Variant report

Variant	nsv456737
Chromosome Location	chr15:29812777-29875999
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	ATF1	chr15:29832798-29832976	K562	blood:	n/a	n/a
2	BACH1	chr15:29863413-29863698	H1-hESC	embryonic stem cell:	n/a	n/a
3	BRCA1	chr15:29817858-29817874	GM12878	blood:	n/a	n/a
4	CEBPB	chr15:29843109-29843359	ECC-1	luminal epithelium:	n/a	chr15:29843169-29843182 chr15:29843234-29843245
5	CEBPB	chr15:29823826-29824001	A549	lung:	n/a	n/a
6	CEBPB	chr15:29843055-29843417	K562	blood:	n/a	chr15:29843169-29843182 chr15:29843234-29843245
7	CEBPB	chr15:29834820-29835020	K562	blood:	n/a	chr15:29834859-29834870
8	CEBPB	chr15:29834833-29834915	H1-hESC	embryonic stem cell:	n/a	chr15:29834859-29834870
9	CEBPB	chr15:29843077-29843415	HepG2	liver:	n/a	chr15:29843169-29843182 chr15:29843234-29843245
10	CEBPB	chr15:29843093-29843368	IMR90	lung:	n/a	chr15:29843169-29843182 chr15:29843234-29843245
11	CEBPB	chr15:29832931-29832995	HepG2	liver:	n/a	n/a
12	CEBPB	chr15:29843050-29843422	Hela-S3	cervix:	n/a	chr15:29843169-29843182 chr15:29843234-29843245
13	CEBPB	chr15:29825926-29826312	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr15:29823808-29824072	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr15:29843049-29843366	A549	lung:	n/a	chr15:29843169-29843182 chr15:29843234-29843245
16	CEBPB	chr15:29834710-29835015	HepG2	liver:	n/a	chr15:29834859-29834870
17	CEBPB	chr15:29843061-29843430	H1-hESC	embryonic stem cell:	n/a	chr15:29843169-29843182 chr15:29843234-29843245
18	CHD1	chr15:29863333-29863897	H1-hESC	embryonic stem cell:	n/a	chr15:29863399-29863409
19	CHD1	chr15:29862452-29862734	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD2	chr15:29863366-29863659	H1-hESC	embryonic stem cell:	n/a	chr15:29863399-29863409
21	CREB1	chr15:29861919-29862235	H1-hESC	embryonic stem cell:	n/a	n/a
22	CREB1	chr15:29861838-29862236	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr15:29862645-29862668	LNCaP	prostate:	n/a	n/a
24	CTCF	chr15:29861110-29861288	MCF-7	breast:	n/a	chr15:29861205-29861223
25	CTCF	chr15:29863386-29863447	MCF-7	breast:	n/a	n/a
26	CTCF	chr15:29861140-29861290	HEK293	kidney:	n/a	chr15:29861205-29861223
27	CTCF	chr15:29861120-29861270	HCPEpiC	choroid plexus:	n/a	chr15:29861205-29861223
28	CTCF	chr15:29861140-29861290	AG04449	skin:	n/a	chr15:29861205-29861223
29	CTCF	chr15:29861091-29861292	A549	lung:	n/a	chr15:29861205-29861223
30	CTCF	chr15:29861110-29861317	Pancreas_OC	pancreas:	n/a	chr15:29861205-29861223
31	CTCF	chr15:29861120-29861270	A549	lung:	n/a	chr15:29861205-29861223
32	CTCF	chr15:29865897-29865923	ProgFib	skin:	n/a	n/a
33	CTCF	chr15:29861093-29861320	A549	lung:	n/a	chr15:29861205-29861223
34	CTCF	chr15:29859220-29859370	HRE	kidney:	n/a	n/a
35	CTCF	chr15:29861120-29861287	A549	lung:	n/a	chr15:29861205-29861223
36	CTCF	chr15:29861140-29861290	SK-N-SH_RA	brain:	n/a	chr15:29861205-29861223
37	CTCF	chr15:29861091-29861387	A549	lung:	n/a	chr15:29861205-29861223
38	CTCF	chr15:29859300-29859450	RPTEC	kidney:	n/a	chr15:29859368-29859376
39	CTCF	chr15:29859300-29859450	HEK293	kidney:	n/a	chr15:29859368-29859376
40	CTCF	chr15:29861150-29861266	HUVEC	blood vessel:	n/a	chr15:29861205-29861223
41	CTCF	chr15:29862724-29862850	MCF-7	breast:	n/a	n/a
42	CTCF	chr15:29861100-29861250	HepG2	liver:	n/a	chr15:29861205-29861223
43	CTCF	chr15:29859320-29859470	BE2_C	brain:	n/a	chr15:29859368-29859376
44	CTCF	chr15:29860906-29861417	HCT-116	colon:	n/a	chr15:29861205-29861223
45	CTCF	chr15:29861160-29861310	NB4	blood:	n/a	chr15:29861205-29861223
46	CTCF	chr15:29861140-29861290	AG09309	skin:	n/a	chr15:29861205-29861223
47	CTCF	chr15:29865100-29865250	HRE	kidney:	n/a	n/a
48	CTCF	chr15:29861061-29861440	MCF-7	breast:	n/a	chr15:29861205-29861223
