Variant report

Variant	nsv482911
Chromosome Location	chr5:45488673-45641913
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:442)
CpG islands
(count:183)
Chromatin interactive
region (count:6)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:442 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr5:45520472-45520538	K562	blood:	n/a	n/a
2	BACH1	chr5:45622547-45622743	K562	blood:	n/a	n/a
3	BACH1	chr5:45622469-45623083	H1-hESC	embryonic stem cell:	n/a	n/a
4	BRCA1	chr5:45624018-45624277	Hela-S3	cervix:	n/a	n/a
5	BRCA1	chr5:45551191-45551382	H1-hESC	embryonic stem cell:	n/a	n/a
6	BRCA1	chr5:45564807-45564864	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr5:45609832-45610172	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr5:45529565-45529645	A549	lung:	n/a	chr5:45529613-45529626 chr5:45529613-45529624 chr5:45529614-45529625 chr5:45529615-45529624
9	CEBPB	chr5:45509316-45509326	A549	lung:	n/a	n/a
10	CEBPB	chr5:45529506-45529762	HepG2	liver:	n/a	chr5:45529613-45529626 chr5:45529613-45529624 chr5:45529614-45529625 chr5:45529615-45529624
11	CEBPB	chr5:45509164-45509380	HepG2	liver:	n/a	n/a
12	CEBPB	chr5:45588337-45588611	HepG2	liver:	n/a	n/a
13	CEBPB	chr5:45623926-45624273	Hela-S3	cervix:	n/a	n/a
14	CHD2	chr5:45509220-45509267	GM12878	blood:	n/a	n/a
15	CTCF	chr5:45639304-45639433	HepG2	liver:	n/a	chr5:45639352-45639359
16	CTCF	chr5:45639320-45639470	HA-sp	spinal cord:	n/a	chr5:45639352-45639359
17	CTCF	chr5:45521204-45521616	MCF-7	breast:	n/a	n/a
18	CTCF	chr5:45521280-45521430	BJ	skin:	n/a	n/a
19	CTCF	chr5:45521280-45521430	HA-sp	spinal cord:	n/a	n/a
20	CTCF	chr5:45521285-45521479	Hela-S3	cervix:	n/a	n/a
21	CTCF	chr5:45521420-45521570	GM12865	blood:	n/a	n/a
22	CTCF	chr5:45639288-45639451	Pancreas_OC	pancreas:	n/a	chr5:45639352-45639359
23	CTCF	chr5:45639320-45639470	HRPEpiC	eye:	n/a	chr5:45639352-45639359
24	CTCF	chr5:45639380-45639530	RPTEC	kidney:	n/a	n/a
25	CTCF	chr5:45639320-45639470	Hela-S3	cervix:	n/a	chr5:45639352-45639359
26	CTCF	chr5:45521320-45521470	NHLF	lung:	n/a	n/a
27	CTCF	chr5:45521320-45521470	HCM	heart:	n/a	n/a
28	CTCF	chr5:45639336-45639421	MCF-7	breast:	n/a	chr5:45639352-45639359
29	CTCF	chr5:45639304-45639416	HepG2	liver:	n/a	chr5:45639352-45639359
30	CTCF	chr5:45521280-45521430	GM06990	blood:	n/a	n/a
31	CTCF	chr5:45521334-45521376	MCF-7	breast:	n/a	n/a
32	CTCF	chr5:45628916-45628943	GM10266	blood:	n/a	n/a
33	CTCF	chr5:45521264-45521474	Kidney_OC	kidney:	n/a	n/a
34	CTCF	chr5:45521257-45521512	HUVEC	blood vessel:	n/a	n/a
35	CTCF	chr5:45639300-45639450	Caco-2	colon:	n/a	chr5:45639352-45639359
36	CTCF	chr5:45639317-45639434	MCF-7	breast:	n/a	chr5:45639352-45639359
37	CTCF	chr5:45639247-45639469	MCF-7	breast:	n/a	chr5:45639352-45639359
38	CTCF	chr5:45639300-45639450	HRE	kidney:	n/a	chr5:45639352-45639359
39	CTCF	chr5:45639130-45639492	MCF-7	breast:	n/a	chr5:45639352-45639359
40	CTCF	chr5:45521270-45521479	LNCaP	prostate:	n/a	n/a
41	CTCF	chr5:45521173-45521556	IMR90	lung:	n/a	n/a
42	CTCF	chr5:45521248-45521527	Gliobla	brain:	n/a	n/a
43	CTCF	chr5:45604382-45604423	Pancreas_OC	pancreas:	n/a	n/a
44	CTCF	chr5:45521295-45521468	Lung_OC	lung:	n/a	n/a
45	CTCF	chr5:45639065-45639699	SK-N-SH	brain:	n/a	chr5:45639352-45639359
46	CTCF	chr5:45521260-45521410	GM12873	blood:	n/a	n/a
47	CTCF	chr5:45639260-45639410	HL-60	blood:	n/a	chr5:45639352-45639359
48	CTCF	chr5:45639260-45639410	SK-N-SH_RA	brain:	n/a	chr5:45639352-45639359
49	CTCF	chr5:45521296-45521476	GM13977	blood:	n/a	n/a
50	CTCF	chr5:45521300-45521450	RPTEC	kidney:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:45569042-45569092	HEEpiC	esophagus:	n/a
2	chr5:45553518-45553568	H1-hESC	embryonic stem cell:	embryo
3	chr5:45553518-45553568	Caco-2	colon:	n/a
4	chr5:45553518-45553568	MCF10A-Er-Src	breast:	n/a
5	chr5:45569042-45569092	HRPEpiC	eye:	n/a
6	chr5:45569042-45569092	NHBE	bronchial:	n/a
7	chr5:45553518-45553568	A549	lung:	n/a
8	chr5:45569042-45569092	HL-60	blood:	n/a
9	chr5:45499395-45499445	HRE	kidney:	n/a
10	chr5:45569042-45569092	AG04450	lung:	fetal
11	chr5:45499395-45499445	Hela-S3	cervix:	n/a
12	chr5:45569042-45569092	RPTEC	kidney:	n/a
13	chr5:45569042-45569092	SK-N-MC	brain:	n/a
14	chr5:45569042-45569092	Jurkat	blood:	n/a
15	chr5:45499395-45499445	Hepatocyte	liver:	n/a
16	chr5:45569042-45569092	MCF10A-Er-Src	breast:	n/a
17	chr5:45553518-45553568	HL-60	blood:	n/a
18	chr5:45553518-45553568	ovcar-3	ovarian:	n/a
19	chr5:45553518-45553568	Hepatocyte	liver:	n/a
20	chr5:45553518-45553568	PFSK-1	brain:	n/a
21	chr5:45499395-45499445	HNPCEpiC	eye:	n/a
22	chr5:45499395-45499445	NHDF-neo	bronchial:	n/a
23	chr5:45569042-45569092	GM12892	blood:	n/a
24	chr5:45569042-45569092	PFSK-1	brain:	n/a
25	chr5:45553518-45553568	GM12892	blood:	n/a
26	chr5:45569042-45569092	Caco-2	colon:	n/a
27	chr5:45553518-45553568	AG04450	lung:	fetal
28	chr5:45569042-45569092	Hela-S3	cervix:	n/a
