Variant report

Variant	esv13877
Chromosome Location	chr15:74044459-74046147
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:22)
CpG islands
(count:367)
Chromatin interactive
region (count:1)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:22 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr15:74044777-74044983	H1-hESC	embryonic stem cell:	n/a	n/a
2	CHD1	chr15:74044765-74044802	H1-hESC	embryonic stem cell:	n/a	n/a
3	GABPA	chr15:74044827-74045270	H1-hESC	embryonic stem cell:	n/a	n/a
4	HMGN3	chr15:74044983-74045057	K562	blood:	n/a	n/a
5	JUND	chr15:74044631-74044716	H1-hESC	embryonic stem cell:	n/a	n/a
6	JUND	chr15:74046041-74046570	H1-hESC	embryonic stem cell:	n/a	n/a
7	MAX	chr15:74045546-74045921	A549	lung:	n/a	n/a
8	MAZ	chr15:74044597-74046256	IMR90	lung:	n/a	chr15:74044619-74044629 chr15:74044615-74044625
9	POLR2A	chr15:74045457-74045575	Gliobla	brain:	n/a	n/a
10	POLR2A	chr15:74045046-74045549	H1-neurons	neurons:	n/a	n/a
11	POLR2A	chr15:74045574-74045930	H1-neurons	neurons:	n/a	n/a
12	POLR2A	chr15:74045605-74045720	Gliobla	brain:	n/a	n/a
13	POLR2A	chr15:74045033-74045901	H1-neurons	neurons:	n/a	n/a
14	POLR2A	chr15:74045646-74045901	H1-hESC	embryonic stem cell:	n/a	n/a
15	REST	chr15:74044416-74045070	H1-neurons	neurons:	n/a	chr15:74044737-74044750 chr15:74044612-74044625 chr15:74045045-74045065
16	SIN3A	chr15:74044621-74045299	H1-hESC	embryonic stem cell:	n/a	chr15:74044971-74044982
17	SIN3A	chr15:74045817-74045819	H1-hESC	embryonic stem cell:	n/a	n/a
18	UBTF	chr15:74045215-74045380	K562	blood:	n/a	n/a
19	ZBTB7A	chr15:74044521-74045350	ECC-1	luminal epithelium:	n/a	n/a
20	ZBTB7A	chr15:74044592-74045458	ECC-1	luminal epithelium:	n/a	n/a
21	ZNF263	chr15:74046058-74047144	HEK293-T-REx	kidney:	n/a	chr15:74046382-74046403
22	ZNF263	chr15:74044856-74045150	HEK293-T-REx	kidney:	n/a	n/a

