Variant report

Variant	nsv1034527
Chromosome Location	chr8:47555136-47751637
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:821)
CpG islands
(count:184)
Chromatin interactive
region (count:6)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:821 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr8:47750627-47750683	H1-hESC	embryonic stem cell:	n/a	n/a
2	BATF	chr8:47742166-47742315	GM12878	blood:	n/a	n/a
3	BATF	chr8:47742552-47742702	GM12878	blood:	n/a	n/a
4	BATF	chr8:47741055-47741204	GM12878	blood:	n/a	n/a
5	BATF	chr8:47738438-47738681	GM12878	blood:	n/a	chr8:47738534-47738545
6	BATF	chr8:47742058-47742352	GM12878	blood:	n/a	n/a
7	BATF	chr8:47742543-47742780	GM12878	blood:	n/a	n/a
8	BCL11A	chr8:47742493-47742715	GM12878	blood:	n/a	n/a
9	BCL11A	chr8:47741063-47741196	GM12878	blood:	n/a	n/a
10	BCL11A	chr8:47742173-47742308	GM12878	blood:	n/a	n/a
11	BCL11A	chr8:47742558-47742696	GM12878	blood:	n/a	n/a
12	BCL11A	chr8:47742011-47742327	GM12878	blood:	n/a	n/a
13	BCL11A	chr8:47741045-47741214	GM12878	blood:	n/a	n/a
14	BHLHE40	chr8:47741998-47742438	HepG2	liver:	n/a	n/a
15	BHLHE40	chr8:47570504-47570636	K562	blood:	n/a	n/a
16	BHLHE40	chr8:47742538-47742866	HepG2	liver:	n/a	n/a
17	BHLHE40	chr8:47741043-47741216	HepG2	liver:	n/a	n/a
18	CEBPB	chr8:47597167-47597429	A549	lung:	n/a	chr8:47597321-47597332 chr8:47597291-47597302
19	CEBPB	chr8:47557908-47558267	HepG2	liver:	n/a	chr8:47558092-47558103
20	CEBPB	chr8:47587362-47587504	K562	blood:	n/a	n/a
21	CEBPB	chr8:47689369-47689570	HepG2	liver:	n/a	n/a
22	CEBPB	chr8:47728857-47729192	A549	lung:	n/a	n/a
23	CEBPB	chr8:47726143-47726477	MCF-7	breast:	n/a	n/a
24	CEBPB	chr8:47554606-47555182	A549	lung:	n/a	n/a
25	CEBPB	chr8:47587262-47587581	IMR90	lung:	n/a	n/a
26	CEBPB	chr8:47610006-47610207	IMR90	lung:	n/a	chr8:47610104-47610115
27	CEBPB	chr8:47732072-47732430	HepG2	liver:	n/a	chr8:47732251-47732262
28	CEBPB	chr8:47554887-47555177	K562	blood:	n/a	n/a
29	CEBPB	chr8:47587299-47587532	A549	lung:	n/a	n/a
30	CEBPB	chr8:47735917-47736098	HepG2	liver:	n/a	n/a
31	CEBPB	chr8:47728521-47729026	HepG2	liver:	n/a	n/a
32	CEBPB	chr8:47731371-47731837	HepG2	liver:	n/a	n/a
33	CEBPB	chr8:47678002-47678303	IMR90	lung:	n/a	chr8:47678131-47678142
34	CEBPB	chr8:47554849-47555188	MCF-7	breast:	n/a	n/a
35	CEBPB	chr8:47565434-47565709	K562	blood:	n/a	chr8:47565589-47565600
36	CEBPB	chr8:47565469-47565705	HepG2	liver:	n/a	chr8:47565589-47565600
37	CEBPB	chr8:47662817-47663112	IMR90	lung:	n/a	chr8:47662934-47662945
38	CEBPB	chr8:47557938-47558285	IMR90	lung:	n/a	chr8:47558092-47558103
39	CEBPB	chr8:47554891-47555151	K562	blood:	n/a	n/a
40	CEBPB	chr8:47579860-47580138	MCF-7	breast:	n/a	n/a
41	CEBPB	chr8:47662835-47663134	MCF-7	breast:	n/a	chr8:47662934-47662945
42	CEBPB	chr8:47562442-47562621	K562	blood:	n/a	chr8:47562536-47562547
43	CEBPB	chr8:47729582-47729782	IMR90	lung:	n/a	chr8:47729734-47729745
44	CEBPB	chr8:47557878-47558315	MCF-7	breast:	n/a	chr8:47558092-47558103
45	CEBPB	chr8:47646735-47647020	MCF-7	breast:	n/a	chr8:47646871-47646882
46	CEBPB	chr8:47557998-47558160	K562	blood:	n/a	chr8:47558092-47558103
47	CEBPB	chr8:47562301-47562634	A549	lung:	n/a	chr8:47562536-47562547
48	CEBPB	chr8:47733759-47733964	A549	lung:	n/a	n/a
49	CEBPB	chr8:47678009-47678239	A549	lung:	n/a	chr8:47678131-47678142
50	CEBPB	chr8:47730645-47730867	HepG2	liver:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:47751623-47751673	PrEC	prostate:	n/a
2	chr8:47751623-47751673	PrEC	prostate:	n/a
3	chr8:47751494-47751544	GM06990	blood:	n/a
4	chr8:47748435-47748485	NH-A	brain:	n/a
5	chr8:47751623-47751673	HNPCEpiC	eye:	n/a
6	chr8:47751494-47751544	HRE	kidney:	n/a
7	chr8:47748435-47748485	ECC-1	luminal epithelium:	n/a
