Variant report

Variant	esv3493409
Chromosome Location	chr8:87085885-87109161
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	chr8:87100789-87101048	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:87100831-87101147	K562	blood:	n/a	n/a
3	BCL3	chr8:87105415-87105669	GM12878	blood:	n/a	n/a
4	BCL3	chr8:87105381-87105750	GM12878	blood:	n/a	n/a
5	CEBPB	chr8:87107691-87107790	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr8:87104595-87104819	HepG2	liver:	n/a	n/a
7	CEBPB	chr8:87098707-87099017	HepG2	liver:	n/a	chr8:87098830-87098841
8	CEBPB	chr8:87098725-87098989	H1-hESC	embryonic stem cell:	n/a	chr8:87098830-87098841
9	CEBPB	chr8:87098686-87099007	IMR90	lung:	n/a	chr8:87098830-87098841
10	CEBPB	chr8:87104701-87104887	K562	blood:	n/a	n/a
11	CEBPB	chr8:87098665-87099004	K562	blood:	n/a	chr8:87098830-87098841
12	CEBPB	chr8:87098682-87099011	A549	lung:	n/a	chr8:87098830-87098841
13	CTCF	chr8:87100880-87101030	GM12873	blood:	n/a	chr8:87100969-87100985 chr8:87100968-87100986 chr8:87100963-87100984
14	CTCF	chr8:87100840-87100990	NHEK	skin:	n/a	chr8:87100969-87100985 chr8:87100968-87100986 chr8:87100963-87100984
15	CTCF	chr8:87100900-87101050	Hela-S3	cervix:	n/a	chr8:87100969-87100985 chr8:87100968-87100986 chr8:87100963-87100984
16	CTCF	chr8:87100860-87101010	GM12866	blood:	n/a	chr8:87100969-87100985 chr8:87100968-87100986 chr8:87100963-87100984
17	CTCF	chr8:87097060-87097210	HEEpiC	esophagus:	n/a	n/a
18	CTCF	chr8:87099980-87100130	BJ	skin:	n/a	n/a
19	CTCF	chr8:87100861-87101092	HUVEC	blood vessel:	n/a	chr8:87100969-87100985 chr8:87100968-87100986 chr8:87100963-87100984
20	CTCF	chr8:87100920-87101070	GM12870	blood:	n/a	chr8:87100969-87100985 chr8:87100968-87100986 chr8:87100963-87100984
21	CTCF	chr8:87097080-87097230	NHEK	skin:	n/a	n/a
22	CTCF	chr8:87100900-87101050	HFF-Myc	foreskin:	n/a	chr8:87100969-87100985 chr8:87100968-87100986 chr8:87100963-87100984
23	CTCF	chr8:87100880-87101030	NB4	blood:	n/a	chr8:87100969-87100985 chr8:87100968-87100986 chr8:87100963-87100984
24	CTCF	chr8:87100880-87101030	A549	lung:	n/a	chr8:87100969-87100985 chr8:87100968-87100986 chr8:87100963-87100984
25	CTCF	chr8:87100900-87101050	HCFaa	heart:	n/a	chr8:87100969-87100985 chr8:87100968-87100986 chr8:87100963-87100984
26	CTCF	chr8:87097100-87097206	Medullo	brain:	n/a	n/a
27	CTCF	chr8:87097120-87097270	HVMF	connective:	n/a	n/a
28	CTCF	chr8:87100920-87101070	GM12872	blood:	n/a	chr8:87100969-87100985 chr8:87100968-87100986 chr8:87100963-87100984
29	CTCF	chr8:87107668-87107695	Hela-S3	cervix:	n/a	n/a
30	CTCF	chr8:87100900-87101050	NHDF-neo	bronchial:	n/a	chr8:87100969-87100985 chr8:87100968-87100986 chr8:87100963-87100984
31	CTCF	chr8:87097100-87097250	HBMEC	blood vessel:	n/a	n/a
32	CTCF	chr8:87100880-87101030	RPTEC	kidney:	n/a	chr8:87100969-87100985 chr8:87100968-87100986 chr8:87100963-87100984
33	CTCF	chr8:87100920-87101070	HepG2	liver:	n/a	chr8:87100969-87100985 chr8:87100968-87100986 chr8:87100963-87100984
34	CTCF	chr8:87097040-87097190	HPF	lung:	n/a	n/a
35	CTCF	chr8:87100704-87101108	HepG2	liver:	n/a	chr8:87100969-87100985 chr8:87100968-87100986 chr8:87100963-87100984
36	CTCF	chr8:87100708-87101186	A549	lung:	n/a	chr8:87100969-87100985 chr8:87100968-87100986 chr8:87100963-87100984
37	CTCF	chr8:87100880-87101030	BJ	skin:	n/a	chr8:87100969-87100985 chr8:87100968-87100986 chr8:87100963-87100984
38	CTCF	chr8:87097020-87097170	Caco-2	colon:	n/a	n/a
39	CTCF	chr8:87100880-87101030	HEEpiC	esophagus:	n/a	chr8:87100969-87100985 chr8:87100968-87100986 chr8:87100963-87100984
40	CTCF	chr8:87100920-87101070	K562	blood:	n/a	chr8:87100969-87100985 chr8:87100968-87100986 chr8:87100963-87100984
41	CTCF	chr8:87100920-87101070	HCM	heart:	n/a	chr8:87100969-87100985 chr8:87100968-87100986 chr8:87100963-87100984
42	CTCF	chr8:87100594-87101196	MCF-7	breast:	n/a	chr8:87100969-87100985 chr8:87100968-87100986 chr8:87100963-87100984
43	CTCF	chr8:87100820-87100970	HA-sp	spinal cord:	n/a	n/a
44	CTCF	chr8:87097040-87097190	RPTEC	kidney:	n/a	n/a
45	CTCF	chr8:87100840-87100990	BE2_C	brain:	n/a	chr8:87100969-87100985 chr8:87100968-87100986 chr8:87100963-87100984
46	CTCF	chr8:87100900-87101050	HVMF	connective:	n/a	chr8:87100969-87100985 chr8:87100968-87100986 chr8:87100963-87100984
47	CTCF	chr8:87100940-87101090	HFF-Myc	foreskin:	n/a	chr8:87100969-87100985 chr8:87100968-87100986 chr8:87100963-87100984
48	CTCF	chr8:87100920-87101070	HCT-116	colon:	n/a	chr8:87100969-87100985 chr8:87100968-87100986 chr8:87100963-87100984
49	CTCF	chr8:87100867-87101073	Gliobla	brain:	n/a	chr8:87100969-87100985 chr8:87100968-87100986 chr8:87100963-87100984
50	CTCF	chr8:87100880-87101030	AoAF	blood vessel:	n/a	chr8:87100969-87100985 chr8:87100968-87100986 chr8:87100963-87100984

