Variant report

Variant	nsv890914
Chromosome Location	chr8:53835535-53885043
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	chr8:53878433-53878817	K562	blood:	n/a	n/a
2	ARID3A	chr8:53878484-53878808	HepG2	liver:	n/a	n/a
3	ATF1	chr8:53849646-53849868	K562	blood:	n/a	n/a
4	BACH1	chr8:53852611-53852810	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr8:53851100-53851301	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr8:53854127-53854469	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr8:53853083-53853227	H1-hESC	embryonic stem cell:	n/a	n/a
8	BHLHE40	chr8:53854274-53854336	GM12878	blood:	n/a	n/a
9	BHLHE40	chr8:53884307-53884596	GM12878	blood:	n/a	n/a
10	BHLHE40	chr8:53883301-53883728	GM12878	blood:	n/a	n/a
11	BRCA1	chr8:53854261-53854544	H1-hESC	embryonic stem cell:	n/a	n/a
12	BRCA1	chr8:53883776-53883853	H1-hESC	embryonic stem cell:	n/a	n/a
13	BRCA1	chr8:53853372-53853513	H1-hESC	embryonic stem cell:	n/a	n/a
14	BRCA1	chr8:53854213-53854414	HepG2	liver:	n/a	n/a
15	CEBPB	chr8:53850499-53850779	K562	blood:	n/a	n/a
16	CEBPB	chr8:53850582-53850783	A549	lung:	n/a	n/a
17	CEBPB	chr8:53854282-53854519	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr8:53879899-53879925	A549	lung:	n/a	n/a
19	CHD1	chr8:53854213-53854389	GM12878	blood:	n/a	n/a
20	CHD1	chr8:53853898-53854325	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD1	chr8:53854039-53854723	IMR90	lung:	n/a	n/a
22	CHD2	chr8:53853125-53853738	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD2	chr8:53851260-53851279	H1-hESC	embryonic stem cell:	n/a	n/a
24	CHD2	chr8:53854239-53854481	HepG2	liver:	n/a	n/a
25	CHD2	chr8:53854284-53854530	H1-hESC	embryonic stem cell:	n/a	n/a
26	CREB1	chr8:53852360-53853460	H1-hESC	embryonic stem cell:	n/a	n/a
27	CREB1	chr8:53853639-53854000	A549	lung:	n/a	n/a
28	CREB1	chr8:53854182-53854464	A549	lung:	n/a	n/a
29	CTBP2	chr8:53851626-53854473	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr8:53853620-53853770	HFF	foreskin:	n/a	n/a
31	CTCF	chr8:53853849-53853893	GM13976	blood:	n/a	n/a
32	CTCF	chr8:53878460-53878610	HAc	cerebellar:	n/a	chr8:53878564-53878573 chr8:53878563-53878584 chr8:53878561-53878579 chr8:53878562-53878578 chr8:53878564-53878577
33	CTCF	chr8:53878480-53878630	SK-N-SH_RA	brain:	n/a	chr8:53878564-53878573 chr8:53878563-53878584 chr8:53878561-53878579 chr8:53878562-53878578 chr8:53878564-53878577
34	CTCF	chr8:53878470-53878642	GM10248	blood:	n/a	chr8:53878564-53878573 chr8:53878563-53878584 chr8:53878561-53878579 chr8:53878562-53878578 chr8:53878564-53878577
35	CTCF	chr8:53853860-53854150	AG04449	skin:	n/a	chr8:53853894-53853907
36	CTCF	chr8:53853890-53853932	Fibrobl	skin:	n/a	chr8:53853894-53853907
37	CTCF	chr8:53878458-53878670	MCF-7	breast:	n/a	chr8:53878564-53878573 chr8:53878563-53878584 chr8:53878561-53878579 chr8:53878562-53878578 chr8:53878564-53878577
38	CTCF	chr8:53853728-53853977	A549	lung:	n/a	chr8:53853894-53853907
39	CTCF	chr8:53883298-53883385	GM13976	blood:	n/a	chr8:53883344-53883352 chr8:53883341-53883359 chr8:53883344-53883357
40	CTCF	chr8:53836760-53836910	AG10803	skin:	n/a	n/a
41	CTCF	chr8:53878500-53878650	BJ	skin:	n/a	chr8:53878564-53878573 chr8:53878563-53878584 chr8:53878561-53878579 chr8:53878562-53878578 chr8:53878564-53878577
42	CTCF	chr8:53853260-53853410	HRPEpiC	eye:	n/a	n/a
43	CTCF	chr8:53854260-53854410	WI-38	lung:	n/a	chr8:53854334-53854347 chr8:53854327-53854348 chr8:53854332-53854350 chr8:53854338-53854347 chr8:53854333-53854349 chr8:53854335-53854345
44	CTCF	chr8:53853796-53853992	SK-N-SH_RA	brain:	n/a	chr8:53853894-53853907
45	CTCF	chr8:53836720-53836870	GM12865	blood:	n/a	n/a
46	CTCF	chr8:53836760-53836910	HRPEpiC	eye:	n/a	n/a
47	CTCF	chr8:53878408-53878797	A549	lung:	n/a	chr8:53878564-53878573 chr8:53878563-53878584 chr8:53878561-53878579 chr8:53878562-53878578 chr8:53878564-53878577
48	CTCF	chr8:53854060-53854210	GM12865	blood:	n/a	n/a
49	CTCF	chr8:53853780-53853930	GM12872	blood:	n/a	chr8:53853894-53853907
50	CTCF	chr8:53878462-53878648	HepG2	liver:	n/a	chr8:53878564-53878573 chr8:53878563-53878584 chr8:53878561-53878579 chr8:53878562-53878578 chr8:53878564-53878577

