Variant report

Variant	esv3405064
Chromosome Location	chr15:75649949-75652747
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:105)
CpG islands
(count:61)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:105 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr15:75651620-75653273	GM12892	blood:	n/a	n/a
2	POLR2A	chr15:75652471-75653021	K562	blood:	n/a	n/a
3	POLR2A	chr15:75651289-75651341	K562	blood:	n/a	n/a
4	POLR2A	chr15:75651556-75651564	HepG2	liver:	n/a	n/a
5	POLR2A	chr15:75651501-75651528	K562	blood:	n/a	n/a
6	POLR2A	chr15:75651747-75651965	MCF-7	breast:	n/a	n/a
7	POLR2A	chr15:75650779-75653551	SK-N-MC	brain:	n/a	n/a
8	POLR2A	chr15:75651531-75655942	GM12892	blood:	n/a	n/a
9	POLR2A	chr15:75651818-75652611	GM12878	blood:	n/a	n/a
10	POLR2A	chr15:75650818-75650827	Hela-S3	cervix:	n/a	n/a
11	POLR2A	chr15:75650640-75651098	GM12891	blood:	n/a	n/a
12	POLR2A	chr15:75652737-75652768	Hela-S3	cervix:	n/a	n/a
13	POLR2A	chr15:75651201-75651215	HUVEC	blood vessel:	n/a	n/a
14	POLR2A	chr15:75652712-75653658	GM12891	blood:	n/a	n/a
15	POLR2A	chr15:75651620-75651961	A549	lung:	n/a	n/a
16	POLR2A	chr15:75650538-75651511	GM12892	blood:	n/a	n/a
17	POLR2A	chr15:75652019-75652138	A549	lung:	n/a	n/a
18	POLR2A	chr15:75651570-75652015	Hela-S3	cervix:	n/a	n/a
19	POLR2A	chr15:75651483-75651489	K562	blood:	n/a	n/a
20	POLR2A	chr15:75650370-75650521	H1-hESC	embryonic stem cell:	n/a	n/a
21	POLR2A	chr15:75652454-75653322	Hela-S3	cervix:	n/a	n/a
22	POLR2A	chr15:75651589-75652590	GM12891	blood:	n/a	n/a
23	POLR2A	chr15:75651615-75652688	K562	blood:	n/a	n/a
24	POLR2A	chr15:75651974-75652278	GM12892	blood:	n/a	n/a
25	POLR2A	chr15:75651872-75652004	MCF-7	breast:	n/a	n/a
26	POLR2A	chr15:75650642-75651479	GM12878	blood:	n/a	n/a
27	POLR2A	chr15:75650778-75651312	A549	lung:	n/a	n/a
28	POLR2A	chr15:75651039-75651206	ProgFib	skin:	n/a	n/a
29	POLR2A	chr15:75652446-75653906	PANC-1	pancreas:	n/a	n/a
30	POLR2A	chr15:75652214-75652450	Hela-S3	cervix:	n/a	n/a
31	POLR2A	chr15:75652019-75652289	ProgFib	skin:	n/a	n/a
32	POLR2A	chr15:75650822-75651370	GM12891	blood:	n/a	n/a
33	POLR2A	chr15:75651870-75652111	A549	lung:	n/a	n/a
34	POLR2A	chr15:75650886-75651515	GM12891	blood:	n/a	n/a
35	POLR2A	chr15:75651609-75651793	GM12878	blood:	n/a	n/a
36	POLR2A	chr15:75650613-75655985	GM12892	blood:	n/a	n/a
37	POLR2A	chr15:75651736-75651915	HepG2	liver:	n/a	n/a
38	POLR2A	chr15:75650792-75650808	Hela-S3	cervix:	n/a	n/a
39	POLR2A	chr15:75650984-75651079	H1-hESC	embryonic stem cell:	n/a	n/a
40	POLR2A	chr15:75651989-75651991	MCF-7	breast:	n/a	n/a
41	POLR2A	chr15:75651372-75651400	HepG2	liver:	n/a	n/a
42	POLR2A	chr15:75651958-75653155	A549	lung:	n/a	n/a
43	POLR2A	chr15:75652121-75652180	H1-hESC	embryonic stem cell:	n/a	n/a
44	POLR2A	chr15:75651320-75651516	H1-hESC	embryonic stem cell:	n/a	n/a