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:74045075-74045125	HUVEC	blood vessel:	n/a
2	chr15:74045075-74045125	HUVEC	blood vessel:	n/a
3	chr15:74045624-74045674	Jurkat	blood:	n/a
4	chr15:74045705-74045755	AoSMC	blood vessel:	n/a
5	chr15:74045083-74045133	T-47D	breast:	n/a
6	chr15:74045705-74045755	HCM	heart:	n/a
7	chr15:74044539-74044589	AG10803	skin:	n/a
8	chr15:74044539-74044589	HNPCEpiC	eye:	n/a
9	chr15:74045624-74045674	MCF-7	breast:	n/a
10	chr15:74044539-74044589	CMK	blood:	n/a
11	chr15:74045624-74045674	SAEC	small airway:	n/a
12	chr15:74045083-74045133	RPTEC	kidney:	n/a
13	chr15:74044815-74044865	MCF-7	breast:	n/a
14	chr15:74044539-74044589	Jurkat	blood:	n/a
15	chr15:74045705-74045755	CMK	blood:	n/a
16	chr15:74044539-74044589	HCT-116	colon:	n/a
17	chr15:74045075-74045125	CMK	blood:	n/a
18	chr15:74045075-74045125	IMR90	lung:	fetal
19	chr15:74045083-74045133	HPAEpiC	pulmonary alveolar:	n/a
20	chr15:74045705-74045755	SKMC	muscle:	n/a
21	chr15:74044539-74044589	HCF	heart:	n/a
22	chr15:74045705-74045755	NHDF-neo	bronchial:	n/a
23	chr15:74045083-74045133	HIPEpiC	eye:	n/a
24	chr15:74045075-74045125	HEEpiC	esophagus:	n/a
25	chr15:74045705-74045755	HRE	kidney:	n/a
26	chr15:74044539-74044589	GM12891	blood:	n/a
27	chr15:74044539-74044589	HepG2	liver:	n/a
28	chr15:74045075-74045125	HAEpiC	amniotic membrane:	n/a
29	chr15:74044815-74044865	SK-N-MC	brain:	n/a
30	chr15:74045075-74045125	HCPEpiC	choroid plexus:	n/a
31	chr15:74045705-74045755	ovcar-3	ovarian:	n/a
32	chr15:74045705-74045755	HCPEpiC	choroid plexus:	n/a
33	chr15:74045075-74045125	GM12891	blood:	n/a
34	chr15:74044539-74044589	NB4	blood:	n/a
35	chr15:74045624-74045674	HCPEpiC	choroid plexus:	n/a
36	chr15:74045624-74045674	GM19239	blood:	n/a
37	chr15:74045705-74045755	ProgFib	skin:	n/a
38	chr15:74045083-74045133	MCF-7	breast:	n/a
39	chr15:74045083-74045133	HEEpiC	esophagus:	n/a
40	chr15:74045083-74045133	HL-60	blood:	n/a
41	chr15:74045075-74045125	AG09319	gingival:	n/a
42	chr15:74045624-74045674	HEK293	kidney:	embryo
43	chr15:74044539-74044589	HAEpiC	amniotic membrane:	n/a
44	chr15:74045624-74045674	A549	lung:	n/a
45	chr15:74045075-74045125	PANC-1	pancreas:	n/a
46	chr15:74045624-74045674	HCT-116	colon:	n/a
47	chr15:74045705-74045755	LNCaP	prostate:	n/a
48	chr15:74045624-74045674	ProgFib	skin:	n/a
49	chr15:74044539-74044589	Hela-S3	cervix:	n/a
50	chr15:74045083-74045133	HRE	kidney:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:74046017..74047520-chr15:74054449..74056140,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C15orf59-2	chr15:74045697-74046276	NONHSAT047155
2	lnc-CD276-2	chr15:74044453-74044737	XLOC_011305

No data

Variant related genes	Relation type
C15orf59	TF binding region
C15orf59	CpG island

Extended variants
information (count: 41 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:41 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs566972344	chr15:74044473-74044474	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
2	rs369670150	chr15:74044567-74044568	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
3	rs537536681	chr15:74044591-74044592	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
4	rs371924651	chr15:74044652-74044653	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
5	rs188683806	chr15:74044673-74044674	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
6	rs571700494	chr15:74044703-74044704	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
7	rs117069008	chr15:74044740-74044741	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs3169102	chr15:74044741-74044742	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs572760563	chr15:74044896-74044897	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs2306208	chr15:74044902-74044903	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs1129484	chr15:74044906-74044907	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs554997802	chr15:74044912-74044913	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs181220179	chr15:74044933-74044934	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs543506639	chr15:74044935-74044936	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs3088341	chr15:74044965-74044966	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs1047399	chr15:74044966-74044967	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs28740916	chr15:74044974-74044975	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs532949167	chr15:74044981-74044982	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs545176453	chr15:74045010-74045011	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs559945792	chr15:74045045-74045046	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs527580232	chr15:74045084-74045085	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
22	rs548907714	chr15:74045112-74045113	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
23	rs549110870	chr15:74045150-74045151	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs186972601	chr15:74045195-74045196	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs113338004	chr15:74045205-74045206	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs117544936	chr15:74045260-74045261	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs549580113	chr15:74045301-74045302	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs571332559	chr15:74045308-74045309	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs538390337	chr15:74045334-74045335	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs554385207	chr15:74045663-74045664	Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
31	rs567229898	chr15:74045705-74045706	Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
32	rs566323655	chr15:74045794-74045795	Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
33	rs138542745	chr15:74045827-74045828	Active TSS Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
34	rs531374359	chr15:74045878-74045879	Active TSS Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
35	rs141517325	chr15:74045909-74045910	Active TSS Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
36	rs543816687	chr15:74045913-74045914	Active TSS Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
37	rs367926699	chr15:74045976-74045977	Active TSS Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
38	rs146406299	chr15:74045989-74045990	Active TSS Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
39	rs372966590	chr15:74046034-74046035	Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
40	rs138890556	chr15:74046111-74046112	Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
41	rs71738026	chr15:74046116-74046117	Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:75)

