Variant report

Variant	nsv521903
Chromosome Location	chr15:33289949-33301508
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	BHLHE40	chr15:33297971-33297975	GM12878	blood:	n/a	n/a
2	CEBPB	chr15:33291617-33291899	IMR90	lung:	n/a	chr15:33291772-33291781 chr15:33291772-33291781 chr15:33291772-33291781 chr15:33291772-33291781 chr15:33291745-33291757 chr15:33291772-33291783 chr15:33291770-33291783
3	CHD2	chr15:33297906-33298083	GM12878	blood:	n/a	n/a
4	CTCF	chr15:33299613-33299755	MCF-7	breast:	n/a	chr15:33299644-33299665 chr15:33299647-33299655
5	CTCF	chr15:33299589-33299707	SK-N-SH_RA	brain:	n/a	chr15:33299644-33299665 chr15:33299647-33299655
6	CTCF	chr15:33299500-33299650	HFF-Myc	foreskin:	n/a	n/a
7	CTCF	chr15:33299446-33299779	A549	lung:	n/a	chr15:33299644-33299665 chr15:33299647-33299655
8	CTCF	chr15:33299600-33299750	BJ	skin:	n/a	chr15:33299644-33299665 chr15:33299647-33299655
9	CTCF	chr15:33299507-33299769	LNCaP	prostate:	n/a	chr15:33299644-33299665 chr15:33299647-33299655
10	CTCF	chr15:33299500-33299650	NHEK	skin:	n/a	n/a
11	CTCF	chr15:33299618-33299726	Lung_OC	lung:	n/a	chr15:33299644-33299665 chr15:33299647-33299655
12	CTCF	chr15:33299580-33299730	AG09319	gingival:	n/a	chr15:33299644-33299665 chr15:33299647-33299655
13	CTCF	chr15:33299560-33299710	AG09309	skin:	n/a	chr15:33299644-33299665 chr15:33299647-33299655
14	CTCF	chr15:33299651-33299720	GM19240	blood:	n/a	n/a
15	CTCF	chr15:33299580-33299730	Caco-2	colon:	n/a	chr15:33299644-33299665 chr15:33299647-33299655
16	CTCF	chr15:33299464-33300128	A549	lung:	n/a	chr15:33299644-33299665 chr15:33299647-33299655
17	CTCF	chr15:33299606-33299757	MCF-7	breast:	n/a	chr15:33299644-33299665 chr15:33299647-33299655
18	CTCF	chr15:33299560-33299710	HMEC	breast:	n/a	chr15:33299644-33299665 chr15:33299647-33299655
19	CTCF	chr15:33299600-33299750	HFF-Myc	foreskin:	n/a	chr15:33299644-33299665 chr15:33299647-33299655
20	CTCF	chr15:33299546-33299790	ProgFib	skin:	n/a	chr15:33299644-33299665 chr15:33299647-33299655
21	CTCF	chr15:33299575-33299743	Medullo	brain:	n/a	chr15:33299644-33299665 chr15:33299647-33299655
22	CTCF	chr15:33299720-33299870	A549	lung:	n/a	n/a
23	CTCF	chr15:33299600-33299750	NHLF	lung:	n/a	chr15:33299644-33299665 chr15:33299647-33299655
24	CTCF	chr15:33299580-33299730	GM12872	blood:	n/a	chr15:33299644-33299665 chr15:33299647-33299655
25	CTCF	chr15:33299600-33299750	HMEC	breast:	n/a	chr15:33299644-33299665 chr15:33299647-33299655
26	CTCF	chr15:33299540-33299690	HRE	kidney:	n/a	chr15:33299644-33299665 chr15:33299647-33299655
27	CTCF	chr15:33299527-33299794	IMR90	lung:	n/a	chr15:33299644-33299665 chr15:33299647-33299655
28	CTCF	chr15:33299580-33299730	MCF-7	breast:	n/a	chr15:33299644-33299665 chr15:33299647-33299655
29	CTCF	chr15:33299543-33299802	A549	lung:	n/a	chr15:33299644-33299665 chr15:33299647-33299655
30	CTCF	chr15:33299569-33299765	NHEK	skin:	n/a	chr15:33299644-33299665 chr15:33299647-33299655
31	CTCF	chr15:33299621-33299699	Pancreas_OC	pancreas:	n/a	chr15:33299644-33299665 chr15:33299647-33299655
32	CTCF	chr15:33299549-33299723	A549	lung:	n/a	chr15:33299644-33299665 chr15:33299647-33299655
33	CTCF	chr15:33299630-33299732	H1-hESC	embryonic stem cell:	n/a	chr15:33299644-33299665 chr15:33299647-33299655
34	CTCF	chr15:33298540-33298690	HCPEpiC	choroid plexus:	n/a	n/a
35	CTCF	chr15:33299460-33299610	HAc	cerebellar:	n/a	n/a
36	CTCF	chr15:33299540-33299690	HCT-116	colon:	n/a	chr15:33299644-33299665 chr15:33299647-33299655
37	CTCF	chr15:33299540-33299690	HCFaa	heart:	n/a	chr15:33299644-33299665 chr15:33299647-33299655
38	CTCF	chr15:33299560-33299710	AG04450	lung:	n/a	chr15:33299644-33299665 chr15:33299647-33299655
39	CTCF	chr15:33299598-33299735	HepG2	liver:	n/a	chr15:33299644-33299665 chr15:33299647-33299655
40	CTCF	chr15:33299660-33299810	AG04450	lung:	n/a	n/a
41	CTCF	chr15:33299592-33299745	GM12878	blood:	n/a	chr15:33299644-33299665 chr15:33299647-33299655
42	CTCF	chr15:33299600-33299750	HAc	cerebellar:	n/a	chr15:33299644-33299665 chr15:33299647-33299655
43	CTCF	chr15:33299540-33299690	HPF	lung:	n/a	chr15:33299644-33299665 chr15:33299647-33299655
44	CTCF	chr15:33299580-33299730	HCM	heart:	n/a	chr15:33299644-33299665 chr15:33299647-33299655
45	CTCF	chr15:33299600-33299750	WERI-Rb-1	eye:	n/a	chr15:33299644-33299665 chr15:33299647-33299655
46	CTCF	chr15:33299560-33299710	HMF	breast:	n/a	chr15:33299644-33299665 chr15:33299647-33299655
