Variant report

Variant	nsv598942
Chromosome Location	chr5:92557969-92611658
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	chr5:92581525-92582684	HepG2	liver:	n/a	chr5:92582527-92582543 chr5:92582528-92582544
2	BATF	chr5:92576157-92576455	GM12878	blood:	n/a	chr5:92576332-92576343
3	BHLHE40	chr5:92582030-92582487	HepG2	liver:	n/a	n/a
4	BHLHE40	chr5:92560290-92560653	HepG2	liver:	n/a	n/a
5	BHLHE40	chr5:92607827-92607942	GM12878	blood:	n/a	n/a
6	BRCA1	chr5:92572719-92573144	Hela-S3	cervix:	n/a	n/a
7	BRCA1	chr5:92565247-92565349	Hela-S3	cervix:	n/a	n/a
8	CBX3	chr5:92593184-92593787	HCT-116	colon:	n/a	n/a
9	CEBPB	chr5:92593461-92593556	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr5:92572805-92573186	IMR90	lung:	n/a	n/a
11	CEBPB	chr5:92572524-92573208	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr5:92609049-92609380	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr5:92610520-92610580	HepG2	liver:	n/a	chr5:92610557-92610568 chr5:92610557-92610570
14	CEBPB	chr5:92582064-92582441	A549	lung:	n/a	chr5:92582278-92582291 chr5:92582279-92582290 chr5:92582278-92582289
15	CEBPB	chr5:92571344-92571911	A549	lung:	n/a	n/a
16	CEBPB	chr5:92582054-92582496	HepG2	liver:	n/a	chr5:92582278-92582291 chr5:92582279-92582290 chr5:92582278-92582289
17	CEBPB	chr5:92582101-92582482	HepG2	liver:	n/a	chr5:92582278-92582291 chr5:92582279-92582290 chr5:92582278-92582289
18	CEBPB	chr5:92571648-92571994	HepG2	liver:	n/a	n/a
19	CEBPB	chr5:92571414-92572128	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr5:92581970-92582541	ECC-1	luminal epithelium:	n/a	chr5:92582278-92582291 chr5:92582279-92582290 chr5:92582278-92582289
21	CEBPB	chr5:92582194-92582394	IMR90	lung:	n/a	chr5:92582278-92582291 chr5:92582279-92582290 chr5:92582278-92582289
22	CEBPB	chr5:92570782-92570940	A549	lung:	n/a	n/a
23	CEBPB	chr5:92582049-92582491	HepG2	liver:	n/a	chr5:92582278-92582291 chr5:92582279-92582290 chr5:92582278-92582289
24	CEBPB	chr5:92571434-92571917	MCF-7	breast:	n/a	n/a
25	CEBPB	chr5:92582053-92582506	ECC-1	luminal epithelium:	n/a	chr5:92582278-92582291 chr5:92582279-92582290 chr5:92582278-92582289
26	CEBPB	chr5:92610027-92610405	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr5:92571504-92571877	MCF-7	breast:	n/a	n/a
28	CEBPB	chr5:92582034-92582543	HepG2	liver:	n/a	chr5:92582278-92582291 chr5:92582279-92582290 chr5:92582278-92582289
29	CEBPB	chr5:92582017-92582417	A549	lung:	n/a	chr5:92582278-92582291 chr5:92582279-92582290 chr5:92582278-92582289
30	CEBPB	chr5:92582117-92582354	H1-hESC	embryonic stem cell:	n/a	chr5:92582278-92582291 chr5:92582279-92582290 chr5:92582278-92582289
31	CEBPD	chr5:92582061-92582426	HepG2	liver:	n/a	n/a
32	CEBPD	chr5:92582084-92582432	HepG2	liver:	n/a	n/a
33	CEBPZ	chr5:92582242-92582332	HepG2	liver:	n/a	n/a
34	CHD2	chr5:92581987-92582384	HepG2	liver:	n/a	n/a
35	CTCF	chr5:92581820-92581970	AG09319	gingival:	n/a	n/a
36	CTCF	chr5:92585540-92585690	HCPEpiC	choroid plexus:	n/a	n/a
37	CTCF	chr5:92587960-92588110	A549	lung:	n/a	n/a
38	CTCF	chr5:92588020-92588170	AG04449	skin:	n/a	n/a
39	CTCF	chr5:92588035-92588099	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr5:92560339-92560517	HepG2	liver:	n/a	n/a
41	CTCF	chr5:92572645-92572745	MCF-7	breast:	n/a	n/a
42	CTCF	chr5:92587917-92588155	SK-N-SH_RA	brain:	n/a	n/a
43	CTCF	chr5:92573442-92573445	A549	lung:	n/a	n/a
44	CTCF	chr5:92588060-92588210	HEEpiC	esophagus:	n/a	n/a
45	CTCF	chr5:92594188-92594219	Lung_OC	lung:	n/a	n/a
46	CTCF	chr5:92572640-92572790	BJ	skin:	n/a	n/a
47	CTCF	chr5:92587950-92588206	MCF-7	breast:	n/a	n/a
48	CTCF	chr5:92588000-92588150	GM12866	blood:	n/a	n/a
49	CTCF	chr5:92572600-92572750	HMEC	breast:	n/a	n/a
50	CTCF	chr5:92609260-92609410	HCPEpiC	choroid plexus:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:92572688-92572738	NT2-D1	testis:	n/a
2	chr5:92603169-92603219	CMK	blood:	n/a
3	chr5:92603169-92603219	HRCEpiC	kidney:	n/a
4	chr5:92582155-92582205	Hela-S3	cervix:	n/a
5	chr5:92603169-92603219	NB4	blood:	n/a
6	chr5:92582155-92582205	LNCaP	prostate:	n/a
7	chr5:92582155-92582205	GM06990	blood:	n/a
8	chr5:92603043-92603093	NHDF-neo	bronchial:	n/a
9	chr5:92603424-92603474	HAEpiC	amniotic membrane:	n/a
10	chr5:92603169-92603219	GM12891	blood:	n/a
11	chr5:92603424-92603474	HIPEpiC	eye:	n/a
12	chr5:92597063-92597113	HEEpiC	esophagus:	n/a
13	chr5:92603424-92603474	GM12891	blood:	n/a
14	chr5:92572688-92572738	ECC-1	luminal epithelium:	n/a
15	chr5:92603424-92603474	K562	blood:	n/a
16	chr5:92572688-92572738	SKMC	muscle:	n/a
17	chr5:92603169-92603219	U87	brain:	n/a
18	chr5:92572688-92572738	NHDF-neo	bronchial:	n/a
19	chr5:92603043-92603093	PFSK-1	brain:	n/a
20	chr5:92582155-92582205	HCT-116	colon:	n/a
21	chr5:92582155-92582205	T-47D	breast:	n/a
22	chr5:92572688-92572738	BJ	skin:	n/a
23	chr5:92603424-92603474	HRCEpiC	kidney:	n/a
