Variant report

Variant	nsv830282
Chromosome Location	chr5:45418260-45573515
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:321)
CpG islands
(count:183)
Chromatin interactive
region (count:12)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:321 , 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	chr5:45520472-45520538	K562	blood:	n/a	n/a
2	BRCA1	chr5:45551191-45551382	H1-hESC	embryonic stem cell:	n/a	n/a
3	BRCA1	chr5:45564807-45564864	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr5:45509316-45509326	A549	lung:	n/a	n/a
5	CEBPB	chr5:45529565-45529645	A549	lung:	n/a	chr5:45529613-45529626 chr5:45529613-45529624 chr5:45529614-45529625 chr5:45529615-45529624
6	CEBPB	chr5:45443698-45444134	HepG2	liver:	n/a	chr5:45444028-45444039 chr5:45443784-45443795 chr5:45443784-45443797
7	CEBPB	chr5:45509164-45509380	HepG2	liver:	n/a	n/a
8	CEBPB	chr5:45454133-45454270	HepG2	liver:	n/a	chr5:45454221-45454232
9	CEBPB	chr5:45529506-45529762	HepG2	liver:	n/a	chr5:45529613-45529626 chr5:45529613-45529624 chr5:45529614-45529625 chr5:45529615-45529624
10	CEBPB	chr5:45443682-45444157	IMR90	lung:	n/a	chr5:45444028-45444039 chr5:45443784-45443795 chr5:45443784-45443797
11	CHD2	chr5:45454268-45454563	H1-hESC	embryonic stem cell:	n/a	n/a
12	CHD2	chr5:45454253-45454550	Hela-S3	cervix:	n/a	n/a
13	CHD2	chr5:45509220-45509267	GM12878	blood:	n/a	n/a
14	CREB1	chr5:45454252-45454607	H1-hESC	embryonic stem cell:	n/a	n/a
15	CREB1	chr5:45454299-45454523	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr5:45521273-45521478	MCF-7	breast:	n/a	n/a
17	CTCF	chr5:45521300-45521450	HRE	kidney:	n/a	n/a
18	CTCF	chr5:45521258-45521446	HepG2	liver:	n/a	n/a
19	CTCF	chr5:45521300-45521450	SK-N-SH_RA	brain:	n/a	n/a
20	CTCF	chr5:45443280-45443430	HRE	kidney:	n/a	n/a
21	CTCF	chr5:45521260-45521410	HRPEpiC	eye:	n/a	n/a
22	CTCF	chr5:45450920-45451070	BE2_C	brain:	n/a	chr5:45450962-45450983 chr5:45450967-45450985 chr5:45450974-45450981
23	CTCF	chr5:45521136-45521616	HCT-116	colon:	n/a	n/a
24	CTCF	chr5:45521296-45521476	GM13977	blood:	n/a	n/a
25	CTCF	chr5:45521280-45521430	BE2_C	brain:	n/a	n/a
26	CTCF	chr5:45450720-45450870	RPTEC	kidney:	n/a	n/a
27	CTCF	chr5:45521260-45521410	HRE	kidney:	n/a	n/a
28	CTCF	chr5:45521257-45521512	HUVEC	blood vessel:	n/a	n/a
29	CTCF	chr5:45521248-45521527	Gliobla	brain:	n/a	n/a
30	CTCF	chr5:45521318-45521437	K562	blood:	n/a	n/a
31	CTCF	chr5:45521340-45521490	HAc	cerebellar:	n/a	n/a
32	CTCF	chr5:45521260-45521410	AG09319	gingival:	n/a	n/a
33	CTCF	chr5:45521280-45521430	HCPEpiC	choroid plexus:	n/a	n/a
34	CTCF	chr5:45521300-45521450	HEK293	kidney:	n/a	n/a
35	CTCF	chr5:45521317-45521440	GM10248	blood:	n/a	n/a
36	CTCF	chr5:45521230-45521521	Medullo	brain:	n/a	n/a
37	CTCF	chr5:45450880-45451023	HUVEC	blood vessel:	n/a	chr5:45450962-45450983 chr5:45450967-45450985 chr5:45450974-45450981
38	CTCF	chr5:45521280-45521430	GM12872	blood:	n/a	n/a
39	CTCF	chr5:45521420-45521570	GM12865	blood:	n/a	n/a
40	CTCF	chr5:45521234-45521434	K562	blood:	n/a	n/a
41	CTCF	chr5:45521300-45521450	HPF	lung:	n/a	n/a
42	CTCF	chr5:45521360-45521510	AG04450	lung:	n/a	n/a
43	CTCF	chr5:45521260-45521410	HBMEC	blood vessel:	n/a	n/a
44	CTCF	chr5:45521204-45521616	MCF-7	breast:	n/a	n/a
45	CTCF	chr5:45521240-45521390	GM12866	blood:	n/a	n/a
46	CTCF	chr5:45521285-45521479	Hela-S3	cervix:	n/a	n/a
47	CTCF	chr5:45521252-45521490	Pancreas_OC	pancreas:	n/a	n/a
48	CTCF	chr5:45521320-45521470	HCPEpiC	choroid plexus:	n/a	n/a
49	CTCF	chr5:45521221-45521531	GM12878	blood:	n/a	n/a
50	CTCF	chr5:45521300-45521450	AG10803	skin:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:45553518-45553568	HCT-116	colon:	n/a
2	chr5:45553518-45553568	IMR90	lung:	fetal
3	chr5:45499395-45499445	MCF-7	breast:	n/a
4	chr5:45569042-45569092	A549	lung:	n/a
