Variant report

Variant	nsv893742
Chromosome Location	chr9:115867276-115910991
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:866)
CpG islands
(count:183)
Chromatin interactive
region (count:44)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:866 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:115905739-115905943	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:115901124-115902211	HepG2	liver:	n/a	n/a
3	BATF	chr9:115875188-115875441	GM12878	blood:	n/a	n/a
4	BATF	chr9:115873657-115873969	GM12878	blood:	n/a	n/a
5	BHLHE40	chr9:115901592-115902043	HepG2	liver:	n/a	n/a
6	CBX3	chr9:115873150-115874076	K562	blood:	n/a	n/a
7	CBX3	chr9:115875083-115875868	K562	blood:	n/a	n/a
8	CEBPB	chr9:115900015-115900371	HepG2	liver:	n/a	chr9:115900196-115900207
9	CEBPB	chr9:115905520-115905886	HepG2	liver:	n/a	chr9:115905698-115905709
10	CEBPB	chr9:115875081-115875193	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr9:115901681-115902131	HepG2	liver:	n/a	n/a
12	CEBPB	chr9:115900103-115900282	Hela-S3	cervix:	n/a	chr9:115900196-115900207
13	CEBPB	chr9:115905556-115905870	K562	blood:	n/a	chr9:115905698-115905709
14	CEBPB	chr9:115905580-115905832	H1-hESC	embryonic stem cell:	n/a	chr9:115905698-115905709
15	CEBPB	chr9:115905565-115905847	A549	lung:	n/a	chr9:115905698-115905709
16	CEBPB	chr9:115899642-115900410	MCF-7	breast:	n/a	chr9:115900196-115900207 chr9:115899687-115899698
17	CEBPB	chr9:115905531-115905836	IMR90	lung:	n/a	chr9:115905698-115905709
18	CEBPB	chr9:115905629-115905817	Hela-S3	cervix:	n/a	chr9:115905698-115905709
19	CEBPZ	chr9:115890537-115890588	HepG2	liver:	n/a	n/a
20	CHD1	chr9:115874170-115874171	GM12878	blood:	n/a	n/a
21	CTCF	chr9:115874790-115875350	K562	blood:	n/a	chr9:115875291-115875309 chr9:115875292-115875308 chr9:115875294-115875307 chr9:115875294-115875307
22	CTCF	chr9:115873960-115874110	BE2_C	brain:	n/a	n/a
23	CTCF	chr9:115873940-115874090	AG04449	skin:	n/a	n/a
24	CTCF	chr9:115873960-115874110	HCPEpiC	choroid plexus:	n/a	n/a
25	CTCF	chr9:115873688-115874036	Lung_OC	lung:	n/a	chr9:115873826-115873839 chr9:115873826-115873839 chr9:115873825-115873841 chr9:115873824-115873842
26	CTCF	chr9:115873864-115874340	MCF-7	breast:	n/a	n/a
27	CTCF	chr9:115873328-115874084	K562	blood:	n/a	chr9:115873826-115873839 chr9:115873826-115873839 chr9:115873825-115873841 chr9:115873824-115873842
28	CTCF	chr9:115874166-115874247	GM19238	blood:	n/a	n/a
29	CTCF	chr9:115873940-115874090	GM12868	blood:	n/a	n/a
30	CTCF	chr9:115874220-115874370	AG04450	lung:	n/a	n/a
31	CTCF	chr9:115875020-115875170	GM06990	blood:	n/a	n/a
32	CTCF	chr9:115874300-115874450	HRE	kidney:	n/a	n/a
33	CTCF	chr9:115876516-115876641	HepG2	liver:	n/a	chr9:115876598-115876611 chr9:115876596-115876614 chr9:115876602-115876611
34	CTCF	chr9:115905843-115905976	MCF-7	breast:	n/a	n/a
35	CTCF	chr9:115875000-115875150	K562	blood:	n/a	n/a
36	CTCF	chr9:115875040-115875190	GM12865	blood:	n/a	n/a
37	CTCF	chr9:115874852-115875269	MCF-7	breast:	n/a	n/a
38	CTCF	chr9:115873920-115874070	HA-sp	spinal cord:	n/a	n/a
39	CTCF	chr9:115873855-115874128	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr9:115873960-115874110	HUVEC	blood vessel:	n/a	n/a
41	CTCF	chr9:115905800-115905950	A549	lung:	n/a	n/a
42	CTCF	chr9:115874980-115875259	T-47D	breast:	n/a	n/a
43	CTCF	chr9:115905820-115905970	HMEC	breast:	n/a	n/a
44	CTCF	chr9:115874500-115874650	HA-sp	spinal cord:	n/a	n/a
45	CTCF	chr9:115875020-115875170	RPTEC	kidney:	n/a	n/a
46	CTCF	chr9:115874440-115874590	GM12875	blood:	n/a	n/a
47	CTCF	chr9:115875020-115875170	HCM	heart:	n/a	n/a
48	CTCF	chr9:115875020-115875170	HFF	foreskin:	n/a	n/a
49	CTCF	chr9:115872226-115872332	MCF-7	breast:	n/a	n/a
50	CTCF	chr9:115873920-115874070	HL-60	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:115910751-115910801	IMR90	lung:	fetal
2	chr9:115875112-115875162	ProgFib	skin:	n/a
3	chr9:115874001-115874051	NHBE	bronchial:	n/a
