Variant report

Variant	nsv891047
Chromosome Location	chr8:78265312-78322329
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	chr8:78311809-78312740	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:78319583-78319789	HepG2	liver:	n/a	n/a
3	BHLHE40	chr8:78312178-78312386	HepG2	liver:	n/a	n/a
4	CBX3	chr8:78296528-78296854	HCT-116	colon:	n/a	n/a
5	CEBPB	chr8:78312043-78312431	HepG2	liver:	n/a	chr8:78312374-78312391
6	CEBPB	chr8:78319565-78319769	HepG2	liver:	n/a	chr8:78319749-78319760 chr8:78319574-78319587
7	CEBPB	chr8:78312096-78312352	HepG2	liver:	n/a	n/a
8	CEBPB	chr8:78312091-78312357	HepG2	liver:	n/a	n/a
9	CEBPB	chr8:78290101-78290301	HepG2	liver:	n/a	chr8:78290167-78290178
10	CTCF	chr8:78310800-78310801	GM13977	blood:	n/a	n/a
11	CTCF	chr8:78310600-78310750	SK-N-SH_RA	brain:	n/a	chr8:78310686-78310707 chr8:78310691-78310709 chr8:78310692-78310708
12	CTCF	chr8:78310660-78310810	HVMF	connective:	n/a	chr8:78310686-78310707 chr8:78310691-78310709 chr8:78310692-78310708
13	CTCF	chr8:78310620-78310770	HUVEC	blood vessel:	n/a	chr8:78310686-78310707 chr8:78310691-78310709 chr8:78310692-78310708
14	CTCF	chr8:78310565-78310818	HUVEC	blood vessel:	n/a	chr8:78310686-78310707 chr8:78310691-78310709 chr8:78310692-78310708
15	CTCF	chr8:78310560-78310710	HEEpiC	esophagus:	n/a	chr8:78310686-78310707 chr8:78310691-78310709 chr8:78310692-78310708
16	CTCF	chr8:78310600-78310750	HA-sp	spinal cord:	n/a	chr8:78310686-78310707 chr8:78310691-78310709 chr8:78310692-78310708
17	CTCF	chr8:78310700-78310850	NB4	blood:	n/a	n/a
18	CTCF	chr8:78291100-78291250	HPAF	blood vessel:	n/a	chr8:78291151-78291164 chr8:78291148-78291166
19	CTCF	chr8:78310600-78310750	HRPEpiC	eye:	n/a	chr8:78310686-78310707 chr8:78310691-78310709 chr8:78310692-78310708
20	CTCF	chr8:78310620-78310770	AG10803	skin:	n/a	chr8:78310686-78310707 chr8:78310691-78310709 chr8:78310692-78310708
21	CTCF	chr8:78291100-78291250	HCPEpiC	choroid plexus:	n/a	chr8:78291151-78291164 chr8:78291148-78291166
22	CTCF	chr8:78310640-78310790	AG04450	lung:	n/a	chr8:78310686-78310707 chr8:78310691-78310709 chr8:78310692-78310708
23	CTCF	chr8:78310640-78310790	GM12865	blood:	n/a	chr8:78310686-78310707 chr8:78310691-78310709 chr8:78310692-78310708
24	CTCF	chr8:78310560-78310710	SAEC	small airway:	n/a	chr8:78310686-78310707 chr8:78310691-78310709 chr8:78310692-78310708
25	CTCF	chr8:78310620-78310770	GM12865	blood:	n/a	chr8:78310686-78310707 chr8:78310691-78310709 chr8:78310692-78310708
26	CTCF	chr8:78310660-78310810	GM12866	blood:	n/a	chr8:78310686-78310707 chr8:78310691-78310709 chr8:78310692-78310708
27	CTCF	chr8:78310562-78310770	SK-N-SH_RA	brain:	n/a	chr8:78310686-78310707 chr8:78310691-78310709 chr8:78310692-78310708
28	CTCF	chr8:78310600-78310750	GM12873	blood:	n/a	chr8:78310686-78310707 chr8:78310691-78310709 chr8:78310692-78310708
29	CTCF	chr8:78310600-78310750	HBMEC	blood vessel:	n/a	chr8:78310686-78310707 chr8:78310691-78310709 chr8:78310692-78310708
30	CTCF	chr8:78310560-78310710	GM12870	blood:	n/a	chr8:78310686-78310707 chr8:78310691-78310709 chr8:78310692-78310708
31	CTCF	chr8:78310640-78310790	HFF-Myc	foreskin:	n/a	chr8:78310686-78310707 chr8:78310691-78310709 chr8:78310692-78310708
32	CTCF	chr8:78310580-78310730	HCPEpiC	choroid plexus:	n/a	chr8:78310686-78310707 chr8:78310691-78310709 chr8:78310692-78310708
33	CTCF	chr8:78291000-78291150	HCFaa	heart:	n/a	n/a
34	CTCF	chr8:78310580-78310730	GM12873	blood:	n/a	chr8:78310686-78310707 chr8:78310691-78310709 chr8:78310692-78310708
35	CTCF	chr8:78310600-78310761	MCF-7	breast:	n/a	chr8:78310686-78310707 chr8:78310691-78310709 chr8:78310692-78310708
36	CTCF	chr8:78310681-78310729	GM20000	blood:	n/a	chr8:78310686-78310707 chr8:78310691-78310709 chr8:78310692-78310708
37	CTCF	chr8:78283863-78283869	GM10248	blood:	n/a	n/a
38	CTCF	chr8:78291100-78291250	HMF	breast:	n/a	chr8:78291151-78291164 chr8:78291148-78291166
39	CTCF	chr8:78310600-78310750	HL-60	blood:	n/a	chr8:78310686-78310707 chr8:78310691-78310709 chr8:78310692-78310708
40	CTCF	chr8:78310620-78310770	HPF	lung:	n/a	chr8:78310686-78310707 chr8:78310691-78310709 chr8:78310692-78310708
41	CTCF	chr8:78310602-78310789	Hela-S3	cervix:	n/a	chr8:78310686-78310707 chr8:78310691-78310709 chr8:78310692-78310708
42	CTCF	chr8:78310580-78310730	AG09309	skin:	n/a	chr8:78310686-78310707 chr8:78310691-78310709 chr8:78310692-78310708
43	CTCF	chr8:78291100-78291250	HBMEC	blood vessel:	n/a	chr8:78291151-78291164 chr8:78291148-78291166
44	CTCF	chr8:78310560-78310710	HAc	cerebellar:	n/a	chr8:78310686-78310707 chr8:78310691-78310709 chr8:78310692-78310708
45	CTCF	chr8:78310620-78310770	HBMEC	blood vessel:	n/a	chr8:78310686-78310707 chr8:78310691-78310709 chr8:78310692-78310708
46	CTCF	chr8:78310580-78310730	GM12878	blood:	n/a	chr8:78310686-78310707 chr8:78310691-78310709 chr8:78310692-78310708
47	CTCF	chr8:78310620-78310770	HRPEpiC	eye:	n/a	chr8:78310686-78310707 chr8:78310691-78310709 chr8:78310692-78310708
48	CTCF	chr8:78310548-78310833	Medullo	brain:	n/a	chr8:78310686-78310707 chr8:78310691-78310709 chr8:78310692-78310708
49	CTCF	chr8:78310557-78310811	H1-hESC	embryonic stem cell:	n/a	chr8:78310686-78310707 chr8:78310691-78310709 chr8:78310692-78310708
50	CTCF	chr8:78291080-78291230	SK-N-SH_RA	brain:	n/a	chr8:78291151-78291164 chr8:78291148-78291166