8	chr8:47751623-47751673	IMR90	lung:	fetal
9	chr8:47751623-47751673	NH-A	brain:	n/a
10	chr8:47748435-47748485	ProgFib	skin:	n/a
11	chr8:47748435-47748485	PrEC	prostate:	n/a
12	chr8:47751623-47751673	PFSK-1	brain:	n/a
13	chr8:47751494-47751544	NB4	blood:	n/a
14	chr8:47748435-47748485	T-47D	breast:	n/a
15	chr8:47751494-47751544	Caco-2	colon:	n/a
16	chr8:47751623-47751673	SAEC	small airway:	n/a
17	chr8:47751623-47751673	HIPEpiC	eye:	n/a
18	chr8:47751494-47751544	PFSK-1	brain:	n/a
19	chr8:47751494-47751544	HIPEpiC	eye:	n/a
20	chr8:47748435-47748485	CMK	blood:	n/a
21	chr8:47751623-47751673	NB4	blood:	n/a
22	chr8:47748435-47748485	GM12878	blood:	n/a
23	chr8:47748435-47748485	BE2_C	brain:	n/a
24	chr8:47751623-47751673	BE2_C	brain:	n/a
25	chr8:47751623-47751673	HCT-116	colon:	n/a
26	chr8:47748435-47748485	AG09309	skin:	n/a
27	chr8:47751494-47751544	AG09309	skin:	n/a
28	chr8:47751494-47751544	HUVEC	blood vessel:	n/a
29	chr8:47751623-47751673	AG09309	skin:	n/a
30	chr8:47751623-47751673	HCF	heart:	n/a
31	chr8:47751494-47751544	HRPEpiC	eye:	n/a
32	chr8:47751623-47751673	Jurkat	blood:	n/a
33	chr8:47751623-47751673	GM12892	blood:	n/a
34	chr8:47748435-47748485	AoSMC	blood vessel:	n/a
35	chr8:47748435-47748485	PFSK-1	brain:	n/a
36	chr8:47748435-47748485	HCPEpiC	choroid plexus:	n/a
37	chr8:47751494-47751544	NT2-D1	testis:	n/a
38	chr8:47751494-47751544	RPTEC	kidney:	n/a
39	chr8:47748435-47748485	HRPEpiC	eye:	n/a
40	chr8:47748435-47748485	SAEC	small airway:	n/a
41	chr8:47751494-47751544	NH-A	brain:	n/a
42	chr8:47748435-47748485	GM06990	blood:	n/a
43	chr8:47748435-47748485	HEEpiC	esophagus:	n/a
44	chr8:47751623-47751673	SK-N-MC	brain:	n/a
45	chr8:47748435-47748485	HepG2	liver:	n/a
46	chr8:47751494-47751544	H1-hESC	embryonic stem cell:	embryo
47	chr8:47751494-47751544	A549	lung:	n/a
48	chr8:47751623-47751673	HCPEpiC	choroid plexus:	n/a
49	chr8:47751623-47751673	ovcar-3	ovarian:	n/a
50	chr8:47751623-47751673	NHBE	bronchial:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:47618289..47619061-chr8:47868266..47869014,2	MCF-7	breast:
2	chr8:47484279..47485112-chr8:47579488..47580411,3	MCF-7	breast:
3	chr8:47618307..47619237-chr8:47916938..47917469,2	MCF-7	breast:
4	chr8:47619331..47620431-chr8:47868217..47869326,4	MCF-7	breast:
5	chr8:47619682..47620259-chr8:47831736..47832439,2	MCF-7	breast:
6	chr8:47619541..47620262-chr8:47868295..47869178,3	MCF-7	breast:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-350F16.2.1-4	chr8:47749200-47750328	NONHSAT126416
2	lnc-RP11-350F16.2.1-2	chr8:47730635-47730705	XLOC_007078
3	lnc-RP11-350F16.2.1-2	chr8:47722340-47723308	XLOC_007078
4	lnc-RP11-350F16.2.1-5	chr8:47738850-47740031	NONHSAT126413
5	lnc-LINC00293-2	chr8:47704231-47704686	NONHSAT126410
6	lnc-RP11-1134I14.8.1-3	chr8:47748364-47748420	ENSG00000253314.1
7	lnc-RP11-1134I14.8.1-3	chr8:47748371-47748420	NONHSAT126415
8	lnc-RP11-1134I14.8.1-8	chr8:47750410-47750827	NONHSAT126417
9	lnc-LINC00293-2	chr8:47703687-47703942	NONHSAT126410
10	lnc-RP11-1134I14.8.1-3	chr8:47733859-47734050	ENSG00000253314.1

No data

Variant related genes	Relation type
ENSG00000254070	TF binding region
MTND1P7	TF binding region
ENSG00000228984	TF binding region
MTND6P20	TF binding region
TRIM60P15	TF binding region
LINC00293	TF binding region
RNU6-656P	TF binding region
ASNSP4	TF binding region
ENSG00000254118	TF binding region
ENSG00000254070	CpG island
MTND1P7	CpG island
ENSG00000228984	CpG island
MTND6P20	CpG island
TRIM60P15	CpG island
LINC00293	CpG island
RNU6-656P	CpG island
ASNSP4	CpG island
ENSG00000254118	CpG island
USO1	miRNA target sites
PPARGC1A	miRNA target sites

Extended variants
