Variant report

Variant	esv1815351
Chromosome Location	chr15:72939659-72963254
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	BATF	chr15:72962900-72963239	GM12878	blood:	n/a	n/a
2	BCL11A	chr15:72949996-72950169	GM12878	blood:	n/a	n/a
3	BCL11A	chr15:72946954-72947101	GM12878	blood:	n/a	n/a
4	BCL11A	chr15:72962896-72963132	GM12878	blood:	n/a	n/a
5	BCL11A	chr15:72956328-72956499	GM12878	blood:	n/a	n/a
6	BCL3	chr15:72963082-72963565	A549	lung:	n/a	n/a
7	BHLHE40	chr15:72956443-72956660	HepG2	liver:	n/a	n/a
8	BHLHE40	chr15:72962865-72963172	HepG2	liver:	n/a	n/a
9	CEBPB	chr15:72963223-72963523	Hela-S3	cervix:	n/a	n/a
10	CHD2	chr15:72963222-72963396	Hela-S3	cervix:	n/a	n/a
11	CTCF	chr15:72963060-72963210	GM12868	blood:	n/a	n/a
12	CTCF	chr15:72962923-72963463	MCF-7	breast:	n/a	chr15:72963059-72963068 chr15:72963356-72963365 chr15:72963048-72963069 chr15:72963053-72963071 chr15:72963054-72963070
13	CTCF	chr15:72963236-72963460	Medullo	brain:	n/a	chr15:72963356-72963365
14	CTCF	chr15:72963152-72963529	ECC-1	luminal epithelium:	n/a	chr15:72963356-72963365
15	CTCF	chr15:72963060-72963210	BE2_C	brain:	n/a	n/a
16	CTCF	chr15:72962774-72964265	A549	lung:	n/a	chr15:72963517-72963535 chr15:72963059-72963068 chr15:72963356-72963365 chr15:72963048-72963069 chr15:72963053-72963071 chr15:72963054-72963070
17	CTCF	chr15:72956413-72956501	MCF-7	breast:	n/a	chr15:72956458-72956476 chr15:72956461-72956469
18	CTCF	chr15:72962721-72962724	Gliobla	brain:	n/a	n/a
19	CTCF	chr15:72957949-72958297	A549	lung:	n/a	n/a
20	CTCF	chr15:72962280-72962430	SAEC	small airway:	n/a	n/a
21	CTCF	chr15:72963111-72963616	HCT-116	colon:	n/a	chr15:72963517-72963535 chr15:72963356-72963365
22	CTCF	chr15:72962921-72963446	GM19239	blood:	n/a	chr15:72963059-72963068 chr15:72963356-72963365 chr15:72963048-72963069 chr15:72963053-72963071 chr15:72963054-72963070
23	CTCF	chr15:72963080-72963230	GM12878	blood:	n/a	n/a
24	CTCF	chr15:72962895-72963539	A549	lung:	n/a	chr15:72963517-72963535 chr15:72963059-72963068 chr15:72963356-72963365 chr15:72963048-72963069 chr15:72963053-72963071 chr15:72963054-72963070
25	CTCF	chr15:72962708-72962789	GM13977	blood:	n/a	n/a
26	CTCF	chr15:72963060-72963210	GM12869	blood:	n/a	n/a
27	CTCF	chr15:72962893-72963585	GM12878	blood:	n/a	chr15:72963517-72963535 chr15:72963059-72963068 chr15:72963356-72963365 chr15:72963048-72963069 chr15:72963053-72963071 chr15:72963054-72963070
28	CTCF	chr15:72963080-72963230	GM12873	blood:	n/a	n/a
29	CTCF	chr15:72963060-72963210	GM12867	blood:	n/a	n/a
30	CTCF	chr15:72963080-72963230	SAEC	small airway:	n/a	n/a
31	CTCF	chr15:72963183-72963440	SK-N-SH_RA	brain:	n/a	chr15:72963356-72963365
32	CTCF	chr15:72963231-72963456	LNCaP	prostate:	n/a	chr15:72963356-72963365
33	CTCF	chr15:72963080-72963230	SK-N-SH_RA	brain:	n/a	n/a
34	CTCF	chr15:72962909-72963482	MCF-7	breast:	n/a	chr15:72963059-72963068 chr15:72963356-72963365 chr15:72963048-72963069 chr15:72963053-72963071 chr15:72963054-72963070
35	CTCF	chr15:72962959-72963467	GM20000	blood:	n/a	chr15:72963059-72963068 chr15:72963356-72963365 chr15:72963048-72963069 chr15:72963053-72963071 chr15:72963054-72963070
36	CTCF	chr15:72962980-72963130	GM12871	blood:	n/a	chr15:72963059-72963068 chr15:72963048-72963069 chr15:72963053-72963071 chr15:72963054-72963070
37	CTCF	chr15:72962906-72963469	GM12891	blood:	n/a	chr15:72963059-72963068 chr15:72963356-72963365 chr15:72963048-72963069 chr15:72963053-72963071 chr15:72963054-72963070
38	CTCF	chr15:72962800-72963673	A549	lung:	n/a	chr15:72963517-72963535 chr15:72963059-72963068 chr15:72963356-72963365 chr15:72963048-72963069 chr15:72963053-72963071 chr15:72963054-72963070
39	CTCF	chr15:72962947-72963487	GM10266	blood:	n/a	chr15:72963059-72963068 chr15:72963356-72963365 chr15:72963048-72963069 chr15:72963053-72963071 chr15:72963054-72963070
40	CTCF	chr15:72962916-72963451	NHEK	skin:	n/a	chr15:72963059-72963068 chr15:72963356-72963365 chr15:72963048-72963069 chr15:72963053-72963071 chr15:72963054-72963070
41	CTCF	chr15:72963040-72963190	GM12865	blood:	n/a	chr15:72963059-72963068 chr15:72963048-72963069 chr15:72963053-72963071 chr15:72963054-72963070
