Variant report

Variant	nsv1048256
Chromosome Location	chr9:72032381-72067786
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	chr9:72037187-72037443	HepG2	liver:	n/a	n/a
2	BACH1	chr9:72044969-72045003	H1-hESC	embryonic stem cell:	n/a	n/a
3	CBX3	chr9:72046628-72046987	K562	blood:	n/a	n/a
4	CBX3	chr9:72046604-72047163	K562	blood:	n/a	n/a
5	CEBPB	chr9:72062496-72062722	IMR90	lung:	n/a	n/a
6	CEBPB	chr9:72067054-72067658	ECC-1	luminal epithelium:	n/a	n/a
7	CEBPB	chr9:72062134-72062154	IMR90	lung:	n/a	n/a
8	CEBPB	chr9:72037167-72037438	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr9:72066922-72067693	ECC-1	luminal epithelium:	n/a	n/a
10	CEBPB	chr9:72062154-72062778	HepG2	liver:	n/a	n/a
11	CEBPD	chr9:72046554-72047083	K562	blood:	n/a	n/a
12	CEBPD	chr9:72046517-72047194	K562	blood:	n/a	n/a
13	CHD2	chr9:72036898-72036903	GM12878	blood:	n/a	n/a
14	CTCF	chr9:72037133-72037430	Lung_OC	lung:	n/a	chr9:72037274-72037292 chr9:72037279-72037289 chr9:72037277-72037290 chr9:72037276-72037297 chr9:72037277-72037286 chr9:72037277-72037290 chr9:72037275-72037291
15	CTCF	chr9:72043428-72043517	GM19238	blood:	n/a	n/a
16	CTCF	chr9:72037220-72037370	AG10803	skin:	n/a	chr9:72037274-72037292 chr9:72037279-72037289 chr9:72037277-72037290 chr9:72037276-72037297 chr9:72037277-72037286 chr9:72037277-72037290 chr9:72037275-72037291
17	CTCF	chr9:72043426-72043504	A549	lung:	n/a	n/a
18	CTCF	chr9:72037200-72037350	HAc	cerebellar:	n/a	chr9:72037274-72037292 chr9:72037279-72037289 chr9:72037277-72037290 chr9:72037276-72037297 chr9:72037277-72037286 chr9:72037277-72037290 chr9:72037275-72037291
19	CTCF	chr9:72037122-72037454	Medullo	brain:	n/a	chr9:72037274-72037292 chr9:72037279-72037289 chr9:72037277-72037290 chr9:72037276-72037297 chr9:72037277-72037286 chr9:72037277-72037290 chr9:72037275-72037291
20	CTCF	chr9:72056860-72057010	NHEK	skin:	n/a	n/a
21	CTCF	chr9:72056904-72057012	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr9:72037101-72037448	K562	blood:	n/a	chr9:72037274-72037292 chr9:72037279-72037289 chr9:72037277-72037290 chr9:72037276-72037297 chr9:72037277-72037286 chr9:72037277-72037290 chr9:72037275-72037291
23	CTCF	chr9:72037160-72037310	GM12875	blood:	n/a	chr9:72037274-72037292 chr9:72037279-72037289 chr9:72037277-72037290 chr9:72037276-72037297 chr9:72037277-72037286 chr9:72037277-72037290 chr9:72037275-72037291
24	CTCF	chr9:72037220-72037370	HMEC	breast:	n/a	chr9:72037274-72037292 chr9:72037279-72037289 chr9:72037277-72037290 chr9:72037276-72037297 chr9:72037277-72037286 chr9:72037277-72037290 chr9:72037275-72037291
25	CTCF	chr9:72037107-72037417	GM19240	blood:	n/a	chr9:72037274-72037292 chr9:72037279-72037289 chr9:72037277-72037290 chr9:72037276-72037297 chr9:72037277-72037286 chr9:72037277-72037290 chr9:72037275-72037291
26	CTCF	chr9:72043423-72043514	GM12891	blood:	n/a	n/a
27	CTCF	chr9:72037167-72037402	HepG2	liver:	n/a	chr9:72037274-72037292 chr9:72037279-72037289 chr9:72037277-72037290 chr9:72037276-72037297 chr9:72037277-72037286 chr9:72037277-72037290 chr9:72037275-72037291
28	CTCF	chr9:72037180-72037330	HAc	cerebellar:	n/a	chr9:72037274-72037292 chr9:72037279-72037289 chr9:72037277-72037290 chr9:72037276-72037297 chr9:72037277-72037286 chr9:72037277-72037290 chr9:72037275-72037291
29	CTCF	chr9:72040380-72040648	MCF-7	breast:	n/a	n/a
30	CTCF	chr9:72037200-72037350	GM12874	blood:	n/a	chr9:72037274-72037292 chr9:72037279-72037289 chr9:72037277-72037290 chr9:72037276-72037297 chr9:72037277-72037286 chr9:72037277-72037290 chr9:72037275-72037291
31	CTCF	chr9:72065780-72065930	HEK293	kidney:	n/a	n/a
