Variant report

Variant	esv1796249
Chromosome Location	chr9:71862129-71911566
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:325)
CpG islands
(count:244)
Chromatin interactive
region (count:22)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

(count:325 , 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	ATF2	chr9:71893929-71894313	GM12878	blood:	n/a	n/a
2	ATF2	chr9:71893376-71893624	GM12878	blood:	n/a	n/a
3	BATF	chr9:71893984-71894344	GM12878	blood:	n/a	n/a
4	BATF	chr9:71893364-71893636	GM12878	blood:	n/a	n/a
5	BATF	chr9:71893358-71893642	GM12878	blood:	n/a	n/a
6	BATF	chr9:71893950-71894312	GM12878	blood:	n/a	n/a
7	BCL11A	chr9:71894036-71894271	GM12878	blood:	n/a	n/a
8	BCL11A	chr9:71893990-71894275	GM12878	blood:	n/a	n/a
9	BHLHE40	chr9:71893376-71893539	GM12878	blood:	n/a	n/a
10	CEBPB	chr9:71873555-71873808	HepG2	liver:	n/a	n/a
11	CEBPB	chr9:71873511-71873756	K562	blood:	n/a	n/a
12	CEBPB	chr9:71873536-71873784	IMR90	lung:	n/a	n/a
13	CEBPB	chr9:71907486-71907775	HepG2	liver:	n/a	chr9:71907739-71907750
14	CEBPB	chr9:71873544-71873822	MCF-7	breast:	n/a	n/a
15	CEBPB	chr9:71873535-71873780	A549	lung:	n/a	n/a
16	CEBPB	chr9:71873504-71873772	ECC-1	luminal epithelium:	n/a	n/a
17	CEBPB	chr9:71873505-71873812	ECC-1	luminal epithelium:	n/a	n/a
18	CHD1	chr9:71889575-71889591	GM12878	blood:	n/a	n/a
19	CTCF	chr9:71907140-71907290	AG04449	skin:	n/a	n/a
20	CTCF	chr9:71907100-71907250	GM06990	blood:	n/a	n/a
21	CTCF	chr9:71907180-71907330	MCF-7	breast:	n/a	n/a
22	CTCF	chr9:71907060-71907210	GM06990	blood:	n/a	n/a
23	CTCF	chr9:71907080-71907230	AG09309	skin:	n/a	n/a
24	CTCF	chr9:71876718-71876835	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr9:71907203-71907223	GM19238	blood:	n/a	n/a
26	CTCF	chr9:71907080-71907230	SK-N-SH_RA	brain:	n/a	n/a
27	CTCF	chr9:71907108-71907316	MCF-7	breast:	n/a	n/a
28	CTCF	chr9:71907160-71907310	GM12873	blood:	n/a	n/a
29	CTCF	chr9:71907101-71907309	Hela-S3	cervix:	n/a	n/a
30	CTCF	chr9:71911043-71911056	Kidney_OC	kidney:	n/a	n/a
31	CTCF	chr9:71876991-71877000	MCF-7	breast:	n/a	n/a
32	CTCF	chr9:71907120-71907270	Hela-S3	cervix:	n/a	n/a
33	CTCF	chr9:71876699-71876815	MCF-7	breast:	n/a	n/a
34	CTCF	chr9:71907120-71907270	HepG2	liver:	n/a	n/a
35	CTCF	chr9:71907144-71907284	A549	lung:	n/a	n/a
36	CTCF	chr9:71907091-71907326	K562	blood:	n/a	n/a
37	CTCF	chr9:71876880-71877030	HMF	breast:	n/a	n/a
38	CTCF	chr9:71907100-71907250	HMEC	breast:	n/a	n/a
39	CTCF	chr9:71907080-71907230	A549	lung:	n/a	n/a
40	CTCF	chr9:71876936-71877061	K562	blood:	n/a	n/a
41	CTCF	chr9:71907040-71907190	HCT-116	colon:	n/a	n/a
42	CTCF	chr9:71876620-71876770	Hela-S3	cervix:	n/a	n/a
43	CTCF	chr9:71907081-71907368	MCF-7	breast:	n/a	n/a
44	CTCF	chr9:71906901-71907412	A549	lung:	n/a	n/a
45	CTCF	chr9:71876661-71876844	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr9:71907100-71907250	AoAF	blood vessel:	n/a	n/a
47	CTCF	chr9:71903480-71903630	HRE	kidney:	n/a	n/a
48	CTCF	chr9:71907044-71907340	HCT-116	colon:	n/a	n/a
49	CTCF	chr9:71907100-71907250	HCFaa	heart:	n/a	n/a
50	CTCF	chr9:71907089-71907447	MCF-7	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:71862747-71862797	GM12878	blood:	n/a
2	chr9:71862747-71862797	A549	lung:	n/a
3	chr9:71881186-71881236	NHBE	bronchial:	n/a
4	chr9:71863159-71863209	HPAEpiC	pulmonary alveolar:	n/a
5	chr9:71881186-71881236	GM19239	blood:	n/a
6	chr9:71862747-71862797	NT2-D1	testis:	n/a
7	chr9:71881186-71881236	U87	brain:	n/a
8	chr9:71881186-71881236	MCF-7	breast:	n/a
9	chr9:71863002-71863052	SK-N-SH_RA	brain:	n/a
10	chr9:71881186-71881236	HL-60	blood:	n/a
11	chr9:71862747-71862797	BJ	skin:	n/a
12	chr9:71863002-71863052	GM12891	blood:	n/a
13	chr9:71863002-71863052	HCF	heart:	n/a
14	chr9:71863002-71863052	PrEC	prostate:	n/a
15	chr9:71863159-71863209	ProgFib	skin:	n/a
16	chr9:71881186-71881236	ECC-1	luminal epithelium:	n/a
17	chr9:71863002-71863052	IMR90	lung:	fetal
18	chr9:71881186-71881236	NHDF-neo	bronchial:	n/a
19	chr9:71863002-71863052	NHDF-neo	bronchial:	n/a
20	chr9:71881186-71881236	CMK	blood:	n/a
