409	chr9:12283544-12283545	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs533858592	chr9:12283558-12283559	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs34796056	chr9:12283577-12283578	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs553936191	chr9:12283580-12283581	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs148518817	chr9:12283612-12283613	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs539224367	chr9:12283648-12283649	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs556333226	chr9:12283649-12283650	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs576208078	chr9:12283654-12283655	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs542151910	chr9:12283679-12283680	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs560935437	chr9:12283691-12283692	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs184341573	chr9:12283700-12283701	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs112704567	chr9:12283703-12283704	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs560182450	chr9:12283774-12283775	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs532650640	chr9:12283779-12283780	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs144424741	chr9:12283791-12283792	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs190012398	chr9:12283830-12283831	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs563144959	chr9:12283856-12283857	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs181285200	chr9:12283858-12283859	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:111)

Disease	PMID	Source
Disorders of sex development	21048976	CNVD
Honadal dysgenesis	21048976	CNVD
Medulloblastoma	21979893	CNVD
Lung cancer	16740712	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cervical cancer	21063398	CNVD
Retinoblastoma	22278416	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Melanoma	18172304	CNVD
Biliary cancer	19435499	CNVD
Gastric cancer	21586687	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myopathy	18421352	CNVD
Neuroblastoma	18664255	CNVD
Acute lymphoblastic leukemia	18957548	CNVD
Myeloproliferative neoplasm	17564968	CNVD
Malignant meningioma	17937814	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Chronic myeloid leukemia	21384125	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Myelodysplastic syndrome	21251322	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	18803288	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma	19074898	CNVD
Malignant melanoma	19074898	CNVD
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Cancer	20164920	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	21764851	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Colorectal cancer	16272173	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Gastric cancer	16891809	CNVD
Mental retardation	17847001	CNVD
Cutaneous squamous cell carcinomas	17420988	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21611746	CNVD
Melanoma	22183965	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Chordoma	21215367	CNVD
Renal cell carcinoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	21811587	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:1834 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:12280800-12281000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr9:12283000-12284000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr9:12284000-12284400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr9:12284400-12284600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr9:12284600-12285400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr9:12285400-12285600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr9:12285600-12285800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr9:12289600-12290200	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr9:12289600-12290200	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr9:12289600-12290200	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr9:12289600-12290200	Enhancers	iPS-20b Cell Line	embryonic stem cell
12	chr9:12289600-12290400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr9:12289800-12290200	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr9:12289800-12290200	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr9:12289800-12290200	Enhancers	Brain Germinal Matrix	brain
16	chr9:12289800-12290400	Enhancers	Cortex derived primary cultured neurospheres	brain
17	chr9:12289800-12290400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr9:12289800-12290600	Enhancers	Brain Inferior Temporal Lobe	brain
19	chr9:12290000-12290600	Enhancers	Brain Cingulate Gyrus	brain
20	chr9:12290000-12290600	Enhancers	Brain Hippocampus Middle	brain
21	chr9:12290000-12291000	Enhancers	Brain Substantia Nigra	brain
22	chr9:12290200-12290800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr9:12292200-12293000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
24	chr9:12294200-12294600	Active TSS	Fetal Lung	lung
25	chr9:12302000-12302400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr9:12314400-12317200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr9:12318800-12319800	Enhancers	Adipose Nuclei	Adipose
28	chr9:12324000-12324400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr9:12324400-12329000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr9:12328800-12329000	Enhancers	Liver	Liver
31	chr9:12328800-12329000	Enhancers	Pancreas	Pancrea
32	chr9:12329000-12329200	Enhancers	Adipose Nuclei	Adipose
33	chr9:12329000-12329200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
34	chr9:12329000-12329200	Enhancers	Fetal Muscle Trunk	muscle
35	chr9:12329000-12329400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr9:12329000-12329400	Flanking Active TSS	Liver	Liver
37	chr9:12329000-12329600	Active TSS	ES-I3 Cell Line	embryonic stem cell
38	chr9:12329000-12329600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr9:12329000-12329600	Active TSS	Pancreatic Islets	Pancreatic Islet
40	chr9:12329000-12329600	Flanking Active TSS	Pancreas	Pancrea
41	chr9:12329000-12329600	Active TSS	HepG2	liver
42	chr9:12329200-12329400	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr9:12329200-12329400	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
44	chr9:12329200-12329600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr9:12329200-12329600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr9:12329200-12329600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr9:12329200-12329600	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr9:12329200-12329600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr9:12329200-12329600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr9:12329200-12329600	Flanking Active TSS	Adipose Nuclei	Adipose

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