Variant report

Variant	esv2757351
Chromosome Location	chr9:115600623-115632898
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:655)
CpG islands
(count:61)
Chromatin interactive
region (count:45)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:655 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:115603482-115603902	HepG2	liver:	n/a	n/a
2	ATF1	chr9:115611268-115611477	K562	blood:	n/a	n/a
3	ATF2	chr9:115606922-115607303	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr9:115621098-115621235	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr9:115621209-115621488	GM12878	blood:	n/a	n/a
6	BCL11A	chr9:115621246-115621416	GM12878	blood:	n/a	n/a
7	BCL11A	chr9:115600632-115600823	GM12878	blood:	n/a	n/a
8	BCL11A	chr9:115621204-115621471	GM12878	blood:	n/a	n/a
9	BCL3	chr9:115627132-115627467	GM12878	blood:	n/a	n/a
10	BCL3	chr9:115626023-115626414	GM12878	blood:	n/a	n/a
11	BCLAF1	chr9:115607014-115607329	GM12878	blood:	n/a	n/a
12	BCLAF1	chr9:115620709-115621551	GM12878	blood:	n/a	n/a
13	BCLAF1	chr9:115606891-115607373	GM12878	blood:	n/a	n/a
14	BHLHE40	chr9:115607008-115607287	K562	blood:	n/a	n/a
15	BHLHE40	chr9:115606949-115607313	GM12878	blood:	n/a	n/a
16	BHLHE40	chr9:115606891-115607271	HepG2	liver:	n/a	n/a
17	BHLHE40	chr9:115624131-115624331	K562	blood:	n/a	n/a
18	BRCA1	chr9:115629713-115629985	H1-hESC	embryonic stem cell:	n/a	n/a
19	BRCA1	chr9:115629718-115629952	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr9:115628994-115629477	H1-hESC	embryonic stem cell:	n/a	n/a
21	CBX3	chr9:115606922-115607388	K562	blood:	n/a	n/a
22	CBX3	chr9:115606856-115607430	HCT-116	colon:	n/a	n/a
23	CBX3	chr9:115606975-115607333	K562	blood:	n/a	n/a
24	CEBPB	chr9:115625617-115625896	Hela-S3	cervix:	n/a	chr9:115625735-115625746
25	CEBPB	chr9:115615155-115615435	ECC-1	luminal epithelium:	n/a	n/a
26	CEBPB	chr9:115625748-115625788	K562	blood:	n/a	n/a
27	CEBPB	chr9:115630038-115630340	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr9:115621134-115621471	K562	blood:	n/a	chr9:115621295-115621306
29	CEBPB	chr9:115621177-115621336	H1-hESC	embryonic stem cell:	n/a	chr9:115621295-115621306
30	CEBPB	chr9:115621126-115621454	A549	lung:	n/a	chr9:115621295-115621306
31	CEBPB	chr9:115625604-115625904	HepG2	liver:	n/a	chr9:115625735-115625746
32	CEBPB	chr9:115621116-115621479	HepG2	liver:	n/a	chr9:115621295-115621306
33	CEBPB	chr9:115609098-115609519	IMR90	lung:	n/a	n/a
34	CEBPB	chr9:115615246-115615332	K562	blood:	n/a	n/a
35	CEBPB	chr9:115621111-115621485	IMR90	lung:	n/a	chr9:115621295-115621306
36	CEBPB	chr9:115625608-115625925	IMR90	lung:	n/a	chr9:115625735-115625746
37	CEBPB	chr9:115624246-115624791	IMR90	lung:	n/a	n/a
38	CEBPB	chr9:115611114-115611374	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr9:115621202-115621323	HepG2	liver:	n/a	chr9:115621295-115621306
40	CEBPB	chr9:115630030-115630369	IMR90	lung:	n/a	n/a
41	CEBPB	chr9:115621216-115621452	GM12878	blood:	n/a	chr9:115621295-115621306
42	CHD2	chr9:115629100-115630187	Hela-S3	cervix:	n/a	n/a
43	CTCF	chr9:115607080-115607230	GM12869	blood:	n/a	chr9:115607137-115607150 chr9:115607137-115607150 chr9:115607135-115607151 chr9:115607134-115607152 chr9:115607136-115607157
44	CTCF	chr9:115607060-115607210	HVMF	connective:	n/a	chr9:115607137-115607150 chr9:115607137-115607150 chr9:115607135-115607151 chr9:115607134-115607152 chr9:115607136-115607157
45	CTCF	chr9:115607040-115607190	HUVEC	blood vessel:	n/a	chr9:115607137-115607150 chr9:115607137-115607150 chr9:115607135-115607151 chr9:115607134-115607152 chr9:115607136-115607157
46	CTCF	chr9:115606978-115607315	H1-hESC	embryonic stem cell:	n/a	chr9:115607137-115607150 chr9:115607137-115607150 chr9:115607135-115607151 chr9:115607134-115607152 chr9:115607136-115607157
