Variant report

Variant	nsv511557
Chromosome Location	chr15:72386175-72408069
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:86)
CpG islands
(count:183)
Chromatin interactive
region (count:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:72402687-72403203	HepG2	liver:	n/a	n/a
2	BCL3	chr15:72402707-72403203	A549	lung:	n/a	n/a
3	CEBPB	chr15:72390575-72390900	K562	blood:	n/a	chr15:72390741-72390752
4	CEBPB	chr15:72395429-72395522	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr15:72402810-72403001	A549	lung:	n/a	n/a
6	CEBPB	chr15:72395404-72395606	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr15:72390648-72390890	HepG2	liver:	n/a	chr15:72390741-72390752
8	CEBPB	chr15:72395338-72395630	IMR90	lung:	n/a	n/a
9	CEBPB	chr15:72395416-72395749	ECC-1	luminal epithelium:	n/a	n/a
10	CEBPB	chr15:72395417-72395537	K562	blood:	n/a	n/a
11	CEBPB	chr15:72395315-72395674	MCF-7	breast:	n/a	n/a
12	CEBPB	chr15:72395407-72395583	A549	lung:	n/a	n/a
13	CEBPB	chr15:72402709-72403232	A549	lung:	n/a	n/a
14	CEBPB	chr15:72402826-72403026	HepG2	liver:	n/a	n/a
15	CHD2	chr15:72406654-72406661	H1-hESC	embryonic stem cell:	n/a	n/a
16	CUX1	chr15:72400450-72400732	K562	blood:	n/a	n/a
17	EP300	chr15:72405900-72406171	T-47D	breast:	n/a	n/a
18	EP300	chr15:72405799-72406303	T-47D	breast:	n/a	n/a
19	EP300	chr15:72402557-72403271	A549	lung:	n/a	chr15:72402842-72402852
20	EP300	chr15:72402551-72403286	A549	lung:	n/a	chr15:72402842-72402852
21	FOS	chr15:72399440-72399785	MCF10A-Er-Src	breast:	n/a	n/a
22	FOS	chr15:72399499-72399762	MCF10A-Er-Src	breast:	n/a	n/a
23	FOS	chr15:72399439-72399773	MCF10A-Er-Src	breast:	n/a	n/a
24	FOSL2	chr15:72402706-72403138	A549	lung:	n/a	n/a
25	FOSL2	chr15:72402702-72403262	A549	lung:	n/a	n/a
26	FOXA1	chr15:72404575-72404828	T-47D	breast:	n/a	chr15:72404748-72404763
27	FOXA1	chr15:72405937-72406319	T-47D	breast:	n/a	chr15:72406121-72406136
28	FOXA1	chr15:72402675-72403101	HepG2	liver:	n/a	n/a
29	FOXA1	chr15:72405845-72406289	HepG2	liver:	n/a	chr15:72406121-72406136
30	FOXA1	chr15:72404570-72404906	T-47D	breast:	n/a	chr15:72404748-72404763
31	FOXA1	chr15:72405970-72406230	HepG2	liver:	n/a	chr15:72406121-72406136
32	FOXA1	chr15:72405938-72406347	HepG2	liver:	n/a	chr15:72406121-72406136
33	FOXA1	chr15:72402680-72403099	HepG2	liver:	n/a	n/a
34	FOXA1	chr15:72406001-72406326	HepG2	liver:	n/a	chr15:72406121-72406136
35	FOXA1	chr15:72402711-72403022	T-47D	breast:	n/a	n/a
36	FOXA1	chr15:72406856-72407196	HepG2	liver:	n/a	n/a
37	FOXA1	chr15:72405881-72406266	T-47D	breast:	n/a	chr15:72406121-72406136
38	FOXA1	chr15:72402688-72402995	HepG2	liver:	n/a	n/a
39	FOXA2	chr15:72402780-72403269	HepG2	liver:	n/a	n/a
40	FOXA2	chr15:72402584-72403249	A549	lung:	n/a	n/a
41	FOXA2	chr15:72402692-72403043	HepG2	liver:	n/a	n/a
42	FOXA2	chr15:72405988-72406199	HepG2	liver:	n/a	n/a
43	GABPA	chr15:72402725-72403092	A549	lung:	n/a	n/a
44	GATA1	chr15:72388885-72389555	PBDE	blood:	n/a	n/a
45	GATA3	chr15:72405838-72406312	T-47D	breast:	n/a	n/a
46	GATA3	chr15:72402693-72403042	T-47D	breast:	n/a	n/a
47	GATA3	chr15:72405722-72406291	T-47D	breast:	n/a	n/a
48	GATA3	chr15:72402454-72403355	A549	lung:	n/a	n/a
49	GATA3	chr15:72402740-72403112	A549	lung:	n/a	n/a
50	HDAC2	chr15:72402779-72402967	HepG2	liver:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:72406824-72406874	CMK	blood:	n/a
2	chr15:72405733-72405783	GM12892	blood:	n/a
3	chr15:72406824-72406874	Hepatocyte	liver:	n/a
4	chr15:72405733-72405783	AG04449	skin:	fetal
5	chr15:72406367-72406417	HEK293	kidney:	embryo
6	chr15:72406824-72406874	NHBE	bronchial:	n/a
7	chr15:72406824-72406874	Caco-2	colon:	n/a
8	chr15:72406367-72406417	BJ	skin:	n/a
9	chr15:72406367-72406417	AoSMC	blood vessel:	n/a
10	chr15:72406367-72406417	HRPEpiC	eye:	n/a
11	chr15:72405733-72405783	Hela-S3	cervix:	n/a
12	chr15:72405733-72405783	HRPEpiC	eye:	n/a
13	chr15:72405733-72405783	Jurkat	blood:	n/a
14	chr15:72406824-72406874	GM19239	blood:	n/a
15	chr15:72405733-72405783	HIPEpiC	eye:	n/a
16	chr15:72406367-72406417	MCF-7	breast:	n/a
17	chr15:72405733-72405783	PFSK-1	brain:	n/a
