Variant report

Variant	nsv597992
Chromosome Location	chr5:45527476-45573428
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:47)
CpG islands
(count:122)
Chromatin interactive
region (count:2)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:47 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BRCA1	chr5:45564807-45564864	Hela-S3	cervix:	n/a	n/a
2	BRCA1	chr5:45551191-45551382	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr5:45529506-45529762	HepG2	liver:	n/a	chr5:45529613-45529626 chr5:45529613-45529624 chr5:45529614-45529625 chr5:45529615-45529624
4	CEBPB	chr5:45529565-45529645	A549	lung:	n/a	chr5:45529613-45529626 chr5:45529613-45529624 chr5:45529614-45529625 chr5:45529615-45529624
5	E2F4	chr5:45539222-45539459	MCF10A-Er-Src	breast:	n/a	n/a
6	FOS	chr5:45559447-45559859	MCF10A-Er-Src	breast:	n/a	n/a
7	GATA3	chr5:45550913-45551157	SH-SY5Y	brain:	n/a	n/a
8	HDAC2	chr5:45561618-45561914	H1-hESC	embryonic stem cell:	n/a	n/a
9	JUND	chr5:45532979-45533174	H1-hESC	embryonic stem cell:	n/a	n/a
10	KAP1	chr5:45544083-45544278	K562	blood:	n/a	n/a
11	MAFF	chr5:45529556-45529756	HepG2	liver:	n/a	chr5:45529643-45529661
12	MAFK	chr5:45529538-45529808	HepG2	liver:	n/a	chr5:45529645-45529660
13	MAFK	chr5:45573096-45573206	HepG2	liver:	n/a	n/a
14	MAFK	chr5:45529549-45529802	HepG2	liver:	n/a	chr5:45529645-45529660
15	MAFK	chr5:45529501-45529689	K562	blood:	n/a	chr5:45529645-45529660
16	MXI1	chr5:45532939-45533242	H1-hESC	embryonic stem cell:	n/a	n/a
17	MYC	chr5:45569261-45569540	MCF10A-Er-Src	breast:	n/a	n/a
18	MYC	chr5:45570019-45570168	MCF10A-Er-Src	breast:	n/a	n/a
19	POLR2A	chr5:45532887-45533302	H1-neurons	neurons:	n/a	n/a
20	POLR2A	chr5:45542672-45542817	MCF10A-Er-Src	breast:	n/a	n/a
21	POLR2A	chr5:45570968-45570985	MCF10A-Er-Src	breast:	n/a	n/a
22	POLR2A	chr5:45540825-45541025	MCF10A-Er-Src	breast:	n/a	n/a
23	POLR2A	chr5:45569025-45569064	ProgFib	skin:	n/a	n/a
24	POLR2A	chr5:45538836-45538881	MCF10A-Er-Src	breast:	n/a	n/a
25	POLR2A	chr5:45533226-45533254	MCF10A-Er-Src	breast:	n/a	n/a
26	POLR2A	chr5:45532883-45533320	H1-neurons	neurons:	n/a	n/a
27	POLR2A	chr5:45556813-45556822	MCF10A-Er-Src	breast:	n/a	n/a
28	POLR2A	chr5:45541571-45541613	MCF10A-Er-Src	breast:	n/a	n/a
29	POLR2A	chr5:45528596-45528619	MCF10A-Er-Src	breast:	n/a	n/a
30	POLR2A	chr5:45572345-45572545	MCF10A-Er-Src	breast:	n/a	n/a
31	RAD21	chr5:45533050-45533123	H1-hESC	embryonic stem cell:	n/a	n/a
32	REST	chr5:45532622-45533974	H1-neurons	neurons:	n/a	chr5:45533483-45533493
33	REST	chr5:45532905-45533356	H1-neurons	neurons:	n/a	n/a
34	SIN3A	chr5:45532945-45533245	H1-hESC	embryonic stem cell:	n/a	n/a
35	SIN3AK20	chr5:45533009-45533191	H1-hESC	embryonic stem cell:	n/a	n/a
36	SPI1	chr5:45548743-45548856	GM12878	blood:	n/a	n/a
37	SPI1	chr5:45548738-45548861	K562	blood:	n/a	n/a
38	STAT3	chr5:45528289-45528579	MCF10A-Er-Src	breast:	n/a	n/a
39	STAT3	chr5:45547509-45547517	MCF10A-Er-Src	breast:	n/a	n/a
