Variant report

Variant	nsv1030378
Chromosome Location	chr8:51892949-52191830
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:644)
CpG islands
(count:62)
Chromatin interactive
region (count:9)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:644 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr8:52176979-52177063	K562	blood:	n/a	n/a
2	ATF2	chr8:51934062-51934395	GM12878	blood:	n/a	n/a
3	ATF2	chr8:52185915-52186577	GM12878	blood:	n/a	n/a
4	ATF2	chr8:52185956-52186392	GM12878	blood:	n/a	n/a
5	BACH1	chr8:51969835-51969916	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr8:51971660-51971674	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr8:52090617-52090952	GM12878	blood:	n/a	chr8:52090783-52090794
8	BATF	chr8:52090683-52090921	GM12878	blood:	n/a	chr8:52090783-52090794
9	BATF	chr8:51934115-51934341	GM12878	blood:	n/a	chr8:51934250-51934261
10	BATF	chr8:52091287-52091566	GM12878	blood:	n/a	chr8:52091398-52091409
11	BATF	chr8:52186032-52186542	GM12878	blood:	n/a	chr8:52186118-52186126
12	BATF	chr8:51934082-51934330	GM12878	blood:	n/a	chr8:51934250-51934261
13	BCL11A	chr8:51934103-51934327	GM12878	blood:	n/a	n/a
14	BCL3	chr8:52149772-52149992	GM12878	blood:	n/a	n/a
15	BCL3	chr8:52185889-52186677	GM12878	blood:	n/a	n/a
16	BCLAF1	chr8:52186074-52186470	GM12878	blood:	n/a	n/a
17	BHLHE40	chr8:52003729-52003801	K562	blood:	n/a	n/a
18	BRCA1	chr8:52046916-52046945	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr8:51943318-51943587	IMR90	lung:	n/a	n/a
20	CEBPB	chr8:52004186-52004566	IMR90	lung:	n/a	chr8:52004376-52004387
21	CEBPB	chr8:52019932-52020334	MCF-7	breast:	n/a	chr8:52020187-52020198
22	CEBPB	chr8:51995320-51995560	HepG2	liver:	n/a	chr8:51995490-51995501
23	CEBPB	chr8:51949282-51949619	A549	lung:	n/a	n/a
24	CEBPB	chr8:52075268-52075461	HepG2	liver:	n/a	chr8:52075349-52075360
25	CEBPB	chr8:52043786-52044131	A549	lung:	n/a	chr8:52043944-52043955
26	CEBPB	chr8:52106818-52107106	A549	lung:	n/a	chr8:52106985-52107002
27	CEBPB	chr8:52100702-52100902	A549	lung:	n/a	chr8:52100766-52100777 chr8:52100715-52100726
28	CEBPB	chr8:52182642-52182781	HepG2	liver:	n/a	chr8:52182668-52182679 chr8:52182667-52182678
29	CEBPB	chr8:52097233-52097442	IMR90	lung:	n/a	n/a
30	CEBPB	chr8:51949260-51949581	HepG2	liver:	n/a	n/a
31	CEBPB	chr8:52020007-52020384	H1-hESC	embryonic stem cell:	n/a	chr8:52020187-52020198
32	CEBPB	chr8:51949273-51949609	IMR90	lung:	n/a	n/a
33	CEBPB	chr8:51943286-51943588	HepG2	liver:	n/a	n/a
34	CEBPB	chr8:52156035-52156212	A549	lung:	n/a	n/a
35	CEBPB	chr8:52140635-52140825	A549	lung:	n/a	n/a
36	CEBPB	chr8:51977144-51977291	A549	lung:	n/a	chr8:51977198-51977209
37	CEBPB	chr8:52106843-52107146	IMR90	lung:	n/a	chr8:52106985-52107002
38	CEBPB	chr8:51977057-51977338	HepG2	liver:	n/a	chr8:51977198-51977209
39	CEBPB	chr8:51995328-51995636	IMR90	lung:	n/a	chr8:51995490-51995501
40	CEBPB	chr8:52020000-52020372	IMR90	lung:	n/a	chr8:52020187-52020198
41	CEBPB	chr8:52004219-52004550	HepG2	liver:	n/a	chr8:52004376-52004387
42	CEBPB	chr8:51949299-51949587	MCF-7	breast:	n/a	n/a
43	CEBPB	chr8:52043768-52044123	IMR90	lung:	n/a	chr8:52043944-52043955
44	CEBPB	chr8:52004145-52004554	MCF-7	breast:	n/a	chr8:52004376-52004387
45	CEBPB	chr8:52019721-52020341	Hela-S3	cervix:	n/a	chr8:52020187-52020198
46	CEBPB	chr8:51995356-51995614	K562	blood:	n/a	chr8:51995490-51995501
47	CEBPB	chr8:52004226-52004557	A549	lung:	n/a	chr8:52004376-52004387
48	CEBPB	chr8:52020009-52020369	K562	blood:	n/a	chr8:52020187-52020198
49	CEBPB	chr8:52121948-52121963	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr8:52020007-52020380	HepG2	liver:	n/a	chr8:52020187-52020198