4	chr9:115874001-115874051	NB4	blood:	n/a
5	chr9:115910751-115910801	BJ	skin:	n/a
6	chr9:115874001-115874051	PrEC	prostate:	n/a
7	chr9:115910751-115910801	ovcar-3	ovarian:	n/a
8	chr9:115874001-115874051	ovcar-3	ovarian:	n/a
9	chr9:115875112-115875162	SKMC	muscle:	n/a
10	chr9:115874001-115874051	HRE	kidney:	n/a
11	chr9:115910751-115910801	GM12891	blood:	n/a
12	chr9:115874001-115874051	HCT-116	colon:	n/a
13	chr9:115875112-115875162	HMEC	breast:	n/a
14	chr9:115874001-115874051	NT2-D1	testis:	n/a
15	chr9:115874001-115874051	IMR90	lung:	fetal
16	chr9:115874001-115874051	BJ	skin:	n/a
17	chr9:115874001-115874051	LNCaP	prostate:	n/a
18	chr9:115874001-115874051	GM19239	blood:	n/a
19	chr9:115910751-115910801	BE2_C	brain:	n/a
20	chr9:115874001-115874051	U87	brain:	n/a
21	chr9:115874001-115874051	Hepatocyte	liver:	n/a
22	chr9:115875112-115875162	HCT-116	colon:	n/a
23	chr9:115910751-115910801	NH-A	brain:	n/a
24	chr9:115910751-115910801	HNPCEpiC	eye:	n/a
25	chr9:115910751-115910801	GM06990	blood:	n/a
26	chr9:115874001-115874051	HMEC	breast:	n/a
27	chr9:115875112-115875162	GM12892	blood:	n/a
28	chr9:115875112-115875162	HAEpiC	amniotic membrane:	n/a
29	chr9:115874001-115874051	Jurkat	blood:	n/a
30	chr9:115910751-115910801	A549	lung:	n/a
31	chr9:115875112-115875162	GM06990	blood:	n/a
32	chr9:115910751-115910801	NT2-D1	testis:	n/a
33	chr9:115910751-115910801	Hepatocyte	liver:	n/a
34	chr9:115874001-115874051	CMK	blood:	n/a
35	chr9:115874001-115874051	HRCEpiC	kidney:	n/a
36	chr9:115874001-115874051	HepG2	liver:	n/a
37	chr9:115910751-115910801	AG09309	skin:	n/a
38	chr9:115910751-115910801	K562	blood:	n/a
39	chr9:115910751-115910801	HEEpiC	esophagus:	n/a
40	chr9:115910751-115910801	AG04449	skin:	fetal
41	chr9:115875112-115875162	AoSMC	blood vessel:	n/a
42	chr9:115874001-115874051	RPTEC	kidney:	n/a
43	chr9:115875112-115875162	NT2-D1	testis:	n/a
44	chr9:115875112-115875162	ECC-1	luminal epithelium:	n/a
45	chr9:115874001-115874051	GM06990	blood:	n/a
46	chr9:115910751-115910801	HIPEpiC	eye:	n/a
47	chr9:115910751-115910801	HEK293	kidney:	embryo
48	chr9:115875112-115875162	AG04450	lung:	fetal
49	chr9:115875112-115875162	IMR90	lung:	fetal
50	chr9:115874001-115874051	GM12878	blood:	n/a

(count:44 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:115898948..115900526-chr9:115901136..115903192,2	K562	blood:
2	chr9:115882399..115884999-chr9:115891613..115894561,3	MCF-7	breast:
3	chr9:115904166..115905985-chr9:115907508..115909495,2	K562	blood:
4	chr9:115880293..115882518-chr9:115890659..115892988,2	K562	blood:
5	chr9:115887976..115889749-chr9:115910119..115911972,2	MCF-7	breast:
6	chr9:115905880..115908127-chr9:115911738..115913287,2	K562	blood:
7	chr9:115890546..115893506-chr9:115895057..115896950,2	K562	blood:
8	chr9:115886125..115889063-chr9:115896987..115899858,2	K562	blood:
9	chr9:115888448..115891950-chr9:115898465..115901029,3	MCF-7	breast:
10	chr9:115882399..115884999-chr9:115891613..115894561,3	MCF-7	breast:
11	chr19:13262562..13265292-chr9:115900215..115901888,2	MCF-7	breast:
12	chr9:115886125..115889063-chr9:115896987..115899858,2	K562	blood:
13	chr9:115872624..115875532-chr9:115912017..115913734,2	MCF-7	breast:
14	chr9:115904166..115905985-chr9:115907508..115909495,2	K562	blood:
15	chr9:115905644..115908349-chr9:115914691..115916468,2	K562	blood:
16	chr9:115890845..115895225-chr9:115895362..115900277,5	MCF-7	breast:
17	chr9:115890878..115893257-chr9:115912029..115915211,3	MCF-7	breast:
18	chr9:115886679..115889181-chr9:115895702..115897217,2	MCF-7	breast:
19	chr9:115892442..115895400-chr9:115904212..115906056,3	MCF-7	breast:
20	chr9:115884518..115887843-chr9:115899953..115901831,3	MCF-7	breast:
21	chr9:115893647..115895768-chr9:115898797..115900868,2	K562	blood:
22	chr9:115893647..115895768-chr9:115898797..115900868,2	K562	blood:
23	chr9:115875142..115875676-chr9:115912672..115913501,2	MCF-7	breast:
24	chr9:115899892..115901950-chr9:115925051..115926804,2	MCF-7	breast:
25	chr9:115890546..115893506-chr9:115895057..115896950,2	K562	blood:
26	chr9:115687009..115687855-chr9:115874049..115874602,2	MCF-7	breast:
27	chr9:115900227..115901850-chr9:115926488..115929015,2	MCF-7	breast:
28	chr9:115890845..115895225-chr9:115895362..115900277,5	MCF-7	breast:
29	chr9:115886679..115889181-chr9:115895702..115897217,2	MCF-7	breast:
30	chr9:115898948..115900526-chr9:115901136..115903192,2	K562	blood:
31	chr9:115887976..115889749-chr9:115910119..115911972,2	MCF-7	breast:
32	chr9:115884874..115886487-chr9:115927190..115929312,2	K562	blood:
33	chr9:115884518..115887843-chr9:115899953..115901831,3	MCF-7	breast:
34	chr1:224803776..224804276-chr9:115875131..115875670,2	MCF-7	breast:
35	chr9:115881515..115883241-chr9:115913395..115914943,2	MCF-7	breast:
36	chr9:115888226..115890685-chr9:115891498..115893833,2	MCF-7	breast:
37	chr9:115904438..115911145-chr9:115911174..115916685,7	K562	blood:
38	chr9:115888448..115891950-chr9:115898465..115901029,3	MCF-7	breast:
39	chr9:115882894..115884462-chr9:115915677..115917990,2	MCF-7	breast:
40	chr9:115880293..115882518-chr9:115890659..115892988,2	K562	blood:
41	chr9:115892442..115895400-chr9:115904212..115906056,3	MCF-7	breast:
42	chr9:115888226..115890685-chr9:115891498..115893833,2	MCF-7	breast:
43	chr9:115873480..115874076-chr9:115899935..115900570,3	MCF-7	breast:
44	chr9:115887611..115890231-chr9:115913519..115916345,2	MCF-7	breast:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZFP37-2	chr9:115873190-115873296	NONHSAT134034
2	lnc-SLC31A2-1	chr9:115876700-115882126	NONHSAT134170
3	lnc-ZFP37-2	chr9:115873190-115873296	ENSG00000225684
4	lnc-SLC31A2-1	chr9:115876700-115882126	ENSG00000231528
5	lnc-SLC31A2-1	chr9:115875176-115875443	NONHSAT134170
6	lnc-SLC31A2-1	chr9:115875837-115875943	ENSG00000231528
7	lnc-SLC31A2-1	chr9:115875837-115875943	NONHSAT134170
8	lnc-SLC31A2-1	chr9:115875353-115875443	ENSG00000231528
9	lnc-ZFP37-2	chr9:115873690-115873780	ENSG00000225684
10	lnc-ZFP37-2	chr9:115865618-115872433	ENSG00000225684
11	lnc-ZFP37-2	chr9:115873190-115873753	ENSG00000225684
12	lnc-ZFP37-2	chr9:115867003-115872433	NONHSAT134034
13	lnc-ZFP37-2	chr9:115873690-115873957	NONHSAT134034
14	lnc-ZFP37-2	chr9:115867003-115872433	ENSG00000225684

No data

Variant related genes	Relation type
FAM225B	TF binding region
SLC31A2	TF binding region
FAM225A	TF binding region
FAM225B	CpG island
SLC31A2	CpG island
FAM225A	CpG island
ENSG00000143786	chromatin interactions
ENSG00000136867	chromatin interactions
ENSG00000225684	chromatin interactions
ENSG00000160888	chromatin interactions
ENSG00000267598	chromatin interactions
ENSG00000233384	chromatin interactions

Extended variants
information (count: 1332 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:1332 , 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	rs2009977	chr9:115867276-115867277	Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs184819272	chr9:115867279-115867280	Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
3	rs372531448	chr9:115867298-115867299	Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
4	rs540811066	chr9:115867336-115867337	Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
5	rs564184918	chr9:115867359-115867360	Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
6	rs533382316	chr9:115867367-115867368	Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
7	rs77994698	chr9:115867400-115867401	Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
8	rs73656476	chr9:115867407-115867408	Weak transcription Genic enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs373696651	chr9:115867436-115867437	Weak transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
10	rs529495023	chr9:115867445-115867446	Weak transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