42	CTCF	chr15:72962933-72963197	Kidney_OC	kidney:	n/a	chr15:72963059-72963068 chr15:72963048-72963069 chr15:72963053-72963071 chr15:72963054-72963070
43	CTCF	chr15:72956349-72956646	A549	lung:	n/a	chr15:72956458-72956476 chr15:72956461-72956469
44	CTCF	chr15:72962946-72963453	H1-hESC	embryonic stem cell:	n/a	chr15:72963059-72963068 chr15:72963356-72963365 chr15:72963048-72963069 chr15:72963053-72963071 chr15:72963054-72963070
45	CTCF	chr15:72963080-72963230	MCF-7	breast:	n/a	n/a
46	CTCF	chr15:72963240-72963390	BE2_C	brain:	n/a	chr15:72963356-72963365
47	CTCF	chr15:72963080-72963230	HepG2	liver:	n/a	n/a
48	CTCF	chr15:72962926-72963486	GM10248	blood:	n/a	chr15:72963059-72963068 chr15:72963356-72963365 chr15:72963048-72963069 chr15:72963053-72963071 chr15:72963054-72963070
49	CTCF	chr15:72956320-72956470	HEK293	kidney:	n/a	chr15:72956461-72956469
50	CTCF	chr15:72956389-72956504	GM19240	blood:	n/a	chr15:72956458-72956476 chr15:72956461-72956469

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:72958737-72958787	SK-N-SH	brain:	n/a
2	chr15:72956720-72956770	H1-hESC	embryonic stem cell:	embryo
3	chr15:72958737-72958787	AG10803	skin:	n/a
4	chr15:72958737-72958787	GM12878	blood:	n/a
5	chr15:72956720-72956770	AG04450	lung:	fetal
6	chr15:72956720-72956770	HRPEpiC	eye:	n/a
7	chr15:72956720-72956770	Caco-2	colon:	n/a
8	chr15:72956720-72956770	Jurkat	blood:	n/a
9	chr15:72956720-72956770	HCT-116	colon:	n/a
10	chr15:72956720-72956770	MCF10A-Er-Src	breast:	n/a
11	chr15:72958737-72958787	HCT-116	colon:	n/a
12	chr15:72956720-72956770	AG04449	skin:	fetal
13	chr15:72956720-72956770	T-47D	breast:	n/a
14	chr15:72956720-72956770	NH-A	brain:	n/a
15	chr15:72958737-72958787	HRCEpiC	kidney:	n/a
16	chr15:72958737-72958787	NT2-D1	testis:	n/a
17	chr15:72958737-72958787	T-47D	breast:	n/a
18	chr15:72956720-72956770	SK-N-SH_RA	brain:	n/a
19	chr15:72956720-72956770	HNPCEpiC	eye:	n/a
20	chr15:72956720-72956770	HepG2	liver:	n/a
21	chr15:72956720-72956770	NB4	blood:	n/a
22	chr15:72956720-72956770	HEEpiC	esophagus:	n/a
23	chr15:72956720-72956770	AG09309	skin:	n/a
24	chr15:72956720-72956770	AG10803	skin:	n/a
25	chr15:72956720-72956770	HRCEpiC	kidney:	n/a
26	chr15:72956720-72956770	BJ	skin:	n/a
27	chr15:72958737-72958787	HCF	heart:	n/a
28	chr15:72956720-72956770	CMK	blood:	n/a
29	chr15:72958737-72958787	GM06990	blood:	n/a
30	chr15:72958737-72958787	AoSMC	blood vessel:	n/a
31	chr15:72956720-72956770	Hela-S3	cervix:	n/a
32	chr15:72958737-72958787	HIPEpiC	eye:	n/a
33	chr15:72958737-72958787	HAEpiC	amniotic membrane:	n/a
34	chr15:72958737-72958787	GM12891	blood:	n/a
35	chr15:72956720-72956770	HCF	heart:	n/a
36	chr15:72958737-72958787	NH-A	brain:	n/a
37	chr15:72958737-72958787	NB4	blood:	n/a
38	chr15:72958737-72958787	HRPEpiC	eye:	n/a
39	chr15:72958737-72958787	HUVEC	blood vessel:	n/a
40	chr15:72958737-72958787	ProgFib	skin:	n/a
41	chr15:72956720-72956770	PANC-1	pancreas:	n/a
42	chr15:72956720-72956770	AG09319	gingival:	n/a
43	chr15:72958737-72958787	GM12892	blood:	n/a
44	chr15:72956720-72956770	HL-60	blood:	n/a
45	chr15:72956720-72956770	HCM	heart:	n/a
46	chr15:72956720-72956770	HUVEC	blood vessel:	n/a
47	chr15:72958737-72958787	ovcar-3	ovarian:	n/a
48	chr15:72958737-72958787	HNPCEpiC	eye:	n/a
49	chr15:72958737-72958787	Jurkat	blood:	n/a
50	chr15:72958737-72958787	ECC-1	luminal epithelium:	n/a

No.	Distal block	Cell Line	Cell type
1	chr15:72891911..72892848-chr15:72962933..72963848,3	MCF-7	breast:
2	chr15:72961997..72964036-chr15:72977939..72979769,2	MCF-7	breast:
3	chr15:72961874..72963830-chr15:72977494..72979926,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BBS4-2	chr15:72956896-72957171	NONHSAT047115

Variant related genes	Relation type
GOLGA6B	TF binding region
RN7SL853P	TF binding region
GOLGA6B	CpG island
RN7SL853P	CpG island
ENSG00000140463	chromatin interactions
ENSG00000175202	chromatin interactions

Extended variants
