Variant report

Variant	nsv821020
Chromosome Location	chr15:72921261-72966130
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	ATF3	chr15:72929199-72929370	HepG2	liver:	n/a	chr15:72929314-72929323 chr15:72929285-72929294
2	ATF3	chr15:72929193-72929453	GM12878	blood:	n/a	chr15:72929314-72929323 chr15:72929285-72929294
3	ATF3	chr15:72929169-72929468	H1-hESC	embryonic stem cell:	n/a	chr15:72929314-72929323 chr15:72929285-72929294
4	ATF3	chr15:72929209-72929423	K562	blood:	n/a	chr15:72929314-72929323 chr15:72929285-72929294
5	BATF	chr15:72962900-72963239	GM12878	blood:	n/a	n/a
6	BATF	chr15:72925333-72925511	GM12878	blood:	n/a	n/a
7	BCL11A	chr15:72946954-72947101	GM12878	blood:	n/a	n/a
8	BCL11A	chr15:72949996-72950169	GM12878	blood:	n/a	n/a
9	BCL11A	chr15:72929114-72929321	GM12878	blood:	n/a	n/a
10	BCL11A	chr15:72956328-72956499	GM12878	blood:	n/a	n/a
11	BCL11A	chr15:72962896-72963132	GM12878	blood:	n/a	n/a
12	BCL3	chr15:72963082-72963565	A549	lung:	n/a	n/a
13	BHLHE40	chr15:72956443-72956660	HepG2	liver:	n/a	n/a
14	BHLHE40	chr15:72929274-72929469	K562	blood:	n/a	chr15:72929313-72929322 chr15:72929314-72929323 chr15:72929312-72929325 chr15:72929308-72929329 chr15:72929314-72929323
15	BHLHE40	chr15:72929272-72929472	HepG2	liver:	n/a	chr15:72929313-72929322 chr15:72929314-72929323 chr15:72929312-72929325 chr15:72929308-72929329 chr15:72929314-72929323
16	BHLHE40	chr15:72929099-72929473	HepG2	liver:	n/a	chr15:72929313-72929322 chr15:72929314-72929323 chr15:72929312-72929325 chr15:72929308-72929329 chr15:72929314-72929323
17	BHLHE40	chr15:72962865-72963172	HepG2	liver:	n/a	n/a
18	BHLHE40	chr15:72963349-72963614	K562	blood:	n/a	n/a
19	CBX3	chr15:72928995-72929709	K562	blood:	n/a	n/a
20	CBX3	chr15:72929167-72929610	K562	blood:	n/a	n/a
21	CEBPB	chr15:72964819-72964947	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr15:72929283-72929294	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr15:72963223-72963523	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr15:72964807-72964942	K562	blood:	n/a	n/a
25	CEBPB	chr15:72964805-72964921	A549	lung:	n/a	n/a
26	CHD2	chr15:72929278-72929474	GM12878	blood:	n/a	n/a
27	CHD2	chr15:72963438-72963551	GM12878	blood:	n/a	n/a
28	CHD2	chr15:72929269-72929481	Hela-S3	cervix:	n/a	n/a
29	CHD2	chr15:72963222-72963396	Hela-S3	cervix:	n/a	n/a
30	CHD2	chr15:72963257-72963397	K562	blood:	n/a	n/a
31	CHD2	chr15:72963583-72963634	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD2	chr15:72929281-72929477	K562	blood:	n/a	n/a
33	CHD2	chr15:72929278-72929469	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD2	chr15:72929272-72929475	HepG2	liver:	n/a	n/a
35	CTCF	chr15:72962280-72962430	SAEC	small airway:	n/a	n/a
36	CTCF	chr15:72963080-72963230	HepG2	liver:	n/a	n/a
37	CTCF	chr15:72962921-72963446	GM19239	blood:	n/a	chr15:72963059-72963068 chr15:72963356-72963365 chr15:72963048-72963069 chr15:72963053-72963071 chr15:72963054-72963070
38	CTCF	chr15:72963080-72963230	AG04450	lung:	n/a	n/a
39	CTCF	chr15:72956410-72956504	GM12891	blood:	n/a	chr15:72956458-72956476 chr15:72956461-72956469
40	CTCF	chr15:72958114-72958203	LNCaP	prostate:	n/a	n/a
41	CTCF	chr15:72963820-72963970	GM12873	blood:	n/a	n/a
42	CTCF	chr15:72962942-72963503	Spleen_OC	spleen:	n/a	chr15:72963059-72963068 chr15:72963356-72963365 chr15:72963048-72963069 chr15:72963053-72963071 chr15:72963054-72963070
43	CTCF	chr15:72962697-72962819	GM10248	blood:	n/a	n/a
44	CTCF	chr15:72929233-72929235	Spleen_OC	spleen:	n/a	n/a
45	CTCF	chr15:72962911-72963564	IMR90	lung:	n/a	chr15:72963517-72963535 chr15:72963059-72963068 chr15:72963356-72963365 chr15:72963048-72963069 chr15:72963053-72963071 chr15:72963054-72963070
46	CTCF	chr15:72963320-72963470	HFF-Myc	foreskin:	n/a	chr15:72963356-72963365
47	CTCF	chr15:72963300-72963450	GM12875	blood:	n/a	chr15:72963356-72963365
48	CTCF	chr15:72963080-72963230	AG09309	skin:	n/a	n/a
49	CTCF	chr15:72956349-72956646	A549	lung:	n/a	chr15:72956458-72956476 chr15:72956461-72956469
