Variant report

Variant	nsv1027984
Chromosome Location	chr8:51060895-51098808
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:221)
CpG islands
(count:61)
Chromatin interactive
region (count:0)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:221 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr8:51095438-51096474	IMR90	lung:	n/a	n/a
2	CTCF	chr8:51066602-51066814	MCF-7	breast:	n/a	n/a
3	CTCF	chr8:51066600-51066750	WERI-Rb-1	eye:	n/a	n/a
4	CTCF	chr8:51066253-51066493	MCF-7	breast:	n/a	n/a
5	CTCF	chr8:51066600-51066750	HPAF	blood vessel:	n/a	n/a
6	CTCF	chr8:51066300-51066450	WERI-Rb-1	eye:	n/a	n/a
7	CTCF	chr8:51066220-51066370	HAc	cerebellar:	n/a	n/a
8	CTCF	chr8:51066620-51066770	HMEC	breast:	n/a	n/a
9	CTCF	chr8:51066300-51066450	Hela-S3	cervix:	n/a	n/a
10	CTCF	chr8:51066240-51066530	HVMF	connective:	n/a	n/a
11	CTCF	chr8:51066300-51066450	HMEC	breast:	n/a	n/a
12	CTCF	chr8:51066616-51066803	MCF-7	breast:	n/a	n/a
13	CTCF	chr8:51066300-51066450	HRPEpiC	eye:	n/a	n/a
14	CTCF	chr8:51066280-51066430	AG04449	skin:	n/a	n/a
15	CTCF	chr8:51066340-51066490	AoAF	blood vessel:	n/a	n/a
16	CTCF	chr8:51066266-51066472	SK-N-SH_RA	brain:	n/a	n/a
17	CTCF	chr8:51066285-51066525	GM12878	blood:	n/a	n/a
18	CTCF	chr8:51066300-51066450	AG09319	gingival:	n/a	n/a
19	CTCF	chr8:51066640-51066790	SK-N-SH_RA	brain:	n/a	n/a
20	CTCF	chr8:51066460-51066610	WI-38	lung:	n/a	n/a
21	CTCF	chr8:51066710-51066747	GM12891	blood:	n/a	n/a
22	CTCF	chr8:51066203-51066506	T-47D	breast:	n/a	n/a
23	CTCF	chr8:51066271-51066492	MCF-7	breast:	n/a	n/a
24	CTCF	chr8:51066224-51066495	T-47D	breast:	n/a	n/a
25	CTCF	chr8:51066300-51066450	GM12878	blood:	n/a	n/a
26	CTCF	chr8:51066640-51066790	HBMEC	blood vessel:	n/a	n/a
27	CTCF	chr8:51066248-51066433	SK-N-SH_RA	brain:	n/a	n/a
28	CTCF	chr8:51066632-51066707	GM13977	blood:	n/a	n/a
29	CTCF	chr8:51066240-51066390	WI-38	lung:	n/a	n/a
30	CTCF	chr8:51066300-51066450	SAEC	small airway:	n/a	n/a
31	CTCF	chr8:51066277-51066465	Hela-S3	cervix:	n/a	n/a
32	CTCF	chr8:51066260-51066512	LNCaP	prostate:	n/a	n/a
33	CTCF	chr8:51066300-51066450	AG10803	skin:	n/a	n/a
34	CTCF	chr8:51066640-51066790	HPAF	blood vessel:	n/a	n/a
35	CTCF	chr8:51066283-51066458	GM12892	blood:	n/a	n/a
36	CTCF	chr8:51066673-51066748	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr8:51066240-51066390	HRPEpiC	eye:	n/a	n/a
38	CTCF	chr8:51066320-51066409	GM13976	blood:	n/a	n/a
39	CTCF	chr8:51066640-51066790	HEK293	kidney:	n/a	n/a
40	CTCF	chr8:51066316-51066421	Kidney_OC	kidney:	n/a	n/a
41	CTCF	chr8:51066300-51066450	AG04449	skin:	n/a	n/a
42	CTCF	chr8:51066320-51066470	BJ	skin:	n/a	n/a
43	CTCF	chr8:51066320-51066470	HBMEC	blood vessel:	n/a	n/a
