Variant report

Variant	nsv1050714
Chromosome Location	chr9:118619303-118690263
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:118646129-118646327	HepG2	liver:	n/a	n/a
2	ATF3	chr9:118686166-118686684	A549	lung:	n/a	n/a
3	ATF3	chr9:118685936-118686685	A549	lung:	n/a	n/a
4	BCL3	chr9:118685961-118686927	A549	lung:	n/a	n/a
5	BCL3	chr9:118685994-118686701	A549	lung:	n/a	n/a
6	BRCA1	chr9:118686225-118686584	Hela-S3	cervix:	n/a	n/a
7	BRCA1	chr9:118646190-118646208	HepG2	liver:	n/a	n/a
8	BRCA1	chr9:118647249-118647395	Hela-S3	cervix:	n/a	n/a
9	CCNT2	chr9:118690119-118690319	K562	blood:	n/a	n/a
10	CEBPB	chr9:118654614-118654641	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr9:118683398-118684123	A549	lung:	n/a	chr9:118683829-118683838 chr9:118683829-118683838 chr9:118683829-118683838 chr9:118683829-118683838 chr9:118683653-118683662 chr9:118683829-118683840 chr9:118683653-118683662
12	CEBPB	chr9:118645783-118646437	Hela-S3	cervix:	n/a	chr9:118645882-118645899
13	CEBPB	chr9:118630272-118630433	H1-hESC	embryonic stem cell:	n/a	chr9:118630320-118630331
14	CEBPB	chr9:118630229-118630465	A549	lung:	n/a	chr9:118630320-118630331
15	CEBPB	chr9:118654173-118654761	IMR90	lung:	n/a	n/a
16	CEBPB	chr9:118686209-118686586	IMR90	lung:	n/a	n/a
17	CEBPB	chr9:118684667-118685151	Hela-S3	cervix:	n/a	chr9:118685010-118685027 chr9:118684824-118684841 chr9:118684829-118684840
18	CEBPB	chr9:118629844-118629977	IMR90	lung:	n/a	n/a
19	CEBPB	chr9:118664337-118664394	A549	lung:	n/a	n/a
20	CEBPB	chr9:118685907-118686826	A549	lung:	n/a	n/a
21	CEBPB	chr9:118645934-118646336	A549	lung:	n/a	n/a
22	CEBPB	chr9:118683619-118683873	H1-hESC	embryonic stem cell:	n/a	chr9:118683829-118683838 chr9:118683829-118683838 chr9:118683829-118683838 chr9:118683829-118683838 chr9:118683653-118683662 chr9:118683829-118683840 chr9:118683653-118683662
23	CEBPB	chr9:118630220-118630451	HepG2	liver:	n/a	chr9:118630320-118630331
24	CEBPB	chr9:118683502-118684000	A549	lung:	n/a	chr9:118683829-118683838 chr9:118683829-118683838 chr9:118683829-118683838 chr9:118683829-118683838 chr9:118683653-118683662 chr9:118683829-118683840 chr9:118683653-118683662
25	CEBPB	chr9:118683465-118684021	IMR90	lung:	n/a	chr9:118683829-118683838 chr9:118683829-118683838 chr9:118683829-118683838 chr9:118683829-118683838 chr9:118683653-118683662 chr9:118683829-118683840 chr9:118683653-118683662
26	CEBPB	chr9:118683497-118683977	A549	lung:	n/a	chr9:118683829-118683838 chr9:118683829-118683838 chr9:118683829-118683838 chr9:118683829-118683838 chr9:118683653-118683662 chr9:118683829-118683840 chr9:118683653-118683662
27	CEBPB	chr9:118645702-118646471	A549	lung:	n/a	chr9:118645882-118645899
28	CEBPB	chr9:118683497-118683989	HepG2	liver:	n/a	chr9:118683829-118683838 chr9:118683829-118683838 chr9:118683829-118683838 chr9:118683829-118683838 chr9:118683653-118683662 chr9:118683829-118683840 chr9:118683653-118683662
29	CEBPB	chr9:118630292-118630371	Hela-S3	cervix:	n/a	chr9:118630320-118630331
30	CEBPB	chr9:118686118-118686716	A549	lung:	n/a	n/a
31	CEBPB	chr9:118686261-118686589	A549	lung:	n/a	n/a
32	CEBPB	chr9:118686030-118686652	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr9:118683500-118683977	Hela-S3	cervix:	n/a	chr9:118683829-118683838 chr9:118683829-118683838 chr9:118683829-118683838 chr9:118683829-118683838 chr9:118683653-118683662 chr9:118683829-118683840 chr9:118683653-118683662
34	CEBPB	chr9:118642676-118642846	IMR90	lung:	n/a	n/a
35	CHD2	chr9:118684745-118685089	Hela-S3	cervix:	n/a	n/a
36	CHD2	chr9:118685956-118686735	Hela-S3	cervix:	n/a	n/a
37	CHD2	chr9:118646099-118646215	HepG2	liver:	n/a	n/a
38	CREB1	chr9:118686148-118686618	A549	lung:	n/a	n/a
39	CREB1	chr9:118686127-118686579	A549	lung:	n/a	n/a
40	CTCF	chr9:118646120-118646270	HAc	cerebellar:	n/a	chr9:118646194-118646212 chr9:118646196-118646217 chr9:118646195-118646211
41	CTCF	chr9:118646060-118646210	Hela-S3	cervix:	n/a	n/a
42	CTCF	chr9:118646080-118646230	MCF-7	breast:	n/a	chr9:118646194-118646212 chr9:118646196-118646217 chr9:118646195-118646211
43	CTCF	chr9:118665340-118665490	HEK293	kidney:	n/a	n/a
44	CTCF	chr9:118646138-118646254	GM10248	blood:	n/a	chr9:118646194-118646212 chr9:118646196-118646217 chr9:118646195-118646211
45	CTCF	chr9:118646100-118646250	HCM	heart:	n/a	chr9:118646194-118646212 chr9:118646196-118646217 chr9:118646195-118646211
46	CTCF	chr9:118646180-118646330	HAc	cerebellar:	n/a	chr9:118646194-118646212 chr9:118646196-118646217 chr9:118646195-118646211
