Variant report

Variant	nsv831308
Chromosome Location	chr8:47490970-47684786
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:732)
CpG islands
(count:305)
Chromatin interactive
region (count:22)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:47529231-47529761	K562	blood:	n/a	n/a
2	ATF1	chr8:47548283-47548344	K562	blood:	n/a	n/a
3	ATF1	chr8:47551373-47551428	K562	blood:	n/a	n/a
4	ATF3	chr8:47529101-47529363	K562	blood:	n/a	n/a
5	BACH1	chr8:47536608-47536724	K562	blood:	n/a	n/a
6	BHLHE40	chr8:47528443-47529576	K562	blood:	n/a	chr8:47528874-47528890 chr8:47529336-47529352
7	BHLHE40	chr8:47570504-47570636	K562	blood:	n/a	n/a
8	CBX3	chr8:47529072-47529420	K562	blood:	n/a	n/a
9	CCNT2	chr8:47528797-47529481	K562	blood:	n/a	n/a
10	CEBPB	chr8:47554881-47555207	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr8:47570103-47570239	HepG2	liver:	n/a	chr8:47570181-47570192
12	CEBPB	chr8:47678002-47678303	IMR90	lung:	n/a	chr8:47678131-47678142
13	CEBPB	chr8:47547945-47548304	A549	lung:	n/a	n/a
14	CEBPB	chr8:47529077-47529452	K562	blood:	n/a	n/a
15	CEBPB	chr8:47562910-47563178	MCF-7	breast:	n/a	n/a
16	CEBPB	chr8:47587261-47587588	HepG2	liver:	n/a	n/a
17	CEBPB	chr8:47610035-47610215	HepG2	liver:	n/a	chr8:47610104-47610115
18	CEBPB	chr8:47546616-47546808	K562	blood:	n/a	chr8:47546682-47546693
19	CEBPB	chr8:47548607-47548874	A549	lung:	n/a	chr8:47548763-47548774
20	CEBPB	chr8:47504609-47504813	HepG2	liver:	n/a	chr8:47504728-47504745 chr8:47504677-47504688 chr8:47504676-47504689 chr8:47504731-47504743
21	CEBPB	chr8:47554891-47555151	K562	blood:	n/a	n/a
22	CEBPB	chr8:47579903-47580243	HepG2	liver:	n/a	n/a
23	CEBPB	chr8:47493915-47494006	K562	blood:	n/a	n/a
24	CEBPB	chr8:47587262-47587581	IMR90	lung:	n/a	n/a
25	CEBPB	chr8:47560585-47560829	HepG2	liver:	n/a	n/a
26	CEBPB	chr8:47678009-47678239	A549	lung:	n/a	chr8:47678131-47678142
27	CEBPB	chr8:47662835-47663134	MCF-7	breast:	n/a	chr8:47662934-47662945
28	CEBPB	chr8:47534139-47534510	IMR90	lung:	n/a	n/a
29	CEBPB	chr8:47549385-47550207	A549	lung:	n/a	n/a
30	CEBPB	chr8:47557913-47558274	K562	blood:	n/a	chr8:47558092-47558103
31	CEBPB	chr8:47495566-47495807	HepG2	liver:	n/a	n/a
32	CEBPB	chr8:47597167-47597429	A549	lung:	n/a	chr8:47597321-47597332 chr8:47597291-47597302
33	CEBPB	chr8:47587362-47587504	K562	blood:	n/a	n/a
34	CEBPB	chr8:47546537-47546824	A549	lung:	n/a	chr8:47546682-47546693
35	CEBPB	chr8:47554880-47555156	HepG2	liver:	n/a	n/a
36	CEBPB	chr8:47546529-47547110	HepG2	liver:	n/a	chr8:47546682-47546693
37	CEBPB	chr8:47534167-47534483	HepG2	liver:	n/a	n/a
38	CEBPB	chr8:47565434-47565709	K562	blood:	n/a	chr8:47565589-47565600
39	CEBPB	chr8:47491043-47491262	K562	blood:	n/a	chr8:47491158-47491169
40	CEBPB	chr8:47562442-47562621	K562	blood:	n/a	chr8:47562536-47562547
41	CEBPB	chr8:47506841-47507041	K562	blood:	n/a	chr8:47506900-47506917
42	CEBPB	chr8:47529068-47529484	K562	blood:	n/a	n/a
43	CEBPB	chr8:47548637-47548787	HepG2	liver:	n/a	chr8:47548763-47548774
44	CEBPB	chr8:47530129-47530132	K562	blood:	n/a	n/a
45	CEBPB	chr8:47557878-47558315	MCF-7	breast:	n/a	chr8:47558092-47558103
46	CEBPB	chr8:47552473-47553612	HepG2	liver:	n/a	n/a
47	CEBPB	chr8:47552480-47553588	A549	lung:	n/a	n/a
48	CEBPB	chr8:47646735-47647020	MCF-7	breast:	n/a	chr8:47646871-47646882
49	CEBPB	chr8:47525869-47526123	K562	blood:	n/a	n/a
50	CEBPB	chr8:47557938-47558285	IMR90	lung:	n/a	chr8:47558092-47558103