No.	Distal block	Cell Line	Cell type
1	chr8:78268071..78271065-chr8:78271580..78274324,2	K562	blood:
2	chr8:78266597..78268495-chr8:78269805..78272021,2	MCF-7	breast:
3	chr8:78268071..78271065-chr8:78271580..78274324,2	K562	blood:
4	chr8:78266597..78268495-chr8:78269805..78272021,2	MCF-7	breast:
5	chr6:43025757..43028121-chr8:78314973..78317562,2	MCF-7	breast:
6	chr8:77279732..77280710-chr8:78310370..78311176,4	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZFHX4-3	chr8:78290937-78290976	NONHSAT127353
2	lnc-ZFHX4-3	chr8:78311308-78311390	ENSG00000254366.2
3	lnc-ZFHX4-3	chr8:78311309-78311390	XLOC_006852
4	lnc-ZFHX4-3	chr8:78311200-78311372	XLOC_006852
5	lnc-ZFHX4-3	chr8:78290938-78290976	XLOC_006852
6	lnc-ZFHX4-3	chr8:78311308-78311390	ENSG00000254366
7	lnc-ZFHX4-3	chr8:78311199-78311390	NONHSAT127353

Variant related genes	Relation type
ENSG00000254366	TF binding region
ENSG00000112651	chromatin interactions
ENSG00000137171	chromatin interactions
TMEM100	miRNA target sites

