Variant report

Variant	nsv528964
Chromosome Location	chr9:15760822-15875162
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	chr9:15824460-15824492	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:15873620-15873926	HepG2	liver:	n/a	n/a
3	BHLHE40	chr9:15837128-15837398	GM12878	blood:	n/a	n/a
4	CEBPB	chr9:15803787-15803977	A549	lung:	n/a	chr9:15803862-15803873
5	CEBPB	chr9:15817342-15817541	IMR90	lung:	n/a	n/a
6	CEBPB	chr9:15845792-15846013	HepG2	liver:	n/a	chr9:15845914-15845927 chr9:15845914-15845925 chr9:15845916-15845925
7	CEBPB	chr9:15831451-15831723	Hela-S3	cervix:	n/a	chr9:15831596-15831609
8	CEBPB	chr9:15803709-15804025	IMR90	lung:	n/a	chr9:15803862-15803873
9	CEBPB	chr9:15845785-15846037	MCF-7	breast:	n/a	chr9:15845914-15845927 chr9:15845914-15845925 chr9:15845916-15845925
10	CEBPB	chr9:15845846-15845992	A549	lung:	n/a	chr9:15845914-15845927 chr9:15845914-15845925 chr9:15845916-15845925
11	CEBPB	chr9:15803721-15803998	HepG2	liver:	n/a	chr9:15803862-15803873
12	CEBPB	chr9:15856572-15856992	IMR90	lung:	n/a	n/a
13	CEBPB	chr9:15863418-15863420	A549	lung:	n/a	n/a
14	CEBPB	chr9:15850052-15850257	A549	lung:	n/a	chr9:15850110-15850122
15	CEBPB	chr9:15825520-15825732	IMR90	lung:	n/a	chr9:15825609-15825620
16	CEBPB	chr9:15831522-15831716	A549	lung:	n/a	chr9:15831596-15831609
17	CEBPB	chr9:15817338-15817562	A549	lung:	n/a	n/a
18	CEBPB	chr9:15831422-15831741	ECC-1	luminal epithelium:	n/a	chr9:15831596-15831609
19	CEBPB	chr9:15825568-15825724	HepG2	liver:	n/a	chr9:15825609-15825620
20	CEBPB	chr9:15845758-15846062	IMR90	lung:	n/a	chr9:15845914-15845927 chr9:15845914-15845925 chr9:15845916-15845925
21	CTCF	chr9:15806383-15806488	GM10248	blood:	n/a	n/a
22	CTCF	chr9:15873700-15873850	Caco-2	colon:	n/a	chr9:15873756-15873777 chr9:15873754-15873772 chr9:15873757-15873770
23	CTCF	chr9:15837160-15837310	AG04450	lung:	n/a	chr9:15837266-15837274 chr9:15837261-15837279 chr9:15837262-15837278 chr9:15837263-15837284
24	CTCF	chr9:15873616-15873886	ECC-1	luminal epithelium:	n/a	chr9:15873756-15873777 chr9:15873754-15873772 chr9:15873757-15873770
25	CTCF	chr9:15837127-15837417	HUVEC	blood vessel:	n/a	chr9:15837266-15837274 chr9:15837261-15837279 chr9:15837262-15837278 chr9:15837263-15837284
26	CTCF	chr9:15824700-15824850	HFF-Myc	foreskin:	n/a	chr9:15824811-15824820
27	CTCF	chr9:15837220-15837370	HAc	cerebellar:	n/a	chr9:15837266-15837274 chr9:15837261-15837279 chr9:15837262-15837278 chr9:15837263-15837284
28	CTCF	chr9:15837220-15837370	SK-N-SH_RA	brain:	n/a	chr9:15837266-15837274 chr9:15837261-15837279 chr9:15837262-15837278 chr9:15837263-15837284
29	CTCF	chr9:15873680-15873830	SK-N-SH_RA	brain:	n/a	chr9:15873756-15873777 chr9:15873754-15873772 chr9:15873757-15873770
30	CTCF	chr9:15873720-15873870	GM12871	blood:	n/a	chr9:15873756-15873777 chr9:15873754-15873772 chr9:15873757-15873770
31	CTCF	chr9:15824383-15824625	Hela-S3	cervix:	n/a	chr9:15824497-15824515 chr9:15824499-15824512
32	CTCF	chr9:15824420-15824570	BE2_C	brain:	n/a	chr9:15824497-15824515 chr9:15824499-15824512
33	CTCF	chr9:15824420-15824570	RPTEC	kidney:	n/a	chr9:15824497-15824515 chr9:15824499-15824512
34	CTCF	chr9:15873700-15873850	HRPEpiC	eye:	n/a	chr9:15873756-15873777 chr9:15873754-15873772 chr9:15873757-15873770
35	CTCF	chr9:15873720-15873870	HPAF	blood vessel:	n/a	chr9:15873756-15873777 chr9:15873754-15873772 chr9:15873757-15873770
36	CTCF	chr9:15839620-15839770	GM12872	blood:	n/a	n/a
37	CTCF	chr9:15824460-15824610	AG09319	gingival:	n/a	chr9:15824497-15824515 chr9:15824499-15824512
38	CTCF	chr9:15837180-15837330	HBMEC	blood vessel:	n/a	chr9:15837266-15837274 chr9:15837261-15837279 chr9:15837262-15837278 chr9:15837263-15837284
39	CTCF	chr9:15873720-15873870	GM12801	blood:	n/a	chr9:15873756-15873777 chr9:15873754-15873772 chr9:15873757-15873770
40	CTCF	chr9:15873653-15873887	GM12878	blood:	n/a	chr9:15873756-15873777 chr9:15873754-15873772 chr9:15873757-15873770
41	CTCF	chr9:15837156-15837353	HepG2	liver:	n/a	chr9:15837266-15837274 chr9:15837261-15837279 chr9:15837262-15837278 chr9:15837263-15837284
