Variant report

Variant	nsv1050535
Chromosome Location	chr15:53352572-53472957
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:330)
CpG islands
(count:123)
Chromatin interactive
region (count:27)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:330 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr15:53354867-53354946	K562	blood:	n/a	n/a
2	BACH1	chr15:53424601-53424612	K562	blood:	n/a	n/a
3	CBX3	chr15:53364324-53364710	HCT-116	colon:	n/a	n/a
4	CEBPB	chr15:53435728-53436063	HepG2	liver:	n/a	chr15:53435895-53435906
5	CEBPB	chr15:53369787-53369848	A549	lung:	n/a	chr15:53369789-53369800 chr15:53369789-53369802
6	CEBPB	chr15:53435722-53436004	IMR90	lung:	n/a	chr15:53435895-53435906
7	CEBPB	chr15:53394804-53394982	HepG2	liver:	n/a	chr15:53394870-53394881
8	CEBPB	chr15:53450526-53450844	IMR90	lung:	n/a	chr15:53450666-53450677
9	CEBPB	chr15:53423121-53423484	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr15:53450483-53450832	MCF-7	breast:	n/a	chr15:53450666-53450677
11	CEBPB	chr15:53450535-53450833	HepG2	liver:	n/a	chr15:53450666-53450677
12	CEBPB	chr15:53450508-53450855	A549	lung:	n/a	chr15:53450666-53450677
13	CEBPB	chr15:53458663-53458973	HepG2	liver:	n/a	chr15:53458827-53458838 chr15:53458826-53458839
14	CEBPB	chr15:53435690-53436040	MCF-7	breast:	n/a	chr15:53435895-53435906
15	CEBPB	chr15:53456248-53456254	HepG2	liver:	n/a	n/a
16	CEBPB	chr15:53435745-53436076	A549	lung:	n/a	chr15:53435895-53435906
17	CHD1	chr15:53403047-53403168	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD2	chr15:53364346-53364644	Hela-S3	cervix:	n/a	n/a
19	CREB1	chr15:53364391-53364729	A549	lung:	n/a	n/a
20	CTCF	chr15:53385980-53386130	SK-N-SH_RA	brain:	n/a	chr15:53386057-53386064
21	CTCF	chr15:53364420-53364570	GM12864	blood:	n/a	n/a
22	CTCF	chr15:53452520-53452670	A549	lung:	n/a	n/a
23	CTCF	chr15:53386020-53386170	A549	lung:	n/a	chr15:53386057-53386064
24	CTCF	chr15:53470228-53470291	HepG2	liver:	n/a	chr15:53470243-53470264 chr15:53470248-53470266
25	CTCF	chr15:53431477-53431558	GM13977	blood:	n/a	n/a
26	CTCF	chr15:53452400-53452550	HepG2	liver:	n/a	n/a
27	CTCF	chr15:53470220-53470370	MCF-7	breast:	n/a	chr15:53470243-53470264 chr15:53470248-53470266
28	CTCF	chr15:53385940-53386090	MCF-7	breast:	n/a	chr15:53386057-53386064
29	CTCF	chr15:53423320-53423470	A549	lung:	n/a	n/a
30	CTCF	chr15:53439366-53439405	GM13976	blood:	n/a	n/a
31	CTCF	chr15:53378009-53378140	GM10248	blood:	n/a	n/a
32	CTCF	chr15:53452483-53452553	MCF-7	breast:	n/a	n/a
33	CTCF	chr15:53452452-53452602	HepG2	liver:	n/a	n/a
34	CTCF	chr15:53420040-53420190	GM12866	blood:	n/a	n/a
35	CTCF	chr15:53452429-53452600	HepG2	liver:	n/a	n/a
36	CTCF	chr15:53452436-53452597	A549	lung:	n/a	n/a
37	CTCF	chr15:53452480-53452630	HepG2	liver:	n/a	n/a
38	CTCF	chr15:53470240-53470390	MCF-7	breast:	n/a	chr15:53470243-53470264 chr15:53470248-53470266
39	CTCF	chr15:53386020-53386170	MCF-7	breast:	n/a	chr15:53386057-53386064
40	CTCF	chr15:53452440-53452590	WERI-Rb-1	eye:	n/a	n/a
41	CTCF	chr15:53407283-53407349	Pancreas_OC	pancreas:	n/a	n/a
42	CTCF	chr15:53460280-53460430	NB4	blood:	n/a	n/a
43	CTCF	chr15:53378026-53378138	Kidney_OC	kidney:	n/a	n/a
44	E2F4	chr15:53387861-53388070	MCF10A-Er-Src	breast:	n/a	n/a
45	E2F4	chr15:53364424-53364665	MCF10A-Er-Src	breast:	n/a	n/a
46	EBF1	chr15:53384232-53384240	GM12878	blood:	n/a	n/a
47	ELF1	chr15:53463867-53464134	HepG2	liver:	n/a	n/a
48	ELF1	chr15:53363901-53364912	MCF-7	breast:	n/a	n/a
49	ELF1	chr15:53463931-53464177	HepG2	liver:	n/a	n/a
50	EP300	chr15:53364248-53364645	T-47D	breast:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:53422311-53422361	GM19239	blood:	n/a
2	chr15:53422311-53422361	GM19239	blood:	n/a
3	chr15:53372675-53372725	NH-A	brain:	n/a
4	chr15:53372675-53372725	AG09319	gingival:	n/a
5	chr15:53372675-53372725	HCPEpiC	choroid plexus:	n/a
6	chr15:53422311-53422361	HNPCEpiC	eye:	n/a
7	chr15:53372675-53372725	GM06990	blood:	n/a
8	chr15:53372675-53372725	NB4	blood:	n/a
9	chr15:53422311-53422361	GM12878	blood:	n/a
10	chr15:53422311-53422361	PANC-1	pancreas:	n/a
11	chr15:53372675-53372725	HCF	heart:	n/a
12	chr15:53372675-53372725	GM12891	blood:	n/a
13	chr15:53422311-53422361	GM12892	blood:	n/a
14	chr15:53372675-53372725	AG10803	skin:	n/a
15	chr15:53422311-53422361	K562	blood:	n/a
16	chr15:53372675-53372725	AoSMC	blood vessel:	n/a
17	chr15:53422311-53422361	BE2_C	brain:	n/a
18	chr15:53372675-53372725	Jurkat	blood:	n/a