No.	Distal block	Cell Line	Cell type
1	chr8:87099204..87102058-chr8:87106597..87109469,2	MCF-7	breast:
2	chr8:87055024..87057404-chr8:87093302..87095378,2	MCF-7	breast:
3	chr8:87104968..87107537-chr8:87108407..87111374,2	MCF-7	breast:
4	chr8:87058815..87059551-chr8:87097105..87097612,2	MCF-7	breast:
5	chr8:86211068..86212027-chr8:87100896..87101631,2	K562	blood:
6	chr8:87079401..87081548-chr8:87093916..87096819,2	MCF-7	breast:
7	chr8:86374350..86376869-chr8:87092620..87094880,2	MCF-7	breast:

Variant related genes	Relation type
PSKH2	TF binding region
ATP6V0D2	TF binding region
ENSG00000243761	chromatin interactions
ENSG00000147614	chromatin interactions
ENSG00000253549	chromatin interactions
ENSG00000104267	chromatin interactions
ENSG00000147613	chromatin interactions

Extended variants
information (count: 1006 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:1006 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs541848964	chr8:87085905-87085906	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs555370022	chr8:87085949-87085950	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs572344759	chr8:87086014-87086015	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs183421923	chr8:87086018-87086019	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs564279356	chr8:87086027-87086028	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs80068485	chr8:87086030-87086031	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs551815460	chr8:87086034-87086035	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs73688582	chr8:87086042-87086043	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs376013453	chr8:87086045-87086046	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs35645724	chr8:87086049-87086050	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs73688583	chr8:87086064-87086065	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs550035155	chr8:87086074-87086075	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs565039090	chr8:87086075-87086076	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs528871371	chr8:87086079-87086080	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs141477553	chr8:87086144-87086145	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs74973093	chr8:87086176-87086177	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs576443570	chr8:87086238-87086239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs543838965	chr8:87086245-87086246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs188274330	chr8:87086254-87086255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs73255276	chr8:87086260-87086261	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs547794908	chr8:87086262-87086263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs570987443	chr8:87086270-87086271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs74562223	chr8:87086275-87086276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs539679313	chr8:87086298-87086299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs191641259	chr8:87086312-87086313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs569861046	chr8:87086329-87086330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs535447481	chr8:87086331-87086332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs145104484	chr8:87086335-87086336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs138981127	chr8:87086403-87086404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs377339254	chr8:87086405-87086406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs565130997	chr8:87086577-87086578	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs140595191	chr8:87086603-87086604	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs370715817	chr8:87086604-87086605	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs150422504	chr8:87086605-87086606	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs577261513	chr8:87086609-87086610	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs989810	chr8:87086636-87086637	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs71275828	chr8:87086662-87086663	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs35514709	chr8:87086663-87086664	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs397891811	chr8:87086664-87086665	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs398008606	chr8:87086677-87086678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs563366028	chr8:87086719-87086720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs528957600	chr8:87086736-87086737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs372941081	chr8:87086741-87086742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs182344686	chr8:87086780-87086781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs528313196	chr8:87086809-87086810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs559270682	chr8:87086815-87086816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs571526556	chr8:87086854-87086855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs528087431	chr8:87086885-87086886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs186907284	chr8:87086938-87086939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs571085504	chr8:87086945-87086946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:106)