49	CTCF	chr15:29861140-29861290	HCFaa	heart:	n/a	chr15:29861205-29861223
50	CTCF	chr15:29832480-29832630	A549	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:29864169-29864219	HL-60	blood:	n/a
2	chr15:29863572-29863622	HMEC	breast:	n/a
3	chr15:29864169-29864219	HL-60	blood:	n/a
4	chr15:29863572-29863622	HMEC	breast:	n/a
5	chr15:29863572-29863622	Jurkat	blood:	n/a
6	chr15:29863572-29863622	HIPEpiC	eye:	n/a
7	chr15:29825929-29825979	HCT-116	colon:	n/a
8	chr15:29862568-29862618	RPTEC	kidney:	n/a
9	chr15:29863570-29863620	NH-A	brain:	n/a
10	chr15:29866755-29866805	LNCaP	prostate:	n/a
11	chr15:29861165-29861215	AG04449	skin:	fetal
12	chr15:29861165-29861215	A549	lung:	n/a
13	chr15:29825929-29825979	HCPEpiC	choroid plexus:	n/a
14	chr15:29863572-29863622	CMK	blood:	n/a
15	chr15:29862517-29862567	HL-60	blood:	n/a
16	chr15:29825929-29825979	SAEC	small airway:	n/a
17	chr15:29864169-29864219	GM12891	blood:	n/a
18	chr15:29862036-29862086	GM19239	blood:	n/a
19	chr15:29861165-29861215	SAEC	small airway:	n/a
20	chr15:29859427-29859477	HUVEC	blood vessel:	n/a
21	chr15:29861165-29861215	HL-60	blood:	n/a
22	chr15:29863570-29863620	IMR90	lung:	fetal
23	chr15:29825426-29825476	GM12891	blood:	n/a
24	chr15:29862517-29862567	AG04449	skin:	fetal
25	chr15:29863964-29864014	Caco-2	colon:	n/a
26	chr15:29825929-29825979	BJ	skin:	n/a
27	chr15:29863570-29863620	ECC-1	luminal epithelium:	n/a
28	chr15:29825929-29825979	MCF10A-Er-Src	breast:	n/a
29	chr15:29862517-29862567	HCPEpiC	choroid plexus:	n/a
30	chr15:29864140-29864190	HAEpiC	amniotic membrane:	n/a
31	chr15:29864169-29864219	ovcar-3	ovarian:	n/a
32	chr15:29862568-29862618	HCT-116	colon:	n/a
33	chr15:29859427-29859477	NH-A	brain:	n/a
34	chr15:29863964-29864014	BE2_C	brain:	n/a
35	chr15:29862036-29862086	Hela-S3	cervix:	n/a
36	chr15:29863964-29864014	Hepatocyte	liver:	n/a
37	chr15:29825426-29825476	H1-hESC	embryonic stem cell:	embryo
38	chr15:29859427-29859477	HEK293	kidney:	embryo
39	chr15:29863648-29863698	HCT-116	colon:	n/a
40	chr15:29863648-29863698	K562	blood:	n/a
41	chr15:29864140-29864190	HEK293	kidney:	embryo
42	chr15:29862568-29862618	HRE	kidney:	n/a
43	chr15:29864169-29864219	SK-N-SH_RA	brain:	n/a
44	chr15:29866755-29866805	NT2-D1	testis:	n/a
45	chr15:29863570-29863620	SK-N-MC	brain:	n/a
46	chr15:29864140-29864190	PrEC	prostate:	n/a
47	chr15:29861165-29861215	HEEpiC	esophagus:	n/a
48	chr15:29859427-29859477	HL-60	blood:	n/a
49	chr15:29863964-29864014	HPAEpiC	pulmonary alveolar:	n/a
50	chr15:29866755-29866805	HMEC	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr15:29853639..29856310-chr15:29888164..29890119,2	K562	blood:
2	chr15:29743174..29744066-chr15:29860740..29861596,5	MCF-7	breast:
3	chr15:29820815..29822568-chr15:29824443..29826210,2	K562	blood:
4	chr15:29743489..29744057-chr15:29860766..29861643,3	MCF-7	breast:
5	chr15:29820815..29822568-chr15:29824443..29826210,2	K562	blood:

Variant related genes	Relation type
FAM189A1	TF binding region
FAM189A1	CpG island

Extended variants
information (count: 2239 )
Associated
traits (count: 160 )

Variant overlapped rSNPs/rCNVs (count:2239 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs8028924	chr15:29812777-29812778	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs541170616	chr15:29812787-29812788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs79716142	chr15:29812906-29812907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs568686218	chr15:29812907-29812908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs556315100	chr15:29812934-29812935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs185494423	chr15:29812946-29812947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs189358101	chr15:29812971-29812972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs531709374	