Variant report

Variant	nsv1031155
Chromosome Location	chr8:51907530-52173218
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	ATF2	chr8:51934062-51934395	GM12878	blood:	n/a	n/a
2	BACH1	chr8:51969835-51969916	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr8:51971660-51971674	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr8:52090683-52090921	GM12878	blood:	n/a	chr8:52090783-52090794
5	BATF	chr8:52090617-52090952	GM12878	blood:	n/a	chr8:52090783-52090794
6	BATF	chr8:51934082-51934330	GM12878	blood:	n/a	chr8:51934250-51934261
7	BATF	chr8:51934115-51934341	GM12878	blood:	n/a	chr8:51934250-51934261
8	BATF	chr8:52091287-52091566	GM12878	blood:	n/a	chr8:52091398-52091409
9	BCL11A	chr8:51934103-51934327	GM12878	blood:	n/a	n/a
10	BCL3	chr8:52149772-52149992	GM12878	blood:	n/a	n/a
11	BHLHE40	chr8:52003729-52003801	K562	blood:	n/a	n/a
12	BRCA1	chr8:52046916-52046945	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr8:52020011-52020246	A549	lung:	n/a	chr8:52020187-52020198
14	CEBPB	chr8:52106818-52107106	A549	lung:	n/a	chr8:52106985-52107002
15	CEBPB	chr8:52053031-52053080	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr8:52156035-52156212	A549	lung:	n/a	n/a
17	CEBPB	chr8:51995356-51995614	K562	blood:	n/a	chr8:51995490-51995501
18	CEBPB	chr8:51995320-51995560	HepG2	liver:	n/a	chr8:51995490-51995501
19	CEBPB	chr8:52020007-52020380	HepG2	liver:	n/a	chr8:52020187-52020198
20	CEBPB	chr8:52020009-52020369	K562	blood:	n/a	chr8:52020187-52020198
21	CEBPB	chr8:52019721-52020341	Hela-S3	cervix:	n/a	chr8:52020187-52020198
22	CEBPB	chr8:52004186-52004566	IMR90	lung:	n/a	chr8:52004376-52004387
23	CEBPB	chr8:52020007-52020384	H1-hESC	embryonic stem cell:	n/a	chr8:52020187-52020198
24	CEBPB	chr8:52043806-52044133	HepG2	liver:	n/a	chr8:52043944-52043955
25	CEBPB	chr8:52140635-52140825	A549	lung:	n/a	n/a
26	CEBPB	chr8:52068361-52068660	IMR90	lung:	n/a	chr8:52068520-52068533 chr8:52068519-52068536 chr8:52068520-52068533 chr8:52068520-52068533 chr8:52068520-52068531 chr8:52068521-52068532
27	CEBPB	chr8:52043786-52044131	A549	lung:	n/a	chr8:52043944-52043955
28	CEBPB	chr8:51995419-51995546	H1-hESC	embryonic stem cell:	n/a	chr8:51995490-51995501
29	CEBPB	chr8:52020000-52020372	IMR90	lung:	n/a	chr8:52020187-52020198
30	CEBPB	chr8:52068399-52068661	HepG2	liver:	n/a	chr8:52068520-52068533 chr8:52068519-52068536 chr8:52068520-52068533 chr8:52068520-52068533 chr8:52068520-52068531 chr8:52068521-52068532
31	CEBPB	chr8:51943318-51943587	IMR90	lung:	n/a	n/a
32	CEBPB	chr8:52004227-52004570	H1-hESC	embryonic stem cell:	n/a	chr8:52004376-52004387
33	CEBPB	chr8:51943286-51943588	HepG2	liver:	n/a	n/a
34	CEBPB	chr8:51977057-51977338	HepG2	liver:	n/a	chr8:51977198-51977209
35	CEBPB	chr8:51977144-51977291	A549	lung:	n/a	chr8:51977198-51977209
36	CEBPB	chr8:52004145-52004554	MCF-7	breast:	n/a	chr8:52004376-52004387
37	CEBPB	chr8:52043768-52044123	IMR90	lung:	n/a	chr8:52043944-52043955
38	CEBPB	chr8:51949299-51949587	MCF-7	breast:	n/a	n/a
39	CEBPB	chr8:52019932-52020334	MCF-7	breast:	n/a	chr8:52020187-52020198
40	CEBPB	chr8:51949273-51949609	IMR90	lung:	n/a	n/a
41	CEBPB	chr8:51949282-51949619	A549	lung:	n/a	n/a
42	CEBPB	chr8:52097233-52097442	IMR90	lung:	n/a	n/a
43	CEBPB	chr8:51950948-51951182	HepG2	liver:	n/a	chr8:51951003-51951012 chr8:51951001-51951014 chr8:51951001-51951012
44	CEBPB	chr8:51949260-51949581	HepG2	liver:	n/a	n/a
45	CEBPB	chr8:52004226-52004557	A549	lung:	n/a	chr8:52004376-52004387
46	CEBPB	chr8:52004288-52004531	K562	blood:	n/a	chr8:52004376-52004387
47	CEBPB	chr8:52004219-52004550	HepG2	liver:	n/a	chr8:52004376-52004387
48	CEBPB	chr8:52121948-52121963	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr8:52043860-52044101	H1-hESC	embryonic stem cell:	n/a	chr8:52043944-52043955
50	CEBPB	chr8:51950503-51951199	IMR90	lung:	n/a	chr8:51950581-51950592 chr8:51950579-51950592 chr8:51950579-51950592 chr8:51950581-51950592 chr8:51951003-51951012 chr8:51950576-51950593 chr8:51951001-51951014 chr8:51951001-51951012