32	CTCF	chr9:72037075-72037596	MCF-7	breast:	n/a	chr9:72037274-72037292 chr9:72037279-72037289 chr9:72037277-72037290 chr9:72037276-72037297 chr9:72037277-72037286 chr9:72037277-72037290 chr9:72037275-72037291
33	CTCF	chr9:72037007-72037542	HCT-116	colon:	n/a	chr9:72037274-72037292 chr9:72037279-72037289 chr9:72037277-72037290 chr9:72037276-72037297 chr9:72037277-72037286 chr9:72037277-72037290 chr9:72037275-72037291
34	CTCF	chr9:72061580-72061730	HEK293	kidney:	n/a	chr9:72061624-72061637 chr9:72061621-72061639
35	CTCF	chr9:72061480-72061630	WERI-Rb-1	eye:	n/a	n/a
36	CTCF	chr9:72037200-72037350	RPTEC	kidney:	n/a	chr9:72037274-72037292 chr9:72037279-72037289 chr9:72037277-72037290 chr9:72037276-72037297 chr9:72037277-72037286 chr9:72037277-72037290 chr9:72037275-72037291
37	CTCF	chr9:72036900-72037050	SAEC	small airway:	n/a	n/a
38	CTCF	chr9:72037080-72037469	T-47D	breast:	n/a	chr9:72037274-72037292 chr9:72037279-72037289 chr9:72037277-72037290 chr9:72037276-72037297 chr9:72037277-72037286 chr9:72037277-72037290 chr9:72037275-72037291
39	CTCF	chr9:72037122-72037494	A549	lung:	n/a	chr9:72037274-72037292 chr9:72037279-72037289 chr9:72037277-72037290 chr9:72037276-72037297 chr9:72037277-72037286 chr9:72037277-72037290 chr9:72037275-72037291
40	CTCF	chr9:72037160-72037310	GM12867	blood:	n/a	chr9:72037274-72037292 chr9:72037279-72037289 chr9:72037277-72037290 chr9:72037276-72037297 chr9:72037277-72037286 chr9:72037277-72037290 chr9:72037275-72037291
41	CTCF	chr9:72043393-72043541	GM12892	blood:	n/a	n/a
42	CTCF	chr9:72037090-72037446	ECC-1	luminal epithelium:	n/a	chr9:72037274-72037292 chr9:72037279-72037289 chr9:72037277-72037290 chr9:72037276-72037297 chr9:72037277-72037286 chr9:72037277-72037290 chr9:72037275-72037291
43	CTCF	chr9:72037160-72037310	GM12865	blood:	n/a	chr9:72037274-72037292 chr9:72037279-72037289 chr9:72037277-72037290 chr9:72037276-72037297 chr9:72037277-72037286 chr9:72037277-72037290 chr9:72037275-72037291
44	CTCF	chr9:72037063-72037490	K562	blood:	n/a	chr9:72037274-72037292 chr9:72037279-72037289 chr9:72037277-72037290 chr9:72037276-72037297 chr9:72037277-72037286 chr9:72037277-72037290 chr9:72037275-72037291
45	CTCF	chr9:72037152-72037448	HUVEC	blood vessel:	n/a	chr9:72037274-72037292 chr9:72037279-72037289 chr9:72037277-72037290 chr9:72037276-72037297 chr9:72037277-72037286 chr9:72037277-72037290 chr9:72037275-72037291
46	CTCF	chr9:72037220-72037370	Caco-2	colon:	n/a	chr9:72037274-72037292 chr9:72037279-72037289 chr9:72037277-72037290 chr9:72037276-72037297 chr9:72037277-72037286 chr9:72037277-72037290 chr9:72037275-72037291
47	CTCF	chr9:72037150-72037429	LNCaP	prostate:	n/a	chr9:72037274-72037292 chr9:72037279-72037289 chr9:72037277-72037290 chr9:72037276-72037297 chr9:72037277-72037286 chr9:72037277-72037290 chr9:72037275-72037291
48	CTCF	chr9:72037113-72037437	GM19238	blood:	n/a	chr9:72037274-72037292 chr9:72037279-72037289 chr9:72037277-72037290 chr9:72037276-72037297 chr9:72037277-72037286 chr9:72037277-72037290 chr9:72037275-72037291
49	CTCF	chr9:72037200-72037350	AG04450	lung:	n/a	chr9:72037274-72037292 chr9:72037279-72037289 chr9:72037277-72037290 chr9:72037276-72037297 chr9:72037277-72037286 chr9:72037277-72037290 chr9:72037275-72037291
50	CTCF	chr9:72037074-72037084	GM19239	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:72046240-72046290	IMR90	lung:	fetal
2	chr9:72046240-72046290	T-47D	breast:	n/a
3	chr9:72046240-72046290	BE2_C	brain:	n/a
4	chr9:72046240-72046290	ProgFib	skin:	n/a
5	chr9:72046240-72046290	HCF	heart:	n/a
6	chr9:72046240-72046290	U87	brain:	n/a
7	chr9:72046240-72046290	GM12892	blood:	n/a
8	chr9:72046240-72046290	HRE	kidney:	n/a
9	chr9:72046240-72046290	AG09309	skin:	n/a
10	chr9:72046240-72046290	HMEC	breast:	n/a