19	chr15:53422311-53422361	HRE	kidney:	n/a
20	chr15:53422311-53422361	HRCEpiC	kidney:	n/a
21	chr15:53422311-53422361	NHBE	bronchial:	n/a
22	chr15:53422311-53422361	HL-60	blood:	n/a
23	chr15:53422311-53422361	AoSMC	blood vessel:	n/a
24	chr15:53372675-53372725	AG09309	skin:	n/a
25	chr15:53422311-53422361	SK-N-MC	brain:	n/a
26	chr15:53422311-53422361	HCPEpiC	choroid plexus:	n/a
27	chr15:53372675-53372725	SKMC	muscle:	n/a
28	chr15:53372675-53372725	NHBE	bronchial:	n/a
29	chr15:53422311-53422361	ECC-1	luminal epithelium:	n/a
30	chr15:53422311-53422361	HEEpiC	esophagus:	n/a
31	chr15:53372675-53372725	HEEpiC	esophagus:	n/a
32	chr15:53422311-53422361	MCF-7	breast:	n/a
33	chr15:53372675-53372725	ovcar-3	ovarian:	n/a
34	chr15:53422311-53422361	AG04450	lung:	fetal
35	chr15:53372675-53372725	SK-N-MC	brain:	n/a
36	chr15:53422311-53422361	LNCaP	prostate:	n/a
37	chr15:53422311-53422361	HIPEpiC	eye:	n/a
38	chr15:53372675-53372725	AG04449	skin:	fetal
39	chr15:53422311-53422361	AG09319	gingival:	n/a
40	chr15:53422311-53422361	GM06990	blood:	n/a
41	chr15:53422311-53422361	AG10803	skin:	n/a
42	chr15:53422311-53422361	HPAEpiC	pulmonary alveolar:	n/a
43	chr15:53372675-53372725	HPAEpiC	pulmonary alveolar:	n/a
44	chr15:53422311-53422361	SK-N-SH_RA	brain:	n/a
45	chr15:53372675-53372725	RPTEC	kidney:	n/a
46	chr15:53372675-53372725	Caco-2	colon:	n/a
47	chr15:53372675-53372725	GM12892	blood:	n/a
48	chr15:53372675-53372725	CMK	blood:	n/a
49	chr15:53372675-53372725	SK-N-SH	brain:	n/a
50	chr15:53372675-53372725	BJ	skin:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:53364390..53366274-chr15:53368340..53370470,3	MCF-7	breast:
2	chr15:53318089..53321018-chr15:53355252..53357036,2	MCF-7	breast:
3	chr15:53438169..53441367-chr15:53443605..53446504,3	MCF-7	breast:
4	chr15:53463040..53465970-chr15:53466273..53469129,2	MCF-7	breast:
5	chr15:53412161..53414398-chr15:53418222..53421112,2	MCF-7	breast:
6	chr15:53364183..53365120-chr15:53374984..53375519,2	MCF-7	breast:
7	chr15:53398769..53401159-chr15:53403733..53405993,2	K562	blood:
8	chr15:53436114..53438272-chr15:53440682..53443510,2	MCF-7	breast:
9	chr15:53364183..53365120-chr15:53374984..53375519,2	MCF-7	breast:
10	chr15:53369383..53371838-chr15:53381998..53383881,2	K562	blood:
11	chr15:53398769..53401159-chr15:53403733..53405993,2	K562	blood:
12	chr15:53406863..53408730-chr15:53409145..53411501,2	MCF-7	breast:
13	chr15:53412161..53414398-chr15:53418222..53421112,2	MCF-7	breast:
14	chr15:53367799..53369631-chr15:53373514..53375161,2	MCF-7	breast:
15	chr15:53463040..53465970-chr15:53466273..53469129,2	MCF-7	breast:
16	chr15:53363971..53364789-chr15:53374593..53375688,3	MCF-7	breast:
17	chr15:53452155..53452718-chr15:53489026..53490168,3	MCF-7	breast:
18	chr15:53146326..53147158-chr15:53363981..53364531,2	MCF-7	breast:
19	chr15:53363971..53364789-chr15:53374593..53375688,3	MCF-7	breast:
20	chr15:53447164..53449219-chr15:53451381..53453427,2	K562	blood:
21	chr15:53447164..53449219-chr15:53451381..53453427,2	K562	blood:
22	chr15:53364390..53366274-chr15:53368340..53370470,3	MCF-7	breast:
23	chr15:53367799..53369631-chr15:53373514..53375161,2	MCF-7	breast:
24	chr15:53438169..53441367-chr15:53443605..53446504,3	MCF-7	breast:
25	chr15:53364212..53364797-chr15:53623796..53624629,2	MCF-7	breast:
26	chr15:53436114..53438272-chr15:53440682..53443510,2	MCF-7	breast:
27	chr15:53369383..53371838-chr15:53381998..53383881,2	K562	blood:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UNC13C-1	chr15:53410416-53410462	ENSG00000259237.1
2	lnc-UNC13C-2	chr15:53392927-53393040	XLOC_011259
3	lnc-ONECUT1-4	chr15:53397038-53397355	expReg_chr15_3758_-
4	lnc-UNC13C-1	chr15:53421436-53421895	ENSG00000259237.1
5	lnc-UNC13C-2	chr15:53375073-53375267	XLOC_011259
6	lnc-UNC13C-2	chr15:53392927-53393040	XLOC_011259
7	lnc-UNC13C-6	chr15:53360686-53360774	NONHSAT043960
8	lnc-UNC13C-6	chr15:53362262-53362447	NONHSAT043960
9	lnc-UNC13C-2	chr15:53393714-53393924	NONHSAT043961
10	lnc-UNC13C-2	chr15:53393715-53393924	XLOC_011259
11	lnc-UNC13C-2	chr15:53392926-53393040	NONHSAT043961
12	lnc-UNC13C-1	chr15:53408562-53408655	ENSG00000259237.1
13	lnc-UNC13C-2	chr15:53375035-53375267	NONHSAT043961
14	lnc-UNC13C-2	chr15:53375036-53375267	XLOC_011259

No data

Variant related genes	Relation type
ENSG00000259237	TF binding region
ENSG00000259237	CpG island
ENSG00000259237	chromatin interactions
PWP1	miRNA target sites