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:52003919-52003969	LNCaP	prostate:	n/a
2	chr8:52003919-52003969	PFSK-1	brain:	n/a
3	chr8:52003919-52003969	AG09319	gingival:	n/a
4	chr8:52003919-52003969	SK-N-SH	brain:	n/a
5	chr8:52003919-52003969	HEEpiC	esophagus:	n/a
6	chr8:52003919-52003969	HNPCEpiC	eye:	n/a
7	chr8:52003919-52003969	HUVEC	blood vessel:	n/a
8	chr8:52003919-52003969	HMEC	breast:	n/a
9	chr8:52003919-52003969	NHBE	bronchial:	n/a
10	chr8:52003919-52003969	NT2-D1	testis:	n/a
11	chr8:52003919-52003969	HEK293	kidney:	embryo
12	chr8:52003919-52003969	A549	lung:	n/a
13	chr8:52003919-52003969	MCF-7	breast:	n/a
14	chr8:52003919-52003969	ovcar-3	ovarian:	n/a
15	chr8:52003919-52003969	AG09309	skin:	n/a
16	chr8:52003919-52003969	HIPEpiC	eye:	n/a
17	chr8:52003919-52003969	HPAEpiC	pulmonary alveolar:	n/a
18	chr8:52003919-52003969	ECC-1	luminal epithelium:	n/a
19	chr8:52003919-52003969	RPTEC	kidney:	n/a
20	chr8:52003919-52003969	HCPEpiC	choroid plexus:	n/a
21	chr8:52003919-52003969	PANC-1	pancreas:	n/a
22	chr8:52003919-52003969	BE2_C	brain:	n/a
23	chr8:52003919-52003969	SKMC	muscle:	n/a
24	chr8:52003919-52003969	GM19239	blood:	n/a
25	chr8:52003919-52003969	NH-A	brain:	n/a
26	chr8:52003919-52003969	BJ	skin:	n/a
27	chr8:52003919-52003969	Caco-2	colon:	n/a
28	chr8:52003919-52003969	HRCEpiC	kidney:	n/a
29	chr8:52003919-52003969	HCF	heart:	n/a
30	chr8:52003919-52003969	CMK	blood:	n/a
31	chr8:52003919-52003969	AG04449	skin:	fetal
32	chr8:52003919-52003969	Hepatocyte	liver:	n/a
33	chr8:52003919-52003969	MCF10A-Er-Src	breast:	n/a
34	chr8:52003919-52003969	GM12891	blood:	n/a
35	chr8:52003919-52003969	HepG2	liver:	n/a
36	chr8:52003919-52003969	K562	blood:	n/a
37	chr8:52003919-52003969	HL-60	blood:	n/a
38	chr8:52003919-52003969	H1-hESC	embryonic stem cell:	embryo
39	chr8:52003919-52003969	U87	brain:	n/a
40	chr8:52003919-52003969	AG10803	skin:	n/a
41	chr8:52003919-52003969	HRE	kidney:	n/a
42	chr8:52003919-52003969	GM12892	blood:	n/a
43	chr8:52003919-52003969	SK-N-MC	brain:	n/a
44	chr8:52003919-52003969	NHDF-neo	bronchial:	n/a
45	chr8:52003919-52003969	HCM	heart:	n/a
46	chr8:52003919-52003969	Jurkat	blood:	n/a
47	chr8:52003919-52003969	HAEpiC	amniotic membrane:	n/a
48	chr8:52003919-52003969	T-47D	breast:	n/a
49	chr8:52003919-52003969	HRPEpiC	eye:	n/a
50	chr8:52003919-52003969	HCT-116	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:51957221..51959868-chr8:51967147..51969241,2	MCF-7	breast:
2	chr17:41466381..41468590-chr8:52157758..52159258,2	MCF-7	breast:
3	chr8:52104614..52105495-chr9:79531675..79532265,2	MCF-7	breast:
4	chr17:41398392..41400915-chr8:52157758..52159278,2	K562	blood:
5	chr8:51957221..51959868-chr8:51967147..51969241,2	MCF-7	breast:
6	chr8:52085245..52087687-chr8:52096002..52098496,2	K562	blood:
7	chr8:52085245..52087687-chr8:52096002..52098496,2	K562	blood:
8	chr17:41400152..41402660-chr8:52157778..52160758,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SNTG1-1	chr8:52170248-52170367	ENSG00000253664.1

Variant related genes	Relation type
ENSG00000253664	TF binding region
ENSG00000201316	TF binding region
ENSG00000253664	CpG island
ENSG00000201316	CpG island
ENSG00000188825	chromatin interactions

Extended variants
information (count: 2880 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:2880 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs537529273	chr8:51926516-51926517	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs555286238	chr8:51926518-51926519	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs6998342	chr8:51926533-51926534	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs550975783	chr8:51932055-51932056	Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs76672651	chr8:51932056-51932057	Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs375606532	chr8:51932079-51932080	Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs368320452	chr8:51932086-51932087	Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs530715102	chr8:51932112-51932113	Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs184748659	chr8:51932152-51932153	Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs189063913	chr8:51932194-51932195	Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs534855579	chr8:51932200-51932201	Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs534943175	chr8:51933214-51933215	Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs553151852	chr8:51933215-51933216	Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs577860825	chr8:51933361-51933362	Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs545189491	chr8:51933397-51933398	Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs563079483	chr8:51933426-51933427	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs575230199	chr8:51933428-51933429	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs375024358	chr8:51933440-51933441	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs184303668	chr8:51933454-51933455	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs370743862	chr8:51933544-51933545	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs75458919	chr8:51933614-51933615	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs78092404	chr8:51933633-51933634	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs546870693	chr8:51933649-51933650	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs565177014	chr8:51933650-51933651	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs201106088	chr8:51933705-51933706	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs11782445	chr8:51933728-51933729	Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs550772507	chr8:51933775-51933776	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs570154771	chr8:51933793-51933794	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs537115508	chr8:51933802-51933803	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs139878127	chr8:51933804-51933805	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs117348599	chr8:51933810-51933811	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs114037509	chr8:51933835-51933836	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs553290779	chr8:51933849-51933850	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs370097811	chr8:51933886-51933887	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs572911232	chr8:51933895-51933896	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs577903994	chr8:51933900-51933901	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs558057450	chr8:51933922-51933923	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs144952910	chr8:51933953-51933954	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs35689808	chr8:51933955-51933956	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs188786620	chr8:51934022-51934023	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs575316801	chr8:51934055-51934056	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs373422927	chr8:51934070-51934071	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs147952236	chr8:51934075-51934076	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs560943207	chr8:51934107-51934108	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs577143185	chr8:51934111-51934112	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs141819895	chr8:51934115-51934116	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs181566163	chr8:51934129-51934130	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs371666275	chr8:51934152-51934153	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs73584083	chr8:51934160-51934161	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs7000380	chr8:51944616-51944617	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	22286061	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Melanoma	17363583	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Sezary syndrome	18413736	CNVD