47	CTCF	chr9:115607060-115607210	GM12864	blood:	n/a	chr9:115607137-115607150 chr9:115607137-115607150 chr9:115607135-115607151 chr9:115607134-115607152 chr9:115607136-115607157
48	CTCF	chr9:115607014-115607263	MCF-7	breast:	n/a	chr9:115607137-115607150 chr9:115607137-115607150 chr9:115607135-115607151 chr9:115607134-115607152 chr9:115607136-115607157
49	CTCF	chr9:115612620-115612770	AG09309	skin:	n/a	chr9:115612685-115612694
50	CTCF	chr9:115607040-115607190	HL-60	blood:	n/a	chr9:115607137-115607150 chr9:115607137-115607150 chr9:115607135-115607151 chr9:115607134-115607152 chr9:115607136-115607157

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:115631083-115631133	HCT-116	colon:	n/a
2	chr9:115631083-115631133	Jurkat	blood:	n/a
3	chr9:115631083-115631133	MCF-7	breast:	n/a
4	chr9:115631083-115631133	NB4	blood:	n/a
5	chr9:115631083-115631133	HEEpiC	esophagus:	n/a
6	chr9:115631083-115631133	AG10803	skin:	n/a
7	chr9:115631083-115631133	HRPEpiC	eye:	n/a
8	chr9:115631083-115631133	ECC-1	luminal epithelium:	n/a
9	chr9:115631083-115631133	IMR90	lung:	fetal
10	chr9:115631083-115631133	T-47D	breast:	n/a
11	chr9:115631083-115631133	HAEpiC	amniotic membrane:	n/a
12	chr9:115631083-115631133	SKMC	muscle:	n/a
13	chr9:115631083-115631133	PFSK-1	brain:	n/a
14	chr9:115631083-115631133	GM12878	blood:	n/a
15	chr9:115631083-115631133	HMEC	breast:	n/a
16	chr9:115631083-115631133	HNPCEpiC	eye:	n/a
17	chr9:115631083-115631133	SK-N-MC	brain:	n/a
18	chr9:115631083-115631133	CMK	blood:	n/a
19	chr9:115631083-115631133	HL-60	blood:	n/a
20	chr9:115631083-115631133	GM06990	blood:	n/a
21	chr9:115631083-115631133	ovcar-3	ovarian:	n/a
22	chr9:115631083-115631133	A549	lung:	n/a
23	chr9:115631083-115631133	HCF	heart:	n/a
24	chr9:115631083-115631133	RPTEC	kidney:	n/a
25	chr9:115631083-115631133	HEK293	kidney:	embryo
26	chr9:115631083-115631133	HPAEpiC	pulmonary alveolar:	n/a
27	chr9:115631083-115631133	HRCEpiC	kidney:	n/a
28	chr9:115631083-115631133	AG09309	skin:	n/a
29	chr9:115631083-115631133	PrEC	prostate:	n/a
30	chr9:115631083-115631133	GM12891	blood:	n/a
31	chr9:115631083-115631133	MCF10A-Er-Src	breast:	n/a
32	chr9:115631083-115631133	HCM	heart:	n/a
33	chr9:115631083-115631133	AG04450	lung:	fetal
34	chr9:115631083-115631133	Caco-2	colon:	n/a
35	chr9:115631083-115631133	BJ	skin:	n/a
36	chr9:115631083-115631133	Hela-S3	cervix:	n/a
37	chr9:115631083-115631133	K562	blood:	n/a
38	chr9:115631083-115631133	LNCaP	prostate:	n/a
39	chr9:115631083-115631133	Hepatocyte	liver:	n/a
40	chr9:115631083-115631133	H1-hESC	embryonic stem cell:	embryo
41	chr9:115631083-115631133	AG09319	gingival:	n/a
42	chr9:115631083-115631133	HRE	kidney:	n/a
43	chr9:115631083-115631133	HCPEpiC	choroid plexus:	n/a
44	chr9:115631083-115631133	NT2-D1	testis:	n/a
45	chr9:115631083-115631133	AG04449	skin:	fetal
46	chr9:115631083-115631133	HUVEC	blood vessel:	n/a
47	chr9:115631083-115631133	U87	brain:	n/a
48	chr9:115631083-115631133	NHDF-neo	bronchial:	n/a
49	chr9:115631083-115631133	GM12892	blood:	n/a
50	chr9:115631083-115631133	BE2_C	brain:	n/a

(count:45 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:115606178..115608888-chr9:115665655..115667772,2	K562	blood:
2	chr9:115628888..115632126-chr9:115633392..115636528,4	K562	blood:
3	chr9:115606591..115607824-chr9:115664991..115666131,23	MCF-7	breast:
4	chr9:115512658..115514289-chr9:115605391..115606971,2	K562	blood:
5	chr9:115622331..115624612-chr9:115626867..115628416,2	K562	blood:
6	chr9:115606716..115607610-chr9:115664880..115666423,8	MCF-7	breast:
7	chr9:115606797..115607665-chr9:115683466..115683976,2	MCF-7	breast:
8	chr9:115605115..115608085-chr9:115663970..115666331,4	MCF-7	breast:
9	chr9:115606672..115607642-chr9:115665315..115666036,4	K562	blood:
10	chr9:115605264..115607754-chr9:115609316..115612065,2	MCF-7	breast:
11	chr9:115598488..115601038-chr9:115603652..115606343,4	MCF-7	breast:
12	chr9:115630001..115632301-chr9:115634628..115637570,3	MCF-7	breast:
13	chr9:115614764..115617679-chr9:115622672..115625535,2	K562	blood:
14	chr9:115625288..115627848-chr9:115629822..115631773,2	K562	blood:
15	chr9:115606663..115607630-chr9:115649377..115650352,3	K562	blood:
16	chr9:115615876..115617436-chr9:115625877..115628749,2	MCF-7	breast:
17	chr9:115607030..115607606-chr9:115644620..115645220,2	MCF-7	breast:
18	chr9:115616161..115618077-chr9:115630043..115631979,2	MCF-7	breast:
19	chr9:115616179..115618234-chr9:115622844..115625535,2	K562	blood:
20	chr9:115607502..115609208-chr9:115615429..115617354,2	MCF-7	breast:
21	chr9:115623112..115625247-chr9:115625662..115630540,4	K562	blood:
22	chr9:115588210..115591138-chr9:115628992..115630690,2	MCF-7	breast:
23	chr9:115606700..115607559-chr9:115646453..115647076,3	MCF-7	breast:
24	chr9:115615772..115618098-chr9:115620406..115622597,2	K562	blood:
25	chr9:115615876..115617436-chr9:115625877..115628749,2	MCF-7	breast:
26	chr9:115612240..115614238-chr9:115614501..115616948,2	K562	blood:
27	chr9:115616161..115618077-chr9:115630043..115631979,2	MCF-7	breast:
28	chr9:115625288..115627848-chr9:115629822..115631773,2	K562	blood:
29	chr9:115629889..115631673-chr9:115633392..115635288,2	K562	blood:
30	chr9:115612240..115614238-chr9:115614501..115616948,2	K562	blood:
31	chr9:115608067..115608649-chr9:115665121..115665685,2	MCF-7	breast:
32	chr9:115568175..115570231-chr9:115604790..115606325,2	K562	blood:
33	chr9:115606627..115607225-chr9:115774405..115774960,2	K562	blood:
34	chr9:115609355..115610986-chr9:115659802..115661844,2	MCF-7	breast:
35	chr9:115615772..115618098-chr9:115620406..115622597,2	K562	blood:
36	chr9:115632762..115634297-chr9:115636411..115638284,2	K562	blood:
37	chr9:115607502..115609208-chr9:115615429..115617354,2	MCF-7	breast:
38	chr9:115614764..115617679-chr9:115622672..115625535,2	K562	blood:
39	chr9:115606376..115607335-chr9:115649571..115650256,3	MCF-7	breast:
40	chr9:115607981..115610113-chr9:115651782..115654095,2	MCF-7	breast:
41	chr9:115606728..115607289-chr9:115644336..115645178,2	MCF-7	breast:
42	chr9:115622331..115624612-chr9:115626867..115628416,2	K562	blood:
43	chr9:115623112..115625247-chr9:115625662..115630540,4	K562	blood:
44	chr9:115605264..115607754-chr9:115609316..115612065,2	MCF-7	breast:
45	chr9:115616179..115618234-chr9:115622844..115625535,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC46A2-1	chr9:115631918-115632206	ENSG00000249440

No data

Variant related genes	Relation type
SNX30	TF binding region
SNX30	CpG island
ENSG00000228623	chromatin interactions
ENSG00000148158	chromatin interactions
ENSG00000226609	chromatin interactions
ENSG00000119457	chromatin interactions
S100A7A	miRNA target sites

Extended variants
information (count: 1312 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:1312 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10732374	chr9:115600623-115600624	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs143283453	chr9:115600643-115600644	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs563555153	chr9:115600646-115600647	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs529185045	chr9:115600677-115600678	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs548966450	chr9:115600679-115600680	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs189745142	chr9:115600746-115600747	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs374697212	chr9:115600756-115600757	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs111658028	chr9:115600803-115600804	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs192545589	chr9:115600817-115600818	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs41280189	chr9:115600827-115600828	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs377422322	chr9:115600828-115600829	