Extended variants
information (count: 951 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:951 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7816973	chr8:78265312-78265313	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs182568251	chr8:78265317-78265318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs551448797	chr8:78265388-78265389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs563485415	chr8:78265394-78265395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs189228859	chr8:78265405-78265406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs530795012	chr8:78265433-78265434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs572526549	chr8:78265442-78265443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs191986665	chr8:78265449-78265450	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs371103999	chr8:78265468-78265469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs59773332	chr8:78265469-78265470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs567568376	chr8:78265524-78265525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs12546860	chr8:78265607-78265608	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs532132801	chr8:78265669-78265670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs554960237	chr8:78265724-78265725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs571772814	chr8:78265864-78265865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs183862474	chr8:78265896-78265897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs557089780	chr8:78265972-78265973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs187441519	chr8:78266058-78266059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs191933221	chr8:78266059-78266060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs202135860	chr8:78266104-78266105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs145644272	chr8:78266105-78266106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs73691673	chr8:78266113-78266114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs60739236	chr8:78266115-78266116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs572753115	chr8:78266136-78266137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs374557887	chr8:78266140-78266141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs75300247	chr8:78266215-78266216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs56386822	chr8:78266242-78266243	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs576961603	chr8:78266262-78266263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs544027133	chr8:78266275-78266276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs186924359	chr8:78266312-78266313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs149020466	chr8:78266316-78266317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs12677220	chr8:78266342-78266343	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs570282929	chr8:78266350-78266351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs59944236	chr8:78266364-78266365	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs547263908	chr8:78266368-78266369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs577441049	chr8:78266383-78266384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs571893489	chr8:78266407-78266408	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs545209588	chr8:78266444-78266445	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs532737207	chr8:78266449-78266450	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs375905514	chr8:78266456-78266457	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs559958133	chr8:78266461-78266462	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs192806020	chr8:78266471-78266472	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs143209100	chr8:78266535-78266536	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs573447244	chr8:78266545-78266546	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs7825472	chr8:78266576-78266577	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs548653443	chr8:78266595-78266596	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs148270402	chr8:78266621-78266622	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs566451295	chr8:78266657-78266658	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs538971642	chr8:78266672-78266673	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs141278274	chr8:78266674-78266675	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:109)

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
primary effusion lymphomas	17116491	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
Salivary gland tumor	18059337	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
Acute myeloid leukemia	21251322	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
Melanoma	22183965	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
Sezary syndrome	18413736	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
Hepatocellular carcinoma	16750200	CNVD
Prostate cancer	17016436	CNVD
Colorectal cancer	16774939	CNVD
Colorectal cancer	19455253	CNVD
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Urothelial cell carcinoma	18451213	CNVD
Intellectual disability	21802062	CNVD
Myelodysplastic syndrome	18508791	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:66 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:78263000-78266400	Weak transcription	HUVEC	blood vessel
2	chr8:78266400-78267400	Enhancers	HUVEC	blood vessel
3	chr8:78267400-78267800	Flanking Active TSS	HUVEC	blood vessel
4	chr8:78267800-78268600	Active TSS	HUVEC	blood vessel
5	chr8:78268600-78270400	Flanking Active TSS	HUVEC	blood vessel
6	chr8:78269400-78270600	Enhancers	Muscle Satellite Cultured Cells	--
7	chr8:78270400-78271200	Weak transcription	HUVEC	blood vessel
8	chr8:78271200-78271400	ZNF genes & repeats	HUVEC	blood vessel
9	chr8:78271400-78272200	Weak transcription	HUVEC	blood vessel
10	chr8:78272200-78272400	ZNF genes & repeats	HUVEC	blood vessel
11	chr8:78290400-78291600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr8:78290600-78291000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr8:78290800-78291000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr8:78293600-78293800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr8:78300800-78301800	Enhancers	Muscle Satellite Cultured Cells	--
16	chr8:78308200-78309200	Enhancers	HepG2	liver
17	chr8:78309200-78310800	Weak transcription	HepG2	liver
18	chr8:78309800-78310400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr8:78309800-78310600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr8:78309800-78311200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr8:78309800-78311400	Enhancers	Muscle Satellite Cultured Cells	--
22	chr8:78310400-78310800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr8:78310600-78311200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr8:78310800-78311000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr8:78310800-78311400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr8:78310800-78311600	Enhancers	Liver	Liver
27	chr8:78310800-78311600	Enhancers	HepG2	liver
28	chr8:78311000-78311600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr8:78311200-78311400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr8:78311200-78311800	Enhancers	Fetal Intestine Large	intestine
31	chr8:78311200-78312000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr8:78311200-78312400	Active TSS	Fetal Muscle Trunk	muscle
33	chr8:78311200-78313800	Active TSS	Adipose Nuclei	Adipose
34	chr8:78311400-78311600	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr8:78311400-78311800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr8:78311400-78312600	Weak transcription	Muscle Satellite Cultured Cells	--
37	chr8:78311400-78315800	Active TSS	Fetal Muscle Leg	muscle
38	chr8:78311600-78311800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr8:78311600-78312000	Flanking Active TSS	Liver	Liver
40	chr8:78311600-78312000	Flanking Active TSS	HepG2	liver
41	chr8:78311600-78314800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr8:78311800-78312000	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr8:78311800-78312600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr8:78312000-78312400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr8:78312000-78312800	Enhancers	HepG2	liver
46	chr8:78312000-78313000	Active TSS	Liver	Liver
47	chr8:78312000-78313800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr8:78312600-78312800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr8:78312800-78313400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr8:78313000-78313200	Enhancers	Muscle Satellite Cultured Cells	--

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