DMXL1	miRNA target sites
RBM10	miRNA target sites
DMTF1	miRNA target sites
SMG1	miRNA target sites

Extended variants
information (count: 2203 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:2203 , 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	rs370645241	chr15:53352610-53352611	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs562143331	chr15:53352617-53352618	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs530898593	chr15:53352636-53352637	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs551060841	chr15:53352657-53352658	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs550754982	chr15:53352703-53352704	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs570907069	chr15:53352737-53352738	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs533585624	chr15:53352771-53352772	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs547279564	chr15:53352782-53352783	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs185447396	chr15:53352789-53352790	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs536182629	chr15:53352793-53352794	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs140276156	chr15:53352854-53352855	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs568090197	chr15:53352868-53352869	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs536707473	chr15:53352895-53352896	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs7165208	chr15:53352914-53352915	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs547095154	chr15:53352924-53352925	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs571030094	chr15:53352959-53352960	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs576934324	chr15:53352990-53352991	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs438069	chr15:53353038-53353039	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs145280294	chr15:53353054-53353055	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs61460460	chr15:53353164-53353165	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs146412183	chr15:53353176-53353177	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs541771166	chr15:53353180-53353181	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs371595501	chr15:53353185-53353186	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs561892351	chr15:53353195-53353196	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs575595515	chr15:53353223-53353224	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs544348841	chr15:53353266-53353267	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs564617576	chr15:53353305-53353306	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs16965401	chr15:53353311-53353312	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs80120390	chr15:53353317-53353318	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs371394853	chr15:53353346-53353347	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs115433649	chr15:53353428-53353429	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs549660876	chr15:53353468-53353469	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs190137721	chr15:53353472-53353473	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs181999011	chr15:53353483-53353484	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs537072202	chr15:53353494-53353495	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs186539151	chr15:53353510-53353511	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs192381284	chr15:53353516-53353517	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs140727636	chr15:53353522-53353523	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs552748454	chr15:53353545-53353546	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs183262136	chr15:53353620-53353621	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs450081	chr15:53353634-53353635	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs555652876	chr15:53353660-53353661	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs9920517	chr15:53353664-53353665	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs138323968	chr15:53353666-53353667	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs564351486	chr15:53353759-53353760	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs371575959	chr15:53353781-53353782	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs199729448	chr15:53353800-53353801	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs114911040	chr15:53353816-53353817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs540769522	chr15:53353817-53353818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs560629717	chr15:53353848-53353849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	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
