Variant report

Variant	nsv892633
Chromosome Location	chr9:15604746-15889411
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1620)
CpG islands
(count:61)
Chromatin interactive
region (count:18)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1620 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:15606729-15607013	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:15738069-15738699	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:15824460-15824492	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:15642421-15642732	HepG2	liver:	n/a	n/a
5	ARID3A	chr9:15873620-15873926	HepG2	liver:	n/a	n/a
6	ATF1	chr9:15606159-15606277	K562	blood:	n/a	n/a
7	BACH1	chr9:15722850-15723205	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr9:15712591-15712742	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr9:15724284-15724315	K562	blood:	n/a	n/a
10	BATF	chr9:15612994-15613254	GM12878	blood:	n/a	chr9:15613158-15613169
11	BATF	chr9:15613003-15613305	GM12878	blood:	n/a	chr9:15613158-15613169
12	BHLHE40	chr9:15837128-15837398	GM12878	blood:	n/a	n/a
13	CEBPB	chr9:15817338-15817562	A549	lung:	n/a	n/a
14	CEBPB	chr9:15741024-15741393	HepG2	liver:	n/a	chr9:15741201-15741212
15	CEBPB	chr9:15856572-15856992	IMR90	lung:	n/a	n/a
16	CEBPB	chr9:15730933-15731218	HepG2	liver:	n/a	chr9:15731094-15731105
17	CEBPB	chr9:15741023-15741380	IMR90	lung:	n/a	chr9:15741201-15741212
18	CEBPB	chr9:15755700-15755790	HepG2	liver:	n/a	n/a
19	CEBPB	chr9:15825520-15825732	IMR90	lung:	n/a	chr9:15825609-15825620
20	CEBPB	chr9:15634610-15635086	IMR90	lung:	n/a	chr9:15634719-15634730
21	CEBPB	chr9:15845792-15846013	HepG2	liver:	n/a	chr9:15845914-15845927 chr9:15845914-15845925 chr9:15845916-15845925
22	CEBPB	chr9:15863418-15863420	A549	lung:	n/a	n/a
23	CEBPB	chr9:15831422-15831741	ECC-1	luminal epithelium:	n/a	chr9:15831596-15831609
24	CEBPB	chr9:15734335-15734526	A549	lung:	n/a	n/a
25	CEBPB	chr9:15803721-15803998	HepG2	liver:	n/a	chr9:15803862-15803873
26	CEBPB	chr9:15845785-15846037	MCF-7	breast:	n/a	chr9:15845914-15845927 chr9:15845914-15845925 chr9:15845916-15845925
27	CEBPB	chr9:15696978-15698055	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr9:15697348-15697947	IMR90	lung:	n/a	n/a
29	CEBPB	chr9:15616839-15617368	HepG2	liver:	n/a	chr9:15617185-15617196
30	CEBPB	chr9:15755596-15756068	IMR90	lung:	n/a	n/a
31	CEBPB	chr9:15741125-15741305	K562	blood:	n/a	chr9:15741201-15741212
32	CEBPB	chr9:15735045-15735794	IMR90	lung:	n/a	chr9:15735616-15735627
33	CEBPB	chr9:15831522-15831716	A549	lung:	n/a	chr9:15831596-15831609
34	CEBPB	chr9:15735009-15735843	A549	lung:	n/a	chr9:15735616-15735627
35	CEBPB	chr9:15714960-15715003	A549	lung:	n/a	n/a
36	CEBPB	chr9:15735056-15735385	ECC-1	luminal epithelium:	n/a	n/a
37	CEBPB	chr9:15734342-15734549	IMR90	lung:	n/a	n/a
38	CEBPB	chr9:15845846-15845992	A549	lung:	n/a	chr9:15845914-15845927 chr9:15845914-15845925 chr9:15845916-15845925
39	CEBPB	chr9:15730933-15731271	IMR90	lung:	n/a	chr9:15731094-15731105
40	CEBPB	chr9:15730990-15731258	A549	lung:	n/a	chr9:15731094-15731105
41	CEBPB	chr9:15735107-15735781	A549	lung:	n/a	chr9:15735616-15735627
42	CEBPB	chr9:15634650-15635051	HepG2	liver:	n/a	chr9:15634719-15634730
43	CEBPB	chr9:15724070-15724406	Hela-S3	cervix:	n/a	chr9:15724219-15724230 chr9:15724219-15724230
44	CEBPB	chr9:15741051-15741354	A549	lung:	n/a	chr9:15741201-15741212
45	CEBPB	chr9:15803787-15803977	A549	lung:	n/a	chr9:15803862-15803873
46	CEBPB	chr9:15803709-15804025	IMR90	lung:	n/a	chr9:15803862-15803873
47	CEBPB	chr9:15741073-15741357	Hela-S3	cervix:	n/a	chr9:15741201-15741212
48	CEBPB	chr9:15850052-15850257	A549	lung:	n/a	chr9:15850110-15850122
49	CEBPB	chr9:15831451-15831723	Hela-S3	cervix:	n/a	chr9:15831596-15831609
50	CEBPB	chr9:15741109-15741261	HepG2	liver:	n/a	chr9:15741201-15741212