40	STAT3	chr5:45535770-45536141	MCF10A-Er-Src	breast:	n/a	chr5:45535826-45535834
41	STAT3	chr5:45529242-45529314	MCF10A-Er-Src	breast:	n/a	n/a
42	STAT3	chr5:45559605-45559650	MCF10A-Er-Src	breast:	n/a	n/a
43	STAT3	chr5:45558155-45558258	MCF10A-Er-Src	breast:	n/a	n/a
44	TEAD4	chr5:45534227-45534570	H1-hESC	embryonic stem cell:	n/a	n/a
45	TEAD4	chr5:45534206-45534607	H1-hESC	embryonic stem cell:	n/a	n/a
46	TEAD4	chr5:45534313-45534651	ECC-1	luminal epithelium:	n/a	n/a
47	TEAD4	chr5:45534298-45534688	ECC-1	luminal epithelium:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:45569042-45569092	GM06990	blood:	n/a
2	chr5:45553518-45553568	HUVEC	blood vessel:	n/a
3	chr5:45569042-45569092	HEEpiC	esophagus:	n/a
4	chr5:45553518-45553568	AG04449	skin:	fetal
5	chr5:45569042-45569092	SK-N-SH_RA	brain:	n/a
6	chr5:45553518-45553568	HCT-116	colon:	n/a
7	chr5:45553518-45553568	NH-A	brain:	n/a
8	chr5:45569042-45569092	SKMC	muscle:	n/a
9	chr5:45553518-45553568	ECC-1	luminal epithelium:	n/a
10	chr5:45553518-45553568	PANC-1	pancreas:	n/a
11	chr5:45569042-45569092	PFSK-1	brain:	n/a
12	chr5:45569042-45569092	AG09319	gingival:	n/a
13	chr5:45553518-45553568	CMK	blood:	n/a
14	chr5:45569042-45569092	GM12878	blood:	n/a
15	chr5:45569042-45569092	SK-N-MC	brain:	n/a
16	chr5:45569042-45569092	GM19239	blood:	n/a
17	chr5:45569042-45569092	HPAEpiC	pulmonary alveolar:	n/a
18	chr5:45553518-45553568	AG09309	skin:	n/a
19	chr5:45569042-45569092	CMK	blood:	n/a
20	chr5:45553518-45553568	T-47D	breast:	n/a
21	chr5:45569042-45569092	LNCaP	prostate:	n/a
22	chr5:45569042-45569092	HMEC	breast:	n/a
23	chr5:45553518-45553568	H1-hESC	embryonic stem cell:	embryo
24	chr5:45553518-45553568	LNCaP	prostate:	n/a
25	chr5:45553518-45553568	HCM	heart:	n/a
26	chr5:45569042-45569092	A549	lung:	n/a
27	chr5:45569042-45569092	SK-N-SH	brain:	n/a
28	chr5:45553518-45553568	SK-N-MC	brain:	n/a
29	chr5:45553518-45553568	GM12891	blood:	n/a
30	chr5:45569042-45569092	Hepatocyte	liver:	n/a
31	chr5:45569042-45569092	HUVEC	blood vessel:	n/a
32	chr5:45553518-45553568	AG09319	gingival:	n/a
33	chr5:45569042-45569092	HCM	heart:	n/a
34	chr5:45553518-45553568	SAEC	small airway:	n/a
35	chr5:45569042-45569092	HCF	heart:	n/a
36	chr5:45553518-45553568	HL-60	blood:	n/a
37	chr5:45569042-45569092	BE2_C	brain:	n/a
38	chr5:45569042-45569092	AG04450	lung:	fetal
39	chr5:45553518-45553568	NB4	blood:	n/a
40	chr5:45553518-45553568	K562	blood:	n/a
41	chr5:45569042-45569092	MCF10A-Er-Src	breast:	n/a
42	chr5:45553518-45553568	HRE	kidney:	n/a
43	chr5:45569042-45569092	ProgFib	skin:	n/a
44	chr5:45569042-45569092	HRCEpiC	kidney:	n/a
45	chr5:45569042-45569092	NT2-D1	testis:	n/a
46	chr5:45569042-45569092	T-47D	breast:	n/a
47	chr5:45569042-45569092	HEK293	kidney:	embryo
48	chr5:45569042-45569092	ECC-1	luminal epithelium:	n/a
49	chr5:45553518-45553568	HEK293	kidney:	embryo
50	chr5:45569042-45569092	AG04449	skin:	fetal