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
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Prostate cancer	16573809	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
Breast cancer	21364760	CNVD
Epilepsy	22083797	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Bipolar disorder	19114987	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD

Chromatin state (count:250 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:74043200-74046000	Active TSS	H9 Cell Line	embryonic stem cell
2	chr15:74043400-74044800	Bivalent/Poised TSS	Fetal Lung	lung
3	chr15:74043400-74045000	Enhancers	Spleen	Spleen
4	chr15:74043400-74045400	Active TSS	Brain Substantia Nigra	brain
5	chr15:74043600-74044800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr15:74043600-74045000	Flanking Active TSS	Right Ventricle	heart
7	chr15:74043600-74045200	Bivalent/Poised TSS	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr15:74043600-74045400	Active TSS	Brain Cingulate Gyrus	brain
9	chr15:74043600-74045800	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
10	chr15:74043600-74046000	Active TSS	Pancreatic Islets	Pancreatic Islet
11	chr15:74043800-74044600	Bivalent/Poised TSS	Brain Dorsolateral Prefrontal Cortex	brain
12	chr15:74043800-74044800	Enhancers	Fetal Heart	heart
13	chr15:74043800-74045000	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr15:74043800-74045200	Active TSS	Fetal Kidney	kidney
15	chr15:74043800-74045400	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
16	chr15:74043800-74045800	Active TSS	Right Atrium	heart
17	chr15:74043800-74046000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr15:74044000-74044600	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
19	chr15:74044000-74044600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr15:74044000-74044600	Active TSS	Brain Hippocampus Middle	brain
21	chr15:74044000-74044600	Enhancers	Pancreas	Pancrea
22	chr15:74044000-74044600	Active TSS	NH-A	brain
23	chr15:74044000-74045400	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr15:74044000-74045400	Active TSS	Brain Angular Gyrus	brain
25	chr15:74044000-74045400	Active TSS	Brain Anterior Caudate	brain
26	chr15:74044000-74045800	Active TSS	iPS-15b Cell Line	embryonic stem cell
27	chr15:74044000-74045800	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr15:74044000-74045800	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr15:74044000-74045800	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
30	chr15:74044000-74046000	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
31	chr15:74044000-74046000	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
32	chr15:74044000-74046000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr15:74044000-74046000	Active TSS	Brain Germinal Matrix	brain
34	chr15:74044000-74046000	Active TSS	Fetal Brain Female	brain
35	chr15:74044200-74044600	Bivalent/Poised TSS	Colonic Mucosa	Colon
36	chr15:74044200-74044600	Bivalent/Poised TSS	Skeletal Muscle Male	skeletal muscle
37	chr15:74044200-74044600	Active TSS	Stomach Smooth Muscle	stomach
38	chr15:74044200-74044800	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr15:74044200-74044800	Enhancers	Lung	lung
40	chr15:74044200-74045200	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
41	chr15:74044200-74045800	Active TSS	Cortex derived primary cultured neurospheres	brain
42	chr15:74044200-74045800	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr15:74044200-74045800	Active TSS	Brain Inferior Temporal Lobe	brain
44	chr15:74044200-74045800	Weak transcription	Fetal Brain Male	brain
45	chr15:74044200-74045800	Bivalent/Poised TSS	Fetal Stomach	stomach
46	chr15:74044200-74045800	Active TSS	Left Ventricle	heart
47	chr15:74044200-74045800	Active TSS	Rectal Smooth Muscle	rectum
48	chr15:74044200-74046000	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
49	chr15:74044200-74046000	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr15:74044200-74046000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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