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:15810627-15810677	LNCaP	prostate:	n/a
2	chr9:15810627-15810677	AoSMC	blood vessel:	n/a
3	chr9:15810627-15810677	ovcar-3	ovarian:	n/a
4	chr9:15810627-15810677	Hepatocyte	liver:	n/a
5	chr9:15810627-15810677	SK-N-MC	brain:	n/a
6	chr9:15810627-15810677	CMK	blood:	n/a
7	chr9:15810627-15810677	ProgFib	skin:	n/a
8	chr9:15810627-15810677	NT2-D1	testis:	n/a
9	chr9:15810627-15810677	NHBE	bronchial:	n/a
10	chr9:15810627-15810677	K562	blood:	n/a
11	chr9:15810627-15810677	SK-N-SH	brain:	n/a
12	chr9:15810627-15810677	AG04449	skin:	fetal
13	chr9:15810627-15810677	H1-hESC	embryonic stem cell:	embryo
14	chr9:15810627-15810677	BE2_C	brain:	n/a
15	chr9:15810627-15810677	HCF	heart:	n/a
16	chr9:15810627-15810677	HepG2	liver:	n/a
17	chr9:15810627-15810677	IMR90	lung:	fetal
18	chr9:15810627-15810677	HNPCEpiC	eye:	n/a
19	chr9:15810627-15810677	SKMC	muscle:	n/a
20	chr9:15810627-15810677	HL-60	blood:	n/a
21	chr9:15810627-15810677	AG09309	skin:	n/a
22	chr9:15810627-15810677	Hela-S3	cervix:	n/a
23	chr9:15810627-15810677	AG04450	lung:	fetal
24	chr9:15810627-15810677	RPTEC	kidney:	n/a
25	chr9:15810627-15810677	NH-A	brain:	n/a
26	chr9:15810627-15810677	HAEpiC	amniotic membrane:	n/a
27	chr9:15810627-15810677	ECC-1	luminal epithelium:	n/a
28	chr9:15810627-15810677	MCF10A-Er-Src	breast:	n/a
29	chr9:15810627-15810677	PFSK-1	brain:	n/a
30	chr9:15810627-15810677	HCT-116	colon:	n/a
31	chr9:15810627-15810677	U87	brain:	n/a
32	chr9:15810627-15810677	A549	lung:	n/a
33	chr9:15810627-15810677	BJ	skin:	n/a
34	chr9:15810627-15810677	HEEpiC	esophagus:	n/a
35	chr9:15810627-15810677	AG09319	gingival:	n/a
36	chr9:15810627-15810677	PrEC	prostate:	n/a
37	chr9:15810627-15810677	SAEC	small airway:	n/a
38	chr9:15810627-15810677	HRCEpiC	kidney:	n/a
39	chr9:15810627-15810677	GM12892	blood:	n/a
40	chr9:15810627-15810677	HCM	heart:	n/a
41	chr9:15810627-15810677	PANC-1	pancreas:	n/a
42	chr9:15810627-15810677	GM06990	blood:	n/a
43	chr9:15810627-15810677	HIPEpiC	eye:	n/a