47	CTCF	chr15:33299580-33299730	HEEpiC	esophagus:	n/a	chr15:33299644-33299665 chr15:33299647-33299655
48	CTCF	chr15:33299580-33299730	HBMEC	blood vessel:	n/a	chr15:33299644-33299665 chr15:33299647-33299655
49	CTCF	chr15:33299560-33299710	HEEpiC	esophagus:	n/a	chr15:33299644-33299665 chr15:33299647-33299655
50	CTCF	chr15:33299580-33299730	HEK293	kidney:	n/a	chr15:33299644-33299665 chr15:33299647-33299655

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:33300472-33300522	HNPCEpiC	eye:	n/a
2	chr15:33300472-33300522	MCF-7	breast:	n/a
3	chr15:33300472-33300522	AG10803	skin:	n/a
4	chr15:33300472-33300522	AoSMC	blood vessel:	n/a
5	chr15:33300472-33300522	GM12878	blood:	n/a
6	chr15:33300472-33300522	PFSK-1	brain:	n/a
7	chr15:33300472-33300522	A549	lung:	n/a
8	chr15:33300472-33300522	Hepatocyte	liver:	n/a
9	chr15:33300472-33300522	CMK	blood:	n/a
10	chr15:33300472-33300522	Jurkat	blood:	n/a
11	chr15:33300472-33300522	Caco-2	colon:	n/a
12	chr15:33300472-33300522	GM19239	blood:	n/a
13	chr15:33300472-33300522	BJ	skin:	n/a
14	chr15:33300472-33300522	ovcar-3	ovarian:	n/a
15	chr15:33300472-33300522	HPAEpiC	pulmonary alveolar:	n/a
16	chr15:33300472-33300522	H1-hESC	embryonic stem cell:	embryo
17	chr15:33300472-33300522	T-47D	breast:	n/a
18	chr15:33300472-33300522	HAEpiC	amniotic membrane:	n/a
19	chr15:33300472-33300522	HCPEpiC	choroid plexus:	n/a
20	chr15:33300472-33300522	AG09309	skin:	n/a
21	chr15:33300472-33300522	HIPEpiC	eye:	n/a
22	chr15:33300472-33300522	HRCEpiC	kidney:	n/a
23	chr15:33300472-33300522	NHDF-neo	bronchial:	n/a
24	chr15:33300472-33300522	RPTEC	kidney:	n/a
25	chr15:33300472-33300522	Hela-S3	cervix:	n/a
26	chr15:33300472-33300522	SK-N-SH_RA	brain:	n/a
27	chr15:33300472-33300522	GM06990	blood:	n/a
28	chr15:33300472-33300522	HMEC	breast:	n/a
29	chr15:33300472-33300522	HL-60	blood:	n/a
30	chr15:33300472-33300522	ProgFib	skin:	n/a
31	chr15:33300472-33300522	PANC-1	pancreas:	n/a
32	chr15:33300472-33300522	ECC-1	luminal epithelium:	n/a
33	chr15:33300472-33300522	HEEpiC	esophagus:	n/a
34	chr15:33300472-33300522	SKMC	muscle:	n/a
35	chr15:33300472-33300522	NH-A	brain:	n/a
36	chr15:33300472-33300522	HRE	kidney:	n/a
37	chr15:33300472-33300522	IMR90	lung:	fetal
38	chr15:33300472-33300522	LNCaP	prostate:	n/a
39	chr15:33300472-33300522	NHBE	bronchial:	n/a
40	chr15:33300472-33300522	AG04450	lung:	fetal
41	chr15:33300472-33300522	SAEC	small airway:	n/a
42	chr15:33300472-33300522	U87	brain:	n/a
43	chr15:33300472-33300522	SK-N-MC	brain:	n/a
44	chr15:33300472-33300522	HRPEpiC	eye:	n/a
45	chr15:33300472-33300522	NB4	blood:	n/a
46	chr15:33300472-33300522	SK-N-SH	brain:	n/a
47	chr15:33300472-33300522	MCF10A-Er-Src	breast:	n/a
48	chr15:33300472-33300522	PrEC	prostate:	n/a
49	chr15:33300472-33300522	HUVEC	blood vessel:	n/a
50	chr15:33300472-33300522	GM12891	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr15:33276577..33278445-chr15:33292733..33295082,2	MCF-7	breast:
2	chr15:33300871..33303669-chr15:33360060..33362322,2	MCF-7	breast:
3	chr15:33301497..33303169-chr15:33347240..33349716,2	MCF-7	breast:
4	chr15:33298305..33300128-chr15:33304629..33307307,2	MCF-7	breast:
5	chr15:33299011..33299669-chr15:33424327..33425140,2	MCF-7	breast:
6	chr15:33287991..33290554-chr15:33293399..33295008,2	K562	blood:
7	chr15:33299875..33302830-chr15:33303027..33306565,4	MCF-7	breast:
8	chr15:33287991..33290554-chr15:33293399..33295008,2	K562	blood:
9	chr15:33289408..33292508-chr15:33359912..33362781,5	MCF-7	breast:
10	chr15:33297830..33309224-chr15:33355310..33362883,25	MCF-7	breast:
11	chr15:33298321..33300066-chr15:33361018..33362893,2	MCF-7	breast:

Variant related genes	Relation type
HNRNPA1P71	TF binding region
HNRNPA1P71	CpG island
ENSG00000259686	chromatin interactions
ENSG00000248905	chromatin interactions

Extended variants