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:47529545-47529595	CMK	blood:	n/a
2	chr8:47529280-47529330	HUVEC	blood vessel:	n/a
3	chr8:47529280-47529330	Jurkat	blood:	n/a
4	chr8:47529280-47529330	LNCaP	prostate:	n/a
5	chr8:47526309-47526359	NHDF-neo	bronchial:	n/a
6	chr8:47529545-47529595	NB4	blood:	n/a
7	chr8:47527657-47527707	GM12878	blood:	n/a
8	chr8:47529280-47529330	AG09319	gingival:	n/a
9	chr8:47526309-47526359	PFSK-1	brain:	n/a
10	chr8:47529280-47529330	AG04449	skin:	fetal
11	chr8:47527657-47527707	AG09309	skin:	n/a
12	chr8:47527657-47527707	H1-hESC	embryonic stem cell:	embryo
13	chr8:47529280-47529330	RPTEC	kidney:	n/a
14	chr8:47529015-47529065	GM12891	blood:	n/a
15	chr8:47529015-47529065	HIPEpiC	eye:	n/a
16	chr8:47526309-47526359	GM12892	blood:	n/a
17	chr8:47529545-47529595	SKMC	muscle:	n/a
18	chr8:47526309-47526359	H1-hESC	embryonic stem cell:	embryo
19	chr8:47529280-47529330	HEK293	kidney:	embryo
20	chr8:47529545-47529595	LNCaP	prostate:	n/a
21	chr8:47527657-47527707	HL-60	blood:	n/a
22	chr8:47527657-47527707	Hepatocyte	liver:	n/a
23	chr8:47526309-47526359	HEK293	kidney:	embryo
24	chr8:47527657-47527707	T-47D	breast:	n/a
25	chr8:47526309-47526359	Hepatocyte	liver:	n/a
26	chr8:47529280-47529330	HCT-116	colon:	n/a
27	chr8:47529015-47529065	U87	brain:	n/a
28	chr8:47527657-47527707	NHDF-neo	bronchial:	n/a
29	chr8:47527657-47527707	SK-N-SH	brain:	n/a
30	chr8:47529545-47529595	IMR90	lung:	fetal
31	chr8:47529280-47529330	K562	blood:	n/a
32	chr8:47529015-47529065	A549	lung:	n/a
33	chr8:47527657-47527707	HUVEC	blood vessel:	n/a
34	chr8:47526309-47526359	HNPCEpiC	eye:	n/a
35	chr8:47529015-47529065	HPAEpiC	pulmonary alveolar:	n/a
36	chr8:47527657-47527707	RPTEC	kidney:	n/a
37	chr8:47529280-47529330	Caco-2	colon:	n/a
38	chr8:47527657-47527707	HCM	heart:	n/a
39	chr8:47527657-47527707	GM12891	blood:	n/a
40	chr8:47529015-47529065	HepG2	liver:	n/a
41	chr8:47529015-47529065	HRE	kidney:	n/a
42	chr8:47529545-47529595	PFSK-1	brain:	n/a
43	chr8:47526309-47526359	SK-N-MC	brain:	n/a
44	chr8:47527657-47527707	MCF10A-Er-Src	breast:	n/a
45	chr8:47529545-47529595	HEK293	kidney:	embryo
46	chr8:47527657-47527707	NT2-D1	testis:	n/a
47	chr8:47526309-47526359	CMK	blood:	n/a
48	chr8:47526309-47526359	GM19239	blood:	n/a
49	chr8:47529280-47529330	SAEC	small airway:	n/a
50	chr8:47527657-47527707	SK-N-SH_RA	brain:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:47512649..47514644-chr8:47529072..47530746,2	K562	blood:
2	chr8:47619682..47620259-chr8:47831736..47832439,2	MCF-7	breast:
3	chr8:47618289..47619061-chr8:47868266..47869014,2	MCF-7	breast:
4	chr8:47491632..47493538-chr8:47505350..47507971,2	K562	blood:
5	chr8:47515437..47518605-chr8:47528973..47530959,3	K562	blood:
6	chr8:47528106..47530039-chr8:47536064..47537656,2	MCF-7	breast:
7	chr7:97495363..97496869-chr8:47517938..47519464,2	K562	blood:
8	chr8:47506585..47508657-chr8:47510206..47513067,2	K562	blood:
9	chr8:47515437..47518605-chr8:47528973..47530959,3	K562	blood:
10	chr8:47506585..47508657-chr8:47510206..47513067,2	K562	blood:
11	chr8:47528106..47530039-chr8:47536064..47537656,2	MCF-7	breast:
12	chr8:47491632..47493538-chr8:47505350..47507971,2	K562	blood:
13	chr8:47619331..47620431-chr8:47868217..47869326,4	MCF-7	breast:
14	chr8:47524927..47529861-chr8:47530508..47536088,6	K562	blood:
15	chr8:47519082..47521588-chr8:47524616..47530066,4	K562	blood:
16	chr8:47512649..47514644-chr8:47529072..47530746,2	K562	blood:
17	chr8:47618307..47619237-chr8:47916938..47917469,2	MCF-7	breast:
18	chr8:47517410..47521817-chr8:47524226..47528650,6	K562	blood:
19	chr8:47487702..47490248-chr8:47515594..47517867,2	K562	blood:
20	chr8:47619541..47620262-chr8:47868295..47869178,3	MCF-7	breast:
21	chr8:47484279..47485112-chr8:47579488..47580411,3	MCF-7	breast:
22	chr7:97501587..97502366-chr8:47529051..47529557,3	HCT-116	colon:

No data

Variant related genes	Relation type
ASNSP4	TF binding region
ENSG00000254070	TF binding region
ASNSP1	TF binding region
ASNSP4	CpG island
ENSG00000254070	CpG island
ASNSP1	CpG island
ENSG00000070669	chromatin interactions
ENSG00000248498	chromatin interactions

Extended variants
information (count: 2192 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:2192 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs180823283	chr8:47490972-47490973	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs7008539	chr8:47490997-47490998	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs112063828	chr8:47491026-47491027	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs528673322	chr8:47491027-47491028	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs548709157	chr8:47491041-47491042	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs1852082	chr8:47491073-47491074	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs1049845	chr8:47491097-47491098	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs550702156	chr8:47491109-47491110	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs570484535	chr8:47491167-47491168	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs369139990	chr8:47498215-47498216	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs184888435	chr8:47498247-47498248	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs528746845	chr8:47498259-47498260	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs190862897	chr8:47498263-47498264	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs538056041	chr8:47498312-47498313	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs565515988	chr8:47498313-47498314	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs530991852	chr8:47498371-47498372	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs138659225	chr8:47498433-47498434	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs578063045	chr8:47498447-47498448	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs35321362	chr8:47498456-47498457	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs549871431	chr8:47498524-47498525	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs142721154	chr8:47498542-47498543	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs554174318	chr8:47498568-47498569	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs573931983	chr8:47498584-47498585	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs376913377	chr8:47514207-47514208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs370003420	chr8:47514211-47514212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs373506248	chr8:47514229-47514230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs79067176	chr8:47514280-47514281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs201572379	chr8:47514308-47514309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs560011100	chr8:47514312-47514313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs4483169	chr8:47514596-47514597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs75600954	chr8:47514876-47514877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs528955136	chr8:47514987-47514988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs542286526	chr8:47514994-47514995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs562489323	chr8:47515042-47515043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs556196889	chr8:47515043-47515044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs531149562	chr8:47515070-47515071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs554446754	chr8:47515151-47515152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs568182195	chr8:47515290-47515291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs9773686	chr8:47515314-47515315	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs570762881	chr8:47515315-47515316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs533357209	chr8:47515316-47515317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs546755394	chr8:47515378-47515379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs9693304	chr8:47515543-47515544	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs566872551	chr8:47515556-47515557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs9692834	chr8:47515571-47515572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs535919388	chr8:47515579-47515580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs191502535	chr8:47515688-47515689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs568119779	chr8:47515706-47515707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs377240847	chr8:47515717-47515718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs370156284	chr8:47515748-47515749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

