Variant report

Variant	nsv537711
Chromosome Location	chr5:28951390-29139719
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	chr5:28990432-28990436	K562	blood:	n/a	n/a
2	ARID3A	chr5:29070987-29071060	K562	blood:	n/a	n/a
3	ATF1	chr5:29114649-29114850	K562	blood:	n/a	n/a
4	ATF1	chr5:29134593-29134792	K562	blood:	n/a	n/a
5	ATF1	chr5:29089739-29090287	K562	blood:	n/a	n/a
6	ATF1	chr5:29005496-29006030	K562	blood:	n/a	n/a
7	BATF	chr5:29099772-29100098	GM12878	blood:	n/a	n/a
8	BATF	chr5:29099732-29100010	GM12878	blood:	n/a	n/a
9	BHLHE40	chr5:29089838-29090224	K562	blood:	n/a	n/a
10	BHLHE40	chr5:29114706-29114820	K562	blood:	n/a	n/a
11	BRCA1	chr5:29077488-29077830	Hela-S3	cervix:	n/a	n/a
12	CBX3	chr5:29134584-29134844	K562	blood:	n/a	n/a
13	CCNT2	chr5:29051731-29051997	K562	blood:	n/a	chr5:29051832-29051852
14	CCNT2	chr5:29089941-29090240	K562	blood:	n/a	n/a
15	CCNT2	chr5:29079757-29080002	K562	blood:	n/a	n/a
16	CCNT2	chr5:29017623-29017823	K562	blood:	n/a	n/a
17	CEBPB	chr5:29005633-29005968	IMR90	lung:	n/a	chr5:29005787-29005798
18	CEBPB	chr5:29096184-29096509	IMR90	lung:	n/a	chr5:29096332-29096343 chr5:29096327-29096344 chr5:29096330-29096343 chr5:29096332-29096341 chr5:29096332-29096341 chr5:29096332-29096341 chr5:29096332-29096341 chr5:29096330-29096341
19	CEBPB	chr5:28996802-28996842	K562	blood:	n/a	n/a
20	CEBPB	chr5:29040534-29040845	A549	lung:	n/a	chr5:29040710-29040721
21	CEBPB	chr5:29096282-29096449	H1-hESC	embryonic stem cell:	n/a	chr5:29096332-29096343 chr5:29096327-29096344 chr5:29096330-29096343 chr5:29096332-29096341 chr5:29096332-29096341 chr5:29096332-29096341 chr5:29096332-29096341 chr5:29096330-29096341
22	CEBPB	chr5:29040539-29040883	HepG2	liver:	n/a	chr5:29040710-29040721
23	CEBPB	chr5:29005532-29005991	Hela-S3	cervix:	n/a	chr5:29005787-29005798
24	CEBPB	chr5:29077957-29078214	A549	lung:	n/a	n/a
25	CEBPB	chr5:29096194-29096516	A549	lung:	n/a	chr5:29096332-29096343 chr5:29096327-29096344 chr5:29096330-29096343 chr5:29096332-29096341 chr5:29096332-29096341 chr5:29096332-29096341 chr5:29096332-29096341 chr5:29096330-29096341
26	CEBPB	chr5:29077432-29078233	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr5:29072750-29072805	HepG2	liver:	n/a	chr5:29072772-29072783
28	CEBPB	chr5:29040539-29040883	IMR90	lung:	n/a	chr5:29040710-29040721
29	CEBPB	chr5:29037785-29038205	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr5:28996805-28996847	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr5:29005619-29005973	HepG2	liver:	n/a	chr5:29005787-29005798
32	CEBPB	chr5:28996799-28997003	HepG2	liver:	n/a	n/a
33	CEBPB	chr5:29005612-29005970	K562	blood:	n/a	chr5:29005787-29005798
34	CEBPB	chr5:29096172-29096477	K562	blood:	n/a	chr5:29096332-29096343 chr5:29096327-29096344 chr5:29096330-29096343 chr5:29096332-29096341 chr5:29096332-29096341 chr5:29096332-29096341 chr5:29096332-29096341 chr5:29096330-29096341
35	CEBPB	chr5:28955763-28956009	A549	lung:	n/a	chr5:28955901-28955914 chr5:28955901-28955912
36	CEBPB	chr5:28996795-28996999	A549	lung:	n/a	n/a
37	CEBPB	chr5:28955759-28956080	HepG2	liver:	n/a	chr5:28955901-28955914 chr5:28955901-28955912
38	CEBPB	chr5:28955727-28956050	IMR90	lung:	n/a	chr5:28955901-28955914 chr5:28955901-28955912
39	CEBPB	chr5:29130906-29131232	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr5:29134625-29134899	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr5:29134588-29134823	K562	blood:	n/a	n/a
42	CEBPB	chr5:29096209-29096500	HepG2	liver:	n/a	chr5:29096332-29096343 chr5:29096327-29096344 chr5:29096330-29096343 chr5:29096332-29096341 chr5:29096332-29096341 chr5:29096332-29096341 chr5:29096332-29096341 chr5:29096330-29096341
43	CEBPB	chr5:29025866-29026131	HepG2	liver:	n/a	chr5:29026021-29026032
44	CEBPB	chr5:29085361-29085554	HepG2	liver:	n/a	n/a
45	CEBPB	chr5:29040551-29040876	K562	blood:	n/a	chr5:29040710-29040721
46	CEBPB	chr5:29134586-29134903	K562	blood:	n/a	n/a
47	CEBPB	chr5:29096216-29096495	Hela-S3	cervix:	n/a	chr5:29096332-29096343 chr5:29096327-29096344 chr5:29096330-29096343 chr5:29096332-29096341 chr5:29096332-29096341 chr5:29096332-29096341 chr5:29096332-29096341 chr5:29096330-29096341
48	CEBPB	chr5:29005648-29005964	A549	lung:	n/a	chr5:29005787-29005798
49	CHD1	chr5:29048762-29048773	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD1	chr5:29095636-29095675	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:29128011-29128061	NHBE	bronchial:	n/a
2	chr5:29128011-29128061	HEK293	kidney:	embryo
3	chr5:29128011-29128061	HepG2	liver:	n/a
4	chr5:29128011-29128061	HCT-116	colon:	n/a
5	chr5:29128011-29128061	NH-A	brain:	n/a
6	chr5:29128011-29128061	RPTEC	kidney:	n/a
7	chr5:29128011-29128061	PrEC	prostate:	n/a
