Variant report

Variant	nsv9277
Chromosome Location	chr15:75545225-75583588
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	ARID3A	chr15:75566765-75567085	HepG2	liver:	n/a	n/a
2	BATF	chr15:75566750-75567078	GM12878	blood:	n/a	n/a
3	BATF	chr15:75571142-75571340	GM12878	blood:	n/a	n/a
4	BCL11A	chr15:75571092-75571384	GM12878	blood:	n/a	chr15:75571302-75571309
5	BCL11A	chr15:75560181-75560352	GM12878	blood:	n/a	n/a
6	BCL11A	chr15:75553856-75554029	GM12878	blood:	n/a	n/a
7	BCL11A	chr15:75550815-75550962	GM12878	blood:	n/a	n/a
8	BCL11A	chr15:75575109-75575293	GM12878	blood:	n/a	n/a
9	BCL11A	chr15:75578133-75578306	GM12878	blood:	n/a	n/a
10	CTCF	chr15:75566920-75567070	GM12878	blood:	n/a	n/a
11	CTCF	chr15:75566940-75567090	HAc	cerebellar:	n/a	n/a
12	CTCF	chr15:75566920-75567210	AoAF	blood vessel:	n/a	n/a
13	CTCF	chr15:75566900-75567050	BE2_C	brain:	n/a	chr15:75566904-75566920 chr15:75566909-75566918 chr15:75566903-75566921
14	CTCF	chr15:75566920-75567070	SAEC	small airway:	n/a	n/a
15	CTCF	chr15:75566620-75566770	GM12872	blood:	n/a	n/a
16	CTCF	chr15:75566766-75567084	GM19238	blood:	n/a	chr15:75566904-75566920 chr15:75566909-75566918 chr15:75566898-75566919 chr15:75566903-75566921
17	CTCF	chr15:75566788-75567064	Medullo	brain:	n/a	chr15:75566904-75566920 chr15:75566909-75566918 chr15:75566898-75566919 chr15:75566903-75566921
18	CTCF	chr15:75560225-75560419	GM10248	blood:	n/a	n/a
19	CTCF	chr15:75566920-75567210	GM12872	blood:	n/a	n/a
20	CTCF	chr15:75566920-75567070	HL-60	blood:	n/a	n/a
21	CTCF	chr15:75566920-75567070	Hela-S3	cervix:	n/a	n/a
22	CTCF	chr15:75566920-75567210	GM12875	blood:	n/a	n/a
23	CTCF	chr15:75566794-75567054	H1-hESC	embryonic stem cell:	n/a	chr15:75566904-75566920 chr15:75566909-75566918 chr15:75566898-75566919 chr15:75566903-75566921
24	CTCF	chr15:75566847-75567049	SK-N-SH_RA	brain:	n/a	chr15:75566904-75566920 chr15:75566909-75566918 chr15:75566898-75566919 chr15:75566903-75566921
25	CTCF	chr15:75560209-75560418	Pancreas_OC	pancreas:	n/a	n/a
26	CTCF	chr15:75566920-75567070	HEEpiC	esophagus:	n/a	n/a
27	CTCF	chr15:75561806-75562154	A549	lung:	n/a	n/a