45	POLR2A	chr15:75651578-75652281	PANC-1	pancreas:	n/a	n/a
46	POLR2A	chr15:75651988-75652001	Hela-S3	cervix:	n/a	n/a
47	POLR2A	chr15:75651179-75651180	GM12878	blood:	n/a	n/a
48	POLR2A	chr15:75652461-75652501	HUVEC	blood vessel:	n/a	n/a
49	POLR2A	chr15:75652272-75652560	GM12878	blood:	n/a	n/a
50	POLR2A	chr15:75650299-75650555	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:75651821-75651871	AoSMC	blood vessel:	n/a
2	chr15:75651821-75651871	SK-N-MC	brain:	n/a
3	chr15:75651821-75651871	LNCaP	prostate:	n/a
4	chr15:75651821-75651871	HEEpiC	esophagus:	n/a
5	chr15:75651821-75651871	HNPCEpiC	eye:	n/a
6	chr15:75651821-75651871	Hepatocyte	liver:	n/a
7	chr15:75651821-75651871	A549	lung:	n/a
8	chr15:75651821-75651871	PFSK-1	brain:	n/a
9	chr15:75651821-75651871	SAEC	small airway:	n/a
10	chr15:75651821-75651871	K562	blood:	n/a
11	chr15:75651821-75651871	ovcar-3	ovarian:	n/a
12	chr15:75651821-75651871	MCF10A-Er-Src	breast:	n/a
13	chr15:75651821-75651871	HCM	heart:	n/a
14	chr15:75651821-75651871	ProgFib	skin:	n/a
15	chr15:75651821-75651871	AG10803	skin:	n/a
16	chr15:75651821-75651871	T-47D	breast:	n/a
17	chr15:75651821-75651871	GM12892	blood:	n/a
18	chr15:75651821-75651871	PrEC	prostate:	n/a
19	chr15:75651821-75651871	AG09319	gingival:	n/a
20	chr15:75651821-75651871	CMK	blood:	n/a
21	chr15:75651821-75651871	IMR90	lung:	fetal
22	chr15:75651821-75651871	Caco-2	colon:	n/a
23	chr15:75651821-75651871	Jurkat	blood:	n/a
24	chr15:75651821-75651871	HRPEpiC	eye:	n/a
25	chr15:75651821-75651871	U87	brain:	n/a
26	chr15:75651821-75651871	SK-N-SH	brain:	n/a
27	chr15:75651821-75651871	SK-N-SH_RA	brain:	n/a
28	chr15:75651821-75651871	PANC-1	pancreas:	n/a
29	chr15:75651821-75651871	HEK293	kidney:	embryo
30	chr15:75651821-75651871	HCF	heart:	n/a
31	chr15:75651821-75651871	NH-A	brain:	n/a
32	chr15:75651821-75651871	HPAEpiC	pulmonary alveolar:	n/a
33	chr15:75651821-75651871	NHBE	bronchial:	n/a
34	chr15:75651821-75651871	HRCEpiC	kidney:	n/a
35	chr15:75651821-75651871	HIPEpiC	eye:	n/a
36	chr15:75651821-75651871	HL-60	blood:	n/a
37	chr15:75651821-75651871	BE2_C	brain:	n/a
38	chr15:75651821-75651871	MCF-7	breast:	n/a
39	chr15:75651821-75651871	Hela-S3	cervix:	n/a
40	chr15:75651821-75651871	HCPEpiC	choroid plexus:	n/a
41	chr15:75651821-75651871	H1-hESC	embryonic stem cell:	embryo
42	chr15:75651821-75651871	NB4	blood:	n/a
43	chr15:75651821-75651871	ECC-1	luminal epithelium:	n/a
44	chr15:75651821-75651871	NHDF-neo	bronchial:	n/a
45	chr15:75651821-75651871	HepG2	liver:	n/a
46	chr15:75651821-75651871	HAEpiC	amniotic membrane:	n/a
47	chr15:75651821-75651871	HRE	kidney:	n/a
48	chr15:75651821-75651871	HUVEC	blood vessel:	n/a
49	chr15:75651821-75651871	AG09309	skin:	n/a
50	chr15:75651821-75651871	BJ	skin:	n/a