44	chr9:15810627-15810677	Jurkat	blood:	n/a
45	chr9:15810627-15810677	HEK293	kidney:	embryo
46	chr9:15810627-15810677	AG10803	skin:	n/a
47	chr9:15810627-15810677	MCF-7	breast:	n/a
48	chr9:15810627-15810677	HRE	kidney:	n/a
49	chr9:15810627-15810677	HUVEC	blood vessel:	n/a
50	chr9:15810627-15810677	HPAEpiC	pulmonary alveolar:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:15732005..15734234-chr9:15736903..15738825,2	K562	blood:
2	chr9:15732005..15734234-chr9:15736903..15738825,2	K562	blood:
3	chr9:15690406..15691946-chr9:15692582..15695063,2	MCF-7	breast:
4	chr9:15509144..15511285-chr9:15608383..15610950,2	MCF-7	breast:
5	chr9:15876069..15878996-chr9:15881161..15882668,2	MCF-7	breast:
6	chr9:15510294..15512690-chr9:15720146..15721868,2	MCF-7	breast:
7	chr9:15609722..15611520-chr9:15613088..15614614,2	MCF-7	breast:
8	chr9:15778842..15781676-chr9:15783903..15785972,2	MCF-7	breast:
9	chr9:15873671..15874276-chr9:16131035..16131676,2	MCF-7	breast:
10	chr9:15873337..15874253-chr9:16131080..16131915,3	MCF-7	breast:
11	chr9:15876069..15878996-chr9:15881161..15882668,2	MCF-7	breast:
12	chr9:15551936..15552629-chr9:15619996..15620642,2	MCF-7	breast:
13	chr9:15421567..15424446-chr9:15606338..15608598,2	MCF-7	breast:
14	chr9:15778842..15781676-chr9:15783903..15785972,2	MCF-7	breast:
15	chr9:15836820..15837651-chr9:16133566..16134324,2	MCF-7	breast:
16	chr9:15551939..15552527-chr9:15606365..15606962,2	MCF-7	breast:
17	chr9:15690406..15691946-chr9:15692582..15695063,2	MCF-7	breast:
18	chr9:15609722..15611520-chr9:15613088..15614614,2	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C9orf92-3	chr9:15864309-15864521	uc_251_-
2	lnc-SNAPC3-1	chr9:15888035-15888086	NONHSAT130281
3	lnc-SNAPC3-1	chr9:15874539-15874661	NONHSAT130279
4	lnc-SNAPC3-1	chr9:15888981-15890761	NONHSAT130281
5	lnc-SNAPC3-5	chr9:15864309-15864521	uc_251_+
6	lnc-SNAPC3-6	chr9:15878981-15880761	ucscGeneNc_uc003zmg_2
7	lnc-SNAPC3-6	chr9:15878035-15878086	ucscGeneNc_uc003zmg_2

