Variant report

Variant	nsv1032081
Chromosome Location	chr9:15845902-15878115
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	chr9:15873620-15873926	HepG2	liver:	n/a	n/a
2	CEBPB	chr9:15845792-15846013	HepG2	liver:	n/a	chr9:15845914-15845927 chr9:15845914-15845925 chr9:15845916-15845925
3	CEBPB	chr9:15850052-15850257	A549	lung:	n/a	chr9:15850110-15850122
4	CEBPB	chr9:15863418-15863420	A549	lung:	n/a	n/a
5	CEBPB	chr9:15845785-15846037	MCF-7	breast:	n/a	chr9:15845914-15845927 chr9:15845914-15845925 chr9:15845916-15845925
6	CEBPB	chr9:15845758-15846062	IMR90	lung:	n/a	chr9:15845914-15845927 chr9:15845914-15845925 chr9:15845916-15845925
7	CEBPB	chr9:15845846-15845992	A549	lung:	n/a	chr9:15845914-15845927 chr9:15845914-15845925 chr9:15845916-15845925
8	CEBPB	chr9:15856572-15856992	IMR90	lung:	n/a	n/a
9	CEBPB	chr9:15875974-15876186	A549	lung:	n/a	n/a
10	CTCF	chr9:15873900-15874050	GM12870	blood:	n/a	n/a
11	CTCF	chr9:15873727-15873872	MCF-7	breast:	n/a	chr9:15873756-15873777 chr9:15873754-15873772 chr9:15873757-15873770
12	CTCF	chr9:15873680-15873830	SAEC	small airway:	n/a	chr9:15873756-15873777 chr9:15873754-15873772 chr9:15873757-15873770
13	CTCF	chr9:15873700-15873850	Caco-2	colon:	n/a	chr9:15873756-15873777 chr9:15873754-15873772 chr9:15873757-15873770
14	CTCF	chr9:15873600-15873750	HFF	foreskin:	n/a	n/a
15	CTCF	chr9:15873712-15873833	GM20000	blood:	n/a	chr9:15873756-15873777 chr9:15873754-15873772 chr9:15873757-15873770
16	CTCF	chr9:15873720-15873870	AoAF	blood vessel:	n/a	chr9:15873756-15873777 chr9:15873754-15873772 chr9:15873757-15873770
17	CTCF	chr9:15873720-15873870	HCT-116	colon:	n/a	chr9:15873756-15873777 chr9:15873754-15873772 chr9:15873757-15873770
18	CTCF	chr9:15873820-15873970	HAc	cerebellar:	n/a	n/a
19	CTCF	chr9:15873820-15873970	HFF-Myc	foreskin:	n/a	n/a
20	CTCF	chr9:15873528-15873952	A549	lung:	n/a	chr9:15873756-15873777 chr9:15873754-15873772 chr9:15873757-15873770
21	CTCF	chr9:15873680-15873830	WERI-Rb-1	eye:	n/a	chr9:15873756-15873777 chr9:15873754-15873772 chr9:15873757-15873770
22	CTCF	chr9:15873700-15873850	AG09309	skin:	n/a	chr9:15873756-15873777 chr9:15873754-15873772 chr9:15873757-15873770
23	CTCF	chr9:15873345-15874223	A549	lung:	n/a	chr9:15873756-15873777 chr9:15873754-15873772 chr9:15873757-15873770
24	CTCF	chr9:15873680-15873830	BJ	skin:	n/a	chr9:15873756-15873777 chr9:15873754-15873772 chr9:15873757-15873770
25	CTCF	chr9:15873700-15873850	HepG2	liver:	n/a	chr9:15873756-15873777 chr9:15873754-15873772 chr9:15873757-15873770
26	CTCF	chr9:15873631-15873889	Spleen_OC	spleen:	n/a	chr9:15873756-15873777 chr9:15873754-15873772 chr9:15873757-15873770