29	chr5:45569042-45569092	HPAEpiC	pulmonary alveolar:	n/a
30	chr5:45553518-45553568	ProgFib	skin:	n/a
31	chr5:45553518-45553568	U87	brain:	n/a
32	chr5:45569042-45569092	SAEC	small airway:	n/a
33	chr5:45499395-45499445	MCF-7	breast:	n/a
34	chr5:45499395-45499445	BJ	skin:	n/a
35	chr5:45569042-45569092	HCT-116	colon:	n/a
36	chr5:45569042-45569092	HRE	kidney:	n/a
37	chr5:45553518-45553568	RPTEC	kidney:	n/a
38	chr5:45553518-45553568	AG10803	skin:	n/a
39	chr5:45499395-45499445	HCT-116	colon:	n/a
40	chr5:45499395-45499445	NT2-D1	testis:	n/a
41	chr5:45553518-45553568	LNCaP	prostate:	n/a
42	chr5:45569042-45569092	HCPEpiC	choroid plexus:	n/a
43	chr5:45499395-45499445	SK-N-MC	brain:	n/a
44	chr5:45569042-45569092	HepG2	liver:	n/a
45	chr5:45553518-45553568	HPAEpiC	pulmonary alveolar:	n/a
46	chr5:45569042-45569092	A549	lung:	n/a
47	chr5:45553518-45553568	NHBE	bronchial:	n/a
48	chr5:45499395-45499445	T-47D	breast:	n/a
49	chr5:45499395-45499445	HIPEpiC	eye:	n/a
50	chr5:45553518-45553568	CMK	blood:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:45038409..45039119-chr5:45520902..45521831,4	MCF-7	breast:
2	chr15:66571588..66572090-chr5:45541388..45542303,2	MCF-7	breast:
3	chr5:45635537..45637341-chr5:45642108..45644494,2	K562	blood:
4	chr5:44952326..44952886-chr5:45639183..45639775,2	MCF-7	breast:
5	chr5:44952200..44952811-chr5:45521283..45521849,2	MCF-7	breast:
6	chr13:55537336..55537947-chr5:45562607..45563107,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MRPS30-13	chr5:45574692-45576714	NONHSAT101361
2	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: 3413 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:3413 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs184475067	chr5:45491031-45491032	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs567248253	chr5:45491048-45491049	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs543782493	chr5:45491058-45491059	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs534753953	chr5:45491065-45491066	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs77505492	chr5:45491146-45491147	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs187817156	chr5:45491169-45491170	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs199917076	chr5:45491171-45491172	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs549159565	chr5:45491172-45491173	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs561875817	chr5:45491190-45491191	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs527450527	chr5:45491230-45491231	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs138893263	chr5:45491231-45491232	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs114206363	chr5:45491256-45491257	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs192786107	chr5:45491273-45491274	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs149416285	chr5:45491297-45491298	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs569698220	chr5:45491312-45491313	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs78266485	chr5:45491326-45491327	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs111630901	chr5:45491395-45491396	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs565755439	chr5:45491440-45491441	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs114634363	chr5:45491447-45491448	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs555009363	chr5:45491452-45491453	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs377257840	chr5:45491518-45491519	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs79498246	chr5:45491572-45491573	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs143946103	chr5:45491573-45491574	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs558064370	chr5:45491644-45491645	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs376557077	chr5:45491700-45491701	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs386687789	chr5:45491723-45491724	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs75150349	chr5:45491724-45491725	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs370612001	chr5:45491732-45491733	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs573908319	chr5:45491787-45491788	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs543161170	chr5:45491802-45491803	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs564684570	chr5:45491870-45491871	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs183980125	chr5:45491898-45491899	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs188367018	chr5:45491905-45491906	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs530478060	chr5:45491925-45491926	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs1483307	chr5:45491939-45491940	Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