information (count: 583 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:583 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs747349	chr15:33289949-33289950	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs76701377	chr15:33289950-33289951	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs559105120	chr15:33289982-33289983	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs560511495	chr15:33289983-33289984	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs372882578	chr15:33289995-33289996	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs142631408	chr15:33290012-33290013	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs747350	chr15:33290016-33290017	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs73374808	chr15:33290038-33290039	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs538864594	chr15:33290046-33290047	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs149307187	chr15:33290086-33290087	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs568200085	chr15:33290095-33290096	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs569158539	chr15:33290103-33290104	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs536126865	chr15:33290135-33290136	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs144491740	chr15:33290228-33290229	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs148442149	chr15:33290241-33290242	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs76725	chr15:33290270-33290271	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs59310964	chr15:33290282-33290283	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs577257808	chr15:33290312-33290313	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs544825680	chr15:33290361-33290362	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs550624490	chr15:33290371-33290372	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs115566711	chr15:33290503-33290504	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs71462834	chr15:33290540-33290541	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs371351997	chr15:33290544-33290545	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs555774594	chr15:33290553-33290554	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs74012449	chr15:33290555-33290556	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs191631771	chr15:33290587-33290588	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs56203939	chr15:33290607-33290608	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs532085726	chr15:33290623-33290624	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs550772041	chr15:33290637-33290638	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs112409471	chr15:33290646-33290647	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs568926359	chr15:33290649-33290650	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs140310555	chr15:33290653-33290654	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs343918	chr15:33290655-33290656	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs17816633	chr15:33290666-33290667	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs534226458	chr15:33290680-33290681	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs369524817	chr15:33290698-33290699	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs558978016	chr15:33290745-33290746	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs199629564	chr15:33290752-33290753	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs570954358	chr15:33290761-33290762	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs144896188	chr15:33290794-33290795	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs556725589	chr15:33290826-33290827	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs574888197	chr15:33290828-33290829	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs56153957	chr15:33290855-33290856	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs554084107	chr15:33290864-33290865	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs572386779	chr15:33290865-33290866	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs4780061	chr15:33290875-33290876	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs539868237	chr15:33290881-33290882	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs564695879	chr15:33290915-33290916	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs377517593	chr15:33290956-33290957	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs140543555	chr15:33290957-33290958	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
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
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Angelman syndrome	16183798	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
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
Intellectual disability	22102821	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	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
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Abnormal corpus callosum	21572526	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Autism	19204725	CNVD
