Variant report

Variant	nsv892620
Chromosome Location	chr9:14922877-15086021
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:788)
CpG islands
(count:305)
Chromatin interactive
region (count:11)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:788 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:15079916-15080552	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:15081278-15081815	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:14967513-14968337	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:14925038-14925148	HepG2	liver:	n/a	n/a
5	ARID3A	chr9:14960946-14962339	HepG2	liver:	n/a	n/a
6	ATF1	chr9:14992118-14992479	K562	blood:	n/a	n/a
7	ATF1	chr9:14926973-14927434	K562	blood:	n/a	n/a
8	ATF1	chr9:14993152-14993450	K562	blood:	n/a	n/a
9	ATF1	chr9:15057885-15057984	K562	blood:	n/a	n/a
10	BATF	chr9:14992095-14992275	GM12878	blood:	n/a	n/a
11	BCL3	chr9:14974056-14974338	GM12878	blood:	n/a	n/a
12	BHLHE40	chr9:15079998-15080418	HepG2	liver:	n/a	n/a
13	BHLHE40	chr9:14961666-14961683	K562	blood:	n/a	n/a
14	BHLHE40	chr9:14993063-14993414	K562	blood:	n/a	n/a
15	CBX3	chr9:14993086-14993431	K562	blood:	n/a	n/a
16	CCNT2	chr9:14926887-14927432	K562	blood:	n/a	n/a
17	CCNT2	chr9:14993093-14993468	K562	blood:	n/a	chr9:14993195-14993204
18	CEBPB	chr9:14993420-14993444	K562	blood:	n/a	n/a
19	CEBPB	chr9:15044267-15044502	HepG2	liver:	n/a	chr9:15044351-15044362
20	CEBPB	chr9:15079942-15080517	HepG2	liver:	n/a	n/a
21	CEBPB	chr9:15045847-15046039	K562	blood:	n/a	n/a
22	CEBPB	chr9:15045815-15045862	H1-hESC	embryonic stem cell:	n/a	chr9:15045833-15045844
23	CEBPB	chr9:14924966-14925246	A549	lung:	n/a	chr9:14925029-14925040 chr9:14925086-14925097
24	CEBPB	chr9:15045687-15045972	HepG2	liver:	n/a	chr9:15045833-15045844
25	CEBPB	chr9:15079977-15080474	HepG2	liver:	n/a	n/a
26	CEBPB	chr9:15044264-15044450	A549	lung:	n/a	chr9:15044351-15044362
27	CEBPB	chr9:14945585-14945795	HepG2	liver:	n/a	chr9:14945603-14945614
28	CEBPB	chr9:14924936-14925115	K562	blood:	n/a	chr9:14925029-14925040 chr9:14925086-14925097
29	CEBPB	chr9:14974108-14974375	HepG2	liver:	n/a	chr9:14974218-14974229
30	CEBPB	chr9:14978581-14978815	HepG2	liver:	n/a	chr9:14978687-14978698
31	CEBPB	chr9:15044258-15044505	IMR90	lung:	n/a	chr9:15044351-15044362
32	CEBPB	chr9:14978650-14978695	A549	lung:	n/a	n/a
33	CEBPB	chr9:15078367-15078703	HepG2	liver:	n/a	n/a
34	CEBPB	chr9:15044270-15044442	HepG2	liver:	n/a	chr9:15044351-15044362
35	CEBPB	chr9:15078435-15078628	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr9:15010647-15010868	HepG2	liver:	n/a	chr9:15010746-15010757 chr9:15010745-15010758
37	CEBPB	chr9:14949391-14949419	K562	blood:	n/a	n/a
38	CEBPB	chr9:14924863-14925268	HepG2	liver:	n/a	chr9:14925029-14925040 chr9:14925086-14925097
39	CEBPB	chr9:15044258-15044401	H1-hESC	embryonic stem cell:	n/a	chr9:15044351-15044362
40	CEBPB	chr9:14992111-14992396	K562	blood:	n/a	n/a
41	CEBPB	chr9:14941573-14941825	HepG2	liver:	n/a	chr9:14941720-14941731 chr9:14941718-14941731 chr9:14941718-14941729 chr9:14941720-14941729
42	CEBPB	chr9:15078408-15078724	MCF-7	breast:	n/a	n/a
43	CEBPB	chr9:15078420-15078697	IMR90	lung:	n/a	n/a
44	CEBPB	chr9:14924866-14925231	IMR90	lung:	n/a	chr9:14925029-14925040 chr9:14925086-14925097
45	CEBPB	chr9:14924869-14925229	Hela-S3	cervix:	n/a	chr9:14925029-14925040 chr9:14925086-14925097
46	CEBPB	chr9:15045696-15046018	IMR90	lung:	n/a	chr9:15045833-15045844
47	CEBPB	chr9:14975880-14976085	HepG2	liver:	n/a	n/a
48	CEBPB	chr9:15080090-15080421	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr9:14978624-14978819	IMR90	lung:	n/a	chr9:14978687-14978698