information (count: 151 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:151 , 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	rs3869336	chr15:72942822-72942823	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs28461654	chr15:72943176-72943177	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs561194991	chr15:72943195-72943196	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs531621805	chr15:72943223-72943224	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs550119399	chr15:72943239-72943240	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs200189264	chr15:72943240-72943241	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs200613770	chr15:72946017-72946018	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs2554750	chr15:72947308-72947309	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs201605437	chr15:72948635-72948636	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs565403951	chr15:72948842-72948843	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs532632858	chr15:72949675-72949676	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs548058907	chr15:72949720-72949721	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs566282943	chr15:72949730-72949731	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs530275748	chr15:72949793-72949794	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs141352025	chr15:72949837-72949838	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs368941261	chr15:72949967-72949968	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs537471527	chr15:72950005-72950006	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs372659786	chr15:72952701-72952702	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs376933029	chr15:72952729-72952730	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs555725598	chr15:72952885-72952886	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs554588146	chr15:72953610-72953611	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs576261418	chr15:72953624-72953625	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs368326605	chr15:72953625-72953626	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs543869566	chr15:72953637-72953638	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs201343526	chr15:72953639-72953640	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs202082690	chr15:72953663-72953664	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs201808410	chr15:72953667-72953668	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs199952103	chr15:72953676-72953677	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs200737156	chr15:72953692-72953693	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs565278904	chr15:72953753-72953754	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs532504909	chr15:72953755-72953756	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs201629755	chr15:72953901-72953902	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs541549066	chr15:72954178-72954179	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs3985426	chr15:72954211-72954212	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs559766998	chr15:72954243-72954244	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs199545027	chr15:72954745-72954746	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs369624486	chr15:72954754-72954755	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs373395322	chr15:72954784-72954785	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs377567997	chr15:72954789-72954790	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs370204292	chr15:72954790-72954791	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs146527756	chr15:72954796-72954797	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs201618622	chr15:72954797-72954798	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs554730481	chr15:72954798-72954799	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs376212280	chr15:72954808-72954809	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs201440577	chr15:72954815-72954816	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs375343704	chr15:72954837-72954838	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs201770146	chr15:72954838-72954839	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs577326920	chr15:72954847-72954848	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs200411021	chr15:72954848-72954849	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs201546063	chr15:72954864-72954865	Inactive region	TF binding region	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