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
Oral cancer	21386901	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
Lung cancer	18438408	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
Acute myeloid leukemia	21251322	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
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Medulloblastoma	20607354	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
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	20409316	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
Tetralogy of Fallot	22912587	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD

Chromatin state (count:46 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:47489800-47491200	Enhancers	Skeletal Muscle Male	skeletal muscle
2	chr8:47498200-47498600	Enhancers	Placenta	Placenta
3	chr8:47514200-47518600	Weak transcription	K562	blood
4	chr8:47518600-47520200	Strong transcription	K562	blood
5	chr8:47520200-47525800	Weak transcription	K562	blood
6	chr8:47525800-47526000	Genic enhancers	K562	blood
7	chr8:47526000-47526200	Enhancers	K562	blood
8	chr8:47526200-47527000	Weak transcription	K562	blood
9	chr8:47527000-47529400	Active TSS	K562	blood
10	chr8:47528200-47529200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr8:47528200-47529200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr8:47528600-47528800	Bivalent/Poised TSS	Skeletal Muscle Male	skeletal muscle
13	chr8:47528600-47529400	Active TSS	Pancreas	Pancrea
14	chr8:47528800-47529200	ZNF genes & repeats	Placenta	Placenta
15	chr8:47529000-47529200	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
16	chr8:47529200-47529600	Active TSS	ES-I3 Cell Line	embryonic stem cell
17	chr8:47529400-47529800	Flanking Active TSS	K562	blood
18	chr8:47529400-47531400	Weak transcription	Pancreas	Pancrea
19	chr8:47529800-47531000	Enhancers	K562	blood
20	chr8:47531600-47535200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
21	chr8:47531800-47532200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
22	chr8:47534800-47535200	Enhancers	Skeletal Muscle Male	skeletal muscle
23	chr8:47539400-47539800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr8:47547400-47549400	Enhancers	Skeletal Muscle Female	skeletal muscle
25	chr8:47547400-47549600	Enhancers	Skeletal Muscle Male	skeletal muscle
26	chr8:47548000-47549200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
27	chr8:47549400-47554800	Weak transcription	Skeletal Muscle Female	skeletal muscle
28	chr8:47549600-47555000	Weak transcription	Skeletal Muscle Male	skeletal muscle
29	chr8:47554800-47555600	Enhancers	Skeletal Muscle Female	skeletal muscle
30	chr8:47555000-47556600	Enhancers	Skeletal Muscle Male	skeletal muscle
31	chr8:47555600-47560600	Weak transcription	Skeletal Muscle Female	skeletal muscle
32	chr8:47556600-47560600	Weak transcription	Skeletal Muscle Male	skeletal muscle
33	chr8:47560600-47564400	Enhancers	Skeletal Muscle Male	skeletal muscle
34	chr8:47560600-47564400	Enhancers	Skeletal Muscle Female	skeletal muscle
35	chr8:47567200-47567600	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
36	chr8:47578800-47579200	Active TSS	Fetal Heart	heart
37	chr8:47596600-47596800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr8:47596800-47597800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr8:47597800-47598400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr8:47619600-47620600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
41	chr8:47658600-47658800	ZNF genes & repeats	Aorta	Aorta
42	chr8:47658800-47662200	Weak transcription	Aorta	Aorta
43	chr8:47662200-47662400	ZNF genes & repeats	Aorta	Aorta
44	chr8:47669200-47669800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr8:47676600-47678000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
46	chr8:47683600-47684200	Active TSS	Fetal Heart	heart

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