Variant report

Variant	nsv892635
Chromosome Location	chr9:15731775-15876507
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	chr9:15738069-15738699	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:15824460-15824492	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:15873620-15873926	HepG2	liver:	n/a	n/a
4	BHLHE40	chr9:15837128-15837398	GM12878	blood:	n/a	n/a
5	CEBPB	chr9:15825520-15825732	IMR90	lung:	n/a	chr9:15825609-15825620
6	CEBPB	chr9:15875974-15876186	A549	lung:	n/a	n/a
7	CEBPB	chr9:15825568-15825724	HepG2	liver:	n/a	chr9:15825609-15825620
8	CEBPB	chr9:15831522-15831716	A549	lung:	n/a	chr9:15831596-15831609
9	CEBPB	chr9:15735009-15735843	A549	lung:	n/a	chr9:15735616-15735627
10	CEBPB	chr9:15735042-15735513	MCF-7	breast:	n/a	n/a
11	CEBPB	chr9:15803721-15803998	HepG2	liver:	n/a	chr9:15803862-15803873
12	CEBPB	chr9:15735040-15735683	ECC-1	luminal epithelium:	n/a	chr9:15735616-15735627
13	CEBPB	chr9:15856572-15856992	IMR90	lung:	n/a	n/a
14	CEBPB	chr9:15735107-15735781	A549	lung:	n/a	chr9:15735616-15735627
15	CEBPB	chr9:15755596-15756068	IMR90	lung:	n/a	n/a
16	CEBPB	chr9:15831451-15831723	Hela-S3	cervix:	n/a	chr9:15831596-15831609
17	CEBPB	chr9:15755700-15755790	HepG2	liver:	n/a	n/a
18	CEBPB	chr9:15850052-15850257	A549	lung:	n/a	chr9:15850110-15850122
19	CEBPB	chr9:15741023-15741380	IMR90	lung:	n/a	chr9:15741201-15741212
20	CEBPB	chr9:15741073-15741357	Hela-S3	cervix:	n/a	chr9:15741201-15741212
21	CEBPB	chr9:15803709-15804025	IMR90	lung:	n/a	chr9:15803862-15803873
22	CEBPB	chr9:15741051-15741354	A549	lung:	n/a	chr9:15741201-15741212
23	CEBPB	chr9:15831422-15831741	ECC-1	luminal epithelium:	n/a	chr9:15831596-15831609
24	CEBPB	chr9:15845846-15845992	A549	lung:	n/a	chr9:15845914-15845927 chr9:15845914-15845925 chr9:15845916-15845925
25	CEBPB	chr9:15734342-15734549	IMR90	lung:	n/a	n/a
26	CEBPB	chr9:15845792-15846013	HepG2	liver:	n/a	chr9:15845914-15845927 chr9:15845914-15845925 chr9:15845916-15845925
27	CEBPB	chr9:15803787-15803977	A549	lung:	n/a	chr9:15803862-15803873
28	CEBPB	chr9:15741109-15741261	HepG2	liver:	n/a	chr9:15741201-15741212
29	CEBPB	chr9:15817338-15817562	A549	lung:	n/a	n/a
30	CEBPB	chr9:15741024-15741393	HepG2	liver:	n/a	chr9:15741201-15741212
31	CEBPB	chr9:15735000-15735439	MCF-7	breast:	n/a	n/a
32	CEBPB	chr9:15734822-15735983	Hela-S3	cervix:	n/a	chr9:15735616-15735627
33	CEBPB	chr9:15734335-15734526	A549	lung:	n/a	n/a
34	CEBPB	chr9:15863418-15863420	A549	lung:	n/a	n/a
35	CEBPB	chr9:15845758-15846062	IMR90	lung:	n/a	chr9:15845914-15845927 chr9:15845914-15845925 chr9:15845916-15845925
36	CEBPB	chr9:15735045-15735794	IMR90	lung:	n/a	chr9:15735616-15735627
37	CEBPB	chr9:15817342-15817541	IMR90	lung:	n/a	n/a
38	CEBPB	chr9:15735056-15735385	ECC-1	luminal epithelium:	n/a	n/a
39	CEBPB	chr9:15845785-15846037	MCF-7	breast:	n/a	chr9:15845914-15845927 chr9:15845914-15845925 chr9:15845916-15845925
40	CEBPB	chr9:15741125-15741305	K562	blood:	n/a	chr9:15741201-15741212
41	CEBPB	chr9:15741050-15741339	H1-hESC	embryonic stem cell:	n/a	chr9:15741201-15741212
42	CTCF	chr9:15839640-15839790	NHDF-neo	bronchial:	n/a	n/a
43	CTCF	chr9:15873528-15873952	A549	lung:	n/a	chr9:15873756-15873777 chr9:15873754-15873772 chr9:15873757-15873770
44	CTCF	chr9:15839500-15839650	RPTEC	kidney:	n/a	n/a
45	CTCF	chr9:15837100-15837250	HCM	heart:	n/a	n/a
46	CTCF	chr9:15824440-15824590	HCPEpiC	choroid plexus:	n/a	chr9:15824497-15824515 chr9:15824499-15824512
47	CTCF	chr9:15837186-15837310	Fibrobl	skin:	n/a	chr9:15837266-15837274 chr9:15837261-15837279 chr9:15837262-15837278 chr9:15837263-15837284
48	CTCF	chr9:15824480-15824553	GM13976	blood:	n/a	chr9:15824497-15824515 chr9:15824499-15824512
49	CTCF	chr9:15873640-15873790	GM12868	blood:	n/a	chr9:15873756-15873777 chr9:15873754-15873772 chr9:15873757-15873770
50	CTCF	chr9:15824400-15824550	BJ	skin:	n/a	chr9:15824497-15824515 chr9:15824499-15824512