21	chr9:71863002-71863052	AoSMC	blood vessel:	n/a
22	chr9:71862747-71862797	IMR90	lung:	fetal
23	chr9:71881186-71881236	HEK293	kidney:	embryo
24	chr9:71862747-71862797	GM12892	blood:	n/a
25	chr9:71881186-71881236	BJ	skin:	n/a
26	chr9:71863002-71863052	HRE	kidney:	n/a
27	chr9:71881186-71881236	HIPEpiC	eye:	n/a
28	chr9:71862747-71862797	AG09309	skin:	n/a
29	chr9:71862747-71862797	PFSK-1	brain:	n/a
30	chr9:71862747-71862797	MCF10A-Er-Src	breast:	n/a
31	chr9:71863159-71863209	RPTEC	kidney:	n/a
32	chr9:71863002-71863052	Jurkat	blood:	n/a
33	chr9:71863159-71863209	IMR90	lung:	fetal
34	chr9:71863002-71863052	HCPEpiC	choroid plexus:	n/a
35	chr9:71863159-71863209	HUVEC	blood vessel:	n/a
36	chr9:71863159-71863209	AG10803	skin:	n/a
37	chr9:71863159-71863209	GM06990	blood:	n/a
38	chr9:71863002-71863052	U87	brain:	n/a
39	chr9:71881186-71881236	HEEpiC	esophagus:	n/a
40	chr9:71863159-71863209	MCF-7	breast:	n/a
41	chr9:71863002-71863052	Hela-S3	cervix:	n/a
42	chr9:71862747-71862797	HAEpiC	amniotic membrane:	n/a
43	chr9:71881186-71881236	MCF10A-Er-Src	breast:	n/a
44	chr9:71863159-71863209	NH-A	brain:	n/a
45	chr9:71863002-71863052	AG09309	skin:	n/a
46	chr9:71862747-71862797	HRCEpiC	kidney:	n/a
47	chr9:71881186-71881236	H1-hESC	embryonic stem cell:	embryo
48	chr9:71862747-71862797	SK-N-SH_RA	brain:	n/a
49	chr9:71881186-71881236	SK-N-MC	brain:	n/a
50	chr9:71863002-71863052	AG10803	skin:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:71877776..71879849-chr9:71881788..71883583,2	MCF-7	breast:
2	chr9:71893881..71896810-chr9:71896857..71898912,2	MCF-7	breast:
3	chr9:71908251..71910034-chr9:71912759..71914347,2	MCF-7	breast:
4	chr9:71877776..71879849-chr9:71881788..71883583,2	MCF-7	breast:
5	chr9:71863242..71865900-chr9:71875148..71877546,2	K562	blood:
6	chr9:71907874..71908421-chr9:71999104..71999650,2	MCF-7	breast:
7	chr9:71907168..71909242-chr9:71938119..71941510,4	MCF-7	breast:
8	chr9:71864548..71866057-chr9:71866161..71868827,2	MCF-7	breast:
9	chr9:71887365..71889715-chr9:71890239..71892748,2	K562	blood:
10	chr9:71857960..71860439-chr9:71866424..71869302,2	K562	blood:
11	chr9:71905994..71910591-chr9:71938596..71942963,12	MCF-7	breast:
12	chr9:71863242..71865900-chr9:71875148..71877546,2	K562	blood:
13	chr9:71902826..71905528-chr9:71906383..71908994,3	MCF-7	breast:
14	chr9:71907771..71908503-chr9:72004389..72005167,3	MCF-7	breast:
15	chr9:71902826..71905528-chr9:71906383..71908994,3	MCF-7	breast:
16	chr9:71887365..71889715-chr9:71890239..71892748,2	K562	blood:
17	chr9:71893881..71896810-chr9:71896857..71898912,2	MCF-7	breast:
18	chr9:71905657..71909249-chr9:72003453..72006230,4	MCF-7	breast:
19	chr9:71907137..71907714-chr9:72027328..72028069,2	MCF-7	breast:
20	chr9:71864548..71866057-chr9:71866161..71868827,2	MCF-7	breast:
21	chr9:71907675..71910028-chr9:71950545..71953084,2	MCF-7	breast:
22	chr9:71910612..71916795-chr9:71938109..71942701,9	MCF-7	breast:

No data

(count:4 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	TJP2	hsa-miR-124-3p	chr9:71869744-71869750
2	TJP2	hsa-miR-193b-3p	chr9:71869241-71869262
3	TJP2	hsa-miR-124-3p	chr9:71869732-71869751
4	TJP2	hsa-miR-203a	chr9:71863586-71863605

Variant related genes	Relation type
ENSG00000269295	TF binding region
ENSG00000269295	CpG island
ENSG00000135063	chromatin interactions

Extended variants
information (count: 1982 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:1982 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3750551	chr9:71862129-71862130	Strong transcription Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs192761356	chr9:71862130-71862131	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs375675408	chr9:71862150-71862151	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs76780859	chr9:71862181-71862182	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs11788841	chr9:71862217-71862218	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs182688858	chr9:71862306-71862307	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs576243110	