28	CTCF	chr15:75566840-75566990	NHDF-neo	bronchial:	n/a	chr15:75566904-75566920 chr15:75566909-75566918 chr15:75566898-75566919 chr15:75566903-75566921
29	CTCF	chr15:75566920-75567210	AG10803	skin:	n/a	n/a
30	CTCF	chr15:75566940-75567090	HFF-Myc	foreskin:	n/a	n/a
31	CTCF	chr15:75566863-75566978	HepG2	liver:	n/a	chr15:75566904-75566920 chr15:75566909-75566918 chr15:75566898-75566919 chr15:75566903-75566921
32	CTCF	chr15:75560269-75560409	LNCaP	prostate:	n/a	n/a
33	CTCF	chr15:75566600-75566750	WI-38	lung:	n/a	n/a
34	CTCF	chr15:75566920-75567210	AG09319	gingival:	n/a	n/a
35	CTCF	chr15:75567480-75567630	HCFaa	heart:	n/a	n/a
36	CTCF	chr15:75568040-75568190	HepG2	liver:	n/a	n/a
37	CTCF	chr15:75560258-75560366	GM20000	blood:	n/a	n/a
38	CTCF	chr15:75566697-75567137	K562	blood:	n/a	chr15:75566904-75566920 chr15:75566909-75566918 chr15:75566898-75566919 chr15:75566903-75566921
39	CTCF	chr15:75566900-75567050	NB4	blood:	n/a	chr15:75566904-75566920 chr15:75566909-75566918 chr15:75566903-75566921
40	CTCF	chr15:75567120-75567270	SAEC	small airway:	n/a	n/a
41	CTCF	chr15:75566920-75567190	HUVEC	blood vessel:	n/a	n/a
42	CTCF	chr15:75566920-75567210	HMF	breast:	n/a	n/a
43	CTCF	chr15:75566797-75567060	LNCaP	prostate:	n/a	chr15:75566904-75566920 chr15:75566909-75566918 chr15:75566898-75566919 chr15:75566903-75566921
44	CTCF	chr15:75566920-75567210	GM12878	blood:	n/a	n/a
45	CTCF	chr15:75566840-75566990	GM12864	blood:	n/a	chr15:75566904-75566920 chr15:75566909-75566918 chr15:75566898-75566919 chr15:75566903-75566921
46	CTCF	chr15:75566840-75566990	RPTEC	kidney:	n/a	chr15:75566904-75566920 chr15:75566909-75566918 chr15:75566898-75566919 chr15:75566903-75566921
47	CTCF	chr15:75566840-75566990	GM12866	blood:	n/a	chr15:75566904-75566920 chr15:75566909-75566918 chr15:75566898-75566919 chr15:75566903-75566921
48	CTCF	chr15:75567060-75567210	NHDF-neo	bronchial:	n/a	n/a
49	CTCF	chr15:75566640-75566790	HVMF	connective:	n/a	n/a
50	CTCF	chr15:75566727-75567094	A549	lung:	n/a	chr15:75566904-75566920 chr15:75566909-75566918 chr15:75566898-75566919 chr15:75566903-75566921