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
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 ductal adenocarcinoma	19077451	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:113 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:72962400-72962800	Enhancers	iPS-20b Cell Line	embryonic stem cell
2	chr15:72962800-72963000	Enhancers	Primary T cells fromperipheralblood	blood
3	chr15:72962800-72963000	Enhancers	Skeletal Muscle Female	skeletal muscle
4	chr15:72963000-72963200	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr15:72963000-72963200	Bivalent/Poised TSS	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr15:72963000-72963200	Active TSS	Primary neutrophils fromperipheralblood	blood
7	chr15:72963000-72963200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
8	chr15:72963000-72963200	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
9	chr15:72963000-72963200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr15:72963000-72963200	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr15:72963000-72963200	Active TSS	Muscle Satellite Cultured Cells	--
12	chr15:72963000-72963200	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr15:72963000-72963200	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr15:72963000-72963200	Flanking Active TSS	Adipose Nuclei	Adipose
15	chr15:72963000-72963200	Active TSS	Brain Hippocampus Middle	brain
16	chr15:72963000-72963200	Active TSS	Fetal Muscle Trunk	muscle
17	chr15:72963000-72963200	Active TSS	Stomach Smooth Muscle	stomach
18	chr15:72963000-72963400	Active TSS	ES-I3 Cell Line	embryonic stem cell
19	chr15:72963000-72963400	Active TSS	H1 Cell Line	embryonic stem cell
20	chr15:72963000-72963400	Active TSS	H9 Cell Line	embryonic stem cell
21	chr15:72963000-72963400	Active TSS	HUES48 Cell Line	embryonic stem cell
22	chr15:72963000-72963400	Active TSS	HUES6 Cell Line	embryonic stem cell
23	chr15:72963000-72963400	Active TSS	HUES64 Cell Line	embryonic stem cell
24	chr15:72963000-72963400	Active TSS	iPS-15b Cell Line	embryonic stem cell
25	chr15:72963000-72963400	Active TSS	iPS-18 Cell Line	embryonic stem cell
26	chr15:72963000-72963400	Active TSS	iPS-20b Cell Line	embryonic stem cell
27	chr15:72963000-72963400	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr15:72963000-72963400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr15:72963000-72963400	Flanking Active TSS	Primary T cells fromperipheralblood	blood
30	chr15:72963000-72963400	Active TSS	Primary T helper naive cells fromperipheralblood	blood
31	chr15:72963000-72963400	Active TSS	Primary T helper cells fromperipheralblood	blood
32	chr15:72963000-72963400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr15:72963000-72963400	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr15:72963000-72963400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr15:72963000-72963400	Active TSS	Brain Angular Gyrus	brain
36	chr15:72963000-72963400	Active TSS	Duodenum Mucosa	Duodenum
37	chr15:72963000-72963400	Active TSS	Fetal Adrenal Gland	Adrenal Gland
38	chr15:72963000-72963400	Active TSS	Fetal Intestine Small	intestine
39	chr15:72963000-72963400	Active TSS	Fetal Kidney	kidney
40	chr15:72963000-72963400	Active TSS	Left Ventricle	heart
41	chr15:72963000-72963400	Active TSS	Pancreas	Pancrea
42	chr15:72963000-72963400	Active TSS	Rectal Mucosa Donor 29	rectum
43	chr15:72963000-72963400	Active TSS	Rectal Mucosa Donor 31	rectum
44	chr15:72963000-72963400	Active TSS	Skeletal Muscle Male	skeletal muscle
45	chr15:72963000-72963400	Active TSS	Stomach Mucosa	stomach
46	chr15:72963000-72963400	Active TSS	A549	lung
47	chr15:72963000-72963400	Active TSS	Hela-S3	cervix
48	chr15:72963000-72963400	Active TSS	HepG2	liver
49	chr15:72963000-72963400	Active TSS	HMEC	breast
50	chr15:72963000-72963400	Active TSS	HSMM	muscle

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