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:15810627-15810677	HAEpiC	amniotic membrane:	n/a
2	chr9:15810627-15810677	HAEpiC	amniotic membrane:	n/a
3	chr9:15810627-15810677	H1-hESC	embryonic stem cell:	embryo
4	chr9:15810627-15810677	NB4	blood:	n/a
5	chr9:15810627-15810677	LNCaP	prostate:	n/a
6	chr9:15810627-15810677	ovcar-3	ovarian:	n/a
7	chr9:15810627-15810677	Caco-2	colon:	n/a
8	chr9:15810627-15810677	HUVEC	blood vessel:	n/a
9	chr9:15810627-15810677	SK-N-SH	brain:	n/a
10	chr9:15810627-15810677	MCF10A-Er-Src	breast:	n/a
11	chr9:15810627-15810677	AG09319	gingival:	n/a
12	chr9:15810627-15810677	PFSK-1	brain:	n/a
13	chr9:15810627-15810677	HCF	heart:	n/a
14	chr9:15810627-15810677	Jurkat	blood:	n/a
15	chr9:15810627-15810677	HIPEpiC	eye:	n/a
16	chr9:15810627-15810677	HCM	heart:	n/a
17	chr9:15810627-15810677	SKMC	muscle:	n/a
18	chr9:15810627-15810677	MCF-7	breast:	n/a
19	chr9:15810627-15810677	Hela-S3	cervix:	n/a
20	chr9:15810627-15810677	HCPEpiC	choroid plexus:	n/a
21	chr9:15810627-15810677	GM12891	blood:	n/a
22	chr9:15810627-15810677	PrEC	prostate:	n/a
23	chr9:15810627-15810677	NH-A	brain:	n/a
24	chr9:15810627-15810677	SAEC	small airway:	n/a
25	chr9:15810627-15810677	GM12878	blood:	n/a
26	chr9:15810627-15810677	GM19239	blood:	n/a
27	chr9:15810627-15810677	HEK293	kidney:	embryo
28	chr9:15810627-15810677	RPTEC	kidney:	n/a
29	chr9:15810627-15810677	BE2_C	brain:	n/a
30	chr9:15810627-15810677	IMR90	lung:	fetal
31	chr9:15810627-15810677	HRPEpiC	eye:	n/a
32	chr9:15810627-15810677	AoSMC	blood vessel:	n/a
33	chr9:15810627-15810677	HepG2	liver:	n/a
34	chr9:15810627-15810677	ECC-1	luminal epithelium:	n/a
35	chr9:15810627-15810677	SK-N-SH_RA	brain:	n/a
36	chr9:15810627-15810677	Hepatocyte	liver:	n/a
37	chr9:15810627-15810677	A549	lung:	n/a
38	chr9:15810627-15810677	PANC-1	pancreas:	n/a
39	chr9:15810627-15810677	T-47D	breast:	n/a
40	chr9:15810627-15810677	NT2-D1	testis:	n/a
41	chr9:15810627-15810677	ProgFib	skin:	n/a
42	chr9:15810627-15810677	AG04449	skin:	fetal
43	chr9:15810627-15810677	HPAEpiC	pulmonary alveolar:	n/a
44	chr9:15810627-15810677	SK-N-MC	brain:	n/a
45	chr9:15810627-15810677	AG04450	lung:	fetal
46	chr9:15810627-15810677	NHDF-neo	bronchial:	n/a
47	chr9:15810627-15810677	NHBE	bronchial:	n/a
48	chr9:15810627-15810677	HMEC	breast:	n/a
49	chr9:15810627-15810677	CMK	blood:	n/a
50	chr9:15810627-15810677	HCT-116	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:15873671..15874276-chr9:16131035..16131676,2	MCF-7	breast:
2	chr9:15778842..15781676-chr9:15783903..15785972,2	MCF-7	breast:
3	chr9:15732005..15734234-chr9:15736903..15738825,2	K562	blood:
4	chr9:15836820..15837651-chr9:16133566..16134324,2	MCF-7	breast:
5	chr9:15876069..15878996-chr9:15881161..15882668,2	MCF-7	breast:
6	chr9:15873337..15874253-chr9:16131080..16131915,3	MCF-7	breast:
7	chr9:15732005..15734234-chr9:15736903..15738825,2	K562	blood:
8	chr9:15778842..15781676-chr9:15783903..15785972,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SNAPC3-5	chr9:15864309-15864521	uc_251_+
2	lnc-C9orf92-3	chr9:15864309-15864521	uc_251_-
3	lnc-SNAPC3-1	chr9:15874539-15874661	NONHSAT130279

Variant related genes	Relation type
RNU6-14P	TF binding region
CCDC171	TF binding region
RNU6-14P	CpG island
CCDC171	CpG island

Extended variants
information (count: 6854 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:6854 , 50 per page) page: 1 2 3 4 5 6 7 ... 138