36	rs527513784	chr5:45492051-45492052	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs541214752	chr5:45492091-45492092	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs564413869	chr5:45492119-45492120	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs377343104	chr5:45492121-45492122	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs536432728	chr5:45492177-45492178	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs549763823	chr5:45492204-45492205	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs6451804	chr5:45492205-45492206	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs573248103	chr5:45492210-45492211	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs140434977	chr5:45492218-45492219	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs144176341	chr5:45492239-45492240	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs80064126	chr5:45492262-45492263	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs576843146	chr5:45492304-45492305	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs534925374	chr5:45492375-45492376	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs375423075	chr5:45492398-45492399	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs375738599	chr5:45492399-45492400	Weak transcription Enhancers	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:197 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:45491000-45492000	Enhancers	Liver	Liver
2	chr5:45491000-45492000	Enhancers	Rectal Mucosa Donor 31	rectum
3	chr5:45491000-45492400	Enhancers	Fetal Intestine Large	intestine
4	chr5:45492000-45500200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr5:45505800-45509600	Enhancers	Fetal Brain Female	brain
6	chr5:45506400-45506600	Enhancers	Fetal Brain Male	brain
7	chr5:45506600-45507600	Weak transcription	Fetal Brain Male	brain
8	chr5:45507200-45507600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr5:45507200-45507800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr5:45507200-45508400	Enhancers	Brain Germinal Matrix	brain
11	chr5:45507400-45507600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr5:45507400-45507600	Enhancers	Skeletal Muscle Male	skeletal muscle
13	chr5:45507600-45510000	Enhancers	Fetal Brain Male	brain
14	chr5:45509600-45510800	Weak transcription	Fetal Brain Female	brain
15	chr5:45510800-45511000	Enhancers	Fetal Brain Female	brain
16	chr5:45515400-45516200	Enhancers	Fetal Heart	heart
17	chr5:45518200-45518600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr5:45518600-45524000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr5:45520800-45521200	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr5:45520800-45521200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr5:45521000-45521400	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr5:45521400-45521800	Enhancers	Skeletal Muscle Male	skeletal muscle
23	chr5:45521400-45521800	Enhancers	Skeletal Muscle Female	skeletal muscle
24	chr5:45524000-45524200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr5:45524200-45526400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr5:45525800-45532800	Weak transcription	Fetal Heart	heart
27	chr5:45526400-45526800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr5:45526400-45526800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr5:45529000-45529400	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr5:45529400-45532800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
31	chr5:45531200-45531400	Enhancers	iPS-20b Cell Line	embryonic stem cell
32	chr5:45531400-45532600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
33	chr5:45532600-45533000	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr5:45532600-45533600	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr5:45532600-45533800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr5:45532600-45534800	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr5:45532800-45533200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
38	chr5:45532800-45533400	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr5:45532800-45533800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr5:45532800-45534000	Enhancers	iPS-18 Cell Line	embryonic stem cell
41	chr5:45532800-45534000	Enhancers	Brain Germinal Matrix	brain
42	chr5:45532800-45535000	Enhancers	Fetal Heart	heart
43	chr5:45533000-45533400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
44	chr5:45533000-45533600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr5:45533000-45533600	Enhancers	Fetal Brain Female	brain
46	chr5:45533000-45534000	Enhancers	H1 Cell Line	embryonic stem cell
47	chr5:45533000-45534000	Enhancers	H9 Cell Line	embryonic stem cell
48	chr5:45533000-45534200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr5:45533200-45533800	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr5:45533200-45533800	Enhancers	HUES6 Cell Line	embryonic stem cell

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