Variant report

Variant	nsv466532
Chromosome Location	chr9:116930100-116957958
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:330)
CpG islands
(count:244)
Chromatin interactive
region (count:24)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:330 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:116936786-116937998	HepG2	liver:	n/a	n/a
2	ATF1	chr9:116940037-116940379	K562	blood:	n/a	n/a
3	BHLHE40	chr9:116946473-116946646	K562	blood:	n/a	n/a
4	BHLHE40	chr9:116936906-116938103	HepG2	liver:	n/a	chr9:116937779-116937795
5	BRCA1	chr9:116937024-116937983	HepG2	liver:	n/a	n/a
6	CEBPB	chr9:116935491-116935794	IMR90	lung:	n/a	n/a
7	CEBPB	chr9:116936825-116938017	HepG2	liver:	n/a	n/a
8	CEBPD	chr9:116937125-116937783	HepG2	liver:	n/a	n/a
9	CEBPD	chr9:116946466-116946712	K562	blood:	n/a	n/a
10	CEBPZ	chr9:116938212-116938525	HepG2	liver:	n/a	n/a
11	CHD2	chr9:116936827-116937766	HepG2	liver:	n/a	n/a
12	CTCF	chr9:116935897-116935902	HepG2	liver:	n/a	n/a
13	CTCF	chr9:116949278-116949468	MCF-7	breast:	n/a	chr9:116949369-116949387
14	CTCF	chr9:116949322-116949440	HepG2	liver:	n/a	chr9:116949369-116949387
15	CTCF	chr9:116949280-116949430	HMF	breast:	n/a	chr9:116949369-116949387
16	CTCF	chr9:116937040-116937190	BJ	skin:	n/a	chr9:116937067-116937075
17	CTCF	chr9:116949271-116949476	MCF-7	breast:	n/a	chr9:116949369-116949387
18	CTCF	chr9:116940191-116940231	Kidney_OC	kidney:	n/a	n/a
19	CTCF	chr9:116937100-116937250	AG04449	skin:	n/a	n/a
20	CTCF	chr9:116949317-116949428	A549	lung:	n/a	chr9:116949369-116949387
21	CTCF	chr9:116949273-116949470	MCF-7	breast:	n/a	chr9:116949369-116949387
22	CTCF	chr9:116949273-116949467	MCF-7	breast:	n/a	chr9:116949369-116949387
23	CTCF	chr9:116949347-116949409	Gliobla	brain:	n/a	chr9:116949369-116949387
24	CTCF	chr9:116949300-116949450	HepG2	liver:	n/a	chr9:116949369-116949387
25	CTCF	chr9:116937080-116937230	HepG2	liver:	n/a	n/a
26	CTCF	chr9:116949279-116949475	MCF-7	breast:	n/a	chr9:116949369-116949387
27	CTCF	chr9:116949320-116949470	RPTEC	kidney:	n/a	chr9:116949369-116949387
28	CTCF	chr9:116949260-116949410	Caco-2	colon:	n/a	chr9:116949369-116949387
29	CTCF	chr9:116949333-116949442	Fibrobl	skin:	n/a	chr9:116949369-116949387
30	CTCF	chr9:116949100-116949250	BE2_C	brain:	n/a	n/a
31	CTCF	chr9:116938780-116938930	HAc	cerebellar:	n/a	n/a
32	CTCF	chr9:116949314-116949440	Hela-S3	cervix:	n/a	chr9:116949369-116949387
33	CTCF	chr9:116937100-116937250	HepG2	liver:	n/a	n/a
34	CTCF	chr9:116949349-116949424	H1-hESC	embryonic stem cell:	n/a	chr9:116949369-116949387
35	CTCF	chr9:116949340-116949490	SK-N-SH_RA	brain:	n/a	chr9:116949369-116949387
36	CTCF	chr9:116949260-116949410	MCF-7	breast:	n/a	chr9:116949369-116949387
37	CTCF	chr9:116949290-116949444	NHEK	skin:	n/a	chr9:116949369-116949387
38	CTCF	chr9:116935906-116935930	HepG2	liver:	n/a	n/a
39	CTCF	chr9:116949260-116949410	Hela-S3	cervix:	n/a	chr9:116949369-116949387
40	CTCF	chr9:116940120-116940270	AG04449	skin:	n/a	n/a
41	CTCF	chr9:116949280-116949430	HepG2	liver:	n/a	chr9:116949369-116949387
42	CTCF	chr9:116949280-116949430	WERI-Rb-1	eye:	n/a	chr9:116949369-116949387
43	CTCF	chr9:116949280-116949430	A549	lung:	n/a	chr9:116949369-116949387
44	CTCF	chr9:116949300-116949450	WERI-Rb-1	eye:	n/a	chr9:116949369-116949387
45	CTCF	chr9:116949346-116949438	K562	blood:	n/a	chr9:116949369-116949387
46	CTCF	chr9:116949280-116949430	HEK293	kidney:	n/a	chr9:116949369-116949387
47	CTCF	chr9:116943780-116943930	HPAF	blood vessel:	n/a	n/a
48	CTCF	chr9:116949300-116949450	HBMEC	blood vessel:	n/a	chr9:116949369-116949387
49	CTCF	chr9:116949140-116949290	GM12873	blood:	n/a	n/a
50	CTCF	chr9:116949320-116949470	HPAF	blood vessel:	n/a	chr9:116949369-116949387

