Variant report

Variant	nsv891048
Chromosome Location	chr8:78271372-78322329
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	chr8:78319583-78319789	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:78311809-78312740	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	chr8:78312096-78312352	HepG2	liver:	n/a	n/a
6	CEBPB	chr8:78290101-78290301	HepG2	liver:	n/a	chr8:78290167-78290178
7	CEBPB	chr8:78312043-78312431	HepG2	liver:	n/a	chr8:78312374-78312391
8	CEBPB	chr8:78312091-78312357	HepG2	liver:	n/a	n/a
9	CEBPB	chr8:78319565-78319769	HepG2	liver:	n/a	chr8:78319749-78319760 chr8:78319574-78319587
10	CTCF	chr8:78310640-78310790	AG04450	lung:	n/a	chr8:78310686-78310707 chr8:78310691-78310709 chr8:78310692-78310708
11	CTCF	chr8:78310548-78310833	Medullo	brain:	n/a	chr8:78310686-78310707 chr8:78310691-78310709 chr8:78310692-78310708
12	CTCF	chr8:78310680-78310830	GM12871	blood:	n/a	chr8:78310686-78310707 chr8:78310691-78310709 chr8:78310692-78310708
13	CTCF	chr8:78310580-78310730	NHEK	skin:	n/a	chr8:78310686-78310707 chr8:78310691-78310709 chr8:78310692-78310708
14	CTCF	chr8:78310681-78310729	GM20000	blood:	n/a	chr8:78310686-78310707 chr8:78310691-78310709 chr8:78310692-78310708
15	CTCF	chr8:78310620-78310770	WERI-Rb-1	eye:	n/a	chr8:78310686-78310707 chr8:78310691-78310709 chr8:78310692-78310708
16	CTCF	chr8:78291060-78291210	HBMEC	blood vessel:	n/a	chr8:78291151-78291164 chr8:78291148-78291166
17	CTCF	chr8:78310557-78310811	H1-hESC	embryonic stem cell:	n/a	chr8:78310686-78310707 chr8:78310691-78310709 chr8:78310692-78310708
18	CTCF	chr8:78310414-78310916	HCT-116	colon:	n/a	chr8:78310686-78310707 chr8:78310691-78310709 chr8:78310692-78310708
19	CTCF	chr8:78310580-78310730	HCT-116	colon:	n/a	chr8:78310686-78310707 chr8:78310691-78310709 chr8:78310692-78310708
20	CTCF	chr8:78310501-78310788	SK-N-SH_RA	brain:	n/a	chr8:78310686-78310707 chr8:78310691-78310709 chr8:78310692-78310708
21	CTCF	chr8:78283863-78283869	GM10248	blood:	n/a	n/a
22	CTCF	chr8:78310631-78310735	MCF-7	breast:	n/a	chr8:78310686-78310707 chr8:78310691-78310709 chr8:78310692-78310708
23	CTCF	chr8:78310465-78310873	MCF-7	breast:	n/a	chr8:78310686-78310707 chr8:78310691-78310709 chr8:78310692-78310708
24	CTCF	chr8:78310600-78310750	GM12873	blood:	n/a	chr8:78310686-78310707 chr8:78310691-78310709 chr8:78310692-78310708
25	CTCF	chr8:78310640-78310790	AG09319	gingival:	n/a	chr8:78310686-78310707 chr8:78310691-78310709 chr8:78310692-78310708
26	CTCF	chr8:78310620-78310770	AG09309	skin:	n/a	chr8:78310686-78310707 chr8:78310691-78310709 chr8:78310692-78310708
27	CTCF	chr8:78291120-78291270	HCPEpiC	choroid plexus:	n/a	chr8:78291151-78291164 chr8:78291148-78291166
28	CTCF	chr8:78310597-78310798	GM13977	blood:	n/a	chr8:78310686-78310707 chr8:78310691-78310709 chr8:78310692-78310708
29	CTCF	chr8:78310620-78310770	HRPEpiC	eye:	n/a	chr8:78310686-78310707 chr8:78310691-78310709 chr8:78310692-78310708
30	CTCF	chr8:78310634-78310693	Lung_OC	lung:	n/a	n/a
31	CTCF	chr8:78291060-78291210	HMF	breast:	n/a	chr8:78291151-78291164 chr8:78291148-78291166
32	CTCF	chr8:78310660-78310810	HVMF	connective:	n/a	chr8:78310686-78310707 chr8:78310691-78310709 chr8:78310692-78310708
33	CTCF	chr8:78310660-78310810	A549	lung:	n/a	chr8:78310686-78310707 chr8:78310691-78310709 chr8:78310692-78310708
34	CTCF	chr8:78310600-78310750	HL-60	blood:	n/a	chr8:78310686-78310707 chr8:78310691-78310709 chr8:78310692-78310708
35	CTCF	chr8:78310620-78310770	Caco-2	colon:	n/a	chr8:78310686-78310707 chr8:78310691-78310709 chr8:78310692-78310708
36	CTCF	chr8:78291115-78291188	MCF-7	breast:	n/a	chr8:78291151-78291164 chr8:78291148-78291166
37	CTCF	chr8:78310620-78310770	NHDF-neo	bronchial:	n/a	chr8:78310686-78310707 chr8:78310691-78310709 chr8:78310692-78310708
38	CTCF	chr8:78310600-78310750	BE2_C	brain:	n/a	chr8:78310686-78310707 chr8:78310691-78310709 chr8:78310692-78310708
39	CTCF	chr8:78310368-78311415	SK-N-SH	brain:	n/a	chr8:78310686-78310707 chr8:78310691-78310709 chr8:78310692-78310708
40	CTCF	chr8:78310620-78310770	Hela-S3	cervix:	n/a	chr8:78310686-78310707 chr8:78310691-78310709 chr8:78310692-78310708
41	CTCF	chr8:78310580-78310730	GM12875	blood:	n/a	chr8:78310686-78310707 chr8:78310691-78310709 chr8:78310692-78310708
42	CTCF	chr8:78291100-78291250	HMF	breast:	n/a	chr8:78291151-78291164 chr8:78291148-78291166
43	CTCF	chr8:78310620-78310770	AG04449	skin:	n/a	chr8:78310686-78310707 chr8:78310691-78310709 chr8:78310692-78310708
44	CTCF	chr8:78291066-78291408	HCT-116	colon:	n/a	chr8:78291151-78291164 chr8:78291148-78291166
