Variant report

Variant	nsv1032856
Chromosome Location	chr9:16465330-16773471
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2416)
CpG islands
(count:612)
Chromatin interactive
region (count:20)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2416 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:16653619-16654168	HepG2	liver:	n/a	n/a
2	ATF2	chr9:16485817-16486348	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr9:16708535-16709145	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr9:16515971-16516372	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr9:16726542-16727101	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr9:16705170-16705700	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr9:16708465-16709294	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr9:16704572-16705732	A549	lung:	n/a	n/a
9	ATF3	chr9:16626544-16626978	A549	lung:	n/a	n/a
10	ATF3	chr9:16704594-16705717	A549	lung:	n/a	n/a
11	BACH1	chr9:16626901-16626943	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr9:16730241-16730320	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr9:16725246-16725293	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr9:16708624-16709106	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr9:16559422-16559698	GM12878	blood:	n/a	n/a
16	BATF	chr9:16509989-16510195	GM12878	blood:	n/a	chr9:16510088-16510099
17	BCL11A	chr9:16485917-16486264	H1-hESC	embryonic stem cell:	n/a	n/a
18	BCL11A	chr9:16486000-16486235	H1-hESC	embryonic stem cell:	n/a	n/a
19	BCL3	chr9:16701219-16701697	A549	lung:	n/a	n/a
20	BCL3	chr9:16726476-16727092	A549	lung:	n/a	n/a
21	BCL3	chr9:16726555-16727142	A549	lung:	n/a	n/a
22	BCL3	chr9:16704702-16705796	A549	lung:	n/a	n/a
23	BCL3	chr9:16704567-16705721	A549	lung:	n/a	n/a
24	BHLHE40	chr9:16469359-16469365	GM12878	blood:	n/a	n/a
25	BHLHE40	chr9:16483538-16483634	GM12878	blood:	n/a	n/a
26	BHLHE40	chr9:16655674-16655965	GM12878	blood:	n/a	chr9:16655674-16655683 chr9:16655674-16655683 chr9:16655675-16655684
27	BHLHE40	chr9:16542436-16542571	GM12878	blood:	n/a	n/a
28	BHLHE40	chr9:16586351-16586482	GM12878	blood:	n/a	n/a
29	BRCA1	chr9:16727204-16727670	Hela-S3	cervix:	n/a	n/a
30	BRCA1	chr9:16716591-16716814	Hela-S3	cervix:	n/a	n/a
31	BRCA1	chr9:16469251-16469465	GM12878	blood:	n/a	n/a
32	BRCA1	chr9:16515225-16515402	H1-hESC	embryonic stem cell:	n/a	n/a
33	BRCA1	chr9:16704795-16705688	Hela-S3	cervix:	n/a	n/a
34	BRCA1	chr9:16623666-16623719	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr9:16625871-16626165	IMR90	lung:	n/a	n/a
36	CEBPB	chr9:16726598-16727409	ECC-1	luminal epithelium:	n/a	chr9:16726904-16726915
37	CEBPB	chr9:16726770-16726994	K562	blood:	n/a	chr9:16726904-16726915
38	CEBPB	chr9:16506534-16506646	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr9:16704664-16705654	A549	lung:	n/a	n/a
40	CEBPB	chr9:16679433-16679643	A549	lung:	n/a	n/a
41	CEBPB	chr9:16682813-16683078	IMR90	lung:	n/a	chr9:16682940-16682953
42	CEBPB	chr9:16465340-16465409	IMR90	lung:	n/a	chr9:16465385-16465396
43	CEBPB	chr9:16651134-16651299	IMR90	lung:	n/a	n/a
44	CEBPB	chr9:16681134-16681165	IMR90	lung:	n/a	n/a
45	CEBPB	chr9:16647375-16647679	HepG2	liver:	n/a	chr9:16647524-16647533 chr9:16647522-16647533 chr9:16647524-16647535
46	CEBPB	chr9:16726699-16727129	A549	lung:	n/a	chr9:16726904-16726915
47	CEBPB	chr9:16551502-16551702	HepG2	liver:	n/a	n/a
48	CEBPB	chr9:16611997-16612266	HepG2	liver:	n/a	chr9:16612112-16612121 chr9:16612110-16612123 chr9:16612110-16612121 chr9:16612111-16612122
49	CEBPB	chr9:16647398-16647660	A549	lung:	n/a	chr9:16647524-16647533 chr9:16647522-16647533 chr9:16647524-16647535
50	CEBPB	chr9:16626665-16626979	IMR90	lung:	n/a	chr9:16626932-16626944