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7032595	chr9:15731775-15731776	Strong transcription ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs112797099	chr9:15731779-15731780	Strong transcription ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs147100008	chr9:15731784-15731785	Strong transcription ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs372937566	chr9:15731885-15731886	Strong transcription ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs187159828	chr9:15731910-15731911	Strong transcription ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs376045602	chr9:15731934-15731935	Strong transcription ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs138468922	chr9:15732032-15732033	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs10738408	chr9:15732075-15732076	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs35809067	chr9:15732169-15732170	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs546953538	chr9:15732223-15732224	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs112542009	chr9:15732276-15732277	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs536048292	chr9:15732307-15732308	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs4475607	chr9:15732319-15732320	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs1396705	chr9:15732332-15732333	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs569479589	chr9:15732358-15732359	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs537105819	chr9:15732376-15732377	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs1396706	chr9:15732420-15732421	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs376524978	chr9:15732429-15732430	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs75080305	chr9:15732445-15732446	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs199790788	chr9:15732454-15732455	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs34104006	chr9:15732545-15732546	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs534643337	chr9:15732546-15732547	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs564329634	chr9:15732559-15732560	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs192085194	chr9:15732563-15732564	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs562221908	chr9:15732585-15732586	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs552978475	chr9:15732601-15732602	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs113219365	chr9:15732606-15732607	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs35123706	chr9:15732627-15732628	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs183244690	chr9:15732679-15732680	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs188309090	chr9:15732683-15732684	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs569852525	chr9:15732738-15732739	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs575112973	chr9:15732774-15732775	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs545864864	chr9:15732820-15732821	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs372059114	chr9:15732834-15732835	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs564631915	chr9:15732846-15732847	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs528459287	chr9:15732858-15732859	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs547011555	chr9:15732899-15732900	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs376801141	chr9:15732910-15732911	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs528998700	chr9:15732923-15732924	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs549034745	chr9:15732962-15732963	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs529566548	chr9:15733038-15733039	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs551306059	chr9:15733112-15733113	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs191556313	chr9:15733155-15733156	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs533591668	chr9:15733185-15733186	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs182447080	chr9:15733201-15733202	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs148368705	chr9:15733202-15733203	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs186764163	chr9:15733204-15733205	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs191233386	chr9:15733248-15733249	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs10217681	chr9:15733251-15733252	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs141424533	chr9:15733267-15733268	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	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