50	CEBPB	chr9:15078345-15078671	A549	lung:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:15055021-15055071	U87	brain:	n/a
2	chr9:14993584-14993634	ovcar-3	ovarian:	n/a
3	chr9:15055021-15055071	PANC-1	pancreas:	n/a
4	chr9:14978400-14978450	BE2_C	brain:	n/a
5	chr9:14993584-14993634	Caco-2	colon:	n/a
6	chr9:14992172-14992222	GM06990	blood:	n/a
7	chr9:14978400-14978450	NB4	blood:	n/a
8	chr9:14993584-14993634	SK-N-SH_RA	brain:	n/a
9	chr9:14993584-14993634	A549	lung:	n/a
10	chr9:14993466-14993516	SK-N-SH_RA	brain:	n/a
11	chr9:14993584-14993634	RPTEC	kidney:	n/a
12	chr9:14993584-14993634	GM06990	blood:	n/a
13	chr9:15055021-15055071	A549	lung:	n/a
14	chr9:14993466-14993516	HIPEpiC	eye:	n/a
15	chr9:14993466-14993516	ovcar-3	ovarian:	n/a
16	chr9:15055021-15055071	T-47D	breast:	n/a
17	chr9:14993584-14993634	LNCaP	prostate:	n/a
18	chr9:14993466-14993516	NT2-D1	testis:	n/a
19	chr9:14992172-14992222	Caco-2	colon:	n/a
20	chr9:14992172-14992222	AG04449	skin:	fetal
21	chr9:15055021-15055071	HCT-116	colon:	n/a
22	chr9:14978400-14978450	BJ	skin:	n/a
23	chr9:14993466-14993516	AG09309	skin:	n/a
24	chr9:14993584-14993634	GM12892	blood:	n/a
25	chr9:14993584-14993634	MCF-7	breast:	n/a
26	chr9:15055021-15055071	AG10803	skin:	n/a
27	chr9:14978400-14978450	HMEC	breast:	n/a
28	chr9:14993466-14993516	Hela-S3	cervix:	n/a
29	chr9:14993466-14993516	Hepatocyte	liver:	n/a
30	chr9:14993466-14993516	CMK	blood:	n/a
31	chr9:15055021-15055071	SKMC	muscle:	n/a
32	chr9:14993584-14993634	U87	brain:	n/a
33	chr9:14978400-14978450	HEEpiC	esophagus:	n/a
34	chr9:14978400-14978450	Hela-S3	cervix:	n/a
35	chr9:15055021-15055071	ovcar-3	ovarian:	n/a
36	chr9:14992172-14992222	HCM	heart:	n/a
37	chr9:14993466-14993516	HMEC	breast:	n/a
38	chr9:15055021-15055071	GM19239	blood:	n/a
39	chr9:15055021-15055071	GM12878	blood:	n/a
40	chr9:14993466-14993516	HepG2	liver:	n/a
41	chr9:14993584-14993634	HRPEpiC	eye:	n/a
42	chr9:14978400-14978450	GM12878	blood:	n/a
43	chr9:14992172-14992222	HAEpiC	amniotic membrane:	n/a
44	chr9:15055021-15055071	MCF10A-Er-Src	breast:	n/a
45	chr9:14993466-14993516	HAEpiC	amniotic membrane:	n/a
46	chr9:15055021-15055071	Jurkat	blood:	n/a
47	chr9:14992172-14992222	HL-60	blood:	n/a
48	chr9:14992172-14992222	HRE	kidney:	n/a
49	chr9:14993466-14993516	ECC-1	luminal epithelium:	n/a
50	chr9:14978400-14978450	MCF-7	breast:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:41399132..41401887-chr9:15065450..15066950,2	K562	blood:
2	chr4:153844459..153845960-chr9:15065470..15068450,2	K562	blood:
3	chr10:103123110..103126109-chr9:15066951..15068470,2	K562	blood:
4	chr17:41380667..41383523-chr9:15065470..15068471,3	K562	blood:
5	chr9:15036109..15038088-chr9:15043149..15044736,2	MCF-7	breast:
6	chr9:15036109..15038088-chr9:15043149..15044736,2	MCF-7	breast:
7	chr17:41380109..41382138-chr9:15066951..15068451,2	MCF-7	breast:
8	chr9:14914097..14915785-chr9:14923708..14925930,2	K562	blood:
9	chr17:41462152..41463715-chr9:15065450..15066970,3	MCF-7	breast:
10	chr17:41398994..41400824-chr9:15066951..15068451,2	K562	blood:
11	chr17:41380280..41381950-chr9:15066950..15068451,3	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FREM1-1	chr9:14979298-14979338	l_3739_chr9:14977433-14983179_testes
2	lnc-FREM1-1	chr9:14977891-14977954	l_3739_chr9:14977433-14983179_testes
3	lnc-FREM1-1	chr9:14983147-14983179	l_3739_chr9:14977433-14983179_testes
4	lnc-FREM1-1	chr9:14980226-14980343	l_3739_chr9:14977433-14983179_testes
5	lnc-FREM1-1	chr9:14977434-14977699	l_3739_chr9:14977433-14983179_testes