11	rs189328812	chr9:115867453-115867454	Weak transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
12	rs144873424	chr9:115867539-115867540	Weak transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
13	rs148643023	chr9:115867542-115867543	Weak transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
14	rs373312643	chr9:115867548-115867549	Weak transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
15	rs551613700	chr9:115867566-115867567	Weak transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
16	rs571689184	chr9:115867573-115867574	Weak transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
17	rs539274325	chr9:115867598-115867599	Weak transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
18	rs556286331	chr9:115867601-115867602	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
19	rs569970661	chr9:115867610-115867611	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
20	rs535796645	chr9:115867613-115867614	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
21	rs555691553	chr9:115867614-115867615	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
22	rs572106926	chr9:115867633-115867634	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
23	rs540992531	chr9:115867673-115867674	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
24	rs557582316	chr9:115867693-115867694	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
25	rs569453663	chr9:115867707-115867708	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
26	rs10981632	chr9:115867814-115867815	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs370971420	chr9:115867815-115867816	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
28	rs529434290	chr9:115867871-115867872	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
29	rs542946186	chr9:115867887-115867888	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
30	rs559594154	chr9:115867911-115867912	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
31	rs199691755	chr9:115867950-115867951	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
32	rs200740989	chr9:115868654-115868655	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
33	rs372666712	chr9:115868940-115868941	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
34	rs199746738	chr9:115869513-115869514	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
35	rs201733596	chr9:115871089-115871090	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
36	rs551719605	chr9:115871578-115871579	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
37	rs201905251	chr9:115872356-115872357	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
38	rs62574456	chr9:115872875-115872876	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs199898662	chr9:115872929-115872930	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs187056596	chr9:115873000-115873001	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs201992804	chr9:115873402-115873403	Weak transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
42	rs565247131	chr9:115873689-115873690	Weak transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
43	rs530990393	chr9:115873775-115873776	Weak transcription	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
44	rs550793597	chr9:115873811-115873812	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
45	rs11506773	chr9:115873850-115873851	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs573418351	chr9:115873878-115873879	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
47	rs80016582	chr9:115873890-115873891	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
48	rs565945583	chr9:115873971-115873972	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs534331455	chr9:115873984-115873985	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs75660220	chr9:115874044-115874045	ZNF genes & repeats Enhancers Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:57)