45	CTCF	chr8:78291020-78291170	HPAF	blood vessel:	n/a	chr8:78291151-78291164 chr8:78291148-78291166
46	CTCF	chr8:78310640-78310790	HCPEpiC	choroid plexus:	n/a	chr8:78310686-78310707 chr8:78310691-78310709 chr8:78310692-78310708
47	CTCF	chr8:78310485-78310868	IMR90	lung:	n/a	chr8:78310686-78310707 chr8:78310691-78310709 chr8:78310692-78310708
48	CTCF	chr8:78310580-78310730	AG09309	skin:	n/a	chr8:78310686-78310707 chr8:78310691-78310709 chr8:78310692-78310708
49	CTCF	chr8:78310620-78310770	MCF-7	breast:	n/a	chr8:78310686-78310707 chr8:78310691-78310709 chr8:78310692-78310708
50	CTCF	chr8:78310580-78310730	RPTEC	kidney:	n/a	chr8:78310686-78310707 chr8:78310691-78310709 chr8:78310692-78310708

No.	Distal block	Cell Line	Cell type
1	chr8:78266597..78268495-chr8:78269805..78272021,2	MCF-7	breast:
2	chr8:77279732..77280710-chr8:78310370..78311176,4	MCF-7	breast:
3	chr8:78268071..78271065-chr8:78271580..78274324,2	K562	blood:
4	chr6:43025757..43028121-chr8:78314973..78317562,2	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	chr8:78311200-78311372	XLOC_006852
4	lnc-ZFHX4-3	chr8:78311309-78311390	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: 656 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:656 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1154839	chr8:78271372-78271373	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs186355164	chr8:78271402-78271403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs535896045	chr8:78271416-78271417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs554832651	chr8:78271444-78271445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs573020342	chr8:78271475-78271476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs540540613	chr8:78271501-78271502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs73691675	chr8:78271540-78271541	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs565858234	chr8:78271559-78271560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs74765453	chr8:78271560-78271561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs545088512	chr8:78271577-78271578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs563489028	chr8:78271599-78271600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs189300391	chr8:78271671-78271672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs180807418	chr8:78271735-78271736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs561352940	chr8:78271737-78271738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs528751823	chr8:78271765-78271766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs554817056	chr8:78271791-78271792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs547321316	chr8:78271793-78271794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs2338958	chr8:78271818-78271819	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs532800561	chr8:78271824-78271825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs550673006	chr8:78271825-78271826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs186444150	chr8:78271836-78271837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs536361942	chr8:78271860-78271861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs531626607	chr8:78271887-78271888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs547845258	chr8:78271903-78271904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs558569922	chr8:78271931-78271932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs17375107	chr8:78271998-78271999	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs190849975	chr8:78272011-78272012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs554849485	chr8:78272084-78272085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs574897377	chr8:78272153-78272154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs183092255	chr8:78272183-78272184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs10107840	chr8:78272186-78272187	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs13267294	chr8:78272211-78272212	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs575040961	chr8:78272231-78272232	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs185954592	chr8:78272236-78272237	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs78227381	chr8:78272243-78272244	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs543128799	chr8:78272245-78272246	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs191702632	chr8:78272354-78272355	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs573199619	chr8:78272358-78272359	