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs550802917	chr9:115600830-115600831	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs7023478	chr9:115600848-115600849	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs377593324	chr9:115600854-115600855	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs370564061	chr9:115600862-115600863	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs375010038	chr9:115600890-115600891	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs202023916	chr9:115600913-115600914	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs567913929	chr9:115600935-115600936	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs367671239	chr9:115600999-115601000	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs572541801	chr9:115601013-115601014	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs536564453	chr9:115601068-115601069	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs553280650	chr9:115601106-115601107	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs367912253	chr9:115601125-115601126	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs572887725	chr9:115601127-115601128	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs10981520	chr9:115601129-115601130	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs73656444	chr9:115601149-115601150	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs184353754	chr9:115601156-115601157	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs138717327	chr9:115601176-115601177	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs79354162	chr9:115601177-115601178	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs543565677	chr9:115601179-115601180	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs62576432	chr9:115601180-115601181	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs10981521	chr9:115601183-115601184	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs529160546	chr9:115601197-115601198	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs140334222	chr9:115601232-115601233	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs10981522	chr9:115601252-115601253	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs113656965	chr9:115601274-115601275	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs145581003	chr9:115601320-115601321	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs144046148	chr9:115601348-115601349	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs190517374	chr9:115601354-115601355	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs372167535	chr9:115601379-115601380	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs374813990	chr9:115601422-115601423	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs78256720	chr9:115601425-115601426	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs7038684	chr9:115601431-115601432	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs10981523	chr9:115601455-115601456	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs115936294	chr9:115601531-115601532	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs563373283	chr9:115601552-115601553	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs566871498	chr9:115601553-115601554	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs530636030	chr9:115601605-115601606	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs10817393	chr9:115601649-115601650	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs372594036	chr9:115601653-115601654	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:53)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
small cell lung cancer	20016488	CNVD
Cardiac fibroma	18329553	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	21364760	CNVD
Developmental delay	21147756	CNVD
Lung cancer	19147751	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1293 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:115565000-115600800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
