Variant report

Variant	nsv892619
Chromosome Location	chr9:14821819-14866389
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr9:14846813-14847157	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chr9:14822708-14823063	GM12878	blood:	n/a	n/a
3	BHLHE40	chr9:14831736-14831957	K562	blood:	n/a	n/a
4	CEBPB	chr9:14827792-14827904	IMR90	lung:	n/a	chr9:14827827-14827838
5	CEBPB	chr9:14827709-14827960	HepG2	liver:	n/a	chr9:14827827-14827838
6	CHD2	chr9:14846857-14847057	HepG2	liver:	n/a	n/a
7	CHD2	chr9:14846832-14847123	H1-hESC	embryonic stem cell:	n/a	n/a
8	CREB1	chr9:14846723-14847119	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTCF	chr9:14846860-14847010	GM12867	blood:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
10	CTCF	chr9:14846821-14847082	HepG2	liver:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
11	CTCF	chr9:14846860-14847010	HRE	kidney:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
12	CTCF	chr9:14846920-14847070	GM12866	blood:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
13	CTCF	chr9:14846880-14847030	GM12870	blood:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
14	CTCF	chr9:14846858-14847070	GM13976	blood:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
15	CTCF	chr9:14831903-14832009	K562	blood:	n/a	n/a
16	CTCF	chr9:14846900-14847050	AG09309	skin:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
17	CTCF	chr9:14845660-14845810	GM06990	blood:	n/a	n/a
18	CTCF	chr9:14846784-14847104	GM12892	blood:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
19	CTCF	chr9:14846773-14847111	Fibrobl	skin:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
20	CTCF	chr9:14846880-14847030	GM12866	blood:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
21	CTCF	chr9:14831800-14831831	GM10266	blood:	n/a	n/a
22	CTCF	chr9:14846880-14847030	HepG2	liver:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
23	CTCF	chr9:14846900-14847050	GM06990	blood:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
24	CTCF	chr9:14846840-14846990	NHLF	lung:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846949-14846965 chr9:14846943-14846964
25	CTCF	chr9:14846900-14847050	GM12865	blood:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
26	CTCF	chr9:14846880-14847030	HUVEC	blood vessel:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
27	CTCF	chr9:14831780-14831930	NHDF-neo	bronchial:	n/a	n/a
28	CTCF	chr9:14846554-14847343	A549	lung:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
29	CTCF	chr9:14846900-14847050	HBMEC	blood vessel:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
30	CTCF	chr9:14846820-14846970	HEEpiC	esophagus:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846949-14846965 chr9:14846943-14846964
31	CTCF	chr9:14847200-14847350	HEK293	kidney:	n/a	n/a
32	CTCF	chr9:14846829-14847086	Hela-S3	cervix:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
33	CTCF	chr9:14847212-14847311	GM20000	blood:	n/a	n/a
34	CTCF	chr9:14863480-14863630	HepG2	liver:	n/a	chr9:14863553-14863574 chr9:14863556-14863564 chr9:14863551-14863569
35	CTCF	chr9:14846808-14847115	A549	lung:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
36	CTCF	chr9:14846860-14847010	AoAF	blood vessel:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
37	CTCF	chr9:14846838-14847067	LNCaP	prostate:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
38	CTCF	chr9:14846780-14846930	HFF-Myc	foreskin:	n/a	n/a
39	CTCF	chr9:14846812-14847097	HUVEC	blood vessel:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
40	CTCF	chr9:14846745-14847152	H1-hESC	embryonic stem cell:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
41	CTCF	chr9:14846829-14847104	LNCaP	prostate:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
42	CTCF	chr9:14846880-14847030	GM12871	blood:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
43	CTCF	chr9:14846778-14847123	Gliobla	brain:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
44	CTCF	chr9:14846860-14847010	K562	blood:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
45	CTCF	chr9:14846860-14847010	HFF	foreskin:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
46	CTCF	chr9:14846880-14847030	RPTEC	kidney:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
47	CTCF	chr9:14831960-14832110	HFF	foreskin:	n/a	n/a
48	CTCF	chr9:14846860-14847010	GM12872	blood:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
49	CTCF	chr9:14846900-14847050	GM12872	blood:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
50	CTCF	chr9:14846778-14847109	GM12891	blood:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:14838752-14838802	AG04449	skin:	fetal
2	chr9:14838752-14838802	HCT-116	colon:	n/a
3	chr9:14838752-14838802	NT2-D1	testis:	n/a
4	chr9:14838752-14838802	K562	blood:	n/a
5	chr9:14838752-14838802	Jurkat	blood:	n/a
6	chr9:14838752-14838802	NHBE	bronchial:	n/a
7	chr9:14838752-14838802	A549	lung:	n/a
8	chr9:14838752-14838802	HRE	kidney:	n/a
9	chr9:14838752-14838802	ProgFib	skin:	n/a
10	chr9:14838752-14838802	HCPEpiC	choroid plexus:	n/a
11	chr9:14838752-14838802	AG09309	skin:	n/a
12	chr9:14838752-14838802	HEK293	kidney:	embryo
13	chr9:14838752-14838802	HUVEC	blood vessel:	n/a
14	chr9:14838752-14838802	HCF	heart:	n/a
15	chr9:14838752-14838802	AG09319	gingival:	n/a
16	chr9:14838752-14838802	T-47D	breast:	n/a
17	chr9:14838752-14838802	HIPEpiC	eye:	n/a
18	chr9:14838752-14838802	CMK	blood:	n/a