42	CTCF	chr9:15837220-15837370	GM12878	blood:	n/a	chr9:15837266-15837274 chr9:15837261-15837279 chr9:15837262-15837278 chr9:15837263-15837284
43	CTCF	chr9:15837160-15837310	GM12868	blood:	n/a	chr9:15837266-15837274 chr9:15837261-15837279 chr9:15837262-15837278 chr9:15837263-15837284
44	CTCF	chr9:15837160-15837310	GM12874	blood:	n/a	chr9:15837266-15837274 chr9:15837261-15837279 chr9:15837262-15837278 chr9:15837263-15837284
45	CTCF	chr9:15837180-15837330	HMEC	breast:	n/a	chr9:15837266-15837274 chr9:15837261-15837279 chr9:15837262-15837278 chr9:15837263-15837284
46	CTCF	chr9:15837150-15837367	GM10248	blood:	n/a	chr9:15837266-15837274 chr9:15837261-15837279 chr9:15837262-15837278 chr9:15837263-15837284
47	CTCF	chr9:15837180-15837330	HA-sp	spinal cord:	n/a	chr9:15837266-15837274 chr9:15837261-15837279 chr9:15837262-15837278 chr9:15837263-15837284
48	CTCF	chr9:15873760-15873910	GM12865	blood:	n/a	n/a
49	CTCF	chr9:15837138-15837375	GM13977	blood:	n/a	chr9:15837266-15837274 chr9:15837261-15837279 chr9:15837262-15837278 chr9:15837263-15837284
50	CTCF	chr9:15824400-15824550	MCF-7	breast:	n/a	chr9:15824497-15824515 chr9:15824499-15824512

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:15810627-15810677	SAEC	small airway:	n/a
2	chr9:15810627-15810677	SAEC	small airway:	n/a
3	chr9:15810627-15810677	GM12891	blood:	n/a
4	chr9:15810627-15810677	HIPEpiC	eye:	n/a
5	chr9:15810627-15810677	BJ	skin:	n/a
6	chr9:15810627-15810677	HCM	heart:	n/a
7	chr9:15810627-15810677	SK-N-SH	brain:	n/a
8	chr9:15810627-15810677	Hela-S3	cervix:	n/a
9	chr9:15810627-15810677	HEK293	kidney:	embryo
10	chr9:15810627-15810677	MCF10A-Er-Src	breast:	n/a
11	chr9:15810627-15810677	AG04450	lung:	fetal
12	chr9:15810627-15810677	Jurkat	blood:	n/a
13	chr9:15810627-15810677	NHDF-neo	bronchial:	n/a
14	chr9:15810627-15810677	MCF-7	breast:	n/a
15	chr9:15810627-15810677	ovcar-3	ovarian:	n/a
16	chr9:15810627-15810677	AoSMC	blood vessel:	n/a
17	chr9:15810627-15810677	Hepatocyte	liver:	n/a
18	chr9:15810627-15810677	GM06990	blood:	n/a
19	chr9:15810627-15810677	GM19239	blood:	n/a
20	chr9:15810627-15810677	RPTEC	kidney:	n/a
21	chr9:15810627-15810677	AG09319	gingival:	n/a
22	chr9:15810627-15810677	HRCEpiC	kidney:	n/a
23	chr9:15810627-15810677	IMR90	lung:	fetal
24	chr9:15810627-15810677	LNCaP	prostate:	n/a
25	chr9:15810627-15810677	NH-A	brain:	n/a
26	chr9:15810627-15810677	T-47D	breast:	n/a
27	chr9:15810627-15810677	HNPCEpiC	eye:	n/a
28	chr9:15810627-15810677	H1-hESC	embryonic stem cell:	embryo
29	chr9:15810627-15810677	HPAEpiC	pulmonary alveolar:	n/a
30	chr9:15810627-15810677	U87	brain:	n/a
31	chr9:15810627-15810677	PFSK-1	brain:	n/a
32	chr9:15810627-15810677	PANC-1	pancreas:	n/a
33	chr9:15810627-15810677	Caco-2	colon:	n/a
34	chr9:15810627-15810677	A549	lung:	n/a
35	chr9:15810627-15810677	HRE	kidney:	n/a
36	chr9:15810627-15810677	ProgFib	skin:	n/a
37	chr9:15810627-15810677	PrEC	prostate:	n/a
38	chr9:15810627-15810677	AG09309	skin:	n/a
39	chr9:15810627-15810677	HCF	heart:	n/a
40	chr9:15810627-15810677	HL-60	blood:	n/a
41	chr9:15810627-15810677	AG10803	skin:	n/a
42	chr9:15810627-15810677	SKMC	muscle:	n/a
43	chr9:15810627-15810677	AG04449	skin:	fetal
44	chr9:15810627-15810677	HepG2	liver:	n/a
45	chr9:15810627-15810677	GM12892	blood:	n/a
46	chr9:15810627-15810677	HMEC	breast:	n/a
47	chr9:15810627-15810677	ECC-1	luminal epithelium:	n/a
48	chr9:15810627-15810677	K562	blood:	n/a
49	chr9:15810627-15810677	HCPEpiC	choroid plexus:	n/a
50	chr9:15810627-15810677	HRPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:15778842..15781676-chr9:15783903..15785972,2	MCF-7	breast:
2	chr9:15778842..15781676-chr9:15783903..15785972,2	MCF-7	breast:
3	chr9:15836820..15837651-chr9:16133566..16134324,2	MCF-7	breast:
4	chr9:15873337..15874253-chr9:16131080..16131915,3	MCF-7	breast:
5	chr9:15873671..15874276-chr9:16131035..16131676,2	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: 5478 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:5478 , 50 per page) page: 1 2 3 4 5 6 7 ... 110