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:75551123-75551173	Hepatocyte	liver:	n/a
2	chr15:75575161-75575211	A549	lung:	n/a
3	chr15:75575161-75575211	BJ	skin:	n/a
4	chr15:75575161-75575211	HMEC	breast:	n/a
5	chr15:75575161-75575211	LNCaP	prostate:	n/a
6	chr15:75575161-75575211	NHBE	bronchial:	n/a
7	chr15:75575161-75575211	NT2-D1	testis:	n/a
8	chr15:75575161-75575211	MCF10A-Er-Src	breast:	n/a
9	chr15:75551123-75551173	HNPCEpiC	eye:	n/a
10	chr15:75575161-75575211	NH-A	brain:	n/a
11	chr15:75551123-75551173	ovcar-3	ovarian:	n/a
12	chr15:75575161-75575211	SK-N-MC	brain:	n/a
13	chr15:75551123-75551173	MCF10A-Er-Src	breast:	n/a
14	chr15:75551123-75551173	GM12878	blood:	n/a
15	chr15:75575161-75575211	HEEpiC	esophagus:	n/a
16	chr15:75575161-75575211	AG10803	skin:	n/a
17	chr15:75575161-75575211	PANC-1	pancreas:	n/a
18	chr15:75575161-75575211	HEK293	kidney:	embryo
19	chr15:75551123-75551173	HCM	heart:	n/a
20	chr15:75575161-75575211	HRCEpiC	kidney:	n/a
21	chr15:75575161-75575211	SKMC	muscle:	n/a
22	chr15:75575161-75575211	ovcar-3	ovarian:	n/a
23	chr15:75575161-75575211	HUVEC	blood vessel:	n/a
24	chr15:75575161-75575211	AG04449	skin:	fetal
25	chr15:75551123-75551173	HIPEpiC	eye:	n/a
26	chr15:75575161-75575211	Jurkat	blood:	n/a
27	chr15:75551123-75551173	ProgFib	skin:	n/a
28	chr15:75575161-75575211	PrEC	prostate:	n/a
29	chr15:75551123-75551173	HRPEpiC	eye:	n/a
30	chr15:75551123-75551173	SK-N-MC	brain:	n/a
31	chr15:75551123-75551173	HEK293	kidney:	embryo
32	chr15:75551123-75551173	BJ	skin:	n/a
33	chr15:75575161-75575211	BE2_C	brain:	n/a
34	chr15:75575161-75575211	AG04450	lung:	fetal
35	chr15:75575161-75575211	HIPEpiC	eye:	n/a
36	chr15:75575161-75575211	AoSMC	blood vessel:	n/a
37	chr15:75575161-75575211	HL-60	blood:	n/a
38	chr15:75551123-75551173	AG04449	skin:	fetal
39	chr15:75575161-75575211	GM12891	blood:	n/a
40	chr15:75575161-75575211	HNPCEpiC	eye:	n/a
41	chr15:75575161-75575211	HRPEpiC	eye:	n/a
42	chr15:75551123-75551173	H1-hESC	embryonic stem cell:	embryo
43	chr15:75551123-75551173	NHBE	bronchial:	n/a
44	chr15:75575161-75575211	MCF-7	breast:	n/a
45	chr15:75575161-75575211	AG09319	gingival:	n/a
46	chr15:75575161-75575211	HAEpiC	amniotic membrane:	n/a
47	chr15:75551123-75551173	AG09309	skin:	n/a
48	chr15:75551123-75551173	GM06990	blood:	n/a
49	chr15:75575161-75575211	NHDF-neo	bronchial:	n/a
50	chr15:75551123-75551173	HRE	kidney:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:75321592..75322142-chr15:75566565..75567153,2	MCF-7	breast:
2	chr15:74600289..74600861-chr15:75566666..75567634,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MAN2C1-9	chr15:75564454-75564996	ncRnaDb_ncrna_FR096405_1
2	lnc-GOLGA6D-3	chr15:75560749-75561024	NONHSAT047302