(count:612 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:16727830-16727880	HCF	heart:	n/a
2	chr9:16653688-16653738	HIPEpiC	eye:	n/a
3	chr9:16727830-16727880	HCF	heart:	n/a
4	chr9:16653688-16653738	HIPEpiC	eye:	n/a
5	chr9:16729515-16729565	Hepatocyte	liver:	n/a
6	chr9:16705212-16705262	HepG2	liver:	n/a
7	chr9:16504799-16504849	CMK	blood:	n/a
8	chr9:16726860-16726910	SK-N-SH_RA	brain:	n/a
9	chr9:16729103-16729153	AG04449	skin:	fetal
10	chr9:16504799-16504849	PrEC	prostate:	n/a
11	chr9:16704404-16704454	HRE	kidney:	n/a
12	chr9:16504799-16504849	NHBE	bronchial:	n/a
13	chr9:16727830-16727880	AG04450	lung:	fetal
14	chr9:16726860-16726910	SAEC	small airway:	n/a
15	chr9:16718892-16718942	AG09319	gingival:	n/a
16	chr9:16504799-16504849	NHDF-neo	bronchial:	n/a
17	chr9:16729103-16729153	AoSMC	blood vessel:	n/a
18	chr9:16727830-16727880	ProgFib	skin:	n/a
19	chr9:16729515-16729565	SKMC	muscle:	n/a
20	chr9:16704404-16704454	ovcar-3	ovarian:	n/a
21	chr9:16653688-16653738	MCF-7	breast:	n/a
22	chr9:16726860-16726910	ovcar-3	ovarian:	n/a
23	chr9:16704404-16704454	GM19239	blood:	n/a
24	chr9:16718892-16718942	AG04449	skin:	fetal
25	chr9:16704404-16704454	PrEC	prostate:	n/a
26	chr9:16500626-16500676	HCF	heart:	n/a
27	chr9:16726860-16726910	ProgFib	skin:	n/a
28	chr9:16729515-16729565	HRPEpiC	eye:	n/a
29	chr9:16705212-16705262	SK-N-SH	brain:	n/a
30	chr9:16653688-16653738	SKMC	muscle:	n/a
31	chr9:16727830-16727880	HIPEpiC	eye:	n/a
32	chr9:16726860-16726910	GM12891	blood:	n/a
33	chr9:16726860-16726910	LNCaP	prostate:	n/a
34	chr9:16704404-16704454	AG04450	lung:	fetal
35	chr9:16727830-16727880	HUVEC	blood vessel:	n/a
36	chr9:16718892-16718942	Jurkat	blood:	n/a
37	chr9:16500626-16500676	PANC-1	pancreas:	n/a
38	chr9:16653688-16653738	Jurkat	blood:	n/a
39	chr9:16727830-16727880	HRCEpiC	kidney:	n/a
40	chr9:16726860-16726910	HEEpiC	esophagus:	n/a
41	chr9:16704404-16704454	HIPEpiC	eye:	n/a
42	chr9:16718892-16718942	IMR90	lung:	fetal
43	chr9:16726860-16726910	AG10803	skin:	n/a
44	chr9:16718892-16718942	AG10803	skin:	n/a
45	chr9:16704404-16704454	HAEpiC	amniotic membrane:	n/a
46	chr9:16705212-16705262	ProgFib	skin:	n/a
47	chr9:16500626-16500676	GM06990	blood:	n/a
48	chr9:16727830-16727880	GM12892	blood:	n/a
49	chr9:16729515-16729565	SAEC	small airway:	n/a
50	chr9:16729103-16729153	U87	brain:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:16154369..16155237-chr9:16601764..16602655,2	MCF-7	breast:
2	chr9:16518671..16520605-chr9:16526925..16528585,2	MCF-7	breast:
3	chr19:41731896..41732688-chr9:16704803..16705712,2	Hela-S3	cervix:
4	chr9:16550024..16551022-chrX:41301770..41302313,2	MCF-7	breast:
5	chr17:34853813..34854390-chr9:16572137..16572637,2	MCF-7	breast:
6	chr9:16653386..16655989-chr9:16657272..16659036,2	MCF-7	breast:
7	chr6:3068763..3069618-chr9:16726993..16727675,2	Hela-S3	cervix:
8	chr12:52445126..52445753-chr9:16726910..16727745,2	Hela-S3	cervix:
9	chr3:20227400..20228150-chr9:16726744..16727510,2	Hela-S3	cervix:
10	chr9:16520489..16522214-chr9:16551948..16553682,2	MCF-7	breast:
11	chr11:62609031..62609585-chr9:16704767..16705357,2	Hela-S3	cervix:
12	chr9:16704972..16705696-chr9:16726846..16727389,2	Hela-S3	cervix:
13	chr9:16653386..16655989-chr9:16657272..16659036,2	MCF-7	breast:
14	chr9:16191923..16192798-chr9:16648750..16649311,2	MCF-7	breast:
15	chr9:16520489..16522214-chr9:16551948..16553682,2	MCF-7	breast:
16	chr9:16519927..16521803-chr9:16525394..16528325,2	K562	blood:
17	chr7:5569698..5570590-chr9:16726454..16727434,2	Hela-S3	cervix:
18	chr9:16518671..16520605-chr9:16526925..16528585,2	MCF-7	breast:
19	chr9:16519927..16521803-chr9:16525394..16528325,2	K562	blood:
20	chr6:2765596..2766255-chr9:16738649..16739454,2	MCF-7	breast:

(count:15 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C9orf92-4	chr9:16583059-16583083	NONHSAT130290
2	lnc-CNTLN-3	chr9:16626156-16626388	ENSG00000230694.1
3	lnc-C9orf92-4	chr9:16700753-16700983	uc_252_-
4	lnc-CNTLN-2	chr9:16726812-16726953	ENSG00000234779.1
5	lnc-C9orf92-4	chr9:16583059-16583083	NONHSAT130291
6	lnc-C9orf93-2	chr9:16475991-16476235	ENSG00000231756.1
7	lnc-CNTLN-2	chr9:16727029-16727104	ENSG00000234779.1
8	lnc-C9orf93-2	chr9:16473186-16473354	ENSG00000231756.1
9	lnc-C9orf92-4	chr9:16714816-16714976	NONHSAT130291
10	lnc-CNTLN-2	chr9:16727313-16727522	ENSG00000234779.1
11	lnc-C9orf92-4	chr9:16700841-16700919	NONHSAT130291
12	lnc-CNTLN-3	chr9:16625674-16625895	ENSG00000230694.1
13	lnc-C9orf92-4	chr9:16714816-16714976	NONHSAT130290
14	lnc-C9orf92-4	chr9:16665064-16665173	NONHSAT130290
15	lnc-CNTLN-6	chr9:16700753-16700983	uc_252_+

No data

Variant related genes	Relation type
ENSG00000230694	TF binding region
ENSG00000231756	TF binding region
BNC2	TF binding region
ENSG00000234779	TF binding region
ENSG00000230694	CpG island
ENSG00000231756	CpG island
BNC2	CpG island
ENSG00000234779	CpG island
ENSG00000075624	chromatin interactions
ENSG00000129810	chromatin interactions
ENSG00000173068	chromatin interactions
ENSG00000167601	chromatin interactions
ENSG00000124535	chromatin interactions
ENSG00000272277	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000123358	chromatin interactions

Extended variants
information (count: 14282 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:14282 , 50 per page) page: 1 2 3 4 5 6 7 ... 286