No data

Variant related genes	Relation type
LDHAP4	TF binding region
ENSG00000234297	TF binding region
ENSG00000215237	TF binding region
ENSG00000232000	TF binding region
LDHAP4	CpG island
ENSG00000234297	CpG island
ENSG00000215237	CpG island
ENSG00000232000	CpG island
ENSG00000236383	chromatin interactions
ENSG00000222414	chromatin interactions

Extended variants
information (count: 5717 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:5717 , 50 per page) page: 1 2 3 4 5 6 7 ... 115

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10756626	chr9:14922877-14922878	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs369796655	chr9:14922893-14922894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs554708026	chr9:14922896-14922897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs576171529	chr9:14922897-14922898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs142908171	chr9:14922900-14922901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs372751464	chr9:14922904-14922905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs76611461	chr9:14922910-14922911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs145167999	chr9:14922918-14922919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs541426297	chr9:14922928-14922929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs553452868	chr9:14922994-14922995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs78725990	chr9:14923009-14923010	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs185670385	chr9:14923043-14923044	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs537378215	chr9:14923092-14923093	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs139038113	chr9:14923099-14923100	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs531034682	chr9:14923108-14923109	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs546406134	chr9:14923120-14923121	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs373545743	chr9:14923121-14923122	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs528801133	chr9:14923138-14923139	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs546941556	chr9:14923139-14923140	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs565345603	chr9:14923147-14923148	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs189312141	chr9:14923156-14923157	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs142242554	chr9:14923215-14923216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs376962165	chr9:14923235-14923236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs74638793	chr9:14923277-14923278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs558755520	chr9:14923282-14923283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs200940345	chr9:14923289-14923290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs570753460	chr9:14923328-14923329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs73419708	chr9:14923345-14923346	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs553364763	chr9:14923348-14923349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs574904271	chr9:14923452-14923453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs180817732	chr9:14923453-14923454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs557153589	chr9:14923470-14923471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs575727770	chr9:14923504-14923505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs546072961	chr9:14923527-14923528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs530325111	chr9:14923535-14923536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs73642465	chr9:14923580-14923581	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs528719206	chr9:14923592-14923593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs540538495	chr9:14923612-14923613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs187310868	chr9:14923617-14923618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs529619399	chr9:14923621-14923622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs540681925	chr9:14923631-14923632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs73419709	chr9:14923635-14923636	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs569638293	chr9:14923654-14923655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs530675870	chr9:14923661-14923662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs552042236	chr9:14923677-14923678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs148503734	chr9:14923713-14923714	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs115811828	chr9:14923741-14923742	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs560611052	chr9:14923784-14923785	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs2140323	chr9:14923810-14923811	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs12343486	chr9:14923847-14923848	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:92)