5	chr5:45553518-45553568	MCF10A-Er-Src	breast:	n/a
6	chr5:45499395-45499445	Caco-2	colon:	n/a
7	chr5:45569042-45569092	CMK	blood:	n/a
8	chr5:45569042-45569092	K562	blood:	n/a
9	chr5:45553518-45553568	BE2_C	brain:	n/a
10	chr5:45569042-45569092	GM12878	blood:	n/a
11	chr5:45569042-45569092	NHDF-neo	bronchial:	n/a
12	chr5:45499395-45499445	HUVEC	blood vessel:	n/a
13	chr5:45499395-45499445	U87	brain:	n/a
14	chr5:45499395-45499445	HCPEpiC	choroid plexus:	n/a
15	chr5:45499395-45499445	H1-hESC	embryonic stem cell:	embryo
16	chr5:45499395-45499445	HMEC	breast:	n/a
17	chr5:45553518-45553568	HEK293	kidney:	embryo
18	chr5:45553518-45553568	NHBE	bronchial:	n/a
19	chr5:45553518-45553568	HepG2	liver:	n/a
20	chr5:45553518-45553568	AG09319	gingival:	n/a
21	chr5:45569042-45569092	NB4	blood:	n/a
22	chr5:45569042-45569092	HEEpiC	esophagus:	n/a
23	chr5:45569042-45569092	HL-60	blood:	n/a
24	chr5:45499395-45499445	SAEC	small airway:	n/a
25	chr5:45499395-45499445	NH-A	brain:	n/a
26	chr5:45553518-45553568	HNPCEpiC	eye:	n/a
27	chr5:45569042-45569092	SKMC	muscle:	n/a
28	chr5:45553518-45553568	GM06990	blood:	n/a
29	chr5:45553518-45553568	GM19239	blood:	n/a
30	chr5:45569042-45569092	PANC-1	pancreas:	n/a
31	chr5:45569042-45569092	ECC-1	luminal epithelium:	n/a
32	chr5:45499395-45499445	HAEpiC	amniotic membrane:	n/a
33	chr5:45553518-45553568	NT2-D1	testis:	n/a
34	chr5:45499395-45499445	HepG2	liver:	n/a
35	chr5:45499395-45499445	CMK	blood:	n/a
36	chr5:45499395-45499445	NT2-D1	testis:	n/a
37	chr5:45499395-45499445	PANC-1	pancreas:	n/a
38	chr5:45553518-45553568	HRPEpiC	eye:	n/a
39	chr5:45553518-45553568	SK-N-MC	brain:	n/a
40	chr5:45553518-45553568	NB4	blood:	n/a
41	chr5:45569042-45569092	ProgFib	skin:	n/a
42	chr5:45553518-45553568	AG04450	lung:	fetal
43	chr5:45553518-45553568	AG04449	skin:	fetal
44	chr5:45569042-45569092	BE2_C	brain:	n/a
45	chr5:45499395-45499445	SK-N-SH_RA	brain:	n/a
46	chr5:45553518-45553568	PrEC	prostate:	n/a
47	chr5:45569042-45569092	Hela-S3	cervix:	n/a
48	chr5:45569042-45569092	AG04449	skin:	fetal
49	chr5:45569042-45569092	T-47D	breast:	n/a
50	chr5:45499395-45499445	A549	lung:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:44952200..44952811-chr5:45521283..45521849,2	MCF-7	breast:
2	chr5:45435601..45437646-chr5:45441992..45444757,2	K562	blood:
3	chr5:45435601..45437646-chr5:45441992..45444757,2	K562	blood:
4	chr5:45468898..45471467-chr5:45477657..45479826,2	MCF-7	breast:
5	chr5:45487505..45488239-chr6:10695353..10695968,2	MCF-7	breast:
6	chr15:66571588..66572090-chr5:45541388..45542303,2	MCF-7	breast:
7	chr5:45468898..45471467-chr5:45477657..45479826,2	MCF-7	breast:
8	chr5:45423533..45425292-chr5:45434104..45435924,2	MCF-7	breast:
9	chr1:205318512..205319277-chr5:45469628..45470349,2	MCF-7	breast:
10	chr5:45038409..45039119-chr5:45520902..45521831,4	MCF-7	breast:
11	chr13:55537336..55537947-chr5:45562607..45563107,2	MCF-7	breast:
12	chr5:45423533..45425292-chr5:45434104..45435924,2	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: 2256 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:2256 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs139311521	chr5:45418265-45418266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs149997236	chr5:45418286-45418287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs180885182	chr5:45418296-45418297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs185785605	chr5:45418303-45418304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs527301534	chr5:45418310-45418311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs62369062	chr5:45418333-45418334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs563616507	chr5:45418382-45418383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs111652399	chr5:45418402-45418403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs10472404	