Variant report

Variant	nsv1027452
Chromosome Location	chr8:51525439-51725489
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:435)
CpG islands
(count:244)
Chromatin interactive
region (count:11)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:435 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr8:51622516-51622751	H1-hESC	embryonic stem cell:	n/a	chr8:51622657-51622671
2	BACH1	chr8:51549746-51549863	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr8:51551406-51551486	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr8:51553900-51554065	GM12878	blood:	n/a	n/a
5	CEBPB	chr8:51594361-51594688	IMR90	lung:	n/a	n/a
6	CEBPB	chr8:51647599-51647828	IMR90	lung:	n/a	chr8:51647683-51647694
7	CEBPB	chr8:51544182-51544382	IMR90	lung:	n/a	chr8:51544270-51544279 chr8:51544268-51544279
8	CEBPB	chr8:51658455-51658661	HepG2	liver:	n/a	chr8:51658514-51658525
9	CEBPB	chr8:51647559-51647802	HepG2	liver:	n/a	chr8:51647683-51647694
10	CEBPB	chr8:51647578-51647778	K562	blood:	n/a	chr8:51647683-51647694
11	CEBPB	chr8:51629219-51629277	IMR90	lung:	n/a	chr8:51629252-51629261 chr8:51629250-51629261
12	CEBPB	chr8:51658383-51658644	IMR90	lung:	n/a	chr8:51658514-51658525
13	CEBPB	chr8:51590751-51591040	HepG2	liver:	n/a	chr8:51590858-51590871 chr8:51590858-51590869
14	CEBPB	chr8:51576308-51576662	IMR90	lung:	n/a	n/a
15	CEBPZ	chr8:51529649-51529754	HepG2	liver:	n/a	n/a
16	CTCF	chr8:51721569-51721632	MCF-7	breast:	n/a	n/a
17	CTCF	chr8:51683200-51683350	HMF	breast:	n/a	n/a
18	CTCF	chr8:51721528-51721666	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr8:51721569-51721625	GM19238	blood:	n/a	n/a
20	CTCF	chr8:51640780-51640930	MCF-7	breast:	n/a	chr8:51640877-51640884
21	CTCF	chr8:51683238-51683347	LNCaP	prostate:	n/a	n/a
22	CTCF	chr8:51721500-51721650	HEK293	kidney:	n/a	n/a
23	CTCF	chr8:51721580-51721730	HFF-Myc	foreskin:	n/a	n/a
24	CTCF	chr8:51721540-51721690	NB4	blood:	n/a	n/a
25	CTCF	chr8:51640828-51640906	MCF-7	breast:	n/a	chr8:51640877-51640884
26	CTCF	chr8:51721500-51721650	GM12875	blood:	n/a	n/a
27	CTCF	chr8:51721600-51721750	GM06990	blood:	n/a	n/a
28	CTCF	chr8:51627668-51627812	GM13977	blood:	n/a	n/a
29	CTCF	chr8:51721600-51721750	AG04450	lung:	n/a	n/a
30	CTCF	chr8:51721520-51721670	GM12873	blood:	n/a	n/a
31	CTCF	chr8:51721560-51721710	BE2_C	brain:	n/a	n/a
32	CTCF	chr8:51683180-51683330	HAc	cerebellar:	n/a	n/a
33	CTCF	chr8:51721560-51721710	GM12872	blood:	n/a	n/a
34	CTCF	chr8:51683240-51683390	RPTEC	kidney:	n/a	n/a
35	CTCF	chr8:51627549-51627977	MCF-7	breast:	n/a	n/a
36	CTCF	chr8:51721536-51721697	GM13977	blood:	n/a	n/a
37	CTCF	chr8:51539241-51539324	Lung_OC	lung:	n/a	n/a
38	CTCF	chr8:51721580-51721730	K562	blood:	n/a	n/a
39	CTCF	chr8:51640813-51640910	MCF-7	breast:	n/a	chr8:51640877-51640884
40	CTCF	chr8:51721420-51721570	MCF-7	breast:	n/a	n/a
41	CTCF	chr8:51721397-51721711	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr8:51721540-51721690	GM12873	blood:	n/a	n/a
43	CTCF	chr8:51683237-51683355	Hela-S3	cervix:	n/a	n/a
44	CTCF	chr8:51661780-51661930	HCPEpiC	choroid plexus:	n/a	n/a
45	CTCF	chr8:51627674-51627796	GM19238	blood:	n/a	n/a
46	CTCF	chr8:51721659-51721665	LNCaP	prostate:	n/a	n/a
47	CTCF	chr8:51721600-51721750	HFF-Myc	foreskin:	n/a	n/a
48	CTCF	chr8:51721480-51721630	HPAF	blood vessel:	n/a	n/a