50	CTCF	chr15:72956370-72956511	Gliobla	brain:	n/a	chr15:72956458-72956476 chr15:72956461-72956469

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:72929414-72929464	MCF10A-Er-Src	breast:	n/a
2	chr15:72956720-72956770	K562	blood:	n/a
3	chr15:72929414-72929464	H1-hESC	embryonic stem cell:	embryo
4	chr15:72956720-72956770	AoSMC	blood vessel:	n/a
5	chr15:72958737-72958787	IMR90	lung:	fetal
6	chr15:72964110-72964160	HCM	heart:	n/a
7	chr15:72956720-72956770	HL-60	blood:	n/a
8	chr15:72964110-72964160	HMEC	breast:	n/a
9	chr15:72929414-72929464	HMEC	breast:	n/a
10	chr15:72958737-72958787	NH-A	brain:	n/a
11	chr15:72958737-72958787	SK-N-MC	brain:	n/a
12	chr15:72958737-72958787	HCPEpiC	choroid plexus:	n/a
13	chr15:72964110-72964160	ovcar-3	ovarian:	n/a
14	chr15:72964110-72964160	K562	blood:	n/a
15	chr15:72929414-72929464	Caco-2	colon:	n/a
16	chr15:72964110-72964160	NT2-D1	testis:	n/a
17	chr15:72964110-72964160	U87	brain:	n/a
18	chr15:72958737-72958787	HL-60	blood:	n/a
19	chr15:72964110-72964160	NB4	blood:	n/a
20	chr15:72929414-72929464	NH-A	brain:	n/a
21	chr15:72958737-72958787	HCF	heart:	n/a
22	chr15:72958737-72958787	PFSK-1	brain:	n/a
23	chr15:72929414-72929464	HCM	heart:	n/a
24	chr15:72964110-72964160	SK-N-SH	brain:	n/a
25	chr15:72964110-72964160	T-47D	breast:	n/a
26	chr15:72958737-72958787	CMK	blood:	n/a
27	chr15:72958737-72958787	Hepatocyte	liver:	n/a
28	chr15:72956720-72956770	HCPEpiC	choroid plexus:	n/a
29	chr15:72929414-72929464	ECC-1	luminal epithelium:	n/a
30	chr15:72958737-72958787	HAEpiC	amniotic membrane:	n/a
31	chr15:72929414-72929464	T-47D	breast:	n/a
32	chr15:72929414-72929464	K562	blood:	n/a
33	chr15:72956720-72956770	HEEpiC	esophagus:	n/a
34	chr15:72956720-72956770	HCF	heart:	n/a
35	chr15:72956720-72956770	HCT-116	colon:	n/a
36	chr15:72956720-72956770	SK-N-SH	brain:	n/a
37	chr15:72929414-72929464	AG04449	skin:	fetal
38	chr15:72956720-72956770	ovcar-3	ovarian:	n/a
39	chr15:72929414-72929464	HCT-116	colon:	n/a
40	chr15:72964110-72964160	LNCaP	prostate:	n/a
41	chr15:72964110-72964160	HRPEpiC	eye:	n/a
42	chr15:72929414-72929464	AG10803	skin:	n/a
43	chr15:72929414-72929464	GM12892	blood:	n/a
44	chr15:72929414-72929464	HNPCEpiC	eye:	n/a
45	chr15:72929414-72929464	CMK	blood:	n/a
46	chr15:72958737-72958787	HEK293	kidney:	embryo
47	chr15:72964110-72964160	HIPEpiC	eye:	n/a
48	chr15:72964110-72964160	GM06990	blood:	n/a
49	chr15:72964110-72964160	PrEC	prostate:	n/a
50	chr15:72956720-72956770	AG10803	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr15:72961997..72964036-chr15:72977939..72979769,2	MCF-7	breast:
2	chr15:72891911..72892848-chr15:72962933..72963848,3	MCF-7	breast:
3	chr15:72965813..72966410-chr15:72977917..72978863,2	Hela-S3	cervix:
4	chr15:72964421..72966400-chr15:72976788..72978521,2	MCF-7	breast:
5	chr15:72916000..72918571-chr15:72920534..72922418,2	MCF-7	breast:
6	chr15:72961874..72963830-chr15:72977494..72979926,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HIGD2B-1	chr15:72925679-72925747	ENSG00000259783.1
2	lnc-HIGD2B-1	chr15:72925679-72925747	ENSG00000259783.1
3	lnc-BBS4-2	chr15:72956896-72957171	NONHSAT047115
4	lnc-HIGD2B-1	chr15:72929127-72929229	ENSG00000259783.1
5	lnc-HIGD2B-1	chr15:72929127-72929260	ENSG00000259783.1

Variant related genes	Relation type
ENSG00000259783	TF binding region
ENSG00000259909	TF binding region
GOLGA6B	TF binding region
RN7SL853P	TF binding region
ENSG00000259783	CpG island
ENSG00000259909	CpG island
GOLGA6B	CpG island
RN7SL853P	CpG island
ENSG00000175202	chromatin interactions
ENSG00000140463	chromatin interactions

Extended variants