chr5:45418421-45418422	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs148754213	chr5:45418461-45418462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs529092280	chr5:45418536-45418537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs548774713	chr5:45418575-45418576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs549137561	chr5:45418607-45418608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs191478113	chr5:45418680-45418681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs546460113	chr5:45418737-45418738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs78095611	chr5:45418747-45418748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs142264412	chr5:45418751-45418752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs370595088	chr5:45418791-45418792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs117219193	chr5:45418940-45418941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs537041062	chr5:45418973-45418974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs557134776	chr5:45419010-45419011	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs75106937	chr5:45419018-45419019	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs542700296	chr5:45419054-45419055	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs115081907	chr5:45419100-45419101	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs573354696	chr5:45419108-45419109	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs545414351	chr5:45419183-45419184	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs181176561	chr5:45419238-45419239	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs530857451	chr5:45419241-45419242	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs187081134	chr5:45419244-45419245	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs560905027	chr5:45419308-45419309	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs190461840	chr5:45419314-45419315	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs367702342	chr5:45419329-45419330	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs76855774	chr5:45419343-45419344	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs546659961	chr5:45419348-45419349	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs565751285	chr5:45419363-45419364	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs571229242	chr5:45426431-45426432	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs537177336	chr5:45426481-45426482	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs185985533	chr5:45426490-45426491	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs188888561	chr5:45426510-45426511	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs182547869	chr5:45426534-45426535	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs553248492	chr5:45426554-45426555	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs575140156	chr5:45426555-45426556	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs138077705	chr5:45426654-45426655	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs6891513	chr5:45426702-45426703	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs564955611	chr5:45426780-45426781	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs575220985	chr5:45426781-45426782	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs187163571	chr5:45426806-45426807	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs78645523	chr5:45426814-45426815	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs529118939	chr5:45426842-45426843	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs549172016	chr5:45426849-45426850	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
Lung cancer	18438408	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