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13284663	chr9:16465337-16465338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs189489169	chr9:16465354-16465355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs551586589	chr9:16465355-16465356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs566706781	chr9:16465357-16465358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs530592219	chr9:16465371-16465372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs79983037	chr9:16465390-16465391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs544729436	chr9:16465412-16465413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs565299794	chr9:16465430-16465431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs530327240	chr9:16465432-16465433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs368002179	chr9:16465433-16465434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs34834563	chr9:16465450-16465451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs12340350	chr9:16465452-16465453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs113791555	chr9:16465460-16465461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs377477660	chr9:16465462-16465463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs12000878	chr9:16465467-16465468	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs537811945	chr9:16465495-16465496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs180679467	chr9:16465526-16465527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs201237760	chr9:16465534-16465535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs184775440	chr9:16465557-16465558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs578072925	chr9:16465567-16465568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs144142353	chr9:16465603-16465604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs189192001	chr9:16465613-16465614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs181640393	chr9:16465640-16465641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs148678646	chr9:16465660-16465661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs80092004	chr9:16465676-16465677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs530891920	chr9:16465695-16465696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs573868710	chr9:16465725-16465726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs185771488	chr9:16465753-16465754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs562481340	chr9:16465754-16465755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs144212077	chr9:16465829-16465830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs375041209	chr9:16465837-16465838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs563951839	chr9:16465858-16465859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs35349138	chr9:16465892-16465893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs111487662	chr9:16465911-16465912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs560336860	chr9:16465934-16465935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs60663968	chr9:16466000-16466001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs56148125	chr9:16466002-16466003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs529547908	chr9:16466035-16466036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs546759881	chr9:16466038-16466039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs370385609	chr9:16466041-16466042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs527833758	chr9:16466078-16466079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs549660891	chr9:16466122-16466123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs61391155	chr9:16466173-16466174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs567905668	chr9:16466188-16466189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs543261549	chr9:16466202-16466203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs201128726	chr9:16466266-16466267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs10810566	chr9:16466409-16466410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs111873242	chr9:16466596-16466597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs112257929	chr9:16466658-16466659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs200990724	chr9:16466695-16466696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cervical cancer	21063398	CNVD
Retinoblastoma	22278416	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Melanoma	18172304	CNVD
Biliary cancer	19435499	CNVD
Gastric cancer	21586687	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myopathy	18421352	CNVD
Neuroblastoma	18664255	CNVD
Acute lymphoblastic leukemia	18957548	CNVD
Myeloproliferative neoplasm	17564968	CNVD
Malignant meningioma	17937814	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Chronic myeloid leukemia	21384125	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Myelodysplastic syndrome	21251322	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	18803288	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	22183965	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Glycine encephalopathy	21572526	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Non-small cell lung cancer	19010865	CNVD
Myoepithelioma	18604193	CNVD
Glioblastoma multiforme	18628472	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	21611746	CNVD
Pancreatic cancer	21811587	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:5172 , 50 per page) page: 1 2 3 4 5 6 7 ... 104

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:16457800-16493400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr9:16458000-16470400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr9:16459600-16470800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr9:16459600-16482400	Weak transcription	A549	lung
5	chr9:16459600-16499800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr9:16459600-16500000	Weak transcription	NHLF	lung
7	chr9:16460800-16485400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr9:16462000-16470600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr9:16462000-16476400	Weak transcription	Stomach Smooth Muscle	stomach
10	chr9:16462200-16470400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr9:16462200-16474000	Weak transcription	Fetal Lung	lung
12	chr9:16463200-16468400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr9:16463200-16470600	Weak transcription	H1 Cell Line	embryonic stem cell
14	chr9:16463200-16478000	Weak transcription	Ovary	ovary
15	chr9:16463200-16483800	Weak transcription	Fetal Stomach	stomach
16	chr9:16464000-16470400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr9:16468400-16473400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr9:16469000-16469800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr9:16469200-16476000	Weak transcription	Osteobl	bone
20	chr9:16469800-16475600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr9:16470400-16471000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr9:16470400-16471000	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr9:16470400-16471200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr9:16470400-16471200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
25	chr9:16470600-16471200	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
26	chr9:16470600-16471200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr9:16470800-16471200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr9:16471000-16504600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr9:16471200-16471800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr9:16471200-16472000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr9:16471200-16472400	Weak transcription	HSMM	muscle
32	chr9:16471200-16477800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr9:16472000-16473400	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr9:16472200-16472400	Enhancers	Rectal Smooth Muscle	rectum
35	chr9:16472200-16476000	Weak transcription	Muscle Satellite Cultured Cells	--
36	chr9:16472400-16472600	Weak transcription	H1 Cell Line	embryonic stem cell
37	chr9:16472400-16473200	Strong transcription	HSMM	muscle
38	chr9:16472800-16476000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr9:16473200-16484400	Weak transcription	HSMM	muscle
40	chr9:16473400-16475600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr9:16473400-16477600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr9:16474000-16474200	Enhancers	Fetal Lung	lung
43	chr9:16474200-16474600	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr9:16474200-16475400	Weak transcription	NHDF-Ad	bronchial
45	chr9:16474400-16474600	Enhancers	iPS-20b Cell Line	embryonic stem cell
46	chr9:16474600-16477200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
47	chr9:16474600-16478000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
48	chr9:16475400-16476600	Enhancers	NHDF-Ad	bronchial
49	chr9:16475600-16476600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr9:16475600-16477200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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