Variant report

Variant	esv2761543
Chromosome Location	chr9:96857735-96875582
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:208)
CpG islands
(count:122)
Chromatin interactive
region (count:36)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:208 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:96873101-96873841	K562	blood:	n/a	n/a
2	ARID3A	chr9:96862904-96863149	K562	blood:	n/a	n/a
3	ARID3A	chr9:96875134-96875677	K562	blood:	n/a	n/a
4	ATF1	chr9:96875013-96875701	K562	blood:	n/a	n/a
5	ATF1	chr9:96872973-96873553	K562	blood:	n/a	n/a
6	ATF3	chr9:96873201-96873498	K562	blood:	n/a	n/a
7	CBX3	chr9:96875090-96875847	K562	blood:	n/a	n/a
8	CCNT2	chr9:96873159-96873548	K562	blood:	n/a	n/a
9	CCNT2	chr9:96859774-96860136	K562	blood:	n/a	n/a
10	CEBPB	chr9:96858936-96858963	K562	blood:	n/a	chr9:96858939-96858950 chr9:96858937-96858950 chr9:96858937-96858950 chr9:96858937-96858950
11	CEBPB	chr9:96873097-96873603	K562	blood:	n/a	n/a
12	CEBPB	chr9:96865300-96865580	K562	blood:	n/a	chr9:96865427-96865444 chr9:96865428-96865441 chr9:96865429-96865440
13	CEBPB	chr9:96865368-96865451	HepG2	liver:	n/a	chr9:96865427-96865444 chr9:96865428-96865441 chr9:96865429-96865440
14	CEBPB	chr9:96873130-96873720	K562	blood:	n/a	n/a
15	CEBPB	chr9:96875227-96875657	K562	blood:	n/a	n/a
16	CEBPB	chr9:96865307-96865507	A549	lung:	n/a	chr9:96865427-96865444 chr9:96865428-96865441 chr9:96865429-96865440
17	CEBPB	chr9:96873172-96873508	K562	blood:	n/a	n/a
18	CEBPB	chr9:96859969-96860484	IMR90	lung:	n/a	n/a
19	CEBPB	chr9:96873059-96873855	IMR90	lung:	n/a	n/a
20	CEBPB	chr9:96865262-96865552	IMR90	lung:	n/a	chr9:96865427-96865444 chr9:96865428-96865441 chr9:96865429-96865440
21	CEBPD	chr9:96873123-96873594	K562	blood:	n/a	n/a
22	CEBPD	chr9:96873058-96873637	K562	blood:	n/a	n/a
23	CTCF	chr9:96860020-96860170	GM12869	blood:	n/a	n/a
24	CTCF	chr9:96873403-96873537	K562	blood:	n/a	n/a
25	CTCF	chr9:96873880-96874030	HFF-Myc	foreskin:	n/a	n/a
26	CTCF	chr9:96870880-96871030	HPAF	blood vessel:	n/a	n/a
27	CUX1	chr9:96861502-96861644	K562	blood:	n/a	n/a
28	CUX1	chr9:96873242-96873637	K562	blood:	n/a	n/a
29	E2F4	chr9:96859188-96859600	MCF10A-Er-Src	breast:	n/a	n/a
30	E2F4	chr9:96860004-96860283	MCF10A-Er-Src	breast:	n/a	n/a
31	EP300	chr9:96875229-96875717	K562	blood:	n/a	n/a
32	EP300	chr9:96860018-96860515	SK-N-SH_RA	brain:	n/a	n/a
33	EP300	chr9:96873071-96873873	K562	blood:	n/a	n/a
34	EP300	chr9:96859842-96860669	SK-N-SH	brain:	n/a	n/a
35	EP300	chr9:96859983-96860510	SK-N-SH_RA	brain:	n/a	n/a
36	EP300	chr9:96862449-96862778	SK-N-SH_RA	brain:	n/a	n/a
37	EP300	chr9:96873207-96873695	K562	blood:	n/a	n/a
38	EP300	chr9:96873310-96873493	GM12878	blood:	n/a	n/a
39	EP300	chr9:96870680-96870701	K562	blood:	n/a	n/a
40	EP300	chr9:96875497-96875520	GM12878	blood:	n/a	n/a
41	ESR1	chr9:96869564-96869851	T-47D	breast:	n/a	n/a
42	ESR1	chr9:96869552-96869901	ECC-1	luminal epithelium:	n/a	n/a
43	ESR1	chr9:96869622-96869791	T-47D	breast:	n/a	n/a
44	ESR1	chr9:96869533-96869904	T-47D	breast:	n/a	n/a
45	ESR1	chr9:96869532-96869909	T-47D	breast:	n/a	n/a
46	ESR1	chr9:96869564-96869817	ECC-1	luminal epithelium:	n/a	n/a
47	ESR1	chr9:96869568-96869900	ECC-1	luminal epithelium:	n/a	n/a
48	FOS	chr9:96859892-96860405	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr9:96858886-96860404	MCF10A-Er-Src	breast:	n/a	chr9:96859358-96859368 chr9:96859358-96859368 chr9:96859359-96859366 chr9:96859358-96859368 chr9:96859359-96859367 chr9:96859358-96859368 chr9:96859359-96859367
50	FOS	chr9:96873471-96873686	MCF10A-Er-Src	breast:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:96872879-96872929	ovcar-3	ovarian:	n/a