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
Breast cancer	21611746	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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	21811587	CNVD
Breast cancer	22522925	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:796 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:14920600-14924200	Weak transcription	Adipose Nuclei	Adipose
2	chr9:14920600-14935200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr9:14922800-14924400	Weak transcription	HepG2	liver
4	chr9:14924000-14924200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr9:14924000-14924200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr9:14924000-14924200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr9:14924000-14924200	Enhancers	NHDF-Ad	bronchial
8	chr9:14924000-14925200	Enhancers	Fetal Kidney	kidney
9	chr9:14924200-14924400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr9:14924200-14924400	Enhancers	Fetal Stomach	stomach
11	chr9:14924200-14924600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr9:14924200-14924600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr9:14924200-14924600	Enhancers	Adipose Nuclei	Adipose
14	chr9:14924200-14924600	Enhancers	Fetal Lung	lung
15	chr9:14924200-14924600	Enhancers	Skeletal Muscle Male	skeletal muscle
16	chr9:14924200-14924600	Flanking Active TSS	NHDF-Ad	bronchial
17	chr9:14924200-14925400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr9:14924400-14924600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr9:14924400-14924600	Enhancers	Muscle Satellite Cultured Cells	--
20	chr9:14924400-14924600	Enhancers	Skeletal Muscle Female	skeletal muscle
21	chr9:14924400-14924600	Enhancers	HSMMtube	muscle
22	chr9:14924400-14925000	Weak transcription	Fetal Stomach	stomach
23	chr9:14924400-14925200	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr9:14924400-14925400	Enhancers	HepG2	liver
25	chr9:14924600-14924800	Flanking Active TSS	Adipose Nuclei	Adipose
26	chr9:14924600-14924800	Flanking Active TSS	Fetal Lung	lung
27	chr9:14924600-14925000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr9:14924600-14925000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
29	chr9:14924600-14925000	Active TSS	Skeletal Muscle Male	skeletal muscle
30	chr9:14924600-14925000	Active TSS	Skeletal Muscle Female	skeletal muscle
31	chr9:14924600-14925000	Active TSS	HSMM	muscle
32	chr9:14924600-14925000	Active TSS	Osteobl	bone
33	chr9:14924600-14925200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr9:14924600-14925200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr9:14924600-14925200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr9:14924600-14925200	Active TSS	Aorta	Aorta
37	chr9:14924600-14925200	Active TSS	Right Atrium	heart
38	chr9:14924600-14925200	Active TSS	HSMMtube	muscle
39	chr9:14924600-14925200	Active TSS	NHDF-Ad	bronchial
40	chr9:14924600-14925200	Active TSS	NHLF	lung
41	chr9:14924600-14925400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr9:14924800-14925000	Enhancers	Fetal Heart	heart
43	chr9:14924800-14925200	Active TSS	Adipose Nuclei	Adipose
44	chr9:14924800-14925200	Active TSS	Fetal Lung	lung
45	chr9:14925000-14925200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr9:14925000-14925200	Active TSS	Muscle Satellite Cultured Cells	--
47	chr9:14925000-14925200	Enhancers	Fetal Stomach	stomach
48	chr9:14925000-14925400	Enhancers	HSMM	muscle
49	chr9:14925000-14926000	Weak transcription	Fetal Heart	heart
50	chr9:14925000-14927600	Enhancers	Primary hematopoietic stem cells	blood

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