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:116932436-116932486	RPTEC	kidney:	n/a
2	chr9:116932028-116932078	GM19239	blood:	n/a
3	chr9:116932028-116932078	HIPEpiC	eye:	n/a
4	chr9:116943379-116943429	ovcar-3	ovarian:	n/a
5	chr9:116932028-116932078	BE2_C	brain:	n/a
6	chr9:116930367-116930417	HIPEpiC	eye:	n/a
7	chr9:116943379-116943429	ECC-1	luminal epithelium:	n/a
8	chr9:116930367-116930417	K562	blood:	n/a
9	chr9:116932436-116932486	HIPEpiC	eye:	n/a
10	chr9:116932028-116932078	PFSK-1	brain:	n/a
11	chr9:116932436-116932486	HCPEpiC	choroid plexus:	n/a
12	chr9:116932028-116932078	HCM	heart:	n/a
13	chr9:116932436-116932486	HNPCEpiC	eye:	n/a
14	chr9:116943379-116943429	AG10803	skin:	n/a
15	chr9:116932028-116932078	HAEpiC	amniotic membrane:	n/a
16	chr9:116930367-116930417	SAEC	small airway:	n/a
17	chr9:116943379-116943429	HCT-116	colon:	n/a
18	chr9:116932028-116932078	GM06990	blood:	n/a
19	chr9:116932028-116932078	LNCaP	prostate:	n/a
20	chr9:116930367-116930417	T-47D	breast:	n/a
21	chr9:116930367-116930417	AoSMC	blood vessel:	n/a
22	chr9:116932028-116932078	SK-N-SH_RA	brain:	n/a
23	chr9:116932436-116932486	NHDF-neo	bronchial:	n/a
24	chr9:116930367-116930417	Caco-2	colon:	n/a
25	chr9:116943379-116943429	Caco-2	colon:	n/a
26	chr9:116943379-116943429	HRPEpiC	eye:	n/a
27	chr9:116943379-116943429	BJ	skin:	n/a
28	chr9:116930367-116930417	NB4	blood:	n/a
29	chr9:116930367-116930417	SK-N-SH	brain:	n/a
30	chr9:116930367-116930417	Hepatocyte	liver:	n/a
31	chr9:116930367-116930417	NT2-D1	testis:	n/a
32	chr9:116943379-116943429	AoSMC	blood vessel:	n/a
33	chr9:116930367-116930417	PrEC	prostate:	n/a
34	chr9:116932028-116932078	Hepatocyte	liver:	n/a
35	chr9:116932436-116932486	HRE	kidney:	n/a
36	chr9:116932436-116932486	BJ	skin:	n/a
37	chr9:116932436-116932486	SK-N-MC	brain:	n/a
38	chr9:116932028-116932078	HEK293	kidney:	embryo
39	chr9:116943379-116943429	ProgFib	skin:	n/a
40	chr9:116943379-116943429	HEK293	kidney:	embryo
41	chr9:116930367-116930417	AG10803	skin:	n/a
42	chr9:116932028-116932078	CMK	blood:	n/a
43	chr9:116932028-116932078	H1-hESC	embryonic stem cell:	embryo
44	chr9:116943379-116943429	T-47D	breast:	n/a
45	chr9:116943379-116943429	PANC-1	pancreas:	n/a
46	chr9:116930367-116930417	A549	lung:	n/a
47	chr9:116932436-116932486	NT2-D1	testis:	n/a
48	chr9:116930367-116930417	GM12891	blood:	n/a
49	chr9:116943379-116943429	HRE	kidney:	n/a
50	chr9:116932028-116932078	AG04450	lung:	fetal