2	chr9:115565600-115600800	Weak transcription	HMEC	breast
3	chr9:115570600-115608400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr9:115573600-115607800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr9:115575000-115600800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
6	chr9:115577600-115630400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
7	chr9:115579000-115600800	Weak transcription	Fetal Brain Male	brain
8	chr9:115580200-115608400	Weak transcription	Fetal Kidney	kidney
9	chr9:115580600-115601800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr9:115582200-115608600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
11	chr9:115582400-115608600	Weak transcription	NHLF	lung
12	chr9:115582400-115609000	Weak transcription	NHDF-Ad	bronchial
13	chr9:115582400-115630000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
14	chr9:115584400-115608800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr9:115591200-115606800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
16	chr9:115591400-115623200	Weak transcription	Fetal Heart	heart
17	chr9:115592600-115607200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
18	chr9:115593200-115611000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
19	chr9:115593400-115602600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr9:115593600-115607200	Weak transcription	Muscle Satellite Cultured Cells	--
21	chr9:115594000-115602800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr9:115594200-115600800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr9:115594200-115603000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
24	chr9:115594200-115607200	Weak transcription	Fetal Thymus	thymus
25	chr9:115594200-115610800	Weak transcription	Esophagus	oesophagus
26	chr9:115594200-115616000	Weak transcription	Small Intestine	intestine
27	chr9:115594200-115620400	Weak transcription	Thymus	Thymus
28	chr9:115594200-115634400	Weak transcription	NH-A	brain
29	chr9:115594400-115601400	Weak transcription	Fetal Brain Female	brain
30	chr9:115594400-115608600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr9:115594400-115626800	Weak transcription	Colon Smooth Muscle	Colon
32	chr9:115594600-115607200	Weak transcription	Primary B cells from peripheral blood	blood
33	chr9:115594600-115607200	Weak transcription	Skeletal Muscle Male	skeletal muscle
34	chr9:115595600-115602400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr9:115596200-115604000	Strong transcription	Fetal Stomach	stomach
36	chr9:115596400-115613600	Weak transcription	Placenta Amnion	Placenta Amnion
37	chr9:115596600-115601200	Enhancers	Stomach Mucosa	stomach
38	chr9:115597400-115605600	Strong transcription	Primary T cells from cord blood	blood
39	chr9:115598000-115605000	Strong transcription	Fetal Muscle Leg	muscle
40	chr9:115598200-115601000	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr9:115598200-115602400	Strong transcription	Skeletal Muscle Female	skeletal muscle
42	chr9:115598200-115602600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr9:115598400-115601000	Strong transcription	Aorta	Aorta
44	chr9:115598400-115601400	Strong transcription	Cortex derived primary cultured neurospheres	brain
45	chr9:115598400-115602400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
46	chr9:115598400-115602600	Strong transcription	Ovary	ovary
47	chr9:115598400-115602800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
48	chr9:115598400-115603400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr9:115598400-115604800	Strong transcription	Fetal Muscle Trunk	muscle
50	chr9:115598600-115601200	Strong transcription	Brain Hippocampus Middle	brain

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