Disease	PMID	Source
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
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	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
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	CNVD
abnormal development	18461090	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
Cancer	16751803	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
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
small cell lung cancer	20016488	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Epilepsy	20502679	CNVD
Autism	20841430	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	20409316	CNVD
Acute myeloid leukemia	19651601	CNVD
head and neck squamous cell carcinoma	19451471	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD

Chromatin state (count:56 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:87076800-87087200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr8:87082400-87126200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr8:87083800-87086200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr8:87086800-87087200	Weak transcription	Pancreas	Pancrea
5	chr8:87087200-87087400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr8:87087200-87087400	Enhancers	Gastric	stomach
7	chr8:87087400-87087600	Enhancers	Fetal Brain Female	brain
8	chr8:87094800-87095400	Enhancers	Primary monocytes fromperipheralblood	blood
9	chr8:87095400-87098400	Weak transcription	Primary monocytes fromperipheralblood	blood
10	chr8:87096200-87097200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr8:87098400-87098800	Enhancers	Primary monocytes fromperipheralblood	blood
12	chr8:87098400-87098800	Enhancers	Monocytes-CD14+_RO01746	blood
13	chr8:87098800-87100600	Weak transcription	Monocytes-CD14+_RO01746	blood
14	chr8:87100000-87100200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr8:87100200-87102200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr8:87100400-87100600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr8:87100400-87101000	Enhancers	Fetal Lung	lung
18	chr8:87100600-87100800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr8:87100600-87101000	Enhancers	Adipose Nuclei	Adipose
20	chr8:87100600-87101000	Enhancers	Brain Anterior Caudate	brain
21	chr8:87100600-87101000	Enhancers	Brain Inferior Temporal Lobe	brain
22	chr8:87100600-87101000	Enhancers	Stomach Mucosa	stomach
23	chr8:87100600-87101000	Enhancers	Monocytes-CD14+_RO01746	blood
24	chr8:87100600-87105800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr8:87100800-87101000	Enhancers	Primary monocytes fromperipheralblood	blood
26	chr8:87100800-87101200	Enhancers	Breast Myoepithelial Primary Cells	Breast
27	chr8:87101000-87101800	Weak transcription	Stomach Mucosa	stomach
28	chr8:87101000-87102000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr8:87101200-87101600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
30	chr8:87101600-87102200	Enhancers	Breast Myoepithelial Primary Cells	Breast
31	chr8:87101600-87102200	Enhancers	Fetal Heart	heart
32	chr8:87101800-87102000	Enhancers	Stomach Mucosa	stomach
33	chr8:87101800-87103000	Enhancers	NH-A	brain
34	chr8:87102000-87103000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr8:87102200-87102400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr8:87102200-87103000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr8:87102400-87102800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr8:87102600-87102800	Enhancers	HSMM	muscle
39	chr8:87105200-87106400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr8:87105800-87106200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr8:87106200-87108000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr8:87106400-87110800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr8:87106800-87107000	Enhancers	Muscle Satellite Cultured Cells	--
44	chr8:87107000-87114000	Weak transcription	Muscle Satellite Cultured Cells	--
45	chr8:87107400-87107800	Enhancers	Brain Inferior Temporal Lobe	brain
46	chr8:87107400-87108200	Enhancers	HUES64 Cell Line	embryonic stem cell
47	chr8:87107600-87107800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr8:87107600-87108400	Enhancers	HMEC	breast
49	chr8:87107800-87108000	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr8:87107800-87110600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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