information (count: 411 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:411 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs543345712	chr15:72921274-72921275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs570610966	chr15:72921324-72921325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs11855756	chr15:72921371-72921372	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs146486898	chr15:72921372-72921373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs370064397	chr15:72921496-72921497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs530193825	chr15:72921498-72921499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs548846126	chr15:72921545-72921546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs570139639	chr15:72921550-72921551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs71397261	chr15:72921566-72921567	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs552598827	chr15:72921594-72921595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs553294177	chr15:72921603-72921604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs571098142	chr15:72921611-72921612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs538263482	chr15:72921665-72921666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs553337805	chr15:72921677-72921678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs117589804	chr15:72921699-72921700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs535941042	chr15:72921700-72921701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs554791756	chr15:72921703-72921704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs576157264	chr15:72921741-72921742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs543573509	chr15:72921744-72921745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs565047213	chr15:72921751-72921752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs573477630	chr15:72921769-72921770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs577193210	chr15:72921781-72921782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs117669130	chr15:72921819-72921820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs559779075	chr15:72921918-72921919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs555760014	chr15:72921947-72921948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs151251390	chr15:72921990-72921991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs530257976	chr15:72922005-72922006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs541967168	chr15:72922094-72922095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs544808335	chr15:72922149-72922150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs563755268	chr15:72922204-72922205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs531034626	chr15:72922212-72922213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs552705542	chr15:72922227-72922228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs189888812	chr15:72922237-72922238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs116119022	chr15:72922246-72922247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs181160041	chr15:72922289-72922290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs565329536	chr15:72922297-72922298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs535807623	chr15:72922322-72922323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs554386137	chr15:72922323-72922324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs117080652	chr15:72922339-72922340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs187064014	chr15:72922396-72922397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs558694175	chr15:72922448-72922449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs112080281	chr15:72922463-72922464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs71397262	chr15:72922483-72922484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs541322341	chr15:72922497-72922498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs553263184	chr15:72922512-72922513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs574889674	chr15:72922513-72922514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs542178781	chr15:72922514-72922515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs563648555	chr15:72922533-72922534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs531019514	chr15:72922591-72922592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs546109825	chr15:72922617-72922618	ZNF genes & repeats	n/a	n/a	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:289 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:72909400-72922600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr15:72922600-72922800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr15:72922800-72929400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr15:72928600-72929200	Enhancers	Primary B cells from peripheral blood	blood