11	chr9:72046240-72046290	LNCaP	prostate:	n/a
12	chr9:72046240-72046290	HEK293	kidney:	embryo
13	chr9:72046240-72046290	H1-hESC	embryonic stem cell:	embryo
14	chr9:72046240-72046290	AG09319	gingival:	n/a
15	chr9:72046240-72046290	HIPEpiC	eye:	n/a
16	chr9:72046240-72046290	RPTEC	kidney:	n/a
17	chr9:72046240-72046290	AG10803	skin:	n/a
18	chr9:72046240-72046290	NB4	blood:	n/a
19	chr9:72046240-72046290	Hela-S3	cervix:	n/a
20	chr9:72046240-72046290	HRPEpiC	eye:	n/a
21	chr9:72046240-72046290	SAEC	small airway:	n/a
22	chr9:72046240-72046290	ECC-1	luminal epithelium:	n/a
23	chr9:72046240-72046290	PFSK-1	brain:	n/a
24	chr9:72046240-72046290	MCF10A-Er-Src	breast:	n/a
25	chr9:72046240-72046290	SK-N-MC	brain:	n/a
26	chr9:72046240-72046290	HAEpiC	amniotic membrane:	n/a
27	chr9:72046240-72046290	HCT-116	colon:	n/a
28	chr9:72046240-72046290	SK-N-SH_RA	brain:	n/a
29	chr9:72046240-72046290	CMK	blood:	n/a
30	chr9:72046240-72046290	K562	blood:	n/a
31	chr9:72046240-72046290	GM12891	blood:	n/a
32	chr9:72046240-72046290	HCPEpiC	choroid plexus:	n/a
33	chr9:72046240-72046290	Hepatocyte	liver:	n/a
34	chr9:72046240-72046290	HCM	heart:	n/a
35	chr9:72046240-72046290	GM12878	blood:	n/a
36	chr9:72046240-72046290	HUVEC	blood vessel:	n/a
37	chr9:72046240-72046290	AG04449	skin:	fetal
38	chr9:72046240-72046290	SKMC	muscle:	n/a
39	chr9:72046240-72046290	SK-N-SH	brain:	n/a
40	chr9:72046240-72046290	PANC-1	pancreas:	n/a
41	chr9:72046240-72046290	HEEpiC	esophagus:	n/a
42	chr9:72046240-72046290	GM06990	blood:	n/a
43	chr9:72046240-72046290	Jurkat	blood:	n/a
44	chr9:72046240-72046290	AG04450	lung:	fetal
45	chr9:72046240-72046290	NHBE	bronchial:	n/a
46	chr9:72046240-72046290	HNPCEpiC	eye:	n/a
47	chr9:72046240-72046290	HL-60	blood:	n/a
48	chr9:72046240-72046290	MCF-7	breast:	n/a
49	chr9:72046240-72046290	NT2-D1	testis:	n/a
50	chr9:72046240-72046290	HepG2	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:72059861..72061593-chr9:72066565..72068301,2	MCF-7	breast:
2	chr9:72039845..72040903-chr9:72160889..72161458,4	MCF-7	breast:
3	chr9:72036807..72037778-chr9:72056686..72057333,2	MCF-7	breast:
4	chr9:72059861..72061593-chr9:72066565..72068301,2	MCF-7	breast:
5	chr9:72044312..72045985-chr9:72046714..72048470,2	MCF-7	breast:
6	chr9:72036807..72037778-chr9:72056686..72057333,2	MCF-7	breast:
7	chr9:72036812..72037787-chr9:72160880..72161856,6	MCF-7	breast:
8	chr9:72044312..72045985-chr9:72046714..72048470,2	MCF-7	breast:
9	chr9:72036664..72037777-chr9:72163377..72165001,9	K562	blood:
10	chr9:72036895..72038079-chr9:72163773..72164881,7	MCF-7	breast:
11	chr9:72038579..72040872-chr9:72161729..72164338,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-APBA1-1	chr9:72043544-72043637	ENSG00000243888
2	lnc-APBA1-1	chr9:72043164-72043467	ENSG00000243888
3	lnc-APBA1-1	chr9:72042449-72044751	NONHSAT131778

Variant related genes	Relation type
ENSG00000243888	TF binding region
ENSG00000243888	CpG island

Extended variants
information (count: 1493 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:1493 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9410541	chr9:72032490-72032491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs113036407	chr9:72032514-72032515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs111383257	chr9:72032515-72032516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs547589661	chr9:72033129-72033130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs560596656	chr9:72033146-72033147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs527771908	chr9:72033150-72033151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs9410826	chr9:72033167-72033168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs549441334	