49	CTCF	chr8:51640824-51640900	MCF-7	breast:	n/a	chr8:51640877-51640884
50	CTCF	chr8:51721540-51721690	WERI-Rb-1	eye:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:51576109-51576159	HEK293	kidney:	embryo
2	chr8:51576109-51576159	HRE	kidney:	n/a
3	chr8:51553739-51553789	RPTEC	kidney:	n/a
4	chr8:51576109-51576159	NT2-D1	testis:	n/a
5	chr8:51553739-51553789	CMK	blood:	n/a
6	chr8:51555740-51555790	MCF-7	breast:	n/a
7	chr8:51555740-51555790	GM12891	blood:	n/a
8	chr8:51576109-51576159	SK-N-MC	brain:	n/a
9	chr8:51553739-51553789	HepG2	liver:	n/a
10	chr8:51553739-51553789	ProgFib	skin:	n/a
11	chr8:51576109-51576159	ovcar-3	ovarian:	n/a
12	chr8:51555740-51555790	HEEpiC	esophagus:	n/a
13	chr8:51576109-51576159	SKMC	muscle:	n/a
14	chr8:51528401-51528451	ECC-1	luminal epithelium:	n/a
15	chr8:51553739-51553789	GM12891	blood:	n/a
16	chr8:51553739-51553789	MCF-7	breast:	n/a
17	chr8:51528401-51528451	MCF-7	breast:	n/a
18	chr8:51555740-51555790	HRCEpiC	kidney:	n/a
19	chr8:51528401-51528451	RPTEC	kidney:	n/a
20	chr8:51553739-51553789	AG04450	lung:	fetal
21	chr8:51553739-51553789	IMR90	lung:	fetal
22	chr8:51528401-51528451	Caco-2	colon:	n/a
23	chr8:51576109-51576159	SK-N-SH_RA	brain:	n/a
24	chr8:51576109-51576159	Hepatocyte	liver:	n/a
25	chr8:51528401-51528451	HCT-116	colon:	n/a
26	chr8:51553739-51553789	HRPEpiC	eye:	n/a
27	chr8:51528401-51528451	IMR90	lung:	fetal
28	chr8:51528401-51528451	HRE	kidney:	n/a
29	chr8:51555740-51555790	ovcar-3	ovarian:	n/a
30	chr8:51555740-51555790	BJ	skin:	n/a
31	chr8:51553739-51553789	Caco-2	colon:	n/a
32	chr8:51528401-51528451	HRPEpiC	eye:	n/a
33	chr8:51553739-51553789	K562	blood:	n/a
34	chr8:51528401-51528451	ProgFib	skin:	n/a
35	chr8:51553739-51553789	HCM	heart:	n/a
36	chr8:51528401-51528451	H1-hESC	embryonic stem cell:	embryo
37	chr8:51528401-51528451	SKMC	muscle:	n/a
38	chr8:51576109-51576159	HIPEpiC	eye:	n/a
39	chr8:51553739-51553789	HCPEpiC	choroid plexus:	n/a
40	chr8:51576109-51576159	U87	brain:	n/a
41	chr8:51576109-51576159	CMK	blood:	n/a
42	chr8:51553739-51553789	AG04449	skin:	fetal
43	chr8:51555740-51555790	AoSMC	blood vessel:	n/a
44	chr8:51528401-51528451	HCF	heart:	n/a
45	chr8:51555740-51555790	HUVEC	blood vessel:	n/a
46	chr8:51576109-51576159	A549	lung:	n/a
47	chr8:51528401-51528451	HNPCEpiC	eye:	n/a
48	chr8:51576109-51576159	BJ	skin:	n/a
49	chr8:51576109-51576159	NB4	blood:	n/a
50	chr8:51553739-51553789	ovcar-3	ovarian:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:51700925..51703034-chr8:51706252..51708028,2	K562	blood:
2	chr8:51711545..51713227-chr8:51715658..51718026,2	K562	blood:
3	chr8:51590048..51591794-chr8:51592149..51596284,3	K562	blood:
4	chr8:51711545..51713227-chr8:51715658..51718026,2	K562	blood:
5	chr8:51677159..51678716-chr8:51680516..51682123,2	K562	blood:
6	chr1:116959143..116962126-chr8:51573809..51576471,2	MCF-7	breast:
7	chr8:51715941..51718504-chr8:51718568..51721133,2	K562	blood:
8	chr8:51590048..51591794-chr8:51592149..51596284,3	K562	blood:
9	chr8:51700925..51703034-chr8:51706252..51708028,2	K562	blood:
10	chr8:51715941..51718504-chr8:51718568..51721133,2	K562	blood:
11	chr8:51677159..51678716-chr8:51680516..51682123,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PXDNL-4	chr8:51675020-51675358	NONHSAT126529

