Variant report

Variant	nsv1025889
Chromosome Location	chr8:53824529-54047869
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1494)
CpG islands
(count:1466)
Chromatin interactive
region (count:26)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1494 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:53878484-53878808	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:53878433-53878817	K562	blood:	n/a	n/a
3	ATF1	chr8:53835080-53835117	K562	blood:	n/a	n/a
4	ATF1	chr8:53849646-53849868	K562	blood:	n/a	n/a
5	ATF2	chr8:53909866-53910228	GM12878	blood:	n/a	n/a
6	BACH1	chr8:53853083-53853227	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr8:53854127-53854469	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr8:53851100-53851301	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr8:53852611-53852810	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr8:53909878-53910230	GM12878	blood:	n/a	chr8:53910027-53910037 chr8:53910026-53910037
11	BATF	chr8:53932574-53932770	GM12878	blood:	n/a	n/a
12	BCL11A	chr8:53909839-53910302	GM12878	blood:	n/a	chr8:53910131-53910140
13	BCL11A	chr8:53909858-53910582	GM12878	blood:	n/a	chr8:53910131-53910140 chr8:53910301-53910310
14	BHLHE40	chr8:53909862-53910567	GM12878	blood:	n/a	n/a
15	BHLHE40	chr8:53883301-53883728	GM12878	blood:	n/a	n/a
16	BHLHE40	chr8:53917469-53917491	K562	blood:	n/a	n/a
17	BHLHE40	chr8:53884307-53884596	GM12878	blood:	n/a	n/a
18	BHLHE40	chr8:53854274-53854336	GM12878	blood:	n/a	n/a
19	BRCA1	chr8:53967252-53967345	GM12878	blood:	n/a	n/a
20	BRCA1	chr8:53883776-53883853	H1-hESC	embryonic stem cell:	n/a	n/a
21	BRCA1	chr8:53854