chr15:29813020-29813021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs545433867	chr15:29813054-29813055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs73369450	chr15:29813078-29813079	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs527981448	chr15:29813137-29813138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs548117411	chr15:29813170-29813171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs567751171	chr15:29813204-29813205	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs530355474	chr15:29813224-29813225	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs539267210	chr15:29813251-29813252	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs553900866	chr15:29813259-29813260	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs555629739	chr15:29813295-29813296	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs574072686	chr15:29813300-29813301	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs573966632	chr15:29813370-29813371	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs549446536	chr15:29813402-29813403	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs148358656	chr15:29813417-29813418	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs180835775	chr15:29813463-29813464	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs141534296	chr15:29813481-29813482	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs184099519	chr15:29813488-29813489	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs369059169	chr15:29813497-29813498	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs565713857	chr15:29813512-29813513	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs8041598	chr15:29813620-29813621	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs145762199	chr15:29813626-29813627	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs58002844	chr15:29813652-29813653	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs537272586	chr15:29813685-29813686	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs556660799	chr15:29813701-29813702	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs188632158	chr15:29813704-29813705	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs370824649	chr15:29813716-29813717	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs375341226	chr15:29813720-29813721	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs61310132	chr15:29813726-29813727	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs181084750	chr15:29813745-29813746	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs376655996	chr15:29813759-29813760	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs185914711	chr15:29813764-29813765	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs530196295	chr15:29813796-29813797	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs191648274	chr15:29813825-29813826	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs577939070	chr15:29813852-29813853	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs182340588	chr15:29813918-29813919	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs532070990	chr15:29813981-29813982	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs138485537	chr15:29813985-29813986	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs73369460	chr15:29814011-29814012	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs534649449	chr15:29814049-29814050	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs548151705	chr15:29814065-29814066	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs373092961	chr15:29814066-29814067	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs141485301	chr15:29814072-29814073	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs71132890	chr15:29814082-29814083	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:160)