chr9:72033193-72033194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs546394840	chr9:72033269-72033270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs190729267	chr9:72033299-72033300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs10780362	chr9:72033303-72033304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs10780363	chr9:72033304-72033305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs150042372	chr9:72033316-72033317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs9410827	chr9:72033330-72033331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs538868501	chr9:72033409-72033410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs553922587	chr9:72033416-72033417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs565469567	chr9:72033447-72033448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs535930798	chr9:72033477-72033478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs187182018	chr9:72033480-72033481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs575998896	chr9:72033528-72033529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs148648608	chr9:72033529-72033530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs192308827	chr9:72033556-72033557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs142092721	chr9:72033557-72033558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs541262041	chr9:72033590-72033591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs183259994	chr9:72033618-72033619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs527836196	chr9:72033619-72033620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs187576432	chr9:72033627-72033628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs561183778	chr9:72033642-72033643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs10867477	chr9:72033645-72033646	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs190139270	chr9:72033667-72033668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs141096292	chr9:72033684-72033685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs371822832	chr9:72033693-72033694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs112125939	chr9:72033711-72033712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs147650547	chr9:72033716-72033717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs142250018	chr9:72033734-72033735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs150153716	chr9:72033735-72033736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs554667067	chr9:72033746-72033747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs549887672	chr9:72033779-72033780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs112422268	chr9:72033802-72033803	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs111323844	chr9:72033900-72033901	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs537078301	chr9:72033919-72033920	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs558255208	chr9:72033991-72033992	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs577253173	chr9:72033998-72033999	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs541332322	chr9:72033999-72034000	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs553259096	chr9:72034000-72034001	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs371729182	chr9:72034002-72034003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs538318611	chr9:72034004-72034005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs574691662	chr9:72034014-72034015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs182613108	chr9:72034035-72034036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs561453035	chr9:72034068-72034069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:438 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:72027000-72040000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr9:72033800-72034000	Enhancers	Stomach Mucosa	stomach