47	CTCF	chr9:118646140-118646290	Caco-2	colon:	n/a	chr9:118646194-118646212 chr9:118646196-118646217 chr9:118646195-118646211
48	CTCF	chr9:118646100-118646250	RPTEC	kidney:	n/a	chr9:118646194-118646212 chr9:118646196-118646217 chr9:118646195-118646211
49	CTCF	chr9:118646060-118646306	GM19238	blood:	n/a	chr9:118646194-118646212 chr9:118646196-118646217 chr9:118646195-118646211
50	CTCF	chr9:118646120-118646270	HEK293	kidney:	n/a	chr9:118646194-118646212 chr9:118646196-118646217 chr9:118646195-118646211

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:118687465-118687515	Hela-S3	cervix:	n/a
2	chr9:118687465-118687515	Hela-S3	cervix:	n/a
3	chr9:118687694-118687744	AoSMC	blood vessel:	n/a
4	chr9:118687694-118687744	NB4	blood:	n/a
5	chr9:118687943-118687993	SKMC	muscle:	n/a
6	chr9:118687943-118687993	HEK293	kidney:	embryo
7	chr9:118687694-118687744	K562	blood:	n/a
8	chr9:118687694-118687744	HRCEpiC	kidney:	n/a
9	chr9:118687694-118687744	Jurkat	blood:	n/a
10	chr9:118687465-118687515	HEEpiC	esophagus:	n/a
11	chr9:118676023-118676073	NH-A	brain:	n/a
12	chr9:118687943-118687993	AG09319	gingival:	n/a
13	chr9:118676023-118676073	AG09309	skin:	n/a
14	chr9:118687694-118687744	MCF10A-Er-Src	breast:	n/a
15	chr9:118676023-118676073	HMEC	breast:	n/a
16	chr9:118687943-118687993	NH-A	brain:	n/a
17	chr9:118676023-118676073	K562	blood:	n/a
18	chr9:118687943-118687993	HCM	heart:	n/a
19	chr9:118687694-118687744	MCF-7	breast:	n/a
20	chr9:118687465-118687515	HRPEpiC	eye:	n/a
21	chr9:118687943-118687993	HRCEpiC	kidney:	n/a
22	chr9:118676023-118676073	SAEC	small airway:	n/a
23	chr9:118687465-118687515	NT2-D1	testis:	n/a
24	chr9:118687694-118687744	A549	lung:	n/a
25	chr9:118676023-118676073	GM19239	blood:	n/a
26	chr9:118687465-118687515	T-47D	breast:	n/a
27	chr9:118687465-118687515	SK-N-SH_RA	brain:	n/a
28	chr9:118687943-118687993	HRPEpiC	eye:	n/a
29	chr9:118676023-118676073	HAEpiC	amniotic membrane:	n/a
30	chr9:118687943-118687993	T-47D	breast:	n/a
31	chr9:118687943-118687993	SK-N-SH	brain:	n/a
32	chr9:118676023-118676073	CMK	blood:	n/a
33	chr9:118687465-118687515	U87	brain:	n/a
34	chr9:118687465-118687515	HCF	heart:	n/a
35	chr9:118687465-118687515	H1-hESC	embryonic stem cell:	embryo
36	chr9:118687465-118687515	HMEC	breast:	n/a
37	chr9:118687465-118687515	RPTEC	kidney:	n/a
38	chr9:118687943-118687993	HAEpiC	amniotic membrane:	n/a
39	chr9:118687694-118687744	SK-N-SH	brain:	n/a
40	chr9:118676023-118676073	PFSK-1	brain:	n/a
41	chr9:118676023-118676073	SK-N-SH	brain:	n/a
42	chr9:118687943-118687993	SK-N-MC	brain:	n/a
43	chr9:118676023-118676073	HCPEpiC	choroid plexus:	n/a
44	chr9:118687943-118687993	MCF-7	breast:	n/a
45	chr9:118676023-118676073	HCF	heart:	n/a
46	chr9:118676023-118676073	ECC-1	luminal epithelium:	n/a
47	chr9:118687694-118687744	GM06990	blood:	n/a
48	chr9:118687943-118687993	Hepatocyte	liver:	n/a
49	chr9:118676023-118676073	ProgFib	skin:	n/a
50	chr9:118687465-118687515	HRE	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr20:55549199..55549703-chr9:118639807..118640307,2	MCF-7	breast:
2	chr9:118643492..118644178-chr9:119334404..119335018,2	MCF-7	breast:
3	chr9:118645694..118646386-chr9:118874521..118875021,2	MCF-7	breast:
4	chr9:118455999..118456785-chr9:118645700..118646640,3	MCF-7	breast:
5	chr9:118355579..118356098-chr9:118645880..118646443,2	MCF-7	breast:
6	chr9:118645804..118646662-chr9:119253147..119254123,2	MCF-7	breast:
7	chr9:118646069..118646649-chr9:118874353..118875139,3	MCF-7	breast:
8	chr9:118646139..118646652-chr9:118914025..118914897,2	MCF-7	breast:
9	chr9:118645760..118646664-chr9:119333988..119335002,4	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PAPPA-5	chr9:118644482-118645222	ucscGeneNc_uc004bjy_1
2	lnc-PAPPA-AS1-3	chr9:118666650-118666921	ENSG00000204148
3	lnc-PAPPA-AS1-3	chr9:118687302-118687377	NR_024032
4	lnc-PAPPA-AS1-3	chr9:118650544-118650759	NR_024032
5	lnc-PAPPA-3	chr9:118660973-118661023	XLOC_007533
6	lnc-PAPPA-5	chr9:118640561-118641121	ucscGeneNc_uc004bjy_1
7	lnc-PAPPA-AS1-3	chr9:118666650-118666921	NR_024032
8	lnc-PAPPA-AS1-3	chr9:118650546-118650759	XLOC_007836
9	lnc-PAPPA-AS1-3	chr9:118687302-118687486	ENSG00000204148
10	lnc-PAPPA-AS1-3	chr9:118687302-118687377	XLOC_007836
11	lnc-PAPPA-AS1-3	chr9:118666650-118666921	XLOC_007836
12	lnc-PAPPA-AS1-3	chr9:118666650-118667208	XLOC_007836
13	lnc-PAPPA-AS1-3	chr9:118650454-118650759	XLOC_007836
14	lnc-PAPPA-AS1-3	chr9:118650448-118650759	ENSG00000204148
15	lnc-PAPPA-5	chr9:118643529-118643617	ucscGeneNc_uc004bjy_1