Disease	PMID	Source
Ovarian cancer	21720365	CNVD
HDAC8	0	CNVD
NIPBL	0	CNVD
RAD21	0	CNVD
SMC1A	0	CNVD
SMC3	0	CNVD
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
idiopathic generalized epilepsy	19843651	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Prader-willi syndrome	21504564	CNVD
The inv dup or idic syndrome	19019226	CNVD
Prader-willi syndrome	21233802	CNVD
Angelman syndrome	16617304	CNVD
Angelman syndrome	20970697	CNVD
Autism	22958593	CNVD
Prader-willi syndrome	16617304	CNVD
Prader-willi syndrome	18923514	CNVD
Prader-willi syndrome	20970697	CNVD
Angelman syndrome	16183798	CNVD
Angelman syndrome	18923514	CNVD
Prader-willi syndrome	22241247	CNVD
Epilepsy	20970697	CNVD
Autism	20970697	CNVD
Autism	19935738	CNVD
Autism	22930557	CNVD
Autism	19966786	CNVD
Autism	18923514	CNVD
Autism	18925931	CNVD
Autism	18835857	CNVD
Prader-willi syndrome	18835857	CNVD
Prader-willi syndrome	22152151	CNVD
Autism	22241247	CNVD
15q-syndrome	21725066	CNVD
Prader-willi syndrome	21503198	CNVD
Autism	21956041	CNVD
Prader-willi syndrome	16760730	CNVD
Prader-willi syndrome	22470819	CNVD
prenatal diagnosis	20453657	CNVD
Prader-willi syndrome	17867985	CNVD
Angelman syndrome	21072004	CNVD
Acute lymphoblastic leukemia	20067559	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
Hodgkin''s lymphoma	18641027	CNVD
Prader-willi syndrome	18781185	CNVD
Melanoma	18172304	CNVD
Autism	17322880	CNVD
Prader-willi syndrome	19329560	CNVD
Autism	17999366	CNVD
Autism	17901113	CNVD
Neurodevelopmental disorder	17015230	CNVD
Autism	18414403	CNVD
Neurocytoma	17123091	CNVD
Mental retardation	18923513	CNVD
Colorectal cancer	16774939	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
Gastrointestinal stromal cancer	20818650	CNVD
Intellectual disability	22102821	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Schizophrenia	19197363	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
Angelman syndrome	18787571	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Abnormal corpus callosum	21572526	CNVD
Autism	20531469	CNVD
Neuropsychiatric disorder	20506139	CNVD
Austim spectrum disorder	21302340	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Mental retardation	17124404	CNVD
Autism	19204725	CNVD
Schizophrenia	19204725	CNVD
Schizophrenia	19149910	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Autism	19843651	CNVD
Schizophrenia	19843651	CNVD
Schizophrenia	23813976	CNVD
Cognitive impairment	21505072	CNVD
Epilepsy	20502679	CNVD
Autism	22543975	CNVD
small cell lung cancer	20016488	CNVD
Autism	22495309	CNVD
Schizophrenia	20388499	CNVD
Autism	20841430	CNVD
Epilepsy	22499536	CNVD
Schizophrenia	22499536	CNVD
Schizophrenia	18923514	CNVD
Bipolar disorder	19114987	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	22958593	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	20553308	CNVD
Schizophrenia	21956041	CNVD
Schizophrenia	20970697	CNVD
Mental retardation	19951919	CNVD
Mental retardation	21956041	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	21062444	CNVD
Autism	21269290	CNVD
Intellectual disability	21269290	CNVD
Schizophrenia	21269290	CNVD
Colorectal cancer	21128281	CNVD
Epilepsy	19289393	CNVD
Epilepsy	20643615	CNVD
Mental retardation	19289393	CNVD
Mental retardation	20152051	CNVD
Schizophrenia	19289393	CNVD
dysmorphic features	19289393	CNVD
idiopathic epilepsies	19341504	CNVD
idiopathic generalized epilepsy	19592580	CNVD
idiopathic generalized epilepsy	19136953	CNVD
Autism	22094647	CNVD
Developmental delay	19898479	CNVD
Mental retardation	18278044	CNVD
Mental retardation	19898479	CNVD
Prader-willi syndrome	18854863	CNVD
Schizophrenia	19855392	CNVD
Ovarian cancer	22174824	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