5	chr15:72928600-72929600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr15:72928600-72929800	Active TSS	HUES48 Cell Line	embryonic stem cell
7	chr15:72928600-72929800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr15:72928800-72929200	Enhancers	HUVEC	blood vessel
9	chr15:72928800-72929600	Active TSS	Primary neutrophils fromperipheralblood	blood
10	chr15:72928800-72929600	Active TSS	Thymus	Thymus
11	chr15:72928800-72929800	Active TSS	H1 Cell Line	embryonic stem cell
12	chr15:72928800-72929800	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr15:72928800-72929800	Active TSS	HUES6 Cell Line	embryonic stem cell
14	chr15:72928800-72929800	Active TSS	HUES64 Cell Line	embryonic stem cell
15	chr15:72928800-72929800	Active TSS	iPS-20b Cell Line	embryonic stem cell
16	chr15:72928800-72929800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr15:72928800-72929800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr15:72928800-72929800	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr15:72928800-72929800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr15:72928800-72929800	Active TSS	Muscle Satellite Cultured Cells	--
21	chr15:72928800-72929800	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr15:72928800-72929800	Active TSS	Brain Anterior Caudate	brain
23	chr15:72928800-72929800	Active TSS	A549	lung
24	chr15:72928800-72929800	Active TSS	Monocytes-CD14+_RO01746	blood
25	chr15:72929200-72929600	Active TSS	Primary B cells from peripheral blood	blood
26	chr15:72929200-72929600	Active TSS	Primary T cells fromperipheralblood	blood
27	chr15:72929200-72929600	Active TSS	Primary T helper naive cells fromperipheralblood	blood
28	chr15:72929200-72929600	Active TSS	Primary T helper cells PMA-I stimulated	--
29	chr15:72929200-72929600	Active TSS	Primary T helper cells fromperipheralblood	blood
30	chr15:72929200-72929600	Active TSS	Primary T regulatory cells fromperipheralblood	blood
31	chr15:72929200-72929600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr15:72929200-72929600	Active TSS	Placenta	Placenta
33	chr15:72929200-72929600	Active TSS	Skeletal Muscle Female	skeletal muscle
34	chr15:72929200-72929600	Active TSS	HUVEC	blood vessel
35	chr15:72929200-72929800	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr15:72929200-72929800	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr15:72929200-72929800	Active TSS	Primary monocytes fromperipheralblood	blood
38	chr15:72929200-72929800	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
39	chr15:72929200-72929800	Active TSS	Cortex derived primary cultured neurospheres	brain
40	chr15:72929200-72929800	Active TSS	Brain Germinal Matrix	brain
41	chr15:72929200-72929800	Active TSS	Brain Hippocampus Middle	brain
42	chr15:72929200-72929800	Active TSS	Colonic Mucosa	Colon
43	chr15:72929200-72929800	Active TSS	Fetal Adrenal Gland	Adrenal Gland
44	chr15:72929200-72929800	Active TSS	Fetal Brain Female	brain
45	chr15:72929200-72929800	Active TSS	Fetal Intestine Large	intestine
46	chr15:72929200-72929800	Active TSS	Fetal Intestine Small	intestine
47	chr15:72929200-72929800	Active TSS	Fetal Muscle Leg	muscle
48	chr15:72929200-72929800	Active TSS	Fetal Stomach	stomach
49	chr15:72929200-72929800	Active TSS	Fetal Thymus	thymus
50	chr15:72929200-72929800	Active TSS	Psoas Muscle	Psoas

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