Variant related genes	Relation type
LINC00474	TF binding region
LINC00474	CpG island
PLAGL2	miRNA target sites
HSD17B12	miRNA target sites
PLAG1	miRNA target sites
PELI1	miRNA target sites
C16orf70	miRNA target sites

Extended variants
information (count: 2269 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:2269 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10982959	chr9:118619303-118619304	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs9987648	chr9:118619347-118619348	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs150170360	chr9:118619360-118619361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs527569642	chr9:118619368-118619369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs147860215	chr9:118619409-118619410	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs368433259	chr9:118619471-118619472	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs570568840	chr9:118619520-118619521	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs539217687	chr9:118619552-118619553	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs371575504	chr9:118619576-118619577	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs141313431	chr9:118619580-118619581	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs12552988	chr9:118619594-118619595	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs568970022	chr9:118619644-118619645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs537889525	chr9:118619677-118619678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs554663242	chr9:118619687-118619688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs146996556	chr9:118619690-118619691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs59741134	chr9:118619691-118619692	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs138003682	chr9:118619725-118619726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs9987812	chr9:118619728-118619729	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs546376675	chr9:118619804-118619805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs9987941	chr9:118619820-118619821	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs531429156	chr9:118619857-118619858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs541872490	chr9:118619868-118619869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs561511003	chr9:118619972-118619973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs186177239	chr9:118619982-118619983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs547396748	chr9:118620020-118620021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs564357250	chr9:118620036-118620037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs189805188	chr9:118620037-118620038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs182100671	chr9:118620076-118620077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs35602281	chr9:118620091-118620092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs569057647	chr9:118620115-118620116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs541047210	chr9:118620116-118620117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs537927914	chr9:118620135-118620136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs149486593	chr9:118620188-118620189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs10817842	chr9:118620215-118620216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs554771849	chr9:118620218-118620219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs10982960	chr9:118620221-118620222	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs13298987	chr9:118620254-118620255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs566571882	chr9:118620312-118620313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs577601019	chr9:118620313-118620314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs59445383	chr9:118620369-118620370	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs35187107	chr9:118620392-118620393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs10982961	chr9:118620408-118620409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs143003240	chr9:118620411-118620412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs576239221	chr9:118620415-118620416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs546179318	chr9:118620437-118620438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs10982962	chr9:118620452-118620453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs191065238	chr9:118620480-118620481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs564733086	chr9:118620483-118620484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs116471901	chr9:118620484-118620485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs117529329	chr9:118620495-118620496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:65)