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	GOLGA6A	hsa-miR-192-5p	chr15:75562833-75562852

Variant related genes	Relation type
RN7SL327P	TF binding region
GOLGA6D	TF binding region
ENSG00000260104	TF binding region
GOLGA6C	TF binding region
NIFKP4	TF binding region
RN7SL489P	TF binding region
RN7SL327P	CpG island
GOLGA6D	CpG island
ENSG00000260104	CpG island
GOLGA6C	CpG island
NIFKP4	CpG island
RN7SL489P	CpG island

Extended variants
information (count: 297 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:297 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs573034823	chr15:75545287-75545288	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs561789098	chr15:75545313-75545314	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs573930588	chr15:75545322-75545323	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs544414872	chr15:75545332-75545333	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs189295338	chr15:75545341-75545342	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs192546308	chr15:75545346-75545347	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs28733085	chr15:75545358-75545359	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs539186304	chr15:75545386-75545387	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs140939129	chr15:75545396-75545397	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs555249329	chr15:75545436-75545437	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs184182908	chr15:75545474-75545475	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs113987890	chr15:75545506-75545507	Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
13	rs147951805	chr15:75545529-75545530	Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
14	rs369421767	chr15:75545541-75545542	Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
15	rs141897548	chr15:75545565-75545566	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs190082269	chr15:75545567-75545568	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs149876825	chr15:75545596-75545597	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs181151006	chr15:75545641-75545642	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs566074359	chr15:75545665-75545666	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs111831108	chr15:75545670-75545671	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs144893437	chr15:75545683-75545684	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs34788725	chr15:75545715-75545716	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs555679127	chr15:75545728-75545729	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs543824215	chr15:75545754-75545755	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs573958420	chr15:75545786-75545787	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs75596171	chr15:75545797-75545798	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs556405958	chr15:75545838-75545839	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs577868095	chr15:75545841-75545842	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs34389454	chr15:75545863-75545864	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs545100857	chr15:75545875-75545876	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs397854104	chr15:75545876-75545877	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs559984379	chr15:75545884-75545885	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs527329157	chr15:75545917-75545918	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs186296985	chr15:75545921-75545922	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs114275254	chr15:75545931-75545932	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs531898967	chr15:75545943-75545944	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs550033323	chr15:75545952-75545953	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs571510139	chr15:75545990-75545991	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs532527428	chr15:75546000-75546001	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs180845401	chr15:75546077-75546078	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs11072537	chr15:75546134-75546135	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs11072538	chr15:75546166-75546167	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs536677475	chr15:75546191-75546192	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs577700323	chr15:75546198-75546199	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs11072539	chr15:75546200-75546201	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs145490712	chr15:75546211-75546212	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs538157896	chr15:75546290-75546291	Enhancers	TF binding region	3 gene(s)	Overlapped CNVs	n/a
48	rs2899791	chr15:75546406-75546407	Enhancers	TF binding region	3 gene(s)	Overlapped CNVs	n/a
49	rs2899792	chr15:75546437-75546438	Enhancers	TF binding region	3 gene(s)	Overlapped CNVs	n/a
50	rs3985569	chr15:75546439-75546440	Enhancers	TF binding region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:67)

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
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
Congenital diaphragmatic hernia	21085971	CNVD
Autism	17322880	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
Epilepsy	22083797	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Myelofibrosis	22110671	CNVD
Bipolar disorder	19114987	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	16616336	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:44 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:75538000-75545400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr15:75542400-75545400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr15:75544600-75546200	Enhancers	HUES6 Cell Line	embryonic stem cell
4	chr15:75544600-75547000	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr15:75544800-75545400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr15:75545200-75545600	Enhancers	H9 Cell Line	embryonic stem cell
7	chr15:75545400-75545800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr15:75545400-75546200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
9	chr15:75545400-75546200	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr15:75545400-75546200	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr15:75545600-75546200	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr15:75545600-75546200	Enhancers	HepG2	liver
13	chr15:75545600-75546400	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr15:75546000-75546400	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr15:75566200-75567200	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr15:75566400-75568000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr15:75566600-75567200	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr15:75566600-75567200	Enhancers	Cortex derived primary cultured neurospheres	brain
19	chr15:75566800-75567200	Enhancers	Breast Myoepithelial Primary Cells	Breast
20	chr15:75566800-75567400	Enhancers	Liver	Liver
21	chr15:75567000-75567200	Enhancers	Spleen	Spleen
22	chr15:75567000-75567200	Bivalent Enhancer	HepG2	liver
23	chr15:75567000-75567400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr15:75567000-75567400	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
25	chr15:75567000-75567600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr15:75567200-75568000	Weak transcription	Spleen	Spleen
27	chr15:75567200-75571000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
28	chr15:75567200-75571000	Weak transcription	HUES6 Cell Line	embryonic stem cell
29	chr15:75567600-75568000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr15:75568000-75568200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr15:75568000-75568400	Bivalent/Poised TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr15:75568000-75568400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr15:75568000-75568400	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr15:75568000-75568400	Active TSS	Spleen	Spleen
35	chr15:75568200-75568400	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr15:75570800-75571200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr15:75570800-75571200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr15:75570800-75571200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr15:75570800-75571200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr15:75571000-75571200	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr15:75571000-75571200	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr15:75571000-75571200	Enhancers	HUES64 Cell Line	embryonic stem cell
43	chr15:75571000-75571200	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr15:75571000-75571200	Enhancers	HepG2	liver

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