18	chr15:72405733-72405783	NHBE	bronchial:	n/a
19	chr15:72406824-72406874	MCF10A-Er-Src	breast:	n/a
20	chr15:72406367-72406417	ECC-1	luminal epithelium:	n/a
21	chr15:72406824-72406874	HCPEpiC	choroid plexus:	n/a
22	chr15:72406824-72406874	Jurkat	blood:	n/a
23	chr15:72406824-72406874	U87	brain:	n/a
24	chr15:72406367-72406417	Jurkat	blood:	n/a
25	chr15:72405733-72405783	NHDF-neo	bronchial:	n/a
26	chr15:72405733-72405783	HRE	kidney:	n/a
27	chr15:72405733-72405783	ProgFib	skin:	n/a
28	chr15:72406367-72406417	HEEpiC	esophagus:	n/a
29	chr15:72406824-72406874	HEK293	kidney:	embryo
30	chr15:72406824-72406874	HCM	heart:	n/a
31	chr15:72405733-72405783	HEK293	kidney:	embryo
32	chr15:72406824-72406874	HMEC	breast:	n/a
33	chr15:72406367-72406417	HIPEpiC	eye:	n/a
34	chr15:72406367-72406417	HepG2	liver:	n/a
35	chr15:72405733-72405783	LNCaP	prostate:	n/a
36	chr15:72406367-72406417	H1-hESC	embryonic stem cell:	embryo
37	chr15:72405733-72405783	HepG2	liver:	n/a
38	chr15:72406824-72406874	SKMC	muscle:	n/a
39	chr15:72406367-72406417	GM12891	blood:	n/a
40	chr15:72405733-72405783	RPTEC	kidney:	n/a
41	chr15:72406824-72406874	BJ	skin:	n/a
42	chr15:72405733-72405783	PrEC	prostate:	n/a
43	chr15:72406824-72406874	HIPEpiC	eye:	n/a
44	chr15:72405733-72405783	HPAEpiC	pulmonary alveolar:	n/a
45	chr15:72406824-72406874	SK-N-MC	brain:	n/a
46	chr15:72405733-72405783	HRCEpiC	kidney:	n/a
47	chr15:72406367-72406417	NHBE	bronchial:	n/a
48	chr15:72405733-72405783	IMR90	lung:	fetal
49	chr15:72406824-72406874	HRE	kidney:	n/a
50	chr15:72405733-72405783	GM19239	blood:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:72398211..72399947-chr15:72411763..72414182,2	MCF-7	breast:
2	chr15:72393359..72395081-chr15:72408256..72411185,2	K562	blood:
3	chr15:72399130..72400833-chr15:72405712..72408016,2	MCF-7	breast:
4	chr15:72399406..72401734-chr15:72404487..72406226,2	K562	blood:
5	chr15:72394930..72397507-chr15:72409085..72411660,2	MCF-7	breast:
6	chr15:72398905..72401840-chr15:72409196..72411848,3	K562	blood:
7	chr15:72398478..72400917-chr15:72408968..72411115,2	MCF-7	breast:
8	chr15:72399406..72401734-chr15:72404487..72406226,2	K562	blood:
9	chr15:72401062..72403312-chr15:72406877..72409075,2	K562	blood:
10	chr15:72398664..72401840-chr15:72410348..72413852,3	K562	blood:
11	chr15:72401062..72403312-chr15:72406877..72409075,2	K562	blood:
12	chr15:72405635..72407377-chr15:72409076..72410696,2	K562	blood:
13	chr15:72394985..72397263-chr15:72398518..72401032,2	MCF-7	breast:
14	chr15:72394985..72397263-chr15:72398518..72401032,2	MCF-7	breast:

No data

Variant related genes	Relation type
SENP8	TF binding region
SENP8	CpG island
ENSG00000066933	chromatin interactions
ENSG00000166192	chromatin interactions

Extended variants
information (count: 788 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:788 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs573733248	chr15:72386194-72386195	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs537654584	chr15:72386240-72386241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs397764901	chr15:72386248-72386249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs556414877	chr15:72386279-72386280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs370075410	chr15:72386285-72386286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs368870186	chr15:72386311-72386312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs577907188	chr15:72386323-72386324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs545365360	chr15:72386365-72386366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs560150526	chr15:72386367-72386368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs376037828	chr15:72386414-72386415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs572126122	chr15:72386421-72386422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs542686594	chr15:72386422-72386423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs561052572	chr15:72386520-72386521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs190376754	chr15:72386534-72386535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs550151421	