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7869624	chr9:15760822-15760823	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs138518956	chr9:15760830-15760831	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs141843591	chr9:15760861-15760862	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs535068317	chr9:15760866-15760867	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs547044813	chr9:15760876-15760877	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs183450740	chr9:15760965-15760966	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs187798594	chr9:15760976-15760977	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs578025657	chr9:15760983-15760984	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs6474967	chr9:15760988-15760989	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs557145563	chr9:15761017-15761018	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs369884911	chr9:15761019-15761020	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs569448260	chr9:15761044-15761045	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs540066241	chr9:15761064-15761065	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs7872912	chr9:15761077-15761078	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs375556216	chr9:15761079-15761080	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs576559314	chr9:15761121-15761122	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs540700557	chr9:15761134-15761135	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs1935225	chr9:15761162-15761163	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs574051290	chr9:15761244-15761245	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs7873201	chr9:15761288-15761289	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs541722143	chr9:15761312-15761313	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs372398769	chr9:15761421-15761422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs563645231	chr9:15761449-15761450	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs530704402	chr9:15761476-15761477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs150602128	chr9:15761493-15761494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs116604608	chr9:15761509-15761510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs528617391	chr9:15761524-15761525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs192735790	chr9:15761554-15761555	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs568468555	chr9:15761563-15761564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs144503496	chr9:15761611-15761612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs184171178	chr9:15761621-15761622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs550691727	chr9:15761623-15761624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs569570368	chr9:15761646-15761647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs189415627	chr9:15761655-15761656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs558356168	chr9:15761681-15761682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs79977693	chr9:15761698-15761699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs534418680	chr9:15761708-15761709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs62571269	chr9:15761726-15761727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs552599662	chr9:15761727-15761728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs369215737	chr9:15761753-15761754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs574190577	chr9:15761799-15761800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs541847713	chr9:15761802-15761803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs386733037	chr9:15761808-15761809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs575521894	chr9:15761818-15761819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs192624783	chr9:15761867-15761868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs34656827	chr9:15761881-15761882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs397893347	chr9:15761883-15761884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs184655241	chr9:15761919-15761920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs528249169	chr9:15761936-15761937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs540424573	chr9:15761942-15761943	Weak transcription	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:175 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:15742600-15769600	Weak transcription	Psoas Muscle	Psoas