information (count: 1960 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:1960 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs114861025	chr8:47555152-47555153	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs554616585	chr8:47555176-47555177	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs574343570	chr8:47555182-47555183	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs189161527	chr8:47555209-47555210	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs1568848	chr8:47555249-47555250	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs112911324	chr8:47555256-47555257	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs576598872	chr8:47555260-47555261	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs368139431	chr8:47555281-47555282	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs181219277	chr8:47555282-47555283	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs565087310	chr8:47555283-47555284	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs186497098	chr8:47555339-47555340	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs547451892	chr8:47555361-47555362	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs546982129	chr8:47555388-47555389	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs560968218	chr8:47555415-47555416	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs530082321	chr8:47555418-47555419	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs370139622	chr8:47555448-47555449	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs549840136	chr8:47555482-47555483	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs567200717	chr8:47555500-47555501	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs532254957	chr8:47555520-47555521	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs552403338	chr8:47555546-47555547	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs565840283	chr8:47555555-47555556	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs373184894	chr8:47555577-47555578	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs75596730	chr8:47555615-47555616	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs554680158	chr8:47555636-47555637	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs567994197	chr8:47555653-47555654	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs537037325	chr8:47555658-47555659	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs556628714	chr8:47555796-47555797	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs548158695	chr8:47555809-47555810	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs576674886	chr8:47555873-47555874	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs545252890	chr8:47555881-47555882	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs145470012	chr8:47555910-47555911	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs75017432	chr8:47555911-47555912	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs373627718	chr8:47555926-47555927	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs541155142	chr8:47555927-47555928	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs190993395	chr8:47555934-47555935	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs530081616	chr8:47555945-47555946	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs1404628	chr8:47555971-47555972	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs185086226	chr8:47556031-47556032	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs190727601	chr8:47556040-47556041	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs148050115	chr8:47556045-47556046	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs565906565	chr8:47556046-47556047	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs528276138	