2	chr9:96872879-96872929	SAEC	small airway:	n/a
3	chr9:96872879-96872929	HUVEC	blood vessel:	n/a
4	chr9:96858147-96858197	PFSK-1	brain:	n/a
5	chr9:96872879-96872929	A549	lung:	n/a
6	chr9:96858147-96858197	ovcar-3	ovarian:	n/a
7	chr9:96858147-96858197	AG04449	skin:	fetal
8	chr9:96872879-96872929	HRPEpiC	eye:	n/a
9	chr9:96858147-96858197	AG09319	gingival:	n/a
10	chr9:96858147-96858197	MCF10A-Er-Src	breast:	n/a
11	chr9:96858147-96858197	BE2_C	brain:	n/a
12	chr9:96872879-96872929	HIPEpiC	eye:	n/a
13	chr9:96872879-96872929	HRCEpiC	kidney:	n/a
14	chr9:96872879-96872929	HCM	heart:	n/a
15	chr9:96872879-96872929	HNPCEpiC	eye:	n/a
16	chr9:96872879-96872929	Jurkat	blood:	n/a
17	chr9:96872879-96872929	PANC-1	pancreas:	n/a
18	chr9:96872879-96872929	NHBE	bronchial:	n/a
19	chr9:96872879-96872929	HEK293	kidney:	embryo
20	chr9:96858147-96858197	MCF-7	breast:	n/a
21	chr9:96858147-96858197	HMEC	breast:	n/a
22	chr9:96858147-96858197	IMR90	lung:	fetal
23	chr9:96872879-96872929	Caco-2	colon:	n/a
24	chr9:96858147-96858197	Hela-S3	cervix:	n/a
25	chr9:96858147-96858197	HEK293	kidney:	embryo
26	chr9:96872879-96872929	IMR90	lung:	fetal
27	chr9:96872879-96872929	NT2-D1	testis:	n/a
28	chr9:96872879-96872929	RPTEC	kidney:	n/a
29	chr9:96872879-96872929	ProgFib	skin:	n/a
30	chr9:96858147-96858197	ProgFib	skin:	n/a
31	chr9:96858147-96858197	HRE	kidney:	n/a
32	chr9:96872879-96872929	HL-60	blood:	n/a
33	chr9:96872879-96872929	GM06990	blood:	n/a
34	chr9:96872879-96872929	HPAEpiC	pulmonary alveolar:	n/a
35	chr9:96872879-96872929	NB4	blood:	n/a
36	chr9:96872879-96872929	GM12891	blood:	n/a
37	chr9:96872879-96872929	AG04450	lung:	fetal
38	chr9:96858147-96858197	SK-N-MC	brain:	n/a
39	chr9:96858147-96858197	HRPEpiC	eye:	n/a
40	chr9:96858147-96858197	A549	lung:	n/a
41	chr9:96872879-96872929	PFSK-1	brain:	n/a
42	chr9:96858147-96858197	AoSMC	blood vessel:	n/a
43	chr9:96872879-96872929	AG09319	gingival:	n/a
44	chr9:96858147-96858197	RPTEC	kidney:	n/a
45	chr9:96872879-96872929	SKMC	muscle:	n/a
46	chr9:96858147-96858197	Hepatocyte	liver:	n/a
47	chr9:96872879-96872929	MCF10A-Er-Src	breast:	n/a
48	chr9:96858147-96858197	HCF	heart:	n/a
49	chr9:96858147-96858197	HNPCEpiC	eye:	n/a
50	chr9:96858147-96858197	SAEC	small airway:	n/a

(count:36 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:96866936..96868703-chr9:96870555..96872203,2	K562	blood:
2	chr9:96847639..96850039-chr9:96863471..96865147,2	MCF-7	breast:
3	chr9:96858833..96861735-chr9:96944084..96946628,2	K562	blood:
4	chr9:96857107..96860210-chr9:96870662..96873792,3	MCF-7	breast:
5	chr9:96873250..96875198-chr9:96927135..96929620,4	K562	blood:
6	chr9:96847188..96849533-chr9:96856467..96859477,3	K562	blood:
7	chr9:96855901..96860991-chr9:96926600..96930762,9	MCF-7	breast:
8	chr9:96860361..96862564-chr9:96873614..96875631,2	K562	blood:
9	chr9:96860355..96862707-chr9:96868776..96872890,3	K562	blood:
10	chr9:96856357..96859423-chr9:96862063..96865399,3	MCF-7	breast:
11	chr9:96856270..96858806-chr9:96864043..96866239,3	MCF-7	breast:
12	chr9:96855903..96857740-chr9:96900937..96903523,2	MCF-7	breast:
13	chr9:96873433..96875351-chr9:96903210..96905278,2	MCF-7	breast:
14	chr9:96846694..96848203-chr9:96862701..96864601,2	MCF-7	breast:
15	chr9:96866936..96868703-chr9:96870555..96872203,2	K562	blood:
16	chr9:96871070..96874023-chr9:96892477..96895183,2	MCF-7	breast:
17	chr9:96856270..96858806-chr9:96864043..96866239,3	MCF-7	breast:
18	chr9:96859686..96862226-chr9:96927604..96929691,2	K562	blood:
19	chr9:96872510..96875198-chr9:96927204..96929620,4	K562	blood:
20	chr9:96861323..96864485-chr9:96867388..96870622,3	K562	blood:
21	chr9:96873193..96875324-chr9:96934781..96937611,2	K562	blood:
22	chr9:96866436..96868575-chr9:96873729..96876347,3	K562	blood:
23	chr9:96848027..96849533-chr9:96856014..96858976,2	K562	blood:
24	chr9:96858917..96860519-chr9:133389418..133391095,2	K562	blood:
25	chr9:96864692..96867836-chr9:96868310..96870488,3	K562	blood:
26	chr9:96825007..96827841-chr9:96858083..96859846,2	K562	blood:
27	chr9:96864659..96867120-chr9:96928060..96930580,2	K562	blood:
28	chr9:96863435..96865449-chr9:96927688..96930142,2	MCF-7	breast:
29	chr9:96866436..96868575-chr9:96873729..96876347,3	K562	blood:
30	chr9:96856390..96858828-chr9:96926161..96928705,2	K562	blood:
31	chr9:96871682..96874612-chr9:96882240..96883990,2	MCF-7	breast:
32	chr9:96861428..96863422-chr9:96927160..96928732,2	MCF-7	breast:
33	chr9:96864692..96867836-chr9:96868310..96870488,3	K562	blood:
34	chr9:96791853..96794356-chr9:96860367..96862558,2	MCF-7	breast:
35	chr9:96857107..96860210-chr9:96870662..96873792,3	MCF-7	breast:
36	chr9:96791026..96792800-chr9:96856915..96858416,2	MCF-7	breast:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	PTPDC1	hsa-miR-21-5p	chr9:96870389-96870410
2	PTPDC1	hsa-miR-340-5p	chr9:96871285-96871306

Variant related genes	Relation type
PTPDC1	TF binding region
PTPDC1	CpG island
ENSG00000158079	chromatin interactions
ENSG00000269946	chromatin interactions

Extended variants
information (count: 661 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:661 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs370796759	chr9:96857757-96857758	Active TSS Flanking Active TSS Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs373884213	chr9:96857766-96857767	Active TSS Flanking Active TSS Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs182583729	chr9:96857769-96857770	Active TSS Flanking Active TSS Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs371709489	chr9:96857888-96857889	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs562474269	chr9:96857892-96857893	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs374983658	chr9:96857900-96857901	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs116263654	chr9:96857901-96857902	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs551302649	chr9:96857941-96857942	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs566633362	chr9:96857949-96857950	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs7867925	chr9:96857990-96857991	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs535935447	chr9:96858015-96858016	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs549058196	chr9:96858045-96858046	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs138967850	chr9:96858091-96858092	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs537888042	chr9:96858105-96858106	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs142107517	chr9:96858125-96858126	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs373435373	chr9:96858145-96858146	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs578210899	chr9:96858170-96858171	Weak transcription Strong transcription Enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs56948438	chr9:96858182-96858183	Weak transcription Strong transcription Enhancers	CpG island Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs377186533	chr9:96858265-96858266	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs531696161	chr9:96858274-96858275	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs12001755	chr9:96858289-96858290	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs572561806	chr9:96858379-96858380	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs6479527	chr9:96858411-96858412	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