8	chr5:29128011-29128061	PANC-1	pancreas:	n/a
9	chr5:29128011-29128061	GM19239	blood:	n/a
10	chr5:29128011-29128061	PFSK-1	brain:	n/a
11	chr5:29128011-29128061	ovcar-3	ovarian:	n/a
12	chr5:29128011-29128061	HRE	kidney:	n/a
13	chr5:29128011-29128061	SK-N-MC	brain:	n/a
14	chr5:29128011-29128061	NT2-D1	testis:	n/a
15	chr5:29128011-29128061	Caco-2	colon:	n/a
16	chr5:29128011-29128061	HEEpiC	esophagus:	n/a
17	chr5:29128011-29128061	SAEC	small airway:	n/a
18	chr5:29128011-29128061	U87	brain:	n/a
19	chr5:29128011-29128061	AG09309	skin:	n/a
20	chr5:29128011-29128061	Hepatocyte	liver:	n/a
21	chr5:29128011-29128061	GM12892	blood:	n/a
22	chr5:29128011-29128061	AG10803	skin:	n/a
23	chr5:29128011-29128061	SKMC	muscle:	n/a
24	chr5:29128011-29128061	GM12891	blood:	n/a
25	chr5:29128011-29128061	K562	blood:	n/a
26	chr5:29128011-29128061	HUVEC	blood vessel:	n/a
27	chr5:29128011-29128061	HIPEpiC	eye:	n/a
28	chr5:29128011-29128061	HL-60	blood:	n/a
29	chr5:29128011-29128061	Jurkat	blood:	n/a
30	chr5:29128011-29128061	AG04449	skin:	fetal
31	chr5:29128011-29128061	CMK	blood:	n/a
32	chr5:29128011-29128061	NB4	blood:	n/a
33	chr5:29128011-29128061	HNPCEpiC	eye:	n/a
34	chr5:29128011-29128061	HCM	heart:	n/a
35	chr5:29128011-29128061	H1-hESC	embryonic stem cell:	embryo
36	chr5:29128011-29128061	A549	lung:	n/a
37	chr5:29128011-29128061	IMR90	lung:	fetal
38	chr5:29128011-29128061	Hela-S3	cervix:	n/a
39	chr5:29128011-29128061	ProgFib	skin:	n/a
40	chr5:29128011-29128061	SK-N-SH	brain:	n/a
41	chr5:29128011-29128061	AoSMC	blood vessel:	n/a
42	chr5:29128011-29128061	BJ	skin:	n/a
43	chr5:29128011-29128061	MCF-7	breast:	n/a
44	chr5:29128011-29128061	HPAEpiC	pulmonary alveolar:	n/a
45	chr5:29128011-29128061	MCF10A-Er-Src	breast:	n/a
46	chr5:29128011-29128061	HMEC	breast:	n/a
47	chr5:29128011-29128061	HAEpiC	amniotic membrane:	n/a
48	chr5:29128011-29128061	GM06990	blood:	n/a
49	chr5:29128011-29128061	SK-N-SH_RA	brain:	n/a
50	chr5:29128011-29128061	GM12878	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:28961127..28964020-chr5:28970409..28972229,2	K562	blood:
2	chr5:29059482..29062466-chr5:29065874..29068673,2	MCF-7	breast:
3	chr5:28996102..28998420-chr5:29007454..29009412,2	K562	blood:
4	chr20:55853010..55855279-chr5:29022487..29024544,2	MCF-7	breast:
5	chr5:28906947..28909506-chr5:29049292..29051622,2	K562	blood:
6	chr5:29026756..29028723-chr5:29043428..29045918,2	K562	blood:
7	chr5:29003141..29005545-chr5:29008862..29010410,2	K562	blood:
8	chr5:28986098..28988611-chr5:28988993..28991455,2	MCF-7	breast:
9	chr5:29005476..29006055-chr5:29218041..29218711,2	MCF-7	breast:
10	chr5:28986098..28988611-chr5:28988993..28991455,2	MCF-7	breast:
11	chr5:29059482..29062466-chr5:29065874..29068673,2	MCF-7	breast:
12	chr5:29050111..29052926-chr5:29053158..29054737,2	MCF-7	breast:
13	chr5:28999555..29001892-chr5:29014306..29015830,2	K562	blood:
14	chr5:28961127..28964020-chr5:28970409..28972229,2	K562	blood:
15	chr5:29050111..29052926-chr5:29053158..29054737,2	MCF-7	breast:
16	chr5:29005255..29006082-chr5:29217591..29218623,4	MCF-7	breast:
17	chr5:29138046..29139623-chr5:29144117..29145732,2	K562	blood:
18	chr5:28996102..28998420-chr5:29007454..29009412,2	K562	blood:
19	chr5:29026756..29028723-chr5:29043428..29045918,2	K562	blood:
20	chr5:29003141..29005545-chr5:29008862..29010410,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CDH6-11	chr5:29126624-29126682	NONHSAT100835
2	lnc-CDH6-3	chr5:29073007-29073329	ENSG00000249322
3	lnc-CDH6-3	chr5:29066381-29070363	NR_109948
4	lnc-CDH6-12	chr5:29105449-29105545	NONHSAT100833
5	lnc-CDH6-3	chr5:29065351-29065724	NR_109948
6	lnc-CDH6-12	chr5:29104987-29105152	NONHSAT100833
7	lnc-CDH6-3	chr5:29065946-29066069	NR_109948
8	lnc-CDH6-13	chr5:29001867-29002148	NONHSAT100830
9	lnc-CDH6-13	chr5:29002720-29003464	NONHSAT100830
10	lnc-CDH6-3	chr5:29066381-29070363	ENSG00000249322
11	lnc-CDH9-14	chr5:29105675-29106968	NONHSAT100834
12	lnc-CDH6-3	chr5:29065946-29066069	ENSG00000249322
13	lnc-CDH6-3	chr5:29073007-29073330	NR_109948
14	lnc-CDH6-11	chr5:29106999-29107219	NONHSAT100835
15	lnc-CDH6-3	chr5:29065351-29065724	ENSG00000249322

Variant related genes	Relation type
ENSG00000259786	TF binding region
SUCLG2P4	TF binding region
ENSG00000252601	TF binding region
ENSG00000248687	TF binding region
ENSG00000270430	TF binding region
ENSG00000259786	CpG island
SUCLG2P4	CpG island
ENSG00000252601	CpG island
ENSG00000248687	CpG island
ENSG00000270430	CpG island
ENSG00000249226	chromatin interactions
FOXD1	miRNA target sites
CBFB	miRNA target sites

Extended variants