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:116938315..116939926-chr9:116941668..116944207,2	MCF-7	breast:
2	chr9:116932183..116936074-chr9:116938591..116942808,3	K562	blood:
3	chr9:116938018..116940765-chr9:116944712..116947136,2	K562	blood:
4	chr9:116933656..116936282-chr9:116947384..116950321,2	MCF-7	breast:
5	chr9:116938315..116939926-chr9:116941668..116944207,2	MCF-7	breast:
6	chr9:116936810..116939518-chr9:116945636..116948871,3	K562	blood:
7	chr9:116930014..116932339-chr9:116933734..116935674,2	MCF-7	breast:
8	chr9:116922253..116925161-chr9:116948030..116950142,2	MCF-7	breast:
9	chr9:116933656..116936282-chr9:116947384..116950321,2	MCF-7	breast:
10	chr9:116878648..116881578-chr9:116935106..116937121,2	MCF-7	breast:
11	chr9:116927426..116928989-chr9:116941833..116943417,2	K562	blood:
12	chr9:116940947..116942974-chr9:116968939..116970805,2	MCF-7	breast:
13	chr9:116940464..116942565-chr9:116943951..116946533,3	K562	blood:
14	chr9:116930264..116933030-chr9:116933706..116935267,2	MCF-7	breast:
15	chr9:116953109..116955718-chr9:116958854..116961798,2	K562	blood:
16	chr9:116932183..116936074-chr9:116938591..116942808,3	K562	blood:
17	chr9:116938018..116940765-chr9:116944712..116947136,2	K562	blood:
18	chr9:116956254..116958900-chr9:116963428..116965768,2	MCF-7	breast:
19	chr9:116936810..116939518-chr9:116945636..116948871,3	K562	blood:
20	chr9:116943873..116946561-chr9:116991422..116993679,2	MCF-7	breast:
21	chr9:116918121..116920168-chr9:116937255..116940070,3	K562	blood:
22	chr9:116942707..116945654-chr9:116999630..117002329,2	K562	blood:
23	chr9:116940464..116942565-chr9:116943951..116946533,3	K562	blood:
24	chr9:116927944..116931145-chr9:116936589..116939261,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KIF12-3	chr9:116940190-116940509	NONHSAT134369
2	lnc-ZNF618-2	chr9:116933576-116935890	NONHSAT134370

No data

Variant related genes	Relation type
COL27A1	TF binding region
COL27A1	CpG island
ENSG00000196739	chromatin interactions

Extended variants
information (count: 1186 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:1186 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2567707	chr9:116930100-116930101	Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs142192832	chr9:116930111-116930112	Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs150759476	chr9:116930131-116930132	Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs375672077	chr9:116930138-116930139	Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs369829082	chr9:116930139-116930140	Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs201093507	chr9:116930157-116930158	Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs374714030	chr9:116930177-116930178	Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs2567706	chr9:116930194-116930195	Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs372265305	chr9:116930199-116930200	Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs149948860	chr9:116930205-116930206	Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs111969026	chr9:116930226-116930227	Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs377185109	chr9:116930228-116930229	Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs146793976	chr9:116930232-116930233	Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs140539074	chr9:116930234-116930235	Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs147026086	chr9:116930240-116930241	Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs146589272	chr9:116930243-116930244	Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs369477310	chr9:116930252-116930253	Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs373617346	chr9:116930253-116930254	Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs538733879	chr9:116930261-116930262	Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs558626202	chr9:116930262-116930263	Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs377686014	chr9:116930263-116930264	Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs575113764	chr9:116930276-116930277	Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs370978325	chr9:116930283-116930284	Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs143341894	chr9:116930294-116930295	Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs571516072	chr9:116930298-116930299	Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs148339655	chr9:116930318-116930319	Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs200941311	chr9:116930343-116930344	Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs200309675	chr9:116930374-116930375	Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
29	rs140616075	chr9:116930382-116930383	Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
30	rs147106434	chr9:116930394-116930395	Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
31	rs138532151	chr9:116930405-116930406	Weak transcription Strong transcription Genic enhancers Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
32	rs138434112	chr9:116930408-116930409	Weak transcription Strong transcription Genic enhancers Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
33	rs370021079	chr9:116930427-116930428	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs147140199	chr9:116930447-116930448	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs143912297	chr9:116930454-116930455	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs199729771	chr9:116930485-116930486	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs372325271	chr9:116930500-116930501	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs374669935	chr9:116930507-116930508	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs369005326	chr9:116930513-116930514	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs538713049	chr9:116930516-116930517	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs201192948	chr9:116930528-116930529	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs546860616	chr9:116930537-116930538	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs149260799	chr9:116930543-116930544	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs144556713	chr9:116930548-116930549	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs148448277	chr9:116930557-116930558	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs574675570	chr9:116930558-116930559	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs144068722	chr9:116930574-116930575	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs376160858	chr9:116930595-116930596	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs144086565	chr9:116930596-116930597	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs146040174	chr9:116930605-116930606	Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