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:53857047-53857097	GM06990	blood:	n/a
2	chr8:53852274-53852324	HEK293	kidney:	embryo
3	chr8:53857047-53857097	GM06990	blood:	n/a
4	chr8:53852274-53852324	HEK293	kidney:	embryo
5	chr8:53852274-53852324	HEEpiC	esophagus:	n/a
6	chr8:53852443-53852493	SK-N-MC	brain:	n/a
7	chr8:53864533-53864583	AG09309	skin:	n/a
8	chr8:53852661-53852711	PFSK-1	brain:	n/a
9	chr8:53883763-53883813	MCF-7	breast:	n/a
10	chr8:53866689-53866739	Hepatocyte	liver:	n/a
11	chr8:53852661-53852711	GM12878	blood:	n/a
12	chr8:53854425-53854475	GM06990	blood:	n/a
13	chr8:53854425-53854475	ovcar-3	ovarian:	n/a
14	chr8:53852422-53852472	Hepatocyte	liver:	n/a
15	chr8:53857047-53857097	PrEC	prostate:	n/a
16	chr8:53853112-53853162	A549	lung:	n/a
17	chr8:53883763-53883813	PFSK-1	brain:	n/a
18	chr8:53857047-53857097	K562	blood:	n/a
19	chr8:53857047-53857097	HCT-116	colon:	n/a
20	chr8:53852030-53852080	GM06990	blood:	n/a
21	chr8:53864533-53864583	HCM	heart:	n/a
22	chr8:53864533-53864583	BE2_C	brain:	n/a
23	chr8:53883763-53883813	HRPEpiC	eye:	n/a
24	chr8:53854172-53854222	HCF	heart:	n/a
25	chr8:53883763-53883813	RPTEC	kidney:	n/a
26	chr8:53852443-53852493	SKMC	muscle:	n/a
27	chr8:53851613-53851663	SAEC	small airway:	n/a
28	chr8:53852101-53852151	HCF	heart:	n/a
29	chr8:53853604-53853654	SK-N-SH_RA	brain:	n/a
30	chr8:53854425-53854475	NHDF-neo	bronchial:	n/a
31	chr8:53853112-53853162	HNPCEpiC	eye:	n/a
32	chr8:53866529-53866579	GM12892	blood:	n/a
33	chr8:53852274-53852324	NHDF-neo	bronchial:	n/a
34	chr8:53851156-53851206	HL-60	blood:	n/a
35	chr8:53849059-53849109	AG10803	skin:	n/a
36	chr8:53854495-53854545	LNCaP	prostate:	n/a
37	chr8:53851613-53851663	PrEC	prostate:	n/a
38	chr8:53854172-53854222	NHDF-neo	bronchial:	n/a
39	chr8:53864533-53864583	ovcar-3	ovarian:	n/a
40	chr8:53883763-53883813	AG04450	lung:	fetal
41	chr8:53852030-53852080	RPTEC	kidney:	n/a
42	chr8:53851156-53851206	HEEpiC	esophagus:	n/a
43	chr8:53853444-53853494	HCM	heart:	n/a
44	chr8:53852030-53852080	GM12892	blood:	n/a
45	chr8:53883763-53883813	GM12892	blood:	n/a
46	chr8:53864533-53864583	NH-A	brain:	n/a
47	chr8:53852443-53852493	GM19239	blood:	n/a
48	chr8:53851613-53851663	ProgFib	skin:	n/a
49	chr8:53854425-53854475	AG04450	lung:	fetal
50	chr8:53851156-53851206	HRPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:53711623..53712255-chr8:53854248..53854877,2	MCF-7	breast:
2	chr8:53878320..53879023-chr8:54317254..54317896,3	MCF-7	breast:
3	chr8:53649708..53650309-chr8:53861493..53862325,2	MCF-7	breast:
4	chr8:53878521..53879036-chr8:54398874..54399575,2	MCF-7	breast:
5	chr8:53636506..53637243-chr8:53861404..53862378,2	MCF-7	breast:
6	chr8:53878134..53878972-chr8:54721059..54722142,3	K562	blood:
7	chr8:53634696..53637064-chr8:53861267..53863053,2	MCF-7	breast:
8	chr8:53649371..53650945-chr8:53853868..53854778,6	MCF-7	breast:
9	chr8:53824182..53826447-chr8:53833370..53835967,2	K562	blood:
10	chr8:53878057..53878612-chr8:54775599..54776413,2	K562	blood:
11	chr8:53649395..53650276-chr8:53853945..53854772,3	MCF-7	breast:
12	chr8:53490029..53490926-chr8:53861444..53862393,2	MCF-7	breast:
13	chr8:53627445..53629464-chr8:53852538..53854621,2	MCF-7	breast:
14	chr8:53878008..53878947-chr8:55078471..55079402,3	K562	blood:
15	chr8:53649723..53650709-chr8:53861922..53862952,3	MCF-7	breast:

Variant related genes	Relation type
NPBWR1	TF binding region
NPBWR1	CpG island
ENSG00000271555	chromatin interactions

Extended variants
information (count: 1470 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:1470 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs659200	chr8:53835535-53835536	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs571261122	chr8:53835538-53835539	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs538569759	chr8:53835550-53835551	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs141299499	chr8:53835590-53835591	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs144508674	chr8:53835648-53835649	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs375939987	chr8:53835701-53835702	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs536427283	chr8:53835773-53835774	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs184342673	