Ovarian cancer	22174824	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
22q11 deletion syndrome	20357662	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Renal cell carcinoma	21215367	CNVD

Chromatin state (count:128 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:51932000-51932200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
2	chr8:51933200-51933400	Active TSS	GM12878-XiMat	blood
3	chr8:51933400-51933600	Flanking Active TSS	GM12878-XiMat	blood
4	chr8:51933600-51933800	ZNF genes & repeats	GM12878-XiMat	blood
5	chr8:51933600-51934200	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr8:51933800-51934000	Flanking Active TSS	GM12878-XiMat	blood
7	chr8:51944600-51945000	Enhancers	Adipose Nuclei	Adipose
8	chr8:51947600-51949000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr8:51948200-51948800	Enhancers	NH-A	brain
10	chr8:51955800-51957600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr8:51956000-51957800	Enhancers	NH-A	brain
12	chr8:51956600-51957800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr8:51959000-51959600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
14	chr8:51966400-51966600	Enhancers	Esophagus	oesophagus
15	chr8:51966400-51968600	Weak transcription	Gastric	stomach
16	chr8:51968600-51968800	ZNF genes & repeats	Gastric	stomach
17	chr8:51968600-51968800	ZNF genes & repeats	Pancreas	Pancrea
18	chr8:51971400-51972400	Enhancers	Dnd41	blood
19	chr8:51971800-51972200	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr8:51971800-51972200	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr8:51972000-51972400	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr8:51972000-51972400	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr8:51986000-51986400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
24	chr8:51990600-51991000	Active TSS	Primary T helper naive cells from peripheral blood	blood
25	chr8:51997000-51997600	Enhancers	NH-A	brain
26	chr8:51997600-52002400	Weak transcription	NH-A	brain
27	chr8:52001400-52001600	Enhancers	Fetal Lung	lung
28	chr8:52001800-52003000	Weak transcription	Fetal Lung	lung
29	chr8:52002000-52002400	Enhancers	NHDF-Ad	bronchial
30	chr8:52002200-52004800	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr8:52002400-52003200	Enhancers	NH-A	brain
32	chr8:52002800-52003200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr8:52003000-52003400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
34	chr8:52003000-52003400	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr8:52003000-52004200	Enhancers	Fetal Lung	lung
36	chr8:52003000-52004600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr8:52003200-52007400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr8:52003400-52004800	Enhancers	iPS-20b Cell Line	embryonic stem cell
39	chr8:52003600-52003800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr8:52003600-52004000	Enhancers	H1 Cell Line	embryonic stem cell
41	chr8:52003800-52004000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr8:52003800-52004200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr8:52004000-52004200	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
44	chr8:52004000-52004400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr8:52004000-52005000	Weak transcription	H1 Cell Line	embryonic stem cell
46	chr8:52004200-52004800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr8:52004200-52004800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
48	chr8:52007400-52008200	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr8:52008200-52008400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr8:52017800-52018000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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