19	chr9:14838752-14838802	GM12892	blood:	n/a
20	chr9:14838752-14838802	PrEC	prostate:	n/a
21	chr9:14838752-14838802	SK-N-SH	brain:	n/a
22	chr9:14838752-14838802	H1-hESC	embryonic stem cell:	embryo
23	chr9:14838752-14838802	HMEC	breast:	n/a
24	chr9:14838752-14838802	SKMC	muscle:	n/a
25	chr9:14838752-14838802	BE2_C	brain:	n/a
26	chr9:14838752-14838802	GM06990	blood:	n/a
27	chr9:14838752-14838802	NH-A	brain:	n/a
28	chr9:14838752-14838802	Hepatocyte	liver:	n/a
29	chr9:14838752-14838802	ECC-1	luminal epithelium:	n/a
30	chr9:14838752-14838802	MCF-7	breast:	n/a
31	chr9:14838752-14838802	GM12878	blood:	n/a
32	chr9:14838752-14838802	AG10803	skin:	n/a
33	chr9:14838752-14838802	MCF10A-Er-Src	breast:	n/a
34	chr9:14838752-14838802	GM19239	blood:	n/a
35	chr9:14838752-14838802	U87	brain:	n/a
36	chr9:14838752-14838802	HL-60	blood:	n/a
37	chr9:14838752-14838802	IMR90	lung:	fetal
38	chr9:14838752-14838802	NB4	blood:	n/a
39	chr9:14838752-14838802	AG04450	lung:	fetal
40	chr9:14838752-14838802	NHDF-neo	bronchial:	n/a
41	chr9:14838752-14838802	PFSK-1	brain:	n/a
42	chr9:14838752-14838802	HRPEpiC	eye:	n/a
43	chr9:14838752-14838802	Hela-S3	cervix:	n/a
44	chr9:14838752-14838802	PANC-1	pancreas:	n/a
45	chr9:14838752-14838802	AoSMC	blood vessel:	n/a
46	chr9:14838752-14838802	HepG2	liver:	n/a
47	chr9:14838752-14838802	HEEpiC	esophagus:	n/a
48	chr9:14838752-14838802	SK-N-MC	brain:	n/a
49	chr9:14838752-14838802	Caco-2	colon:	n/a
50	chr9:14838752-14838802	RPTEC	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:14850312..14853276-chr9:14856165..14857741,2	MCF-7	breast:
2	chr9:14842932..14845441-chr9:14846633..14848951,2	K562	blood:
3	chr9:14843588..14845441-chr9:14847451..14849631,2	K562	blood:
4	chr9:14843588..14845441-chr9:14847451..14849631,2	K562	blood:
5	chr9:14846510..14847037-chr9:15142689..15143560,2	MCF-7	breast:
6	chr9:14691985..14694492-chr9:14845348..14847282,2	MCF-7	breast:
7	chr9:14842932..14845441-chr9:14846633..14848951,2	K562	blood:

Variant related genes	Relation type
RNU6-1260P	TF binding region
RNU6-1260P	CpG island
ENSG00000251960	chromatin interactions
ENSG00000199814	chromatin interactions
ENSG00000175893	chromatin interactions

Extended variants
information (count: 2281 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:2281 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2779503	chr9:14821819-14821820	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs71476228	chr9:14821833-14821834	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs2779504	chr9:14821878-14821879	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs531243196	chr9:14821897-14821898	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs552946584	chr9:14821900-14821901	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs571262071	chr9:14821915-14821916	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs558176077	chr9:14821919-14821920	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs571159492	chr9:14821920-14821921	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs2642409	chr9:14821930-14821931	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs2779505	chr9:14821937-14821938	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs573520893	chr9:14821983-14821984	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs150655168	chr9:14821985-14821986	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs554345653	chr9:14821988-14821989	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs4741435	chr9:14821996-14821997	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs139871991	chr9:14822010-14822011	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs112276758	chr9:14822042-14822043	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs190284225	chr9:14822045-14822046	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs541099287	chr9:14822062-14822063	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs182504005	chr9:14822082-14822083	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs530156102	chr9:14822099-14822100	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs572941176	chr9:14822115-14822116	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs143936388	chr9:14822127-14822128	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs200462796	chr9:14822221-14822222	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs375394019	chr9:14822234-14822235	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs377088303	chr9:14822247-14822248	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs59768450	chr9:14822268-14822269	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs372685021	chr9:14822275-14822276	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs533635562	chr9:14822306-14822307	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs13292779	chr9:14822314-14822315	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs77211151	chr9:14822336-14822337	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs571093601	chr9:14822345-14822346	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs532100475	chr9:14822358-14822359	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs146871525	chr9:14822370-14822371	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs372337245	chr9:14822378-14822379	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs535950594	chr9:14822379-14822380	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs554284310	chr9:14822401-14822402	