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs143272338	chr8:78272391-78272392	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs565604046	chr8:78272394-78272395	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs148301649	chr8:78272395-78272396	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs183140538	chr8:78272397-78272398	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs545926400	chr8:78290437-78290438	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs557708411	chr8:78290459-78290460	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs576075249	chr8:78290495-78290496	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs543746338	chr8:78290502-78290503	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs559093842	chr8:78290551-78290552	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs529562400	chr8:78290637-78290638	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs114185227	chr8:78290643-78290644	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs560024399	chr8:78290655-78290656	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:59 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:78271200-78271400	ZNF genes & repeats	HUVEC	blood vessel
2	chr8:78271400-78272200	Weak transcription	HUVEC	blood vessel
3	chr8:78272200-78272400	ZNF genes & repeats	HUVEC	blood vessel
4	chr8:78290400-78291600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr8:78290600-78291000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr8:78290800-78291000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr8:78293600-78293800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr8:78300800-78301800	Enhancers	Muscle Satellite Cultured Cells	--
9	chr8:78308200-78309200	Enhancers	HepG2	liver
10	chr8:78309200-78310800	Weak transcription	HepG2	liver
11	chr8:78309800-78310400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr8:78309800-78310600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr8:78309800-78311200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr8:78309800-78311400	Enhancers	Muscle Satellite Cultured Cells	--
15	chr8:78310400-78310800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr8:78310600-78311200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr8:78310800-78311000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr8:78310800-78311400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr8:78310800-78311600	Enhancers	Liver	Liver
20	chr8:78310800-78311600	Enhancers	HepG2	liver
21	chr8:78311000-78311600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr8:78311200-78311400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr8:78311200-78311800	Enhancers	Fetal Intestine Large	intestine
24	chr8:78311200-78312000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr8:78311200-78312400	Active TSS	Fetal Muscle Trunk	muscle
26	chr8:78311200-78313800	Active TSS	Adipose Nuclei	Adipose
27	chr8:78311400-78311600	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr8:78311400-78311800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr8:78311400-78312600	Weak transcription	Muscle Satellite Cultured Cells	--
30	chr8:78311400-78315800	Active TSS	Fetal Muscle Leg	muscle
31	chr8:78311600-78311800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr8:78311600-78312000	Flanking Active TSS	Liver	Liver
33	chr8:78311600-78312000	Flanking Active TSS	HepG2	liver
34	chr8:78311600-78314800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr8:78311800-78312000	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr8:78311800-78312600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr8:78312000-78312400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr8:78312000-78312800	Enhancers	HepG2	liver
39	chr8:78312000-78313000	Active TSS	Liver	Liver
40	chr8:78312000-78313800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr8:78312600-78312800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr8:78312800-78313400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr8:78313000-78313200	Enhancers	Muscle Satellite Cultured Cells	--
44	chr8:78313000-78313200	Flanking Active TSS	Liver	Liver
45	chr8:78313200-78313400	Active TSS	Liver	Liver
46	chr8:78313400-78313800	Flanking Active TSS	Liver	Liver
47	chr8:78313400-78315000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr8:78313800-78314000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr8:78313800-78316200	Weak transcription	Adipose Nuclei	Adipose
50	chr8:78313800-78318000	Weak transcription	Liver	Liver

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