information (count: 2471 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:2471 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs182063588	chr5:28951390-28951391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs186071489	chr5:28951478-28951479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs374738691	chr5:28951512-28951513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs577598162	chr5:28951575-28951576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs78165599	chr5:28951582-28951583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs200045654	chr5:28951583-28951584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs75492908	chr5:28951585-28951586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs544965014	chr5:28951595-28951596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs392197	chr5:28951611-28951612	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs371932	chr5:28951616-28951617	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs531397957	chr5:28951632-28951633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs540431767	chr5:28951678-28951679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs79789846	chr5:28951718-28951719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs529481488	chr5:28951724-28951725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs544614864	chr5:28951725-28951726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs190444869	chr5:28951731-28951732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs533192921	chr5:28951732-28951733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs112076149	chr5:28951733-28951734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs371073791	chr5:28951739-28951740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs145662433	chr5:28951760-28951761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs566978538	chr5:28951772-28951773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs527737406	chr5:28951783-28951784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs183060282	chr5:28951796-28951797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs567506507	chr5:28951805-28951806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs186208611	chr5:28951829-28951830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs556209244	chr5:28951834-28951835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs571488318	chr5:28951875-28951876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs191503444	chr5:28951913-28951914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs553307223	chr5:28951966-28951967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs571706334	chr5:28952001-28952002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs542356715	chr5:28952029-28952030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs554229092	chr5:28952059-28952060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs182480829	chr5:28952127-28952128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs574181349	chr5:28952159-28952160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs371083355	chr5:28952225-28952226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs140384558	chr5:28952226-28952227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs533634661	chr5:28952266-28952267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs545422810	chr5:28952269-28952270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs188001671	chr5:28952296-28952297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs193083089	chr5:28952316-28952317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs527674482	chr5:28952321-28952322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs549531438	chr5:28952410-28952411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs367571331	chr5:28952414-28952415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs567738220	chr5:28952468-28952469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs531426009	chr5:28952471-28952472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs549910060	chr5:28952492-28952493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs183074524	chr5:28952504-28952505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs547049478	chr5:28952508-28952509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs547282859	chr5:28952562-28952563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs28834489	chr5:28952589-28952590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:100)

Disease	PMID	Source
Kartagener syndrome	16639409	CNVD
Medulloblastoma	21979893	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
Non-small cell lung cancer	20864512	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	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
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
Thoracic aortic aneurysm	21092924	CNVD
Multiple myeloma	17550852	CNVD
