Variant report

Variant	nsv893755
Chromosome Location	chr9:117019801-117032189
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:205)
CpG islands
(count:122)
Chromatin interactive
region (count:6)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:205 , 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	BHLHE40	chr9:117023345-117023493	K562	blood:	n/a	chr9:117023417-117023426 chr9:117023417-117023426
2	CEBPB	chr9:117031395-117031693	HepG2	liver:	n/a	n/a
3	CEBPB	chr9:117031491-117031634	HepG2	liver:	n/a	n/a
4	CTCF	chr9:117026577-117026593	Kidney_OC	kidney:	n/a	n/a
5	CTCF	chr9:117026556-117026635	Gliobla	brain:	n/a	n/a
6	CTCF	chr9:117026480-117026630	SAEC	small airway:	n/a	n/a
7	CTCF	chr9:117026500-117026650	BJ	skin:	n/a	n/a
8	CTCF	chr9:117026500-117026650	RPTEC	kidney:	n/a	n/a
9	CTCF	chr9:117026480-117026630	SK-N-SH_RA	brain:	n/a	n/a
10	CTCF	chr9:117026500-117026650	A549	lung:	n/a	n/a
11	CTCF	chr9:117026459-117026700	K562	blood:	n/a	n/a
12	CTCF	chr9:117026580-117026730	GM12871	blood:	n/a	n/a
13	CTCF	chr9:117026527-117026701	Medullo	brain:	n/a	n/a
14	CTCF	chr9:117026596-117026611	Hela-S3	cervix:	n/a	n/a
15	CTCF	chr9:117026536-117026660	GM19238	blood:	n/a	n/a
16	CTCF	chr9:117026460-117026610	HFF-Myc	foreskin:	n/a	n/a
17	CTCF	chr9:117026480-117026630	HCFaa	heart:	n/a	n/a
18	CTCF	chr9:117026520-117026670	NHDF-neo	bronchial:	n/a	n/a
19	CTCF	chr9:117026580-117026730	HAc	cerebellar:	n/a	n/a
20	CTCF	chr9:117026480-117026630	Caco-2	colon:	n/a	n/a
21	CTCF	chr9:117026540-117026690	AG04450	lung:	n/a	n/a
22	CTCF	chr9:117026560-117026710	HEK293	kidney:	n/a	n/a
23	CTCF	chr9:117026519-117026522	GM12891	blood:	n/a	n/a
24	CTCF	chr9:117026458-117026735	K562	blood:	n/a	n/a
25	CTCF	chr9:117026480-117026630	HRE	kidney:	n/a	n/a
26	CTCF	chr9:117026407-117026755	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr9:117026566-117026657	GM19240	blood:	n/a	n/a
28	CTCF	chr9:117026520-117026670	HepG2	liver:	n/a	n/a
29	CTCF	chr9:117026541-117026647	GM19239	blood:	n/a	n/a
30	CTCF	chr9:117026535-117026661	A549	lung:	n/a	n/a
31	CTCF	chr9:117026520-117026670	AG09319	gingival:	n/a	n/a
32	CTCF	chr9:117026412-117026662	A549	lung:	n/a	n/a
33	CTCF	chr9:117026583-117026644	GM10248	blood:	n/a	n/a
34	CTCF	chr9:117026500-117026650	AG10803	skin:	n/a	n/a
35	CTCF	chr9:117026529-117026666	GM12892	blood:	n/a	n/a
36	CTCF	chr9:117026480-117026630	HPAF	blood vessel:	n/a	n/a
37	CTCF	chr9:117026374-117026669	H1-hESC	embryonic stem cell:	n/a	chr9:117026390-117026403
38	CTCF	chr9:117026480-117026630	HRPEpiC	eye:	n/a	n/a
39	CTCF	chr9:117026520-117026670	HFF-Myc	foreskin:	n/a	n/a
40	CTCF	chr9:117026520-117026670	GM06990	blood:	n/a	n/a
41	CTCF	chr9:117026540-117026690	NHDF-neo	bronchial:	n/a	n/a
42	CTCF	chr9:117026540-117026690	HepG2	liver:	n/a	n/a
43	CTCF	chr9:117026525-117026658	GM12878	blood:	n/a	n/a
44	CTCF	chr9:117026560-117026710	HCT-116	colon:	n/a	n/a
45	CTCF	chr9:117026480-117026630	WERI-Rb-1	eye:	n/a	n/a
46	CTCF	chr9:117026438-117026762	IMR90	lung:	n/a	n/a
47	CTCF	chr9:117026480-117026630	HVMF	connective:	n/a	n/a
48	CTCF	chr9:117026540-117026690	AG09319	gingival:	n/a	n/a