27	CTCF	chr9:15873640-15873790	HRE	kidney:	n/a	chr9:15873756-15873777 chr9:15873754-15873772 chr9:15873757-15873770
28	CTCF	chr9:15873680-15873830	GM12873	blood:	n/a	chr9:15873756-15873777 chr9:15873754-15873772 chr9:15873757-15873770
29	CTCF	chr9:15852080-15852230	HPAF	blood vessel:	n/a	n/a
30	CTCF	chr9:15873669-15874024	MCF-7	breast:	n/a	chr9:15873756-15873777 chr9:15873754-15873772 chr9:15873757-15873770
31	CTCF	chr9:15873700-15873850	HBMEC	blood vessel:	n/a	chr9:15873756-15873777 chr9:15873754-15873772 chr9:15873757-15873770
32	CTCF	chr9:15873742-15873858	Gliobla	brain:	n/a	chr9:15873756-15873777 chr9:15873754-15873772 chr9:15873757-15873770
33	CTCF	chr9:15873680-15873830	MCF-7	breast:	n/a	chr9:15873756-15873777 chr9:15873754-15873772 chr9:15873757-15873770
34	CTCF	chr9:15873600-15873750	A549	lung:	n/a	n/a
35	CTCF	chr9:15873700-15873850	Hela-S3	cervix:	n/a	chr9:15873756-15873777 chr9:15873754-15873772 chr9:15873757-15873770
36	CTCF	chr9:15873680-15873830	HVMF	connective:	n/a	chr9:15873756-15873777 chr9:15873754-15873772 chr9:15873757-15873770
37	CTCF	chr9:15873720-15873870	HMF	breast:	n/a	chr9:15873756-15873777 chr9:15873754-15873772 chr9:15873757-15873770
38	CTCF	chr9:15873629-15873911	Medullo	brain:	n/a	chr9:15873756-15873777 chr9:15873754-15873772 chr9:15873757-15873770
39	CTCF	chr9:15873680-15873830	NHDF-neo	bronchial:	n/a	chr9:15873756-15873777 chr9:15873754-15873772 chr9:15873757-15873770
40	CTCF	chr9:15873700-15873850	HCFaa	heart:	n/a	chr9:15873756-15873777 chr9:15873754-15873772 chr9:15873757-15873770
41	CTCF	chr9:15873620-15873770	BE2_C	brain:	n/a	chr9:15873757-15873770
42	CTCF	chr9:15873601-15873918	SK-N-SH_RA	brain:	n/a	chr9:15873756-15873777 chr9:15873754-15873772 chr9:15873757-15873770
43	CTCF	chr9:15873688-15873857	GM13976	blood:	n/a	chr9:15873756-15873777 chr9:15873754-15873772 chr9:15873757-15873770
44	CTCF	chr9:15873700-15873850	A549	lung:	n/a	chr9:15873756-15873777 chr9:15873754-15873772 chr9:15873757-15873770
45	CTCF	chr9:15873700-15873850	GM12875	blood:	n/a	chr9:15873756-15873777 chr9:15873754-15873772 chr9:15873757-15873770
46	CTCF	chr9:15873680-15873830	Caco-2	colon:	n/a	chr9:15873756-15873777 chr9:15873754-15873772 chr9:15873757-15873770
47	CTCF	chr9:15873720-15873870	AG04449	skin:	n/a	chr9:15873756-15873777 chr9:15873754-15873772 chr9:15873757-15873770
48	CTCF	chr9:15873760-15873910	GM12865	blood:	n/a	n/a
49	CTCF	chr9:15873617-15873897	H1-hESC	embryonic stem cell:	n/a	chr9:15873756-15873777 chr9:15873754-15873772 chr9:15873757-15873770
50	CTCF	chr9:15873660-15873810	NB4	blood:	n/a	chr9:15873756-15873777 chr9:15873754-15873772 chr9:15873757-15873770