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
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	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
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	22032731	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Cancer	21129771	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Myelofibrosis	22110671	CNVD
Acute monocytic leukemia	16498392	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Melanoma	21949216	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Ovarian cancer	21781307	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Renal cell carcinoma	21215367	CNVD

Chromatin state (count:141 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:53351200-53352800	Enhancers	HepG2	liver
2	chr15:53352400-53353200	Enhancers	Liver	Liver
3	chr15:53352400-53353800	Enhancers	Dnd41	blood
4	chr15:53353200-53364200	Weak transcription	Liver	Liver
5	chr15:53353800-53356600	Weak transcription	Dnd41	blood
6	chr15:53356600-53357200	Enhancers	Dnd41	blood
7	chr15:53359600-53361800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr15:53360600-53361600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr15:53362200-53363000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr15:53362600-53363200	Enhancers	NHEK	skin
11	chr15:53362800-53364200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr15:53363200-53364000	Weak transcription	NHEK	skin
13	chr15:53363200-53365200	Enhancers	Pancreas	Pancrea
14	chr15:53364000-53364400	Enhancers	Gastric	stomach
15	chr15:53364000-53364400	Enhancers	NH-A	brain
16	chr15:53364000-53364400	Enhancers	NHEK	skin
17	chr15:53364000-53364600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr15:53364000-53364600	Enhancers	Brain Inferior Temporal Lobe	brain
19	chr15:53364200-53364600	Enhancers	Liver	Liver
20	chr15:53364400-53364600	Weak transcription	NHEK	skin
21	chr15:53364600-53365000	Enhancers	NHEK	skin
22	chr15:53372000-53373200	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr15:53372000-53373400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr15:53372000-53373600	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr15:53372200-53373200	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr15:53372200-53373400	Enhancers	H1 Cell Line	embryonic stem cell
27	chr15:53372400-53373400	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr15:53372600-53373400	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr15:53385000-53385800	Enhancers	Liver	Liver
30	chr15:53394600-53395400	Enhancers	Liver	Liver
31	chr15:53395000-53395200	Enhancers	Pancreas	Pancrea
32	chr15:53395200-53399600	Weak transcription	Pancreas	Pancrea
33	chr15:53397800-53398000	Enhancers	H9 Cell Line	embryonic stem cell
34	chr15:53398000-53402600	Weak transcription	H9 Cell Line	embryonic stem cell
35	chr15:53400400-53400600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr15:53400600-53400800	Enhancers	ES-I3 Cell Line	embryonic stem cell
37	chr15:53400600-53400800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
38	chr15:53400600-53401200	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr15:53400800-53402600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
40	chr15:53401000-53402600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr15:53401200-53403000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
42	chr15:53402200-53403400	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr15:53402400-53404400	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr15:53402600-53402800	Enhancers	H9 Cell Line	embryonic stem cell
45	chr15:53402600-53404000	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr15:53402600-53404000	Enhancers	H1 Cell Line	embryonic stem cell
47	chr15:53402600-53404400	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr15:53402600-53404800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
49	chr15:53402800-53403400	Weak transcription	H9 Cell Line	embryonic stem cell
50	chr15:53402800-53403600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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