3	chr9:72036000-72036200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr9:72036000-72037600	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr9:72036200-72043000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr9:72036400-72037200	Enhancers	Skeletal Muscle Female	skeletal muscle
7	chr9:72036600-72082600	Weak transcription	Rectal Smooth Muscle	rectum
8	chr9:72036800-72037000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
9	chr9:72036800-72037200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr9:72036800-72037200	Enhancers	Skeletal Muscle Male	skeletal muscle
11	chr9:72036800-72037200	Enhancers	Stomach Mucosa	stomach
12	chr9:72036800-72037400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr9:72036800-72037600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr9:72036800-72045200	Weak transcription	Fetal Brain Female	brain
15	chr9:72037000-72037200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr9:72037000-72037200	Enhancers	Fetal Lung	lung
17	chr9:72037000-72037200	Enhancers	Fetal Muscle Leg	muscle
18	chr9:72037000-72037600	Enhancers	Brain Angular Gyrus	brain
19	chr9:72037000-72037600	Enhancers	Brain Cingulate Gyrus	brain
20	chr9:72037000-72037600	Enhancers	Brain Hippocampus Middle	brain
21	chr9:72037000-72037600	Enhancers	Brain Inferior Temporal Lobe	brain
22	chr9:72037000-72037600	Enhancers	Brain Substantia Nigra	brain
23	chr9:72037000-72037600	Enhancers	Fetal Stomach	stomach
24	chr9:72037200-72037600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
25	chr9:72037200-72037800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
26	chr9:72037200-72039800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr9:72037200-72040200	Weak transcription	Skeletal Muscle Male	skeletal muscle
28	chr9:72037200-72046600	Weak transcription	Skeletal Muscle Female	skeletal muscle
29	chr9:72037200-72048600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr9:72037200-72055600	Weak transcription	Fetal Lung	lung
31	chr9:72037200-72056200	Weak transcription	Fetal Muscle Leg	muscle
32	chr9:72037400-72037600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
33	chr9:72037400-72037600	Enhancers	Fetal Kidney	kidney
34	chr9:72037400-72037600	Enhancers	Stomach Smooth Muscle	stomach
35	chr9:72037400-72045200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr9:72037600-72039000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr9:72037600-72039400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
38	chr9:72037600-72039600	Weak transcription	Brain Hippocampus Middle	brain
39	chr9:72037600-72039600	Weak transcription	Brain Inferior Temporal Lobe	brain
40	chr9:72037600-72039600	Weak transcription	Brain Substantia Nigra	brain
41	chr9:72037600-72039800	Weak transcription	Brain Angular Gyrus	brain
42	chr9:72037600-72039800	Weak transcription	Brain Cingulate Gyrus	brain
43	chr9:72037600-72044800	Weak transcription	Fetal Stomach	stomach
44	chr9:72037600-72046600	Weak transcription	Fetal Kidney	kidney
45	chr9:72039000-72040000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr9:72039400-72040000	Enhancers	Breast Myoepithelial Primary Cells	Breast
47	chr9:72039600-72040200	Enhancers	Brain Inferior Temporal Lobe	brain
48	chr9:72039600-72040400	Enhancers	Brain Substantia Nigra	brain
49	chr9:72039600-72043200	Enhancers	Brain Hippocampus Middle	brain
50	chr9:72039800-72040200	Enhancers	HUES6 Cell Line	embryonic stem cell

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