chr15:72386549-72386550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs565549206	chr15:72386578-72386579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs112437820	chr15:72386601-72386602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs548125006	chr15:72386610-72386611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs200601867	chr15:72386707-72386708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs35113958	chr15:72386709-72386710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs58547019	chr15:72386713-72386714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs566446649	chr15:72386742-72386743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs181648214	chr15:72386762-72386763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs7169334	chr15:72386938-72386939	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs58115764	chr15:72387012-72387013	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs534312766	chr15:72387162-72387163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs547868409	chr15:72387243-72387244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs187675369	chr15:72387280-72387281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs567675816	chr15:72387284-72387285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs112473017	chr15:72387455-72387456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs71395061	chr15:72387520-72387521	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs556278567	chr15:72387576-72387577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs575873118	chr15:72387592-72387593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs144077948	chr15:72387700-72387701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs112510853	chr15:72387709-72387710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs147306871	chr15:72387745-72387746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs572064177	chr15:72387762-72387763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs78540791	chr15:72387817-72387818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs8034768	chr15:72387818-72387819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs576486518	chr15:72387828-72387829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs189296975	chr15:72387905-72387906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs562215993	chr15:72388048-72388049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs565300523	chr15:72388074-72388075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs532761982	chr15:72388086-72388087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs180883604	chr15:72388092-72388093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs139880278	chr15:72388129-72388130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs111953659	chr15:72388145-72388146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs560099142	chr15:72388146-72388147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs527269952	chr15:72388147-72388148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs549047766	chr15:72388148-72388149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Wilms tumour	21544195	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	16751803	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Prostate cancer	16573809	CNVD
Autism	17322880	CNVD
Autism	20678247	CNVD
Retinoblastoma	21504564	CNVD
Matthew-Wood syndrome	21085971	CNVD
Myelofibrosis	22110671	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Urothelial cell carcinoma	18451213	CNVD
phobic disorder	16773131	CNVD
Autism	21480499	CNVD
Disorders of sex development	22290220	CNVD
Mental retardation	19951919	CNVD
Mental retardation	16773131	CNVD
T-cell lymphomas	19863542	CNVD
15q24 microdeletion syndrome	22180641	CNVD
15q24 microdeletion syndrome	19921647	CNVD
Disease	22216833	CNVD
Mental retardation	17360722	CNVD
15q24 microdeletion syndrome	22216833	CNVD
15q24 microdeletion syndrome	22283845	CNVD
Developmental delay	17932688	CNVD
craniofacial dysmorphism	17932688	CNVD
digital and genital abnormalities	17932688	CNVD