early-passage human iPS cells	21368824	CNVD
Cancer	20164919	CNVD

Chromatin state (count:594 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:29807600-29813200	Weak transcription	Pancreas	Pancrea
2	chr15:29810400-29814800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr15:29811000-29814800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr15:29812200-29822800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr15:29812600-29814800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr15:29813200-29813400	ZNF genes & repeats	Pancreas	Pancrea
7	chr15:29813200-29813600	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr15:29813200-29815400	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr15:29813400-29813800	Enhancers	H1 Cell Line	embryonic stem cell
10	chr15:29813400-29813800	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr15:29813400-29814000	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr15:29813400-29814800	Weak transcription	Pancreas	Pancrea
13	chr15:29813600-29814800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
14	chr15:29813600-29815400	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr15:29813800-29814000	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr15:29813800-29814800	Weak transcription	H1 Cell Line	embryonic stem cell
17	chr15:29813800-29814800	Weak transcription	HUES64 Cell Line	embryonic stem cell
18	chr15:29814000-29814400	Weak transcription	HUES6 Cell Line	embryonic stem cell
19	chr15:29814000-29814600	Weak transcription	HUES48 Cell Line	embryonic stem cell
20	chr15:29814200-29814600	Enhancers	A549	lung
21	chr15:29814400-29815400	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr15:29814600-29815000	Enhancers	Rectal Mucosa Donor 31	rectum
23	chr15:29814600-29815200	Flanking Active TSS	A549	lung
24	chr15:29814600-29815400	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr15:29814600-29815400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr15:29814600-29815400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr15:29814600-29815400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr15:29814600-29815400	Enhancers	NHEK	skin
29	chr15:29814800-29815200	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr15:29814800-29815200	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr15:29814800-29815200	Enhancers	Rectal Mucosa Donor 29	rectum
32	chr15:29814800-29815400	Enhancers	H1 Cell Line	embryonic stem cell
33	chr15:29814800-29815400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr15:29814800-29815400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr15:29814800-29815400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr15:29814800-29815400	Enhancers	Esophagus	oesophagus
37	chr15:29814800-29815400	Enhancers	Pancreas	Pancrea
38	chr15:29814800-29815400	Enhancers	HMEC	breast
39	chr15:29815200-29815400	Enhancers	H9 Cell Line	embryonic stem cell
40	chr15:29815200-29815800	Enhancers	A549	lung
41	chr15:29815400-29815600	Enhancers	Fetal Brain Male	brain
42	chr15:29815400-29815600	Weak transcription	Left Ventricle	heart
43	chr15:29815400-29820000	Weak transcription	Pancreas	Pancrea
44	chr15:29815400-29820200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr15:29815400-29821600	Weak transcription	H1 Cell Line	embryonic stem cell
46	chr15:29815400-29821600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr15:29815400-29823000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
48	chr15:29815400-29823200	Weak transcription	H9 Cell Line	embryonic stem cell
49	chr15:29817800-29818000	Enhancers	Pancreatic Islets	Pancreatic Islet
50	chr15:29818800-29819000	Weak transcription	Fetal Brain Male	brain

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