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:75628778..75631510-chr15:75648708..75650958,2	MCF-7	breast:
2	chr15:75652075..75654560-chr15:75917811..75919944,2	K562	blood:
3	chr15:75651898..75654769-chr15:75870111..75872338,3	MCF-7	breast:

No data

Variant related genes	Relation type
MAN2C1	TF binding region
MIR631	TF binding region
ENSG00000260591	TF binding region
MAN2C1	CpG island
MIR631	CpG island
ENSG00000260591	CpG island
ENSG00000169410	chromatin interactions
ENSG00000140365	chromatin interactions
ENSG00000169371	chromatin interactions

Extended variants
information (count: 183 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:183 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs536494751	chr15:75649964-75649965	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs554815187	chr15:75649999-75650000	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs565191410	chr15:75650062-75650063	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs572042961	chr15:75650087-75650088	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs576259869	chr15:75650088-75650089	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs373027212	chr15:75650105-75650106	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs543176110	chr15:75650106-75650107	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs189165718	chr15:75650112-75650113	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs558588835	chr15:75650121-75650122	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs576798845	chr15:75650161-75650162	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs148395984	chr15:75650237-75650238	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs559660770	chr15:75650240-75650241	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs530337056	chr15:75650249-75650250	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs368880540	chr15:75650267-75650268	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs542069890	chr15:75650307-75650308	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs563560572	chr15:75650331-75650332	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs531097075	chr15:75650342-75650343	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs531757465	chr15:75650371-75650372	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs570899519	chr15:75650406-75650407	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs192894516	chr15:75650444-75650445	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs183173851	chr15:75650454-75650455	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs568427510	chr15:75650486-75650487	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs373810539	chr15:75650506-75650507	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs370122057	chr15:75650518-75650519	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs201620266	chr15:75650545-75650546	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs148147908	chr15:75650573-75650574	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs376142400	chr15:75650612-75650613	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs142008270	chr15:75650631-75650632	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs150703780	chr15:75650634-75650635	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs142370400	chr15:75650635-75650636	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs58557444	chr15:75650636-75650637	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs576870185	chr15:75650675-75650676	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs199538581	chr15:75650680-75650681	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs377537571	chr15:75650683-75650684	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs369428112	chr15:75650686-75650687	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs371342596	chr15:75650699-75650700	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs374209607	chr15:75650720-75650721	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs368927099	chr15:75650756-75650757	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs371151146	chr15:75650771-75650772	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs374480499	chr15:75650787-75650788	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs187023048	chr15:75650791-75650792	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs200817964	chr15:75650794-75650795	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs139868638	chr15:75650796-75650797	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs368053079	chr15:75650797-75650798	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs143005170	chr15:75650822-75650823	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs200935699	chr15:75650825-75650826	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs147475439	chr15:75650828-75650829	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs1128933	chr15:75650836-75650837	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs375508141	chr15:75650845-75650846	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs199641166	chr15:75650862-75650863	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:65)

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
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
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Autism	17322880	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
Epilepsy	22083797	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Myelofibrosis	22110671	CNVD
Bipolar disorder	19114987	CNVD
Lung cancer	18438408	CNVD
Multiple myeloma	16616336	CNVD

Chromatin state (count:166 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:75641200-75655000	Weak transcription	K562	blood
2	chr15:75641400-75651200	Weak transcription	HSMM	muscle
3	chr15:75641400-75655400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr15:75641400-75658600	Weak transcription	HUVEC	blood vessel
5	chr15:75641600-75650400	Weak transcription	Brain Substantia Nigra	brain
6	chr15:75641600-75654200	Weak transcription	Small Intestine	intestine
7	chr15:75641600-75659200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr15:75641600-75659600	Weak transcription	Pancreatic Islets	Pancreatic Islet
9	chr15:75641800-75651400	Weak transcription	Stomach Mucosa	stomach
10	chr15:75641800-75659600	Weak transcription	Fetal Heart	heart
11	chr15:75642000-75659600	Strong transcription	Fetal Intestine Small	intestine
12	chr15:75642200-75659800	Weak transcription	Fetal Brain Male	brain
13	chr15:75642400-75659800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr15:75642800-75650400	Weak transcription	Primary hematopoietic stem cells	blood
15	chr15:75642800-75654000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr15:75643000-75659600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
17	chr15:75643200-75659800	Weak transcription	Right Atrium	heart
18	chr15:75643400-75654400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
19	chr15:75643400-75656800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
20	chr15:75643600-75656200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
21	chr15:75643800-75657000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
22	chr15:75644000-75650400	Weak transcription	HSMMtube	muscle
23	chr15:75644000-75651000	Weak transcription	Primary B cells from cord blood	blood
24	chr15:75644200-75659600	Strong transcription	Fetal Muscle Trunk	muscle
25	chr15:75644200-75659800	Strong transcription	Fetal Stomach	stomach
26	chr15:75644400-75657600	Strong transcription	Gastric	stomach
27	chr15:75644400-75658000	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr15:75644400-75658800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
29	chr15:75644400-75659600	Strong transcription	Colonic Mucosa	Colon
30	chr15:75644400-75659600	Strong transcription	Duodenum Mucosa	Duodenum
31	chr15:75644400-75659800	Strong transcription	Cortex derived primary cultured neurospheres	brain
32	chr15:75644600-75659600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr15:75644800-75659600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr15:75645600-75659800	Strong transcription	Placenta	Placenta
35	chr15:75645800-75659600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr15:75645800-75659600	Strong transcription	Fetal Intestine Large	intestine
37	chr15:75645800-75660000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr15:75646000-75652400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr15:75646000-75659200	Strong transcription	Brain Germinal Matrix	brain
40	chr15:75646000-75659200	Strong transcription	Skeletal Muscle Male	skeletal muscle
41	chr15:75646000-75659400	Strong transcription	Primary T cells from cord blood	blood
42	chr15:75646000-75659400	Strong transcription	Sigmoid Colon	Sigmoid Colon
43	chr15:75646000-75659400	Strong transcription	Skeletal Muscle Female	skeletal muscle
44	chr15:75646000-75659800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr15:75646000-75659800	Strong transcription	NHLF	lung
46	chr15:75646000-75660200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr15:75646200-75659400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr15:75646200-75659400	Strong transcription	Esophagus	oesophagus
49	chr15:75646200-75659600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
50	chr15:75646200-75659600	Strong transcription	Adipose Nuclei	Adipose

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