49	CTCF	chr9:117026500-117026650	GM06990	blood:	n/a	n/a
50	CTCF	chr9:117026540-117026690	BJ	skin:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:117026288-117026338	LNCaP	prostate:	n/a
2	chr9:117026288-117026338	HAEpiC	amniotic membrane:	n/a
3	chr9:117023199-117023249	MCF-7	breast:	n/a
4	chr9:117026288-117026338	SK-N-SH_RA	brain:	n/a
5	chr9:117023199-117023249	Hela-S3	cervix:	n/a
6	chr9:117026288-117026338	Caco-2	colon:	n/a
7	chr9:117026288-117026338	K562	blood:	n/a
8	chr9:117023199-117023249	HRPEpiC	eye:	n/a
9	chr9:117026288-117026338	BJ	skin:	n/a
10	chr9:117026288-117026338	CMK	blood:	n/a
11	chr9:117026288-117026338	H1-hESC	embryonic stem cell:	embryo
12	chr9:117026288-117026338	Jurkat	blood:	n/a
13	chr9:117026288-117026338	HL-60	blood:	n/a
14	chr9:117023199-117023249	GM06990	blood:	n/a
15	chr9:117023199-117023249	HNPCEpiC	eye:	n/a
16	chr9:117023199-117023249	BJ	skin:	n/a
17	chr9:117026288-117026338	AG09309	skin:	n/a
18	chr9:117023199-117023249	HCF	heart:	n/a
19	chr9:117023199-117023249	AG09309	skin:	n/a
20	chr9:117026288-117026338	MCF-7	breast:	n/a
21	chr9:117023199-117023249	NHBE	bronchial:	n/a
22	chr9:117026288-117026338	U87	brain:	n/a
23	chr9:117026288-117026338	GM12891	blood:	n/a
24	chr9:117026288-117026338	HUVEC	blood vessel:	n/a
25	chr9:117026288-117026338	GM12892	blood:	n/a
26	chr9:117023199-117023249	Caco-2	colon:	n/a
27	chr9:117023199-117023249	HL-60	blood:	n/a
28	chr9:117026288-117026338	ECC-1	luminal epithelium:	n/a
29	chr9:117026288-117026338	HNPCEpiC	eye:	n/a
30	chr9:117023199-117023249	HCT-116	colon:	n/a
31	chr9:117023199-117023249	NB4	blood:	n/a
32	chr9:117026288-117026338	Hepatocyte	liver:	n/a
33	chr9:117026288-117026338	Hela-S3	cervix:	n/a
34	chr9:117026288-117026338	AG10803	skin:	n/a
35	chr9:117023199-117023249	HCM	heart:	n/a
36	chr9:117026288-117026338	AG04450	lung:	fetal
37	chr9:117023199-117023249	HCPEpiC	choroid plexus:	n/a
38	chr9:117026288-117026338	HepG2	liver:	n/a
39	chr9:117026288-117026338	SAEC	small airway:	n/a
40	chr9:117023199-117023249	SK-N-MC	brain:	n/a
41	chr9:117026288-117026338	PrEC	prostate:	n/a
42	chr9:117023199-117023249	HEK293	kidney:	embryo
43	chr9:117026288-117026338	NHDF-neo	bronchial:	n/a
44	chr9:117023199-117023249	PFSK-1	brain:	n/a
45	chr9:117023199-117023249	AG04450	lung:	fetal
46	chr9:117023199-117023249	Jurkat	blood:	n/a
47	chr9:117026288-117026338	GM12878	blood:	n/a
48	chr9:117023199-117023249	HRCEpiC	kidney:	n/a
49	chr9:117026288-117026338	HCPEpiC	choroid plexus:	n/a
50	chr9:117026288-117026338	HPAEpiC	pulmonary alveolar:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:117019506..117021498-chr9:117026111..117027904,2	MCF-7	breast:
2	chr9:116869905..116870808-chr9:117026020..117026989,3	MCF-7	breast:
3	chr9:117004138..117006321-chr9:117024518..117026602,2	MCF-7	breast:
4	chr9:117019506..117021498-chr9:117026111..117027904,2	MCF-7	breast:
5	chr9:116869941..116870862-chr9:117026162..117027038,2	K562	blood:
6	chr9:116844543..116845536-chr9:117026114..117026681,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ORM1-2	chr9:117031087-117031574	NONHSAT134373