chr8:47556067-47556068	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs527687244	chr8:47556072-47556073	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs548342165	chr8:47556109-47556110	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs183286358	chr8:47556131-47556132	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs141789285	chr8:47556144-47556145	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs573330317	chr8:47556161-47556162	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs556922156	chr8:47556249-47556250	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs558762754	chr8:47556250-47556251	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs150601773	chr8:47556271-47556272	Enhancers 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:39 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:47554800-47555600	Enhancers	Skeletal Muscle Female	skeletal muscle
2	chr8:47555000-47556600	Enhancers	Skeletal Muscle Male	skeletal muscle
3	chr8:47555600-47560600	Weak transcription	Skeletal Muscle Female	skeletal muscle
4	chr8:47556600-47560600	Weak transcription	Skeletal Muscle Male	skeletal muscle
5	chr8:47560600-47564400	Enhancers	Skeletal Muscle Male	skeletal muscle
6	chr8:47560600-47564400	Enhancers	Skeletal Muscle Female	skeletal muscle
7	chr8:47567200-47567600	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
8	chr8:47578800-47579200	Active TSS	Fetal Heart	heart
9	chr8:47596600-47596800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr8:47596800-47597800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr8:47597800-47598400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr8:47619600-47620600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
13	chr8:47658600-47658800	ZNF genes & repeats	Aorta	Aorta
14	chr8:47658800-47662200	Weak transcription	Aorta	Aorta
15	chr8:47662200-47662400	ZNF genes & repeats	Aorta	Aorta
16	chr8:47669200-47669800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr8:47676600-47678000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
18	chr8:47683600-47684200	Active TSS	Fetal Heart	heart
19	chr8:47690800-47693200	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
20	chr8:47692200-47692400	ZNF genes & repeats	Fetal Brain Female	brain
21	chr8:47692800-47693000	Active TSS	Fetal Heart	heart
22	chr8:47693000-47695600	Weak transcription	Fetal Heart	heart
23	chr8:47695600-47696000	Active TSS	Fetal Heart	heart
24	chr8:47695600-47696200	ZNF genes & repeats	Adipose Nuclei	Adipose
25	chr8:47695800-47696800	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr8:47696200-47697400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr8:47696600-47697400	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
28	chr8:47698400-47699200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr8:47698600-47699000	Weak transcription	Fetal Heart	heart
30	chr8:47698800-47700800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
31	chr8:47698800-47700800	ZNF genes & repeats	Adipose Nuclei	Adipose
32	chr8:47699000-47699800	Active TSS	Fetal Heart	heart
33	chr8:47699200-47701600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr8:47699400-47700400	ZNF genes & repeats	Lung	lung
35	chr8:47709000-47709400	Active TSS	ES-I3 Cell Line	embryonic stem cell
36	chr8:47709000-47709400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
37	chr8:47733800-47736400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
38	chr8:47751400-47752000	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
39	chr8:47751400-47753800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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