24	chr5:92603043-92603093	SK-N-MC	brain:	n/a
25	chr5:92603043-92603093	AG09309	skin:	n/a
26	chr5:92582155-92582205	HCM	heart:	n/a
27	chr5:92572688-92572738	HepG2	liver:	n/a
28	chr5:92582155-92582205	RPTEC	kidney:	n/a
29	chr5:92582155-92582205	NB4	blood:	n/a
30	chr5:92582155-92582205	GM12878	blood:	n/a
31	chr5:92603169-92603219	IMR90	lung:	fetal
32	chr5:92603169-92603219	HepG2	liver:	n/a
33	chr5:92603169-92603219	HIPEpiC	eye:	n/a
34	chr5:92597063-92597113	AG10803	skin:	n/a
35	chr5:92582155-92582205	HEEpiC	esophagus:	n/a
36	chr5:92582155-92582205	SK-N-MC	brain:	n/a
37	chr5:92572688-92572738	SK-N-SH	brain:	n/a
38	chr5:92603424-92603474	AG09319	gingival:	n/a
39	chr5:92603424-92603474	NHBE	bronchial:	n/a
40	chr5:92603169-92603219	NHDF-neo	bronchial:	n/a
41	chr5:92603043-92603093	HRPEpiC	eye:	n/a
42	chr5:92603424-92603474	BE2_C	brain:	n/a
43	chr5:92597063-92597113	GM12892	blood:	n/a
44	chr5:92572688-92572738	LNCaP	prostate:	n/a
45	chr5:92603169-92603219	AG09319	gingival:	n/a
46	chr5:92603043-92603093	U87	brain:	n/a
47	chr5:92582155-92582205	AG09319	gingival:	n/a
48	chr5:92572688-92572738	GM12891	blood:	n/a
49	chr5:92582155-92582205	HRPEpiC	eye:	n/a
50	chr5:92597063-92597113	AG04450	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr5:92572759..92575011-chr5:92577902..92579568,2	MCF-7	breast:
2	chr5:92245272..92245812-chr5:92587648..92588348,2	MCF-7	breast:
3	chr5:92572759..92575011-chr5:92577902..92579568,2	MCF-7	breast:
4	chr5:92607951..92610447-chr5:92611670..92614154,2	K562	blood:

Variant related genes	Relation type
POLD2P1	TF binding region
POLD2P1	CpG island

Extended variants
information (count: 1376 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:1376 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12652645	chr5:92557969-92557970	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs375423112	chr5:92557987-92557988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs376607845	chr5:92558137-92558138	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs543449566	chr5:92558146-92558147	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs562933198	chr5:92558147-92558148	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs531938805	chr5:92558177-92558178	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs140015002	chr5:92558180-92558181	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs142079912	chr5:92558189-92558190	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs551127250	chr5:92558198-92558199	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs17083014	chr5:92558213-92558214	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs146331278	chr5:92558247-92558248	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs576872510	chr5:92558284-92558285	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs148522446	chr5:92558324-92558325	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs536937469	chr5:92558442-92558443	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs142929006	chr5:92558466-92558467	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs190074886	chr5:92558470-92558471	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs182857726	chr5:92558471-92558472	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs559107264	chr5:92558504-92558505	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs17083016	chr5:92558518-92558519	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs66614167	chr5:92558553-92558554	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs151081442	chr5:92558555-92558556	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs187490848	chr5:92558615-92558616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs543765831	chr5:92558624-92558625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs563591003	chr5:92558628-92558629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs576449094	chr5:92558707-92558708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs536290641	chr5:92558734-92558735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs545380046	chr5:92558736-92558737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs553085325	chr5:92558811-92558812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs192673656	chr5:92558815-92558816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs528172317	chr5:92558819-92558820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs185675490	chr5:92558842-92558843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs78115658	chr5:92558895-92558896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs530684427	chr5:92558921-92558922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs550917139	chr5:92558935-92558936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs570724438	chr5:92558982-92558983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs532584389	