No data

Variant related genes	Relation type
CYCSP22	TF binding region
CYCSP22	CpG island
ENSG00000203865	chromatin interactions

Extended variants
information (count: 5800 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:5800 , 50 per page) page: 1 2 3 4 5 6 7 ... 116

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs375655776	chr8:51525457-51525458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs76008462	chr8:51525534-51525535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs372652893	chr8:51525538-51525539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs536514974	chr8:51525548-51525549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs550146835	chr8:51525610-51525611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs189460744	chr8:51525661-51525662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs535705346	chr8:51525678-51525679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs78406974	chr8:51525688-51525689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs182062765	chr8:51525725-51525726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs554811186	chr8:51525755-51525756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs534060499	chr8:51525762-51525763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs149291698	chr8:51525774-51525775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs577066713	chr8:51525784-51525785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs544403023	chr8:51525805-51525806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs558947414	chr8:51525816-51525817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs563055979	chr8:51525839-51525840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs9298342	chr8:51525852-51525853	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs542482326	chr8:51525855-51525856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs559923715	chr8:51525881-51525882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs112389943	chr8:51525937-51525938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs558727461	chr8:51525962-51525963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs76609437	chr8:51525981-51525982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs564167159	chr8:51526036-51526037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs530324942	chr8:51526094-51526095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs143534638	chr8:51526100-51526101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs183732341	chr8:51526135-51526136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs188164068	chr8:51526142-51526143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs535411989	chr8:51526146-51526147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs547653989	chr8:51526169-51526170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs566790535	chr8:51526200-51526201	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs533926148	chr8:51526201-51526202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs558474880	chr8:51526246-51526247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs576931794	chr8:51526270-51526271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs138138798	chr8:51526300-51526301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs556504360	chr8:51526310-51526311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs150578477	chr8:51526313-51526314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs142621300	chr8:51526334-51526335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs576352973	chr8:51526353-51526354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs13256324	chr8:51526355-51526356	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs572118540	chr8:51526361-51526362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs80090039	chr8:51526366-51526367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs77338873	chr8:51526368-51526369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs543635333	chr8:51526373-51526374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs545819385	chr8:51526379-51526380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs564031456	chr8:51526380-51526381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs561011674	chr8:51526399-51526400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs573518999	chr8:51526456-51526457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs531455687	chr8:51526458-51526459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs543481629	chr8:51526476-51526477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs542698125	chr8:51526565-51526566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

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
Pancreatic ductal adenocarcinoma	19077451	CNVD
22q11 deletion syndrome	20357662	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:199 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:51518200-51529000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr8:51528200-51529400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr8:51528200-51530000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
4	chr8:51528200-51530200	Enhancers	Brain Germinal Matrix	brain
5	chr8:51528200-51530200	Enhancers	HUVEC	blood vessel
6	chr8:51528400-51530200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr8:51528800-51529600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr8:51528800-51529600	Enhancers	H9 Cell Line	embryonic stem cell
9	chr8:51528800-51529600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr8:51528800-51529600	Enhancers	Brain Angular Gyrus	brain
11	chr8:51528800-51529800	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr8:51528800-51529800	Enhancers	Fetal Lung	lung
13	chr8:51528800-51530200	Enhancers	Fetal Brain Female	brain
14	chr8:51529000-51529600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr8:51529000-51529600	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr8:51529000-51529600	Enhancers	Cortex derived primary cultured neurospheres	brain
17	chr8:51529000-51529800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr8:51529000-51529800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr8:51529200-51529600	Enhancers	Duodenum Mucosa	Duodenum
20	chr8:51529200-51529800	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr8:51529200-51530600	Enhancers	Hela-S3	cervix
22	chr8:51529400-51538800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr8:51529600-51530000	Enhancers	Fetal Kidney	kidney
24	chr8:51529600-51530200	Weak transcription	Duodenum Mucosa	Duodenum
25	chr8:51530200-51530600	Active TSS	Duodenum Mucosa	Duodenum
26	chr8:51530200-51533000	Weak transcription	HUVEC	blood vessel
27	chr8:51533000-51534200	Enhancers	HUVEC	blood vessel
28	chr8:51533400-51534200	Enhancers	Primary B cells from cord blood	blood
29	chr8:51533600-51534400	Enhancers	Liver	Liver
30	chr8:51537400-51537800	Active TSS	Fetal Heart	heart
31	chr8:51542200-51543400	Enhancers	HUVEC	blood vessel
32	chr8:51542800-51544800	Enhancers	Primary B cells from cord blood	blood
33	chr8:51543200-51543600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr8:51543200-51544600	Enhancers	Primary B cells from peripheral blood	blood
35	chr8:51543400-51544200	Flanking Active TSS	HUVEC	blood vessel
36	chr8:51543400-51544400	Enhancers	Dnd41	blood
37	chr8:51543600-51544000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr8:51544000-51544200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr8:51544200-51545800	Enhancers	HUVEC	blood vessel
40	chr8:51544200-51552600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr8:51544800-51545000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr8:51545000-51553800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr8:51545800-51548600	Weak transcription	HUVEC	blood vessel
44	chr8:51548600-51549400	Enhancers	HUVEC	blood vessel
45	chr8:51549400-51550600	Weak transcription	HUVEC	blood vessel
46	chr8:51550600-51555600	Enhancers	HUVEC	blood vessel
47	chr8:51551000-51551600	Enhancers	Primary B cells from cord blood	blood
48	chr8:51551600-51552000	Weak transcription	Primary B cells from cord blood	blood
49	chr8:51552000-51554000	Enhancers	Primary B cells from cord blood	blood
50	chr8:51552400-51552600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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