24	rs6479528	chr9:96858429-96858430	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs376848857	chr9:96858450-96858451	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs576108574	chr9:96858457-96858458	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs186905691	chr9:96858464-96858465	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs191596276	chr9:96858482-96858483	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs533099262	chr9:96858485-96858486	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs183750084	chr9:96858538-96858539	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs560098257	chr9:96858548-96858549	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs370721429	chr9:96858611-96858612	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs73518290	chr9:96858618-96858619	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs549195301	chr9:96858630-96858631	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs146399756	chr9:96858642-96858643	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs73518291	chr9:96858651-96858652	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs113939458	chr9:96858680-96858681	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs138492600	chr9:96858691-96858692	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs571192984	chr9:96858764-96858765	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs143040987	chr9:96858810-96858811	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs189429152	chr9:96858816-96858817	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs7869121	chr9:96858842-96858843	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs536479745	chr9:96858885-96858886	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs150624804	chr9:96858932-96858933	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs572421602	chr9:96858948-96858949	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs559407362	chr9:96859066-96859067	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs193152239	chr9:96859088-96859089	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs35156495	chr9:96859112-96859113	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs576145053	chr9:96859265-96859266	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs139689729	chr9:96859273-96859274	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:74)

Disease	PMID	Source
Chordoma	18071362	CNVD
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
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Melanoma	18172304	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
Leukemia	18688285	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
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Bipolar disorder	18458673	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Biliary cancer	19435499	CNVD
small cell lung cancer	20016488	CNVD
Intracranial aneurysm	16715129	CNVD
Cardiac fibroma	18329553	CNVD
Mental retardation	21693067	CNVD
Breast cancer	17133270	CNVD
Basal cell nevus syndrome	21572526	CNVD
Mental retardation	19951919	CNVD
Retinoblastoma	22278416	CNVD
9q22.3 microdeletion syndrome	22283845	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Microcephaly	18830227	CNVD
overgrowth syndrome	16570072	CNVD
Breast cancer	22522925	CNVD
Effusion lymphoma	18079361	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:467 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:96822400-96859800	Weak transcription	Psoas Muscle	Psoas