2	chr9:15756200-15790800	Weak transcription	Primary hematopoietic stem cells	blood
3	chr9:15757800-15763200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr9:15759200-15784400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr9:15760800-15761400	Enhancers	Fetal Heart	heart
6	chr9:15763200-15763600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr9:15763600-15774400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr9:15766000-15770600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr9:15768200-15768600	Enhancers	Fetal Brain Male	brain
10	chr9:15768800-15769200	Enhancers	Pancreatic Islets	Pancreatic Islet
11	chr9:15769400-15769800	Enhancers	Fetal Lung	lung
12	chr9:15769600-15769800	Enhancers	Psoas Muscle	Psoas
13	chr9:15774400-15774600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr9:15774600-15781800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr9:15775800-15786600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
16	chr9:15777000-15810600	Weak transcription	Pancreas	Pancrea
17	chr9:15778200-15782600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr9:15779000-15791200	Weak transcription	Stomach Smooth Muscle	stomach
19	chr9:15781200-15790800	Weak transcription	Fetal Thymus	thymus
20	chr9:15781800-15782800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr9:15782600-15783600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr9:15782800-15784600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr9:15783000-15783200	Enhancers	Primary hematopoietic stem cells short term culture	blood
24	chr9:15783200-15788600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
25	chr9:15783600-15802000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr9:15784400-15785800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr9:15784600-15790200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr9:15785000-15808600	Weak transcription	Aorta	Aorta
29	chr9:15785400-15786800	Weak transcription	Esophagus	oesophagus
30	chr9:15785600-15788000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr9:15785600-15788000	Weak transcription	Duodenum Mucosa	Duodenum
32	chr9:15785800-15786800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr9:15785800-15786800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr9:15786000-15786800	Weak transcription	Gastric	stomach
35	chr9:15786200-15786600	Weak transcription	Left Ventricle	heart
36	chr9:15786200-15789200	Weak transcription	Psoas Muscle	Psoas
37	chr9:15786600-15787000	ZNF genes & repeats	Left Ventricle	heart
38	chr9:15786600-15787200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
39	chr9:15786600-15789600	Weak transcription	Ovary	ovary
40	chr9:15786800-15787000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr9:15786800-15787000	Genic enhancers	Esophagus	oesophagus
42	chr9:15786800-15787000	ZNF genes & repeats	Gastric	stomach
43	chr9:15786800-15787200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr9:15787000-15787200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr9:15787000-15790600	Weak transcription	Left Ventricle	heart
46	chr9:15787000-15791200	Weak transcription	Esophagus	oesophagus
47	chr9:15787200-15796800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr9:15787200-15799600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
49	chr9:15790200-15800000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr9:15799600-15799800	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast

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