chr9:71862382-71862383	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs188987694	chr9:71862543-71862544	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs558324111	chr9:71862574-71862575	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs577751954	chr9:71862647-71862648	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs545078588	chr9:71862650-71862651	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs34992883	chr9:71862657-71862658	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs111671780	chr9:71862669-71862670	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs11789323	chr9:71862679-71862680	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs150947360	chr9:71862681-71862682	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs376071439	chr9:71862747-71862748	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs367811890	chr9:71862748-71862749	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs532029086	chr9:71862765-71862766	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs193140540	chr9:71862778-71862779	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs41308892	chr9:71862817-71862818	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs117754658	chr9:71862838-71862839	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs78728942	chr9:71862839-71862840	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs565732133	chr9:71862849-71862850	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs535876148	chr9:71862861-71862862	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs554499438	chr9:71862866-71862867	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs140714085	chr9:71862894-71862895	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs113671582	chr9:71862898-71862899	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs372881973	chr9:71862907-71862908	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs373270518	chr9:71862913-71862914	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs377138769	chr9:71862936-71862937	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs149969431	chr9:71862951-71862952	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs374830612	chr9:71862958-71862959	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs201976717	chr9:71862961-71862962	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs145703764	chr9:71862966-71862967	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs2282336	chr9:71862975-71862976	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs149659876	chr9:71862980-71862981	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs146761713	chr9:71862986-71862987	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs2095876	chr9:71862987-71862988	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs370164683	chr9:71863002-71863003	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs184519036	chr9:71863011-71863012	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs374453976	chr9:71863035-71863036	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs140442228	chr9:71863038-71863039	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs552732939	chr9:71863049-71863050	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs189082774	chr9:71863050-71863051	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs139276234	chr9:71863051-71863052	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs28556975	chr9:71863070-71863071	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs199852211	chr9:71863079-71863080	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs191634088	chr9:71863092-71863093	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs368776552	chr9:71863112-71863113	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs201287214	chr9:71863113-71863114	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Breast cancer	17133270	CNVD
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
Melanoma	22183965	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