2	chr9:96824200-96860000	Weak transcription	Aorta	Aorta
3	chr9:96824200-96869600	Weak transcription	Skeletal Muscle Male	skeletal muscle
4	chr9:96828200-96859600	Weak transcription	Primary T helper cells PMA-I stimulated	--
5	chr9:96828200-96860800	Weak transcription	Primary T helper cells fromperipheralblood	blood
6	chr9:96828200-96862000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
7	chr9:96828200-96868200	Weak transcription	Rectal Mucosa Donor 31	rectum
8	chr9:96829600-96872400	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr9:96832000-96859800	Weak transcription	Rectal Mucosa Donor 29	rectum
10	chr9:96834400-96859800	Weak transcription	Duodenum Mucosa	Duodenum
11	chr9:96835400-96861800	Weak transcription	Primary B cells from cord blood	blood
12	chr9:96837200-96858600	Weak transcription	Dnd41	blood
13	chr9:96837200-96859800	Weak transcription	Fetal Intestine Small	intestine
14	chr9:96837400-96860200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr9:96837600-96859200	Weak transcription	Primary T cells from cord blood	blood
16	chr9:96840200-96863600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr9:96842600-96858200	Weak transcription	HSMMtube	muscle
18	chr9:96845600-96858200	Weak transcription	Right Ventricle	heart
19	chr9:96845600-96858400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
20	chr9:96845600-96885400	Weak transcription	Gastric	stomach
21	chr9:96846000-96870600	Weak transcription	Rectal Smooth Muscle	rectum
22	chr9:96846200-96859800	Weak transcription	Ovary	ovary
23	chr9:96847000-96859000	Weak transcription	Lung	lung
24	chr9:96847000-96859800	Weak transcription	Pancreas	Pancrea
25	chr9:96847000-96860200	Weak transcription	Fetal Muscle Trunk	muscle
26	chr9:96847200-96859000	Weak transcription	Fetal Brain Male	brain
27	chr9:96847200-96859000	Weak transcription	Fetal Brain Female	brain
28	chr9:96847600-96859200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr9:96847800-96859800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr9:96847800-96859800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr9:96847800-96860200	Weak transcription	Cortex derived primary cultured neurospheres	brain
32	chr9:96847800-96860200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
33	chr9:96847800-96860400	Weak transcription	Spleen	Spleen
34	chr9:96847800-96862600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr9:96848000-96863200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr9:96848600-96858600	Weak transcription	Brain Inferior Temporal Lobe	brain
37	chr9:96849000-96859600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
38	chr9:96849000-96868800	Weak transcription	HepG2	liver
39	chr9:96849200-96858400	Weak transcription	Fetal Intestine Large	intestine
40	chr9:96849200-96859800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr9:96849200-96859800	Weak transcription	NHLF	lung
42	chr9:96849400-96858200	Weak transcription	Duodenum Smooth Muscle	Duodenum
43	chr9:96849400-96859000	Weak transcription	Muscle Satellite Cultured Cells	--
44	chr9:96849400-96859000	Weak transcription	HMEC	breast
45	chr9:96849400-96859000	Weak transcription	NH-A	brain
46	chr9:96849400-96859800	Weak transcription	NHDF-Ad	bronchial
47	chr9:96849400-96866800	Weak transcription	Fetal Kidney	kidney
48	chr9:96849400-96869600	Weak transcription	HUVEC	blood vessel
49	chr9:96849400-96869800	Weak transcription	Colon Smooth Muscle	Colon
50	chr9:96849400-96883800	Weak transcription	Brain Germinal Matrix	brain

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