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
Pancreatic cancer	17952125	CNVD
Breast cancer	21509527	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Cervical cancer	16585170	CNVD
Ependymoma	19289631	CNVD
Melanoma	17363583	CNVD
Melanoma	20688739	CNVD

Chromatin state (count:832 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:116919000-116936600	Weak transcription	Brain Hippocampus Middle	brain
2	chr9:116919000-116937600	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr9:116919200-116972000	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr9:116919600-116939600	Weak transcription	Hela-S3	cervix
5	chr9:116921800-116931600	Weak transcription	Aorta	Aorta
6	chr9:116925800-116931800	Weak transcription	Duodenum Smooth Muscle	Duodenum
7	chr9:116926000-116931600	Weak transcription	Spleen	Spleen
8	chr9:116926000-116937200	Weak transcription	Gastric	stomach
9	chr9:116926200-116930400	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr9:116926200-116934800	Weak transcription	Rectal Smooth Muscle	rectum
11	chr9:116926200-116937400	Weak transcription	Right Ventricle	heart
12	chr9:116926200-116943800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
13	chr9:116926400-116931000	Weak transcription	NH-A	brain
14	chr9:116926400-116931600	Weak transcription	Muscle Satellite Cultured Cells	--
15	chr9:116926400-116932000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr9:116926400-116934400	Weak transcription	Colon Smooth Muscle	Colon
17	chr9:116926400-116935200	Weak transcription	Left Ventricle	heart
18	chr9:116926400-116935400	Weak transcription	Right Atrium	heart
19	chr9:116926400-116937000	Weak transcription	Stomach Mucosa	stomach
20	chr9:116926400-116950200	Weak transcription	HUES64 Cell Line	embryonic stem cell
21	chr9:116926400-116950400	Weak transcription	H1 Cell Line	embryonic stem cell
22	chr9:116926600-116930400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
23	chr9:116926600-116932400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
24	chr9:116926600-116939400	Weak transcription	Fetal Kidney	kidney
25	chr9:116926800-116930200	Weak transcription	Lung	lung
26	chr9:116926800-116930200	Weak transcription	Skeletal Muscle Female	skeletal muscle
27	chr9:116926800-116930400	Weak transcription	A549	lung
28	chr9:116926800-116930600	Weak transcription	Fetal Thymus	thymus
29	chr9:116926800-116934600	Weak transcription	HMEC	breast
30	chr9:116926800-116937000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
31	chr9:116927000-116931400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr9:116927000-116932400	Weak transcription	Pancreatic Islets	Pancreatic Islet
33	chr9:116927000-116933400	Strong transcription	HepG2	liver
34	chr9:116928200-116932400	Strong transcription	Fetal Intestine Large	intestine
35	chr9:116928400-116932800	Enhancers	NHDF-Ad	bronchial
36	chr9:116928600-116930200	Weak transcription	Stomach Smooth Muscle	stomach
37	chr9:116928800-116931000	Strong transcription	Fetal Intestine Small	intestine
38	chr9:116928800-116935600	Enhancers	Skeletal Muscle Male	skeletal muscle
39	chr9:116929000-116931000	Strong transcription	Fetal Stomach	stomach
40	chr9:116929000-116932400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr9:116929000-116933400	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr9:116929000-116933600	Strong transcription	NHEK	skin
43	chr9:116929000-116937000	Weak transcription	HSMM	muscle
44	chr9:116929200-116931400	Weak transcription	Ovary	ovary
45	chr9:116929200-116931800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr9:116929200-116934600	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr9:116929200-116937800	Weak transcription	HUVEC	blood vessel
48	chr9:116929400-116930600	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr9:116929400-116932000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
50	chr9:116929400-116932200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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