44	CTCF	chr8:51066320-51066470	HCPEpiC	choroid plexus:	n/a	n/a
45	CTCF	chr8:51066024-51066908	SK-N-SH	brain:	n/a	n/a
46	CTCF	chr8:51066270-51066612	LNCaP	prostate:	n/a	n/a
47	CTCF	chr8:51066240-51066390	HCM	heart:	n/a	n/a
48	CTCF	chr8:51066420-51066570	NB4	blood:	n/a	n/a
49	CTCF	chr8:51086832-51086914	GM13976	blood:	n/a	n/a
50	CTCF	chr8:51066220-51066370	HFF-Myc	foreskin:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:51095593-51095643	HPAEpiC	pulmonary alveolar:	n/a
2	chr8:51095593-51095643	K562	blood:	n/a
3	chr8:51095593-51095643	MCF10A-Er-Src	breast:	n/a
4	chr8:51095593-51095643	Caco-2	colon:	n/a
5	chr8:51095593-51095643	NH-A	brain:	n/a
6	chr8:51095593-51095643	Hepatocyte	liver:	n/a
7	chr8:51095593-51095643	HCF	heart:	n/a
8	chr8:51095593-51095643	ovcar-3	ovarian:	n/a
9	chr8:51095593-51095643	GM19239	blood:	n/a
10	chr8:51095593-51095643	ECC-1	luminal epithelium:	n/a
11	chr8:51095593-51095643	HIPEpiC	eye:	n/a
12	chr8:51095593-51095643	HepG2	liver:	n/a
13	chr8:51095593-51095643	NB4	blood:	n/a
14	chr8:51095593-51095643	HL-60	blood:	n/a
15	chr8:51095593-51095643	IMR90	lung:	fetal
16	chr8:51095593-51095643	HCT-116	colon:	n/a
17	chr8:51095593-51095643	HRPEpiC	eye:	n/a
18	chr8:51095593-51095643	PANC-1	pancreas:	n/a
19	chr8:51095593-51095643	A549	lung:	n/a
20	chr8:51095593-51095643	HNPCEpiC	eye:	n/a
21	chr8:51095593-51095643	GM12892	blood:	n/a
22	chr8:51095593-51095643	SKMC	muscle:	n/a
23	chr8:51095593-51095643	NHBE	bronchial:	n/a
24	chr8:51095593-51095643	MCF-7	breast:	n/a
25	chr8:51095593-51095643	SAEC	small airway:	n/a
26	chr8:51095593-51095643	AG09309	skin:	n/a
27	chr8:51095593-51095643	LNCaP	prostate:	n/a
28	chr8:51095593-51095643	AoSMC	blood vessel:	n/a
29	chr8:51095593-51095643	GM12878	blood:	n/a
30	chr8:51095593-51095643	HEEpiC	esophagus:	n/a
31	chr8:51095593-51095643	Jurkat	blood:	n/a
32	chr8:51095593-51095643	PFSK-1	brain:	n/a
33	chr8:51095593-51095643	HCM	heart:	n/a
34	chr8:51095593-51095643	AG04450	lung:	fetal
35	chr8:51095593-51095643	GM06990	blood:	n/a
36	chr8:51095593-51095643	AG04449	skin:	fetal
37	chr8:51095593-51095643	HCPEpiC	choroid plexus:	n/a
38	chr8:51095593-51095643	AG10803	skin:	n/a
39	chr8:51095593-51095643	BE2_C	brain:	n/a
40	chr8:51095593-51095643	BJ	skin:	n/a
41	chr8:51095593-51095643	AG09319	gingival:	n/a
42	chr8:51095593-51095643	NHDF-neo	bronchial:	n/a
43	chr8:51095593-51095643	HRE	kidney:	n/a
44	chr8:51095593-51095643	GM12891	blood:	n/a
45	chr8:51095593-51095643	HEK293	kidney:	embryo
46	chr8:51095593-51095643	Hela-S3	cervix:	n/a
47	chr8:51095593-51095643	SK-N-SH	brain:	n/a
48	chr8:51095593-51095643	NT2-D1	testis:	n/a
49	chr8:51095593-51095643	PrEC	prostate:	n/a
50	chr8:51095593-51095643	HUVEC	blood vessel:	n/a