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr13:55537336..55537947-chr5:45562607..45563107,2	MCF-7	breast:
2	chr15:66571588..66572090-chr5:45541388..45542303,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MRPS30-12	chr5:45558021-45560088	NONHSAT101360

No data

Variant related genes	Relation type
ENSG00000250422	TF binding region
ENSG00000250017	TF binding region
ENSG00000250422	CpG island
ENSG00000250017	CpG island

Extended variants
information (count: 1065 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:1065 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs192160799	chr5:45527492-45527493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs372853691	chr5:45527535-45527536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs139532339	chr5:45527547-45527548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs534576569	chr5:45527560-45527561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs184247136	chr5:45527590-45527591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs201490314	chr5:45527647-45527648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs199529085	chr5:45527657-45527658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs538941492	chr5:45527658-45527659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs374667663	chr5:45527667-45527668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs369041569	chr5:45527675-45527676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs544123056	chr5:45527701-45527702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs369936097	chr5:45527704-45527705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs149659742	chr5:45527710-45527711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs34086253	chr5:45527732-45527733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs189445790	chr5:45527744-45527745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs543265665	chr5:45527757-45527758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs374652135	chr5:45527769-45527770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs182328019	chr5:45527802-45527803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs186123375	chr5:45527809-45527810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs1825325	chr5:45527826-45527827	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs530855479	chr5:45527880-45527881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs549647041	chr5:45527897-45527898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs189459588	chr5:45527920-45527921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs145469720	chr5:45527985-45527986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs548778831	chr5:45528021-45528022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs201551558	chr5:45528035-45528036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs67834483	chr5:45528048-45528049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs148892762	chr5:45528113-45528114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs575420040	chr5:45528130-45528131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs180708600	chr5:45528134-45528135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs571144881	chr5:45528136-45528137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs537073700	chr5:45528247-45528248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs368908667	chr5:45528296-45528297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs557660664	chr5:45528319-45528320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs574401748	chr5:45528338-45528339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs536804913	chr5:45528376-45528377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs71616294	chr5:45528404-45528405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs58986238	chr5:45528425-45528426	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs573432476	chr5:45528443-45528444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs185751234	chr5:45528576-45528577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs536317065	chr5:45528693-45528694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs376299382	chr5:45528796-45528797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs371082180	chr5:45528799-45528800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs576174212	chr5:45528820-45528821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs143604594	chr5:45528851-45528852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs575211074	chr5:45528901-45528902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs16902160	chr5:45528912-45528913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs563204881	chr5:45528988-45528989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs373016274	chr5:45529172-45529173	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs548024444	chr5:45529229-45529230	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Bladder cancer	21909424	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Cancer	16751803	CNVD
Breast cancer	16608533	CNVD
Autism	22495311	CNVD
Intellectual disability	22102821	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Esophageal cancer	20955586	CNVD
Breast cancer	17133270	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Breast cancer	17393978	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Hirschsprung''s Disease	21712996	CNVD
Intellectual disability	21811512	CNVD
Lung adenocarcinoma	21935476	CNVD
Myelofibrosis	22110671	CNVD
Intracranial aneurysm	16715129	CNVD
Multiple myeloma	16616336	CNVD
Cancer	21359685	CNVD
adenomatous polyposis	22470819	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164920	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:117 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:45525800-45532800	Weak transcription	Fetal Heart	heart
2	chr5:45529000-45529400	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr5:45529400-45532800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
4	chr5:45531200-45531400	Enhancers	iPS-20b Cell Line	embryonic stem cell
5	chr5:45531400-45532600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chr5:45532600-45533000	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr5:45532600-45533600	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr5:45532600-45533800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr5:45532600-45534800	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr5:45532800-45533200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
11	chr5:45532800-45533400	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr5:45532800-45533800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr5:45532800-45534000	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr5:45532800-45534000	Enhancers	Brain Germinal Matrix	brain
15	chr5:45532800-45535000	Enhancers	Fetal Heart	heart
16	chr5:45533000-45533400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
17	chr5:45533000-45533600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr5:45533000-45533600	Enhancers	Fetal Brain Female	brain
19	chr5:45533000-45534000	Enhancers	H1 Cell Line	embryonic stem cell
20	chr5:45533000-45534000	Enhancers	H9 Cell Line	embryonic stem cell
21	chr5:45533000-45534200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr5:45533200-45533800	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr5:45533200-45533800	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr5:45533400-45534200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr5:45533400-45534400	Enhancers	Left Ventricle	heart
26	chr5:45533400-45534800	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr5:45533800-45534600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
28	chr5:45534000-45534800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
29	chr5:45534600-45534800	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr5:45534800-45535000	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr5:45534800-45537000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
32	chr5:45535000-45537000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
33	chr5:45537000-45537200	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr5:45537000-45537200	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr5:45537000-45537200	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr5:45541200-45543400	Enhancers	Fetal Heart	heart
37	chr5:45551000-45551200	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr5:45551600-45553000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
39	chr5:45552400-45552600	Enhancers	HUES64 Cell Line	embryonic stem cell
40	chr5:45552800-45553000	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr5:45553000-45555200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr5:45553000-45555800	Enhancers	iPS-18 Cell Line	embryonic stem cell
43	chr5:45553200-45553400	Enhancers	HUES48 Cell Line	embryonic stem cell
44	chr5:45553200-45553400	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr5:45553200-45554400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
46	chr5:45553400-45554400	Weak transcription	HUES48 Cell Line	embryonic stem cell
47	chr5:45553400-45554400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
48	chr5:45554400-45554800	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr5:45554400-45555000	Enhancers	H1 Cell Line	embryonic stem cell
50	chr5:45554400-45555400	Enhancers	HUES64 Cell Line	embryonic stem cell

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