chr8:53835837-53835838	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs572888111	chr8:53835879-53835880	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs533829178	chr8:53835887-53835888	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs537902447	chr8:53835898-53835899	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs373499881	chr8:53836007-53836008	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs558587666	chr8:53836037-53836038	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs576877178	chr8:53836046-53836047	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs375575462	chr8:53836065-53836066	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs373513880	chr8:53836120-53836121	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs367879757	chr8:53836127-53836128	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs11268667	chr8:53836130-53836131	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs370553895	chr8:53836131-53836132	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs72640848	chr8:53836225-53836226	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs73601233	chr8:53836229-53836230	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs148015901	chr8:53836256-53836257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs576740430	chr8:53836309-53836310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs543203118	chr8:53836330-53836331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs561284108	chr8:53836363-53836364	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs369051782	chr8:53836369-53836370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs72640849	chr8:53836430-53836431	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs546662112	chr8:53836431-53836432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs564955199	chr8:53836459-53836460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs141620930	chr8:53836630-53836631	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs550491646	chr8:53836655-53836656	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs72640850	chr8:53836681-53836682	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs536100476	chr8:53836718-53836719	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs147150974	chr8:53836722-53836723	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs544155664	chr8:53845994-53845995	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs562365933	chr8:53846072-53846073	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs57777727	chr8:53846094-53846095	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs187318279	chr8:53846110-53846111	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs61269045	chr8:53846128-53846129	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs533486613	chr8:53846183-53846184	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs566868329	chr8:53847414-53847415	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs566440191	chr8:53847450-53847451	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs562642590	chr8:53847939-53847940	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs554719642	chr8:53847955-53847956	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs545849360	chr8:53849059-53849060	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
46	rs565566762	chr8:53849063-53849064	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
47	rs563962321	chr8:53849077-53849078	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
48	rs531203144	chr8:53849092-53849093	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
49	rs550902278	chr8:53849094-53849095	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
50	rs531161408	chr8:53849119-53849120	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:90)

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
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
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
low-grade B-cell lymphoma tumor	18367492	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