Schizophrenia	19204725	CNVD
Schizophrenia	19149910	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Autism	19521722	CNVD
Bipolar disorder	19114987	CNVD
Epilepsy	19521722	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	19521646	CNVD
Autism	19050728	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18668039	CNVD
Schizophrenia	18990708	CNVD
Schizophrenia	19571808	CNVD
Velocardiofacial syndrome	19329560	CNVD
Schizophrenia	19443537	CNVD
Epilepsy	20923578	CNVD
Autism	19955444	CNVD
Autism	20964600	CNVD
Schizophrenia	19955444	CNVD
Olfactory neuroblastoma	18408657	CNVD
Legius syndrome	19443465	CNVD
Holoprosencephaly	21359414	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:178 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:33273200-33294000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr15:33286000-33290000	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr15:33286000-33294000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr15:33286800-33300000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr15:33286800-33301200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr15:33287200-33290200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr15:33287200-33291800	Weak transcription	HSMM	muscle
8	chr15:33287200-33294000	Weak transcription	Osteobl	bone
9	chr15:33287200-33300400	Weak transcription	NHDF-Ad	bronchial
10	chr15:33288800-33290200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr15:33288800-33309200	Weak transcription	Rectal Mucosa Donor 31	rectum
12	chr15:33289000-33291000	Weak transcription	Sigmoid Colon	Sigmoid Colon
13	chr15:33289200-33298800	Weak transcription	Fetal Thymus	thymus
14	chr15:33289400-33290200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr15:33289400-33299400	Weak transcription	NHLF	lung
16	chr15:33289800-33290200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr15:33289800-33292200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr15:33290000-33291000	Enhancers	Pancreatic Islets	Pancreatic Islet
19	chr15:33290200-33291000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr15:33290200-33291400	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr15:33290200-33292000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr15:33291000-33291200	Enhancers	Sigmoid Colon	Sigmoid Colon
23	chr15:33291000-33291400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr15:33291000-33299200	Weak transcription	Pancreatic Islets	Pancreatic Islet
25	chr15:33291200-33301200	Weak transcription	Sigmoid Colon	Sigmoid Colon
26	chr15:33291400-33292000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr15:33291400-33292400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr15:33291400-33292400	Enhancers	Adipose Nuclei	Adipose
29	chr15:33291800-33292400	ZNF genes & repeats	HSMM	muscle
30	chr15:33292000-33292400	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr15:33292000-33292400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr15:33292200-33299200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr15:33292400-33292800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr15:33292400-33293800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr15:33292400-33293800	Weak transcription	HSMM	muscle
36	chr15:33292400-33299400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr15:33292800-33293000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr15:33293000-33293400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr15:33293400-33293600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr15:33293600-33294000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr15:33293800-33294400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr15:33293800-33294400	Enhancers	HSMM	muscle
43	chr15:33293800-33294800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr15:33294000-33294400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr15:33294000-33294400	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr15:33294000-33294800	Enhancers	Muscle Satellite Cultured Cells	--
47	chr15:33294000-33294800	Enhancers	HUVEC	blood vessel
48	chr15:33294000-33294800	Enhancers	NH-A	brain
49	chr15:33294000-33294800	Enhancers	Osteobl	bone
50	chr15:33294000-33295000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

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