prenatal diagnosis	22389664	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
Breast cancer	21858162	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Cancer	16751803	CNVD
Breast cancer	16608533	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Intellectual disability	22102821	CNVD
Renal cell carcinoma	18194544	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Non-small cell lung cancer	19010865	CNVD
Glioblastoma multiforme	22286061	CNVD
Compulsive disorder	18923513	CNVD
Epilepsy	18923513	CNVD
Prader-willi syndrome	18923513	CNVD
small cell lung cancer	20016488	CNVD
Ovarian cancer	21720365	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Esophageal cancer	20955586	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21364760	CNVD
Breast cancer	20409316	CNVD
Medulloblastoma	19270706	CNVD
Breast cancer	19553991	CNVD
Lung cancer	19553991	CNVD
Melanoma	19553991	CNVD
Ovarian cancer	19553991	CNVD
Prostate cancer	19553991	CNVD
Non-small cell lung cancer	17156491	CNVD
Breast cancer	17133270	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:121 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:28935000-28958800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr5:28954000-28954200	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr5:28954000-28954200	Enhancers	HUES6 Cell Line	embryonic stem cell
4	chr5:28954200-28954600	Active TSS	HUES48 Cell Line	embryonic stem cell
5	chr5:28954600-28955000	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr5:28955000-28955200	Active TSS	HUES48 Cell Line	embryonic stem cell
7	chr5:28962200-28962600	Enhancers	NH-A	brain
8	chr5:28967800-28968600	Enhancers	HepG2	liver
9	chr5:28991000-28991600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr5:28998600-28999000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr5:28999000-29002200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr5:29002000-29002400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr5:29002200-29002400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr5:29002400-29003200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr5:29016400-29016600	Enhancers	Pancreas	Pancrea
16	chr5:29016400-29017800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr5:29017400-29017800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr5:29017600-29018200	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr5:29017800-29021000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr5:29021000-29021200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr5:29021200-29023200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr5:29023200-29023600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr5:29036000-29036800	Enhancers	Fetal Heart	heart
24	chr5:29037400-29038200	Enhancers	Hela-S3	cervix
25	chr5:29037400-29038400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr5:29042200-29042600	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr5:29042200-29042600	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr5:29042200-29042800	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr5:29042200-29045000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr5:29042400-29042800	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr5:29042400-29042800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr5:29042800-29045000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr5:29043600-29044000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr5:29044000-29045000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr5:29045000-29045200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr5:29045000-29045200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr5:29045000-29045400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr5:29045400-29045800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr5:29045800-29046400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr5:29051200-29052400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr5:29052400-29054600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr5:29054200-29054400	Enhancers	Fetal Heart	heart
43	chr5:29054400-29054800	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr5:29054400-29054800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr5:29054400-29054800	Flanking Active TSS	Fetal Heart	heart
46	chr5:29054400-29055000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr5:29054400-29055000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr5:29054600-29054800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr5:29054800-29055000	Enhancers	Fetal Heart	heart
50	chr5:29061400-29061800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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