Ovarian cancer	19835627	CNVD
Breast cancer	22522925	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:361 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:15679800-15746800	Weak transcription	Ovary	ovary
2	chr9:15687600-15746600	Weak transcription	Aorta	Aorta
3	chr9:15715200-15746200	Weak transcription	Left Ventricle	heart
4	chr9:15715600-15733800	Weak transcription	Brain Anterior Caudate	brain
5	chr9:15718000-15749600	Weak transcription	Stomach Smooth Muscle	stomach
6	chr9:15718600-15746600	Weak transcription	Thymus	Thymus
7	chr9:15720400-15733400	Weak transcription	Brain Cingulate Gyrus	brain
8	chr9:15720600-15735200	Weak transcription	Adipose Nuclei	Adipose
9	chr9:15725400-15734600	Weak transcription	Muscle Satellite Cultured Cells	--
10	chr9:15727600-15732400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr9:15728000-15732000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
12	chr9:15729000-15746800	Weak transcription	Fetal Thymus	thymus
13	chr9:15731000-15732600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr9:15731200-15732000	Strong transcription	Primary hematopoietic stem cells	blood
15	chr9:15731200-15732000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr9:15732000-15733200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr9:15732000-15734000	Weak transcription	Primary hematopoietic stem cells	blood
18	chr9:15732000-15735200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
19	chr9:15732400-15732800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr9:15732600-15733400	Enhancers	Hela-S3	cervix
21	chr9:15732600-15734400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr9:15732800-15735200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr9:15733200-15739000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr9:15733400-15734800	Weak transcription	Hela-S3	cervix
25	chr9:15734400-15734600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr9:15734600-15735400	Enhancers	Muscle Satellite Cultured Cells	--
27	chr9:15734600-15736000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr9:15734600-15736800	Enhancers	Osteobl	bone
29	chr9:15734800-15735000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr9:15734800-15735000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr9:15734800-15735200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr9:15734800-15735400	Enhancers	HSMMtube	muscle
33	chr9:15734800-15735400	Enhancers	NHLF	lung
34	chr9:15734800-15736000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr9:15734800-15736000	Enhancers	Fetal Heart	heart
36	chr9:15734800-15736000	Enhancers	HSMM	muscle
37	chr9:15734800-15736000	Enhancers	NH-A	brain
38	chr9:15734800-15736200	Enhancers	A549	lung
39	chr9:15734800-15736200	Enhancers	HUVEC	blood vessel
40	chr9:15734800-15736200	Enhancers	NHDF-Ad	bronchial
41	chr9:15734800-15736200	Enhancers	NHEK	skin
42	chr9:15734800-15736400	Enhancers	HMEC	breast
43	chr9:15734800-15736600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr9:15734800-15736600	Enhancers	Hela-S3	cervix
45	chr9:15734800-15737000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr9:15734800-15738400	Enhancers	Fetal Lung	lung
47	chr9:15735000-15735200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr9:15735000-15735200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr9:15735000-15735800	Enhancers	Duodenum Smooth Muscle	Duodenum
50	chr9:15735200-15735400	Enhancers	Breast Myoepithelial Primary Cells	Breast

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