Mental retardation	17621639	CNVD
Autism	20808228	CNVD
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD
Epilepsy	22083797	CNVD
Pancreatic cancer	17952125	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:382 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:72351200-72395800	Weak transcription	Rectal Smooth Muscle	rectum
2	chr15:72361600-72390600	Weak transcription	Aorta	Aorta
3	chr15:72361600-72391400	Weak transcription	Ovary	ovary
4	chr15:72367200-72407600	Weak transcription	Stomach Smooth Muscle	stomach
5	chr15:72372200-72399400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr15:72373600-72394400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
7	chr15:72375000-72408200	Weak transcription	Primary B cells from cord blood	blood
8	chr15:72375800-72395600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr15:72377200-72388200	Weak transcription	Fetal Brain Female	brain
10	chr15:72377800-72397600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr15:72378400-72388400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr15:72378400-72388600	Weak transcription	Fetal Lung	lung
13	chr15:72378800-72391400	Weak transcription	Primary hematopoietic stem cells	blood
14	chr15:72378800-72393200	Weak transcription	Fetal Intestine Large	intestine
15	chr15:72378800-72395800	Weak transcription	Colon Smooth Muscle	Colon
16	chr15:72379000-72388600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr15:72379000-72388600	Weak transcription	Fetal Muscle Leg	muscle
18	chr15:72379000-72395600	Weak transcription	Cortex derived primary cultured neurospheres	brain
19	chr15:72379000-72407800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr15:72379200-72393200	Weak transcription	Primary T helper cells fromperipheralblood	blood
21	chr15:72379200-72395600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
22	chr15:72379600-72388400	Weak transcription	Fetal Intestine Small	intestine
23	chr15:72379800-72388400	Weak transcription	Fetal Muscle Trunk	muscle
24	chr15:72379800-72391000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr15:72379800-72406200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr15:72380000-72388200	Weak transcription	Fetal Stomach	stomach
27	chr15:72380000-72407600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr15:72380200-72388600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr15:72380200-72395600	Weak transcription	Brain Anterior Caudate	brain
30	chr15:72380200-72395600	Weak transcription	Skeletal Muscle Female	skeletal muscle
31	chr15:72380400-72390400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
32	chr15:72380400-72390400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr15:72380600-72393200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
34	chr15:72380800-72395400	Weak transcription	Psoas Muscle	Psoas
35	chr15:72381000-72391400	Weak transcription	Primary T cells from cord blood	blood
36	chr15:72383400-72388400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
37	chr15:72384800-72392400	Weak transcription	Stomach Mucosa	stomach
38	chr15:72386000-72386200	Enhancers	Right Ventricle	heart
39	chr15:72388200-72388800	ZNF genes & repeats	Fetal Stomach	stomach
40	chr15:72388200-72389000	ZNF genes & repeats	Fetal Brain Female	brain
41	chr15:72388200-72395600	Weak transcription	Osteobl	bone
42	chr15:72388400-72388800	ZNF genes & repeats	Fetal Intestine Small	intestine
43	chr15:72388400-72389600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr15:72388400-72389600	Strong transcription	Fetal Muscle Trunk	muscle
45	chr15:72388400-72396200	Weak transcription	Primary B cells from peripheral blood	blood
46	chr15:72388600-72389000	ZNF genes & repeats	Fetal Lung	lung
47	chr15:72388600-72389400	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr15:72388600-72389400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr15:72388600-72389600	ZNF genes & repeats	Fetal Muscle Leg	muscle
50	chr15:72388800-72389200	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain

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