No data

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C8orf22-14	chr8:51076059-51076529	NONHSAT126523
2	lnc-C8orf22-15	chr8:51085121-51085195	NONHSAT126524

No data

Variant related genes	Relation type
SNTG1	TF binding region
SNTG1	CpG island

Extended variants
information (count: 732 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs181376213	chr8:51066403-51066404	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs112563337	chr8:51066443-51066444	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs116967638	chr8:51066447-51066448	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs186564304	chr8:51066453-51066454	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs550345142	chr8:51066467-51066468	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs146685590	chr8:51066498-51066499	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs528387835	chr8:51066499-51066500	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs190294855	chr8:51066503-51066504	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs181978330	chr8:51066538-51066539	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs534001178	chr8:51066555-51066556	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs186359279	chr8:51066573-51066574	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs191204003	chr8:51066586-51066587	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs551223915	chr8:51066594-51066595	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs577076092	chr8:51066599-51066600	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs139085143	chr8:51066607-51066608	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs557120723	chr8:51066625-51066626	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs541417534	chr8:51066628-51066629	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs571202329	chr8:51066657-51066658	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs536686080	chr8:51066669-51066670	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs542745760	chr8:51066676-51066677	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs573658602	chr8:51066681-51066682	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs561060237	chr8:51066684-51066685	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs573072603	chr8:51066712-51066713	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs561724194	chr8:51066727-51066728	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs540473997	chr8:51066752-51066753	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs149938700	chr8:51066756-51066757	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs532739992	chr8:51066780-51066781	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs550527933	chr8:51066781-51066782	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs182290456	chr8:51066791-51066792	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs556665531	chr8:51066818-51066819	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs185337135	chr8:51066819-51066820	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs566572829	chr8:51066839-51066840	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs533944523	chr8:51066868-51066869	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs144995474	chr8:51066870-51066871	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs570724275	chr8:51066892-51066893	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs537781413	chr8:51066930-51066931	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs111319125	chr8:51066940-51066941	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs557310727	chr8:51066945-51066946	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs146062572	chr8:51066965-51066966	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs544154613	chr8:51066979-51066980	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs191027851	chr8:51066995-51066996	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs535938117	chr8:51066998-51066999	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs573011218	chr8:51067019-51067020	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs147882333	chr8:51067053-51067054	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs183333782	chr8:51067126-51067127	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs527339577	chr8:51067137-51067138	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs573433947	chr8:51067138-51067139	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs10098057	chr8:51067154-51067155	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs141506330	chr8:51067160-51067161	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs562361082	chr8:51067162-51067163	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

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
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:77 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:51066400-51067200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr8:51075200-51075600	Enhancers	Spleen	Spleen
3	chr8:51082400-51084600	Weak transcription	NH-A	brain
4	chr8:51082600-51086400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr8:51084400-51085400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr8:51084600-51086000	Enhancers	NH-A	brain
7	chr8:51085200-51086000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr8:51085200-51086000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr8:51085400-51085600	ZNF genes & repeats	ES-WA7 Cell Line	embryonic stem cell
10	chr8:51085600-51091200	Weak transcription	Cortex derived primary cultured neurospheres	brain
11	chr8:51086400-51087000	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr8:51087000-51087200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr8:51087200-51090600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr8:51088400-51088600	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr8:51089000-51090000	Weak transcription	HUES6 Cell Line	embryonic stem cell
16	chr8:51089800-51090600	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr8:51090000-51090200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr8:51090000-51090400	Enhancers	Brain Germinal Matrix	brain
19	chr8:51090000-51090600	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr8:51090000-51090800	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr8:51090200-51090400	Enhancers	iPS-20b Cell Line	embryonic stem cell
22	chr8:51090200-51090800	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr8:51090800-51091800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
24	chr8:51091800-51092200	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr8:51093400-51094000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr8:51093800-51095400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr8:51094000-51095400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr8:51094800-51095400	Enhancers	Osteobl	bone
29	chr8:51095000-51095200	Enhancers	NH-A	brain
30	chr8:51095200-51095800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr8:51095200-51096200	Flanking Active TSS	NH-A	brain
32	chr8:51095200-51096600	Enhancers	HMEC	breast
33	chr8:51095400-51095600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr8:51095400-51096200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr8:51095400-51096200	Enhancers	NHLF	lung
36	chr8:51095400-51096200	Flanking Active TSS	Osteobl	bone
37	chr8:51095400-51096800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr8:51095400-51096800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
39	chr8:51095600-51095800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr8:51095600-51096000	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr8:51095600-51096200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr8:51095600-51096200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr8:51095600-51096200	Enhancers	NHDF-Ad	bronchial
44	chr8:51095600-51096600	Enhancers	HSMM	muscle
45	chr8:51095600-51096600	Enhancers	HSMMtube	muscle
46	chr8:51095600-51096800	Enhancers	Muscle Satellite Cultured Cells	--
47	chr8:51095800-51096200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr8:51095800-51096200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr8:51095800-51096200	Enhancers	Pancreatic Islets	Pancreatic Islet
50	chr8:51095800-51096800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin

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