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	17899364	CNVD
Mantle cell lymphoma	19029149	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	20729466	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Oral cancer	21386901	CNVD
Epilepsy	22083797	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:589 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:71828000-71866000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr9:71828600-71865600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr9:71828800-71874200	Weak transcription	Muscle Satellite Cultured Cells	--
4	chr9:71831400-71868000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
5	chr9:71831400-71872800	Strong transcription	Liver	Liver
6	chr9:71831600-71863200	Weak transcription	Hela-S3	cervix
7	chr9:71836400-71874000	Weak transcription	Fetal Brain Male	brain
8	chr9:71837400-71863000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr9:71838600-71862200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr9:71839000-71872600	Strong transcription	Fetal Intestine Large	intestine
11	chr9:71839600-71863400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
12	chr9:71840200-71870400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr9:71841400-71869800	Weak transcription	Colon Smooth Muscle	Colon
14	chr9:71841400-71869800	Weak transcription	K562	blood
15	chr9:71843000-71862400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr9:71843400-71868000	Weak transcription	Dnd41	blood
17	chr9:71845200-71872000	Weak transcription	Primary T cells fromperipheralblood	blood
18	chr9:71847000-71868800	Weak transcription	Small Intestine	intestine
19	chr9:71847600-71871200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr9:71847600-71879600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
21	chr9:71847800-71867800	Weak transcription	Cortex derived primary cultured neurospheres	brain
22	chr9:71851800-71862400	Weak transcription	Fetal Muscle Leg	muscle
23	chr9:71851800-71870800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
24	chr9:71852000-71876800	Weak transcription	Psoas Muscle	Psoas
25	chr9:71852400-71862400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr9:71852400-71864200	Weak transcription	Stomach Mucosa	stomach
27	chr9:71853000-71862200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr9:71853600-71862400	Weak transcription	Fetal Thymus	thymus
29	chr9:71853600-71863200	Weak transcription	Brain Anterior Caudate	brain
30	chr9:71853600-71868800	Weak transcription	HSMMtube	muscle
31	chr9:71853800-71862400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
32	chr9:71853800-71870800	Weak transcription	Primary T helper cells PMA-I stimulated	--
33	chr9:71854000-71865800	Weak transcription	NH-A	brain
34	chr9:71854400-71862400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
35	chr9:71855200-71863000	Weak transcription	Osteobl	bone
36	chr9:71855400-71864600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
37	chr9:71855600-71865600	Weak transcription	HSMM	muscle
38	chr9:71855800-71863600	Weak transcription	NHDF-Ad	bronchial
39	chr9:71855800-71865800	Weak transcription	Fetal Muscle Trunk	muscle
40	chr9:71855800-71867200	Weak transcription	Spleen	Spleen
41	chr9:71857200-71869400	Strong transcription	Primary monocytes fromperipheralblood	blood
42	chr9:71858600-71870000	Strong transcription	HepG2	liver
43	chr9:71859000-71865000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr9:71859000-71870200	Strong transcription	Duodenum Mucosa	Duodenum
45	chr9:71859200-71870400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
46	chr9:71859200-71872200	Strong transcription	HUES6 Cell Line	embryonic stem cell
47	chr9:71859200-71872600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
48	chr9:71859400-71862600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr9:71859400-71867800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr9:71859400-71873000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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