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Sezary syndrome	18413736	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Uveal melanoma	20484589	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:564 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:53832000-53836600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr8:53834600-53836000	Enhancers	Muscle Satellite Cultured Cells	--
3	chr8:53834800-53836000	Enhancers	HSMMtube	muscle
4	chr8:53835000-53835600	Flanking Active TSS	HSMM	muscle
5	chr8:53835600-53836200	Enhancers	HSMM	muscle
6	chr8:53836600-53836800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr8:53836600-53836800	Enhancers	Brain Germinal Matrix	brain
8	chr8:53850600-53850800	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
9	chr8:53850600-53851000	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
10	chr8:53850600-53851000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr8:53850600-53851000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr8:53850600-53851200	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
13	chr8:53850600-53851400	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
14	chr8:53850800-53851200	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
15	chr8:53850800-53853400	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
16	chr8:53850800-53854400	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
17	chr8:53851000-53851200	Bivalent Enhancer	Primary T cells from cord blood	blood
18	chr8:53851000-53851200	Bivalent/Poised TSS	Primary hematopoietic stem cells	blood
19	chr8:53851000-53851200	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells short term culture	blood
20	chr8:53851000-53851400	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
21	chr8:53851000-53851600	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
22	chr8:53851000-53851800	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
23	chr8:53851000-53851800	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
24	chr8:53851000-53852000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
25	chr8:53851000-53852200	Bivalent Enhancer	Brain Anterior Caudate	brain
26	chr8:53851000-53852200	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
27	chr8:53851000-53854400	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr8:53851000-53854400	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr8:53851000-53854600	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
30	chr8:53851000-53854800	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
31	chr8:53851200-53851400	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
32	chr8:53851200-53851400	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
33	chr8:53851200-53851400	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
34	chr8:53851200-53851400	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
35	chr8:53851200-53851400	Bivalent/Poised TSS	Primary hematopoietic stem cells short term culture	blood
36	chr8:53851200-53851600	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
37	chr8:53851200-53851600	Flanking Bivalent TSS/Enh	Primary T cells from cord blood	blood
38	chr8:53851200-53852600	Bivalent Enhancer	Primary T helper 17 cells PMA-I stimulated	--
39	chr8:53851200-53854400	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells	blood
40	chr8:53851200-53854800	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
41	chr8:53851200-53854800	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
42	chr8:53851400-53851600	Flanking Bivalent TSS/Enh	Primary monocytes fromperipheralblood	blood
43	chr8:53851400-53851600	Bivalent Enhancer	Duodenum Mucosa	Duodenum
44	chr8:53851400-53851800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
45	chr8:53851400-53851800	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
46	chr8:53851400-53852000	Bivalent Enhancer	Primary B cells from cord blood	blood
47	chr8:53851400-53852000	Bivalent Enhancer	Primary T helper naive cells from peripheral blood	blood
48	chr8:53851400-53852000	Bivalent Enhancer	Primary T killer naive cells fromperipheralblood	blood
49	chr8:53851400-53852000	Enhancers	Primary T killer memory cells from peripheral blood	blood
50	chr8:53851400-53852000	Bivalent Enhancer	Fetal Brain Male	brain

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