No data

Variant related genes	Relation type
COL27A1	TF binding region
COL27A1	CpG island

Extended variants
information (count: 605 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:605 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs923601	chr9:117019801-117019802	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
2	rs141027787	chr9:117019802-117019803	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs575812365	chr9:117019824-117019825	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs544823552	chr9:117019857-117019858	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs181689351	chr9:117019862-117019863	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs150352925	chr9:117019869-117019870	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs375470657	chr9:117019878-117019879	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs113235891	chr9:117019892-117019893	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs574924192	chr9:117019938-117019939	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs562807906	chr9:117019966-117019967	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs186312113	chr9:117019998-117019999	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs560172709	chr9:117020007-117020008	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs532376712	chr9:117020016-117020017	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs545766499	chr9:117020043-117020044	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs565202467	chr9:117020079-117020080	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs530702357	chr9:117020097-117020098	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs550796779	chr9:117020135-117020136	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs567337654	chr9:117020180-117020181	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs529871859	chr9:117020187-117020188	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs546718021	chr9:117020202-117020203	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs189673815	chr9:117020211-117020212	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs529803516	chr9:117020230-117020231	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs145163028	chr9:117020234-117020235	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs569560264	chr9:117020296-117020297	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs538155345	chr9:117020307-117020308	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs550604642	chr9:117020317-117020318	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs555186946	chr9:117020328-117020329	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs548410343	chr9:117020336-117020337	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs374988547	chr9:117020352-117020353	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs574943641	chr9:117020373-117020374	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs181358720	chr9:117020382-117020383	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs553873821	chr9:117020383-117020384	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs566435625	chr9:117020398-117020399	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs576894982	chr9:117020414-117020415	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs545830127	chr9:117020420-117020421	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs369948970	chr9:117020421-117020422	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs562719839	chr9:117020435-117020436	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs138993220	chr9:117020443-117020444	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs185957347	chr9:117020468-117020469	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs561186817	chr9:117020506-117020507	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs77482304	chr9:117020514-117020515	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs546782659	chr9:117020533-117020534	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs562493663	chr9:117020536-117020537	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs532821815	chr9:117020548-117020549	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs141988989	chr9:117020583-117020584	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs189996444	chr9:117020589-117020590	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs551875796	chr9:117020611-117020612	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs552198729	chr9:117020619-117020620	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs568751371	chr9:117020654-117020655	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs537808915	chr9:117020671-117020672	Weak transcription Strong transcription Genic enhancers 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
Retinoblastoma	19183342	CNVD

Chromatin state (count:232 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:116973400-117047000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr9:116978600-117041200	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr9:116978800-117027600	Weak transcription	Esophagus	oesophagus
4	chr9:116978800-117027600	Weak transcription	Gastric	stomach
5	chr9:116986600-117022400	Weak transcription	Hela-S3	cervix
6	chr9:116988600-117026200	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr9:116992200-117022000	Weak transcription	H1 Cell Line	embryonic stem cell
8	chr9:116994400-117024000	Weak transcription	Stomach Mucosa	stomach
9	chr9:116998200-117022400	Weak transcription	HUES64 Cell Line	embryonic stem cell
10	chr9:116999800-117034600	Weak transcription	HMEC	breast
11	chr9:117001600-117039400	Weak transcription	HUVEC	blood vessel
12	chr9:117002000-117021400	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr9:117002000-117022200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr9:117002000-117041000	Weak transcription	Aorta	Aorta
15	chr9:117002800-117027000	Weak transcription	Spleen	Spleen
16	chr9:117003400-117026200	Strong transcription	Fetal Intestine Small	intestine
17	chr9:117005000-117022400	Weak transcription	HUES6 Cell Line	embryonic stem cell
18	chr9:117005000-117050200	Weak transcription	HUES48 Cell Line	embryonic stem cell
19	chr9:117008600-117029000	Weak transcription	NHEK	skin
20	chr9:117010800-117022200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr9:117011200-117025800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr9:117011800-117030000	Strong transcription	HepG2	liver
23	chr9:117012400-117054400	Weak transcription	Duodenum Smooth Muscle	Duodenum
24	chr9:117012600-117020600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr9:117013200-117028600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr9:117013200-117028800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr9:117013200-117028800	Weak transcription	HSMM	muscle
28	chr9:117013200-117029200	Weak transcription	Muscle Satellite Cultured Cells	--
29	chr9:117013200-117033600	Weak transcription	NHLF	lung
30	chr9:117013400-117024000	Weak transcription	Stomach Smooth Muscle	stomach
31	chr9:117013400-117027000	Weak transcription	Pancreas	Pancrea
32	chr9:117013400-117039400	Weak transcription	Ovary	ovary
33	chr9:117013400-117067800	Weak transcription	Right Ventricle	heart
34	chr9:117013600-117020800	Weak transcription	Cortex derived primary cultured neurospheres	brain
35	chr9:117013600-117024000	Weak transcription	Left Ventricle	heart
36	chr9:117013600-117027000	Weak transcription	Lung	lung
37	chr9:117013800-117021200	Weak transcription	Fetal Brain Female	brain
38	chr9:117014200-117022000	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr9:117014200-117038400	Weak transcription	NHDF-Ad	bronchial
40	chr9:117015200-117024400	Weak transcription	Fetal Lung	lung
41	chr9:117015400-117020600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr9:117015400-117037600	Weak transcription	A549	lung
43	chr9:117016200-117023000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr9:117016200-117047400	Weak transcription	Fetal Kidney	kidney
45	chr9:117016400-117023200	Strong transcription	Liver	Liver
46	chr9:117016800-117039400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
47	chr9:117017600-117027600	Genic enhancers	Fetal Muscle Trunk	muscle
48	chr9:117018400-117020800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr9:117018400-117021000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr9:117018400-117022400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin

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