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
Breast cancer	21509527	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Cervical cancer	16585170	CNVD
Ependymoma	19289631	CNVD
Schizophrenia	18940311	CNVD
Neuroticism	17667963	CNVD
Cervical cancer	17311676	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Neurodevelopmental disorder	0	CNVD
Intellectual disability	21811512	CNVD
Schizophrenia	20838587	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:161 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:118618600-118619400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
2	chr9:118619200-118625000	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr9:118619400-118619600	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr9:118625000-118625200	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr9:118625200-118625600	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr9:118625600-118626200	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr9:118625600-118626600	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr9:118633200-118634000	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr9:118633600-118634000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr9:118633600-118634000	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr9:118633600-118634000	Enhancers	HMEC	breast
12	chr9:118633600-118634200	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr9:118633600-118634200	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr9:118633600-118634400	Enhancers	NHEK	skin
15	chr9:118633800-118634200	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr9:118633800-118634200	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr9:118633800-118634200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr9:118640000-118640200	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr9:118640000-118640800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr9:118640200-118640400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr9:118640400-118640800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr9:118640400-118641000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
23	chr9:118640600-118641000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr9:118640600-118642000	Enhancers	Esophagus	oesophagus
25	chr9:118640600-118645000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr9:118640800-118641800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr9:118640800-118645400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr9:118641000-118642200	Enhancers	A549	lung
29	chr9:118641600-118643600	Enhancers	Breast Myoepithelial Primary Cells	Breast
30	chr9:118641800-118642000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr9:118641800-118642000	Enhancers	Placenta	Placenta
32	chr9:118642000-118643000	Weak transcription	Esophagus	oesophagus
33	chr9:118642000-118643000	Weak transcription	Placenta	Placenta
34	chr9:118642200-118645000	Weak transcription	A549	lung
35	chr9:118642600-118643000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr9:118642800-118643000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr9:118642800-118643200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr9:118643000-118643400	Enhancers	Placenta	Placenta
39	chr9:118643000-118644800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr9:118643200-118643400	Enhancers	Aorta	Aorta
41	chr9:118643200-118643400	Enhancers	Esophagus	oesophagus
42	chr9:118643200-118645400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr9:118643400-118643600	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr9:118643400-118644600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr9:118643400-118645400	Weak transcription	Placenta	Placenta
46	chr9:118643600-118645200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
47	chr9:118643600-118645200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
48	chr9:118643800-118645000	Weak transcription	Aorta	Aorta
49	chr9:118644600-118646200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr9:118644800-118646000	Enhancers	Muscle Satellite Cultured Cells	--

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