Variant report

Variant	nsv1039762
Chromosome Location	chr15:53354285-53414479
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:234)
CpG islands
(count:61)
Chromatin interactive
region (count:17)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:234 , 50 per page) page: 1 2 3 4 5

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	CBX3	chr15:53364324-53364710	HCT-116	colon:	n/a	n/a
3	CEBPB	chr15:53369787-53369848	A549	lung:	n/a	chr15:53369789-53369800 chr15:53369789-53369802
4	CEBPB	chr15:53394804-53394982	HepG2	liver:	n/a	chr15:53394870-53394881
5	CHD1	chr15:53403047-53403168	H1-hESC	embryonic stem cell:	n/a	n/a
6	CHD2	chr15:53364346-53364644	Hela-S3	cervix:	n/a	n/a
7	CREB1	chr15:53364391-53364729	A549	lung:	n/a	n/a
8	CTCF	chr15:53386020-53386170	A549	lung:	n/a	chr15:53386057-53386064
9	CTCF	chr15:53378026-53378138	Kidney_OC	kidney:	n/a	n/a
10	CTCF	chr15:53385980-53386130	SK-N-SH_RA	brain:	n/a	chr15:53386057-53386064
11	CTCF	chr15:53386020-53386170	MCF-7	breast:	n/a	chr15:53386057-53386064
12	CTCF	chr15:53385940-53386090	MCF-7	breast:	n/a	chr15:53386057-53386064
13	CTCF	chr15:53378009-53378140	GM10248	blood:	n/a	n/a
14	CTCF	chr15:53407283-53407349	Pancreas_OC	pancreas:	n/a	n/a
15	CTCF	chr15:53364420-53364570	GM12864	blood:	n/a	n/a
16	E2F4	chr15:53364424-53364665	MCF10A-Er-Src	breast:	n/a	n/a
17	E2F4	chr15:53387861-53388070	MCF10A-Er-Src	breast:	n/a	n/a
18	EBF1	chr15:53384232-53384240	GM12878	blood:	n/a	n/a
19	ELF1	chr15:53363901-53364912	MCF-7	breast:	n/a	n/a
20	EP300	chr15:53364102-53364765	A549	lung:	n/a	n/a
21	EP300	chr15:53407167-53407538	HepG2	liver:	n/a	n/a
22	EP300	chr15:53364069-53364671	SK-N-SH	brain:	n/a	n/a
23	EP300	chr15:53364343-53364646	Hela-S3	cervix:	n/a	n/a
24	EP300	chr15:53363928-53364810	MCF-7	breast:	n/a	n/a
25	EP300	chr15:53364248-53364645	T-47D	breast:	n/a	n/a
26	EP300	chr15:53363913-53364870	MCF-7	breast:	n/a	n/a
27	FOS	chr15:53364254-53364692	MCF10A-Er-Src	breast:	n/a	chr15:53364472-53364483 chr15:53364474-53364482
28	FOS	chr15:53364224-53364726	MCF10A-Er-Src	breast:	n/a	chr15:53364472-53364483 chr15:53364474-53364482
29	FOS	chr15:53364253-53364697	MCF10A-Er-Src	breast:	n/a	chr15:53364472-53364483 chr15:53364474-53364482
30	FOS	chr15:53364219-53364725	MCF10A-Er-Src	breast:	n/a	chr15:53364472-53364483 chr15:53364474-53364482
31	FOSL1	chr15:53364289-53364704	HCT-116	colon:	n/a	chr15:53364472-53364483 chr15:53364474-53364482
32	FOSL1	chr15:53364172-53364728	HCT-116	colon:	n/a	chr15:53364472-53364483 chr15:53364474-53364482
33	FOSL2	chr15:53363992-53364840	MCF-7	breast:	n/a	chr15:53364472-53364483 chr15:53364474-53364482
34	FOSL2	chr15:53364121-53364772	A549	lung:	n/a	chr15:53364472-53364483 chr15:53364474-53364482
35	FOSL2	chr15:53364160-53364816	SK-N-SH	brain:	n/a	chr15:53364472-53364483 chr15:53364474-53364482
36	FOSL2	chr15:53364227-53364671	A549	lung:	n/a	chr15:53364472-53364483 chr15:53364474-53364482
37	FOSL2	chr15:53364253-53364669	SK-N-SH	brain:	n/a	chr15:53364472-53364483 chr15:53364474-53364482
38	FOSL2	chr15:53363927-53364827	MCF-7	breast:	n/a	chr15:53364472-53364483 chr15:53364474-53364482
39	FOXA1	chr15:53364195-53364731	T-47D	breast:	n/a	n/a
40	FOXA2	chr15:53364144-53364570	A549	lung:	n/a	n/a
41	FOXA2	chr15:53364535-53364722	HepG2	liver:	n/a	n/a
42	FOXA2	chr15:53364187-53364806	A549	lung:	n/a	n/a
43	FOXM1	chr15:53363960-53364790	MCF-7	breast:	n/a	n/a
44	GABPA	chr15:53363994-53364803	MCF-7	breast:	n/a	n/a
45	GATA2	chr15:53364195-53364661	HUVEC	blood vessel:	n/a	chr15:53364472-53364481
46	GATA3	chr15:53364034-53364856	SK-N-SH	brain:	n/a	chr15:53364472-53364481
47	GATA3	chr15:53364154-53364736	T-47D	breast:	n/a	chr15:53364472-53364481
48	GATA3	chr15:53371431-53371822	MCF-7	breast:	n/a	chr15:53371700-53371716 chr15:53371700-53371716
49	GATA3	chr15:53371359-53372053	MCF-7	breast:	n/a	chr15:53371700-53371716 chr15:53371700-53371716
50	GATA3	chr15:53364196-53364640	T-47D	breast:	n/a	chr15:53364472-53364481