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs11788492	chr9:14822411-14822412	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs532268365	chr9:14822450-14822451	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs2642408	chr9:14822454-14822455	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs140532818	chr9:14822479-14822480	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs369144155	chr9:14822527-14822528	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs577076495	chr9:14822540-14822541	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs144183005	chr9:14822560-14822561	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs553093010	chr9:14822578-14822579	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs78851862	chr9:14822579-14822580	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs145251850	chr9:14822603-14822604	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs563803455	chr9:14822658-14822659	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs191192066	chr9:14822659-14822660	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs546437593	chr9:14822686-14822687	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs564773598	chr9:14822687-14822688	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	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
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	22183965	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21611746	CNVD
Glycine encephalopathy	21572526	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Non-small cell lung cancer	19010865	CNVD
Myoepithelioma	18604193	CNVD
Glioblastoma multiforme	18628472	CNVD
Breast cancer	22522925	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:261 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:14779800-14853200	Weak transcription	Placenta	Placenta
2	chr9:14780400-14843200	Weak transcription	Fetal Heart	heart
3	chr9:14782000-14822000	Weak transcription	Fetal Brain Male	brain
4	chr9:14782800-14822000	Weak transcription	Rectal Smooth Muscle	rectum
5	chr9:14793000-14822600	Weak transcription	Duodenum Smooth Muscle	Duodenum
6	chr9:14801800-14857200	Strong transcription	HepG2	liver
7	chr9:14807200-14822800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr9:14807400-14868600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr9:14809200-14847600	Weak transcription	Fetal Intestine Small	intestine
10	chr9:14810200-14831400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr9:14810400-14849600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr9:14813000-14823000	Weak transcription	Fetal Intestine Large	intestine
13	chr9:14814200-14842200	Weak transcription	Pancreas	Pancrea
14	chr9:14815000-14824600	Strong transcription	Adipose Nuclei	Adipose
15	chr9:14815200-14831800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr9:14816400-14824200	Strong transcription	Aorta	Aorta
17	chr9:14816400-14826000	Strong transcription	Fetal Kidney	kidney
18	chr9:14816600-14826200	Strong transcription	Fetal Lung	lung
19	chr9:14818000-14822200	Weak transcription	Fetal Muscle Leg	muscle
20	chr9:14820000-14822400	Strong transcription	Fetal Stomach	stomach
21	chr9:14820200-14823800	Strong transcription	Fetal Muscle Trunk	muscle
22	chr9:14820200-14825400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
23	chr9:14820400-14822400	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr9:14820600-14823400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr9:14821600-14823400	Strong transcription	Duodenum Mucosa	Duodenum
26	chr9:14821800-14822000	Strong transcription	Colon Smooth Muscle	Colon
27	chr9:14822000-14822400	Weak transcription	Colon Smooth Muscle	Colon
28	chr9:14822200-14822800	Strong transcription	Fetal Muscle Leg	muscle
29	chr9:14822400-14823400	Enhancers	Primary B cells from peripheral blood	blood
30	chr9:14822400-14824200	Strong transcription	Colon Smooth Muscle	Colon
31	chr9:14822400-14824600	Enhancers	GM12878-XiMat	blood
32	chr9:14822400-14827800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr9:14822400-14827800	Weak transcription	Fetal Stomach	stomach
34	chr9:14822800-14824000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr9:14822800-14829600	Weak transcription	Fetal Muscle Leg	muscle
36	chr9:14823000-14825000	Strong transcription	Fetal Intestine Large	intestine
37	chr9:14823400-14824800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr9:14823400-14848400	Weak transcription	Duodenum Mucosa	Duodenum
39	chr9:14823800-14826600	Weak transcription	Fetal Muscle Trunk	muscle
40	chr9:14824000-14852800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr9:14824200-14826400	Weak transcription	Colon Smooth Muscle	Colon
42	chr9:14824200-14827800	Weak transcription	Aorta	Aorta
43	chr9:14824600-14826400	Weak transcription	Adipose Nuclei	Adipose
44	chr9:14824800-14829400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr9:14825000-14841400	Weak transcription	Fetal Intestine Large	intestine
46	chr9:14825400-14826400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
47	chr9:14826000-14828800	Weak transcription	Fetal Kidney	kidney
48	chr9:14826000-14849600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
49	chr9:14826200-14826800	Weak transcription	Fetal Lung	lung
50	chr9:14826400-14826800	Strong transcription	Colon Smooth Muscle	Colon

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