small cell lung cancer	20016488	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
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:167 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:45404200-45419200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr5:45419000-45419400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr5:45419200-45419400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr5:45426400-45426800	Enhancers	Skeletal Muscle Male	skeletal muscle
5	chr5:45426600-45427400	Enhancers	Skeletal Muscle Female	skeletal muscle
6	chr5:45436200-45436400	Enhancers	Skeletal Muscle Male	skeletal muscle
7	chr5:45436600-45437600	Weak transcription	Skeletal Muscle Male	skeletal muscle
8	chr5:45437000-45438000	Active TSS	Skeletal Muscle Female	skeletal muscle
9	chr5:45437600-45437800	Active TSS	Skeletal Muscle Male	skeletal muscle
10	chr5:45437800-45438000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
11	chr5:45438000-45438400	Enhancers	Skeletal Muscle Female	skeletal muscle
12	chr5:45438000-45440600	Weak transcription	Skeletal Muscle Male	skeletal muscle
13	chr5:45438400-45439600	Weak transcription	Skeletal Muscle Female	skeletal muscle
14	chr5:45440600-45440800	Enhancers	Lung	lung
15	chr5:45440600-45440800	Enhancers	Skeletal Muscle Female	skeletal muscle
16	chr5:45440600-45441000	Enhancers	Skeletal Muscle Male	skeletal muscle
17	chr5:45443600-45444200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr5:45453800-45454400	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr5:45454000-45454400	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr5:45454000-45454400	Enhancers	Skeletal Muscle Male	skeletal muscle
21	chr5:45454000-45454800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr5:45454400-45454800	Weak transcription	Skeletal Muscle Male	skeletal muscle
23	chr5:45454800-45455200	Enhancers	Skeletal Muscle Male	skeletal muscle
24	chr5:45491000-45492000	Enhancers	Liver	Liver
25	chr5:45491000-45492000	Enhancers	Rectal Mucosa Donor 31	rectum
26	chr5:45491000-45492400	Enhancers	Fetal Intestine Large	intestine
27	chr5:45492000-45500200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr5:45505800-45509600	Enhancers	Fetal Brain Female	brain
29	chr5:45506400-45506600	Enhancers	Fetal Brain Male	brain
30	chr5:45506600-45507600	Weak transcription	Fetal Brain Male	brain
31	chr5:45507200-45507600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr5:45507200-45507800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr5:45507200-45508400	Enhancers	Brain Germinal Matrix	brain
34	chr5:45507400-45507600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr5:45507400-45507600	Enhancers	Skeletal Muscle Male	skeletal muscle
36	chr5:45507600-45510000	Enhancers	Fetal Brain Male	brain
37	chr5:45509600-45510800	Weak transcription	Fetal Brain Female	brain
38	chr5:45510800-45511000	Enhancers	Fetal Brain Female	brain
39	chr5:45515400-45516200	Enhancers	Fetal Heart	heart
40	chr5:45518200-45518600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr5:45518600-45524000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr5:45520800-45521200	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr5:45520800-45521200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr5:45521000-45521400	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr5:45521400-45521800	Enhancers	Skeletal Muscle Male	skeletal muscle
46	chr5:45521400-45521800	Enhancers	Skeletal Muscle Female	skeletal muscle
47	chr5:45524000-45524200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr5:45524200-45526400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr5:45525800-45532800	Weak transcription	Fetal Heart	heart
50	chr5:45526400-45526800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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