No data

Variant related genes	Relation type
RNU6-14P	TF binding region
CCDC171	TF binding region
RNU6-14P	CpG island
CCDC171	CpG island
ENSG00000164975	chromatin interactions
ENSG00000164985	chromatin interactions

Extended variants
information (count: 13709 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:13709 , 50 per page) page: 1 2 3 4 5 6 7 ... 275

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10481557	chr9:15604746-15604747	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs573674408	chr9:15604783-15604784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs561870355	chr9:15604795-15604796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs562627841	chr9:15604806-15604807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs533287618	chr9:15604831-15604832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs560891977	chr9:15604844-15604845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs75184707	chr9:15604850-15604851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs375867399	chr9:15604862-15604863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs368509392	chr9:15604869-15604870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs149977900	chr9:15604873-15604874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs190598233	chr9:15604886-15604887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs372630446	chr9:15604913-15604914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs76251371	chr9:15604942-15604943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs75448207	chr9:15604944-15604945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs116539790	chr9:15604948-15604949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs115831801	chr9:15604952-15604953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs571573167	chr9:15604961-15604962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs182825563	chr9:15604966-15604967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs370596958	chr9:15604989-15604990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs554512272	chr9:15604997-15604998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs115566892	chr9:15605010-15605011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs536892092	chr9:15605109-15605110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs555490201	chr9:15605152-15605153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs573717131	chr9:15605175-15605176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs543843904	chr9:15605187-15605188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs187164166	chr9:15605230-15605231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs577582905	chr9:15605242-15605243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs545248421	chr9:15605252-15605253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs77576371	chr9:15605283-15605284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs527480377	chr9:15605294-15605295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs542455079	chr9:15605313-15605314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs561024018	chr9:15605339-15605340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs531803040	chr9:15605351-15605352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs550021822	chr9:15605366-15605367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs571574019	chr9:15605378-15605379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs532402858	chr9:15605448-15605449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs548102817	chr9:15605488-15605489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs12341196	chr9:15605493-15605494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs370834580	chr9:15605513-15605514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs71325923	chr9:15605535-15605536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs2777947	chr9:15605595-15605596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs12552496	chr9:15605656-15605657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs555232614	chr9:15605672-15605673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs570177528	chr9:15605681-15605682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs374222229	chr9:15605683-15605684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs530405063	chr9:15605688-15605689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs199920480	chr9:15605691-15605692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs200867829	chr9:15605696-15605697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs376836813	chr9:15605742-15605743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs555996365	chr9:15605747-15605748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Chordoma	21215367	CNVD
Renal cell carcinoma	21215367	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:764 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:15587000-15620400	Weak transcription	Pancreas	Pancrea
2	chr9:15589200-15609800	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr9:15589400-15610600	Weak transcription	Thymus	Thymus
4	chr9:15592800-15614000	Weak transcription	Left Ventricle	heart
5	chr9:15599000-15617800	Weak transcription	Aorta	Aorta
6	chr9:15599600-15606200	Weak transcription	Fetal Lung	lung
7	chr9:15600200-15605800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr9:15600200-15614400	Weak transcription	Gastric	stomach
9	chr9:15600600-15617600	Weak transcription	Fetal Stomach	stomach
10	chr9:15601000-15620000	Weak transcription	Ovary	ovary
11	chr9:15601200-15608000	Weak transcription	Fetal Thymus	thymus
12	chr9:15601200-15614000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
13	chr9:15601400-15606000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
14	chr9:15601600-15605800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr9:15605800-15606200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr9:15605800-15606600	Enhancers	Hela-S3	cervix
17	chr9:15605800-15606800	Enhancers	Dnd41	blood
18	chr9:15605800-15607200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr9:15606000-15607800	Enhancers	Primary hematopoietic stem cells	blood
20	chr9:15606000-15607800	Enhancers	Primary hematopoietic stem cells short term culture	blood
21	chr9:15606200-15606400	Enhancers	Fetal Lung	lung
22	chr9:15606200-15606600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr9:15606200-15607200	Enhancers	Muscle Satellite Cultured Cells	--
24	chr9:15606200-15608000	Enhancers	HUVEC	blood vessel
25	chr9:15606400-15606600	Flanking Active TSS	Fetal Lung	lung
26	chr9:15606400-15606800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr9:15606400-15606800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr9:15606400-15606800	Enhancers	Osteobl	bone
29	chr9:15606600-15606800	Enhancers	Fetal Kidney	kidney
30	chr9:15606600-15606800	Active TSS	Fetal Lung	lung
31	chr9:15606600-15608000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr9:15606800-15609000	Weak transcription	Fetal Kidney	kidney
33	chr9:15606800-15609200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr9:15606800-15614000	Weak transcription	Fetal Lung	lung
35	chr9:15607000-15608000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr9:15607200-15608000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr9:15607800-15608200	Genic enhancers	Primary hematopoietic stem cells	blood
38	chr9:15607800-15614000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
39	chr9:15608000-15608200	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr9:15608000-15608400	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr9:15608000-15608600	Strong transcription	Fetal Thymus	thymus
42	chr9:15608000-15618400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr9:15608200-15608600	Strong transcription	Primary hematopoietic stem cells	blood
44	chr9:15608200-15608600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr9:15608400-15613800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr9:15608600-15610600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr9:15608600-15611200	Weak transcription	Primary hematopoietic stem cells	blood
48	chr9:15608600-15614000	Weak transcription	Fetal Thymus	thymus
49	chr9:15609800-15612200	Weak transcription	Stomach Smooth Muscle	stomach
50	chr9:15609800-15625800	Weak transcription	Brain Hippocampus Middle	brain

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