No.	Distal block	Cell Line	Cell type
1	chr9:15876069..15878996-chr9:15881161..15882668,2	MCF-7	breast:
2	chr9:15873337..15874253-chr9:16131080..16131915,3	MCF-7	breast:
3	chr9:15873671..15874276-chr9:16131035..16131676,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SNAPC3-6	chr9:15878035-15878086	ucscGeneNc_uc003zmg_2
2	lnc-SNAPC3-1	chr9:15874539-15874661	NONHSAT130279
3	lnc-SNAPC3-5	chr9:15864309-15864521	uc_251_+
4	lnc-C9orf92-3	chr9:15864309-15864521	uc_251_-

Variant related genes	Relation type
CCDC171	TF binding region

Extended variants
information (count: 1467 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:1467 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs527536516	chr9:15845912-15845913	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs549118780	chr9:15845924-15845925	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs144741734	chr9:15845954-15845955	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs76512002	chr9:15846045-15846046	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs373566177	chr9:15846089-15846090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs549777960	chr9:15846111-15846112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs4741546	chr9:15846112-15846113	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs538626011	chr9:15846148-15846149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs554214293	chr9:15846160-15846161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs566353169	chr9:15846194-15846195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs188125184	chr9:15846198-15846199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs112714408	chr9:15846218-15846219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs555115769	chr9:15846244-15846245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs573668997	chr9:15846245-15846246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs569873998	chr9:15846277-15846278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs181931858	chr9:15846287-15846288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs9407662	chr9:15846288-15846289	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs137923808	chr9:15846319-15846320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs186426045	chr9:15846330-15846331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs545009020	chr9:15846339-15846340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs555468511	chr9:15846340-15846341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs73420384	chr9:15846445-15846446	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs190129354	chr9:15846448-15846449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs181751539	chr9:15846449-15846450	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs377381552	chr9:15846456-15846457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs9407663	chr9:15846459-15846460	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs531388023	chr9:15846509-15846510	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs549892523	chr9:15846513-15846514	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs374865419	chr9:15846536-15846537	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs79617025	chr9:15846539-15846540	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs532411435	chr9:15846549-15846550	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs147893867	chr9:15846572-15846573	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs540643760	chr9:15846577-15846578	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs556498121	chr9:15846635-15846636	Strong transcription Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs376268494	chr9:15846655-15846656	Strong transcription Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs368052933	chr9:15846677-15846678	Strong transcription Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs371947436	chr9:15846680-15846681	Strong transcription Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs375567970	chr9:15846696-15846697	Strong transcription Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs146646466	chr9:15846729-15846730	Strong transcription Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs369463663	chr9:15846737-15846738	Strong transcription Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs548583619	chr9:15846748-15846749	Strong transcription Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs374545016	chr9:15846749-15846750	Strong transcription Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs200368336	chr9:15846763-15846764	Strong transcription Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs368943264	chr9:15846788-15846789	Strong transcription Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs369063179	chr9:15846790-15846791	Strong transcription Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs140792485	chr9:15846793-15846794	Strong transcription Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs35526108	chr9:15846794-15846795	Strong transcription Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs186637736	chr9:15846796-15846797	Strong transcription Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs376236426	chr9:15846832-15846833	Strong transcription Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs151020208	chr9:15846863-15846864	Strong transcription Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:91)

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

Chromatin state (count:86 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:15830200-15857200	Weak transcription	Primary hematopoietic stem cells	blood
2	chr9:15835000-15846600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr9:15844200-15846600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr9:15844800-15850400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr9:15845000-15846600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr9:15845000-15858800	Weak transcription	Thymus	Thymus
7	chr9:15846600-15847000	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr9:15846600-15847000	Enhancers	Brain Germinal Matrix	brain
9	chr9:15846600-15847200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
10	chr9:15846600-15847200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr9:15846600-15847200	Enhancers	Brain Angular Gyrus	brain
12	chr9:15847000-15849000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr9:15847200-15850000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr9:15847200-15857600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
15	chr9:15849000-15850000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr9:15849000-15873800	Weak transcription	Fetal Lung	lung
17	chr9:15850000-15851000	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr9:15850000-15852800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr9:15850400-15851000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr9:15851000-15852600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr9:15851000-15852600	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr9:15852600-15852800	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr9:15852800-15853000	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr9:15852800-15857400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr9:15853000-15853200	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr9:15853200-15853400	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr9:15853400-15854000	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr9:15854000-15855600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr9:15855600-15856200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr9:15856000-15857200	Enhancers	Osteobl	bone
31	chr9:15856200-15856400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr9:15856200-15857000	Enhancers	HSMM	muscle
33	chr9:15856200-15857200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr9:15856400-15857000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr9:15856400-15857400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr9:15857200-15857800	ZNF genes & repeats	Primary hematopoietic stem cells	blood
37	chr9:15857400-15858000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr9:15857400-15858200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr9:15857600-15857800	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
40	chr9:15857800-15885400	Weak transcription	Primary hematopoietic stem cells	blood
41	chr9:15858000-15859600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr9:15858200-15862600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr9:15859200-15860400	Enhancers	HUVEC	blood vessel
44	chr9:15859600-15861200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr9:15861200-15861400	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr9:15862600-15863400	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr9:15862600-15863600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr9:15863000-15863400	ZNF genes & repeats	Aorta	Aorta
49	chr9:15863400-15866000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr9:15863600-15878200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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