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:52003919-52003969	HCT-116	colon:	n/a
2	chr8:52003919-52003969	HCT-116	colon:	n/a
3	chr8:52003919-52003969	HNPCEpiC	eye:	n/a
4	chr8:52003919-52003969	NB4	blood:	n/a
5	chr8:52003919-52003969	SAEC	small airway:	n/a
6	chr8:52003919-52003969	GM19239	blood:	n/a
7	chr8:52003919-52003969	AG04449	skin:	fetal
8	chr8:52003919-52003969	HepG2	liver:	n/a
9	chr8:52003919-52003969	ECC-1	luminal epithelium:	n/a
10	chr8:52003919-52003969	GM12891	blood:	n/a
11	chr8:52003919-52003969	PrEC	prostate:	n/a
12	chr8:52003919-52003969	U87	brain:	n/a
13	chr8:52003919-52003969	Hela-S3	cervix:	n/a
14	chr8:52003919-52003969	Hepatocyte	liver:	n/a
15	chr8:52003919-52003969	AG04450	lung:	fetal
16	chr8:52003919-52003969	BJ	skin:	n/a
17	chr8:52003919-52003969	HRCEpiC	kidney:	n/a
18	chr8:52003919-52003969	GM06990	blood:	n/a
19	chr8:52003919-52003969	HIPEpiC	eye:	n/a
20	chr8:52003919-52003969	NH-A	brain:	n/a
21	chr8:52003919-52003969	SK-N-MC	brain:	n/a
22	chr8:52003919-52003969	AoSMC	blood vessel:	n/a
23	chr8:52003919-52003969	SK-N-SH_RA	brain:	n/a
24	chr8:52003919-52003969	ProgFib	skin:	n/a
25	chr8:52003919-52003969	HEEpiC	esophagus:	n/a
26	chr8:52003919-52003969	CMK	blood:	n/a
27	chr8:52003919-52003969	IMR90	lung:	fetal
28	chr8:52003919-52003969	Jurkat	blood:	n/a
29	chr8:52003919-52003969	PANC-1	pancreas:	n/a
30	chr8:52003919-52003969	BE2_C	brain:	n/a
31	chr8:52003919-52003969	NT2-D1	testis:	n/a
32	chr8:52003919-52003969	MCF10A-Er-Src	breast:	n/a
33	chr8:52003919-52003969	SKMC	muscle:	n/a
34	chr8:52003919-52003969	Caco-2	colon:	n/a
35	chr8:52003919-52003969	K562	blood:	n/a
36	chr8:52003919-52003969	RPTEC	kidney:	n/a
37	chr8:52003919-52003969	NHBE	bronchial:	n/a
38	chr8:52003919-52003969	SK-N-SH	brain:	n/a
39	chr8:52003919-52003969	HUVEC	blood vessel:	n/a
40	chr8:52003919-52003969	HPAEpiC	pulmonary alveolar:	n/a
41	chr8:52003919-52003969	ovcar-3	ovarian:	n/a
42	chr8:52003919-52003969	HL-60	blood:	n/a
43	chr8:52003919-52003969	HCM	heart:	n/a
44	chr8:52003919-52003969	NHDF-neo	bronchial:	n/a
45	chr8:52003919-52003969	PFSK-1	brain:	n/a
46	chr8:52003919-52003969	AG10803	skin:	n/a
47	chr8:52003919-52003969	AG09309	skin:	n/a
48	chr8:52003919-52003969	H1-hESC	embryonic stem cell:	embryo
49	chr8:52003919-52003969	HRPEpiC	eye:	n/a
50	chr8:52003919-52003969	HMEC	breast:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:52085245..52087687-chr8:52096002..52098496,2	K562	blood:
2	chr8:51957221..51959868-chr8:51967147..51969241,2	MCF-7	breast:
3	chr8:51957221..51959868-chr8:51967147..51969241,2	MCF-7	breast:
4	chr8:52189412..52191198-chr8:52195033..52197163,2	MCF-7	breast:
5	chr8:52104614..52105495-chr9:79531675..79532265,2	MCF-7	breast:
6	chr17:41400152..41402660-chr8:52157778..52160758,2	K562	blood:
7	chr8:52085245..52087687-chr8:52096002..52098496,2	K562	blood:
8	chr17:41466381..41468590-chr8:52157758..52159258,2	MCF-7	breast:
9	chr17:41398392..41400915-chr8:52157758..52159278,2	K562	blood:

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

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

No data

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: 3427 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:3427 , 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	rs190582139	chr8:51897829-51897830	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs142578711	chr8:51897835-51897836	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs367929879	chr8:51897837-51897838	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs35781674	chr8:51897859-51897860	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs144177423	chr8:51897978-51897979	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs556142620	chr8:51897986-51897987	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs554233141	chr8:51897990-51897991	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs73578085	chr8:51897991-51897992	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs539944415	chr8:51897998-51897999	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs200847531	chr8:51898027-51898028	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs386725238	chr8:51898028-51898029	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs75001351	chr8:51898029-51898030	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs544153283	chr8:51898063-51898064	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs113892567	chr8:51898083-51898084	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs529835973	chr8:51898122-51898123	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs542049915	chr8:51898176-51898177	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs533638338	chr8:51898178-51898179	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs560390723	chr8:51898222-51898223	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs111979851	chr8:51898276-51898277	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs547129956	chr8:51898281-51898282	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs181999995	chr8:51898289-51898290	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs532565845	chr8:51898290-51898291	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs550975426	chr8:51898363-51898364	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs112206982	chr8:51898383-51898384	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs538908846	chr8:51898396-51898397	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs536444821	chr8:51898398-51898399	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs554697116	chr8:51898412-51898413	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs566733191	chr8:51898434-51898435	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs185292880	chr8:51898465-51898466	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs201957501	chr8:51898470-51898471	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs188431323	chr8:51898477-51898478	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs576744659	chr8:51898512-51898513	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs180903894	chr8:51898540-51898541	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs556178243	chr8:51898555-51898556	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs72649643	chr8:51898568-51898569	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs7846074	chr8:51898577-51898578	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs148694525	chr8:51898581-51898582	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs141819240	chr8:51898604-51898605	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs540708496	chr8:51898607-51898608	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs545952017	chr8:51898616-51898617	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs146302473	chr8:51898621-51898622	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs186307099	chr8:51898638-51898639	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs7830600	chr8:51898644-51898645	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs569162794	chr8:51898651-51898652	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs12674817	chr8:51898660-51898661	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs548487397	chr8:51898683-51898684	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs566697356	chr8:51898747-51898748	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs576613487	chr8:51898765-51898766	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs534153604	chr8:51898775-51898776	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs542217444	chr8:51898804-51898805	Enhancers	n/a	n/a	Overlapped CNVs	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:153 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:51897800-51899000	Enhancers	Dnd41	blood
2	chr8:51932000-51932200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
3	chr8:51933200-51933400	Active TSS	GM12878-XiMat	blood
4	chr8:51933400-51933600	Flanking Active TSS	GM12878-XiMat	blood
5	chr8:51933600-51933800	ZNF genes & repeats	GM12878-XiMat	blood
6	chr8:51933600-51934200	Enhancers	Primary hematopoietic stem cells short term culture	blood
7	chr8:51933800-51934000	Flanking Active TSS	GM12878-XiMat	blood
8	chr8:51944600-51945000	Enhancers	Adipose Nuclei	Adipose
9	chr8:51947600-51949000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr8:51948200-51948800	Enhancers	NH-A	brain
11	chr8:51955800-51957600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr8:51956000-51957800	Enhancers	NH-A	brain
13	chr8:51956600-51957800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr8:51959000-51959600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
15	chr8:51966400-51966600	Enhancers	Esophagus	oesophagus
16	chr8:51966400-51968600	Weak transcription	Gastric	stomach
17	chr8:51968600-51968800	ZNF genes & repeats	Gastric	stomach
18	chr8:51968600-51968800	ZNF genes & repeats	Pancreas	Pancrea
19	chr8:51971400-51972400	Enhancers	Dnd41	blood
20	chr8:51971800-51972200	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr8:51971800-51972200	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr8:51972000-51972400	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr8:51972000-51972400	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr8:51986000-51986400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
25	chr8:51990600-51991000	Active TSS	Primary T helper naive cells from peripheral blood	blood
26	chr8:51997000-51997600	Enhancers	NH-A	brain
27	chr8:51997600-52002400	Weak transcription	NH-A	brain
28	chr8:52001400-52001600	Enhancers	Fetal Lung	lung
29	chr8:52001800-52003000	Weak transcription	Fetal Lung	lung
30	chr8:52002000-52002400	Enhancers	NHDF-Ad	bronchial
31	chr8:52002200-52004800	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr8:52002400-52003200	Enhancers	NH-A	brain
33	chr8:52002800-52003200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr8:52003000-52003400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
35	chr8:52003000-52003400	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr8:52003000-52004200	Enhancers	Fetal Lung	lung
37	chr8:52003000-52004600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr8:52003200-52007400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr8:52003400-52004800	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr8:52003600-52003800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr8:52003600-52004000	Enhancers	H1 Cell Line	embryonic stem cell
42	chr8:52003800-52004000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr8:52003800-52004200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr8:52004000-52004200	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
45	chr8:52004000-52004400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr8:52004000-52005000	Weak transcription	H1 Cell Line	embryonic stem cell
47	chr8:52004200-52004800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr8:52004200-52004800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
49	chr8:52007400-52008200	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr8:52008200-52008400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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