chr5:92559053-92559054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs552583430	chr5:92559083-92559084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs566211307	chr5:92559112-92559113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs545132478	chr5:92559165-92559166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs17367646	chr5:92559173-92559174	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs144904615	chr5:92559200-92559201	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs187756989	chr5:92559216-92559217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs537218717	chr5:92559294-92559295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs192261534	chr5:92559348-92559349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs184201902	chr5:92559365-92559366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs67217436	chr5:92559372-92559373	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs577102679	chr5:92559404-92559405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs188563044	chr5:92559485-92559486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs181183954	chr5:92559518-92559519	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs572757981	chr5:92559523-92559524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	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
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Mental retardation	19471318	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16774939	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:339 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:92555800-92561600	Weak transcription	Ovary	ovary
2	chr5:92556400-92562200	Weak transcription	Fetal Lung	lung
3	chr5:92558000-92558600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr5:92558000-92558600	Enhancers	Adipose Nuclei	Adipose
5	chr5:92560200-92561600	Enhancers	HepG2	liver
6	chr5:92561000-92561800	Enhancers	Brain Hippocampus Middle	brain
7	chr5:92561200-92561800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr5:92561200-92561800	Enhancers	Brain Substantia Nigra	brain
9	chr5:92561200-92562400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr5:92561200-92562800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr5:92561400-92562600	Enhancers	Brain Anterior Caudate	brain
12	chr5:92561600-92562400	Enhancers	Ovary	ovary
13	chr5:92561600-92562600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr5:92561800-92562800	Enhancers	NHDF-Ad	bronchial
15	chr5:92562000-92562600	Enhancers	Colon Smooth Muscle	Colon
16	chr5:92562200-92562600	Enhancers	Fetal Lung	lung
17	chr5:92570800-92573000	Enhancers	Hela-S3	cervix
18	chr5:92572400-92573000	Enhancers	NHLF	lung
19	chr5:92572400-92573200	Enhancers	HMEC	breast
20	chr5:92572400-92573600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr5:92572400-92573600	Enhancers	NHEK	skin
22	chr5:92572600-92573000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr5:92572600-92573000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr5:92572600-92573000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr5:92572600-92573000	Enhancers	NH-A	brain
26	chr5:92573000-92573400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr5:92573000-92579000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr5:92573000-92581000	Weak transcription	NHLF	lung
29	chr5:92573400-92573600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr5:92573600-92581000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr5:92573600-92585400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr5:92577400-92578000	Enhancers	Fetal Kidney	kidney
33	chr5:92577400-92578200	Enhancers	Fetal Lung	lung
34	chr5:92577600-92577800	Enhancers	Fetal Stomach	stomach
35	chr5:92578000-92578200	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr5:92578000-92578800	Weak transcription	Fetal Kidney	kidney
37	chr5:92578200-92578600	Weak transcription	Fetal Lung	lung
38	chr5:92578200-92579000	Weak transcription	HUES6 Cell Line	embryonic stem cell
39	chr5:92578600-92579400	Weak transcription	Fetal Stomach	stomach
40	chr5:92578600-92579800	Enhancers	Fetal Lung	lung
41	chr5:92578800-92579600	Enhancers	ES-I3 Cell Line	embryonic stem cell
42	chr5:92578800-92579600	Enhancers	Fetal Kidney	kidney
43	chr5:92578800-92579800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr5:92578800-92579800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr5:92578800-92579800	Enhancers	HUVEC	blood vessel
46	chr5:92578800-92584000	Enhancers	HepG2	liver
47	chr5:92579000-92579200	Enhancers	Duodenum Smooth Muscle	Duodenum
48	chr5:92579000-92579800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr5:92579000-92579800	Enhancers	HUES6 Cell Line	embryonic stem cell
50	chr5:92579000-92581000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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