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:53372675-53372725	Hela-S3	cervix:	n/a
2	chr15:53372675-53372725	HCF	heart:	n/a
3	chr15:53372675-53372725	BE2_C	brain:	n/a
4	chr15:53372675-53372725	ovcar-3	ovarian:	n/a
5	chr15:53372675-53372725	HPAEpiC	pulmonary alveolar:	n/a
6	chr15:53372675-53372725	NHBE	bronchial:	n/a
7	chr15:53372675-53372725	PANC-1	pancreas:	n/a
8	chr15:53372675-53372725	Jurkat	blood:	n/a
9	chr15:53372675-53372725	CMK	blood:	n/a
10	chr15:53372675-53372725	ECC-1	luminal epithelium:	n/a
11	chr15:53372675-53372725	HEK293	kidney:	embryo
12	chr15:53372675-53372725	HCPEpiC	choroid plexus:	n/a
13	chr15:53372675-53372725	GM12878	blood:	n/a
14	chr15:53372675-53372725	HEEpiC	esophagus:	n/a
15	chr15:53372675-53372725	HepG2	liver:	n/a
16	chr15:53372675-53372725	MCF10A-Er-Src	breast:	n/a
17	chr15:53372675-53372725	NH-A	brain:	n/a
18	chr15:53372675-53372725	HRCEpiC	kidney:	n/a
19	chr15:53372675-53372725	NB4	blood:	n/a
20	chr15:53372675-53372725	HUVEC	blood vessel:	n/a
21	chr15:53372675-53372725	GM19239	blood:	n/a
22	chr15:53372675-53372725	U87	brain:	n/a
23	chr15:53372675-53372725	HIPEpiC	eye:	n/a
24	chr15:53372675-53372725	RPTEC	kidney:	n/a
25	chr15:53372675-53372725	SAEC	small airway:	n/a
26	chr15:53372675-53372725	SK-N-SH	brain:	n/a
27	chr15:53372675-53372725	Caco-2	colon:	n/a
28	chr15:53372675-53372725	HCM	heart:	n/a
29	chr15:53372675-53372725	AoSMC	blood vessel:	n/a
30	chr15:53372675-53372725	GM12891	blood:	n/a
31	chr15:53372675-53372725	NHDF-neo	bronchial:	n/a
32	chr15:53372675-53372725	AG04450	lung:	fetal
33	chr15:53372675-53372725	AG09309	skin:	n/a
34	chr15:53372675-53372725	AG09319	gingival:	n/a
35	chr15:53372675-53372725	HAEpiC	amniotic membrane:	n/a
36	chr15:53372675-53372725	GM12892	blood:	n/a
37	chr15:53372675-53372725	IMR90	lung:	fetal
38	chr15:53372675-53372725	SKMC	muscle:	n/a
39	chr15:53372675-53372725	LNCaP	prostate:	n/a
40	chr15:53372675-53372725	PrEC	prostate:	n/a
41	chr15:53372675-53372725	GM06990	blood:	n/a
42	chr15:53372675-53372725	T-47D	breast:	n/a
43	chr15:53372675-53372725	SK-N-MC	brain:	n/a
44	chr15:53372675-53372725	A549	lung:	n/a
45	chr15:53372675-53372725	BJ	skin:	n/a
46	chr15:53372675-53372725	HL-60	blood:	n/a
47	chr15:53372675-53372725	HRPEpiC	eye:	n/a
48	chr15:53372675-53372725	HNPCEpiC	eye:	n/a
49	chr15:53372675-53372725	AG10803	skin:	n/a
50	chr15:53372675-53372725	Hepatocyte	liver:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:53363971..53364789-chr15:53374593..53375688,3	MCF-7	breast:
2	chr15:53369383..53371838-chr15:53381998..53383881,2	K562	blood:
3	chr15:53364183..53365120-chr15:53374984..53375519,2	MCF-7	breast:
4	chr15:53369383..53371838-chr15:53381998..53383881,2	K562	blood:
5	chr15:53364390..53366274-chr15:53368340..53370470,3	MCF-7	breast:
6	chr15:53363971..53364789-chr15:53374593..53375688,3	MCF-7	breast:
7	chr15:53398769..53401159-chr15:53403733..53405993,2	K562	blood:
8	chr15:53398769..53401159-chr15:53403733..53405993,2	K562	blood:
9	chr15:53146326..53147158-chr15:53363981..53364531,2	MCF-7	breast:
10	chr15:53318089..53321018-chr15:53355252..53357036,2	MCF-7	breast:
11	chr15:53364390..53366274-chr15:53368340..53370470,3	MCF-7	breast:
12	chr15:53367799..53369631-chr15:53373514..53375161,2	MCF-7	breast:
13	chr15:53367799..53369631-chr15:53373514..53375161,2	MCF-7	breast:
14	chr15:53412161..53414398-chr15:53418222..53421112,2	MCF-7	breast:
15	chr15:53364183..53365120-chr15:53374984..53375519,2	MCF-7	breast:
16	chr15:53406863..53408730-chr15:53409145..53411501,2	MCF-7	breast:
17	chr15:53364212..53364797-chr15:53623796..53624629,2	MCF-7	breast:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UNC13C-2	chr15:53393715-53393924	XLOC_011259
2	lnc-UNC13C-2	chr15:53392927-53393040	XLOC_011259
3	lnc-UNC13C-1	chr15:53410416-53410462	ENSG00000259237.1
4	lnc-ONECUT1-4	chr15:53397038-53397355	expReg_chr15_3758_-
5	lnc-UNC13C-6	chr15:53360686-53360774	NONHSAT043960
6	lnc-UNC13C-2	chr15:53393714-53393924	NONHSAT043961
7	lnc-UNC13C-1	chr15:53408562-53408655	ENSG00000259237.1
8	lnc-UNC13C-6	chr15:53362262-53362447	NONHSAT043960
9	lnc-UNC13C-2	chr15:53375073-53375267	XLOC_011259
10	lnc-UNC13C-2	chr15:53375035-53375267	NONHSAT043961
11	lnc-UNC13C-2	chr15:53375036-53375267	XLOC_011259
12	lnc-UNC13C-2	chr15:53392926-53393040	NONHSAT043961
13	lnc-UNC13C-2	chr15:53392927-53393040	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
SMG1	miRNA target sites
DMTF1	miRNA target sites