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
Bladder cancer	21909424	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:185 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:115861600-115874000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr9:115867000-115867400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr9:115867000-115867600	Genic enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr9:115867400-115874000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr9:115867600-115874000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr9:115873800-115874000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr9:115873800-115874000	Active TSS	Adipose Nuclei	Adipose
8	chr9:115873800-115874000	Enhancers	Osteobl	bone
9	chr9:115874000-115874200	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
10	chr9:115874000-115874200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
11	chr9:115874000-115874200	Bivalent Enhancer	Primary T helper naive cells from peripheral blood	blood
12	chr9:115874000-115874200	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood
13	chr9:115874000-115874200	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
14	chr9:115874000-115874200	Bivalent Enhancer	Primary T killer memory cells from peripheral blood	blood
15	chr9:115874000-115874200	Flanking Active TSS	Adipose Nuclei	Adipose
16	chr9:115874000-115874200	Enhancers	Brain Cingulate Gyrus	brain
17	chr9:115874000-115874200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
18	chr9:115874000-115874200	Enhancers	Brain Substantia Nigra	brain
19	chr9:115874000-115874200	Enhancers	Placenta	Placenta
20	chr9:115874000-115874400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr9:115874000-115874400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr9:115874000-115874400	Enhancers	Primary T helper cells PMA-I stimulated	--
23	chr9:115874000-115874400	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
24	chr9:115874000-115874400	Enhancers	Brain Anterior Caudate	brain
25	chr9:115874000-115874400	Enhancers	Brain Inferior Temporal Lobe	brain
26	chr9:115874000-115874400	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
27	chr9:115874000-115874400	Active TSS	HSMMtube	muscle
28	chr9:115874000-115874400	Active TSS	NH-A	brain
29	chr9:115874000-115874400	Flanking Active TSS	Osteobl	bone
30	chr9:115874000-115874600	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
31	chr9:115874000-115874600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr9:115874000-115874600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
33	chr9:115874000-115874600	Enhancers	Spleen	Spleen
34	chr9:115874000-115875000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
35	chr9:115874000-115875000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr9:115874000-115875000	Enhancers	Monocytes-CD14+_RO01746	blood
37	chr9:115874000-115875000	Enhancers	NHEK	skin
38	chr9:115874000-115875200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr9:115874000-115875200	Enhancers	Primary monocytes fromperipheralblood	blood
40	chr9:115874000-115875200	Enhancers	Primary neutrophils fromperipheralblood	blood
41	chr9:115874000-115875200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr9:115874000-115875200	Enhancers	Brain Hippocampus Middle	brain
43	chr9:115874000-115875200	Enhancers	HMEC	breast
44	chr9:115874000-115875200	Enhancers	HSMM	muscle
45	chr9:115874200-115874400	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 2	blood
46	chr9:115874200-115874400	Bivalent Enhancer	Placenta	Placenta
47	chr9:115874200-115875200	Enhancers	Adipose Nuclei	Adipose
48	chr9:115874400-115874600	Bivalent/Poised TSS	Primary B cells from cord blood	blood
49	chr9:115874400-115874800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr9:115874400-115874800	Weak transcription	Brain Anterior Caudate	brain

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