Extended variants
information (count: 1458 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:1458 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs532784515	chr15:53354313-53354314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs34971880	chr15:53354348-53354349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs565011552	chr15:53354394-53354395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs546251449	chr15:53354423-53354424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs566212356	chr15:53354462-53354463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs539911983	chr15:53354522-53354523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs138247618	chr15:53354553-53354554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs182841718	chr15:53354616-53354617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs4142454	chr15:53354646-53354647	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs373527643	chr15:53354647-53354648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs72728931	chr15:53354652-53354653	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs188226929	chr15:53354656-53354657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs571641487	chr15:53354704-53354705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs534199604	chr15:53354714-53354715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs114815222	chr15:53354762-53354763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs574060368	chr15:53354776-53354777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs192564958	chr15:53354780-53354781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs556709460	chr15:53354785-53354786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs79977146	chr15:53354789-53354790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs545266879	chr15:53354838-53354839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs8038973	chr15:53354845-53354846	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs528010048	chr15:53354868-53354869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs539818597	chr15:53354880-53354881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs183697386	chr15:53354910-53354911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs72728932	chr15:53354933-53354934	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs188272126	chr15:53354939-53354940	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs568986524	chr15:53354965-53354966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs531430044	chr15:53354969-53354970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs143739821	chr15:53354970-53354971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs551561193	chr15:53354972-53354973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs571550873	chr15:53354995-53354996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs150599422	chr15:53355006-53355007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs547811885	chr15:53355084-53355085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs567596444	chr15:53355132-53355133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs17659077	chr15:53355161-53355162	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs556387188	chr15:53355191-53355192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs546757103	chr15:53355194-53355195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs576544211	chr15:53355199-53355200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs538830664	chr15:53355274-53355275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs558752227	chr15:53355345-53355346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs572402177	chr15:53355399-53355400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs541365627	chr15:53355404-53355405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs560051995	chr15:53355408-53355409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs573558200	chr15:53355412-53355413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs542680746	chr15:53355424-53355425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs192572006	chr15:53355489-53355490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs551580934	chr15:53355564-53355565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs565126521	chr15:53355584-53355585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs527577370	chr15:53355590-53355591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs139619838	chr15:53355593-53355594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

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

Chromatin state (count:85 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:53353200-53364200	Weak transcription	Liver	Liver
2	chr15:53353800-53356600	Weak transcription	Dnd41	blood
3	chr15:53356600-53357200	Enhancers	Dnd41	blood
4	chr15:53359600-53361800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr15:53360600-53361600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr15:53362200-53363000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr15:53362600-53363200	Enhancers	NHEK	skin
8	chr15:53362800-53364200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr15:53363200-53364000	Weak transcription	NHEK	skin
10	chr15:53363200-53365200	Enhancers	Pancreas	Pancrea
11	chr15:53364000-53364400	Enhancers	Gastric	stomach
12	chr15:53364000-53364400	Enhancers	NH-A	brain
13	chr15:53364000-53364400	Enhancers	NHEK	skin
14	chr15:53364000-53364600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr15:53364000-53364600	Enhancers	Brain Inferior Temporal Lobe	brain
16	chr15:53364200-53364600	Enhancers	Liver	Liver
17	chr15:53364400-53364600	Weak transcription	NHEK	skin
18	chr15:53364600-53365000	Enhancers	NHEK	skin
19	chr15:53372000-53373200	Enhancers	iPS-18 Cell Line	embryonic stem cell
20	chr15:53372000-53373400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr15:53372000-53373600	Enhancers	iPS-20b Cell Line	embryonic stem cell
22	chr15:53372200-53373200	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr15:53372200-53373400	Enhancers	H1 Cell Line	embryonic stem cell
24	chr15:53372400-53373400	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr15:53372600-53373400	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr15:53385000-53385800	Enhancers	Liver	Liver
27	chr15:53394600-53395400	Enhancers	Liver	Liver
28	chr15:53395000-53395200	Enhancers	Pancreas	Pancrea
29	chr15:53395200-53399600	Weak transcription	Pancreas	Pancrea
30	chr15:53397800-53398000	Enhancers	H9 Cell Line	embryonic stem cell
31	chr15:53398000-53402600	Weak transcription	H9 Cell Line	embryonic stem cell
32	chr15:53400400-53400600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr15:53400600-53400800	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr15:53400600-53400800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr15:53400600-53401200	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr15:53400800-53402600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
37	chr15:53401000-53402600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
38	chr15:53401200-53403000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
39	chr15:53402200-53403400	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr15:53402400-53404400	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr15:53402600-53402800	Enhancers	H9 Cell Line	embryonic stem cell
42	chr15:53402600-53404000	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr15:53402600-53404000	Enhancers	H1 Cell Line	embryonic stem cell
44	chr15:53402600-53404400	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr15:53402600-53404800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
46	chr15:53402800-53403400	Weak transcription	H9 Cell Line	embryonic stem cell
47	chr15:53402800-53403600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr15:53402800-53403600	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr15:53403000-53404200	Enhancers	HUES64 Cell Line	embryonic stem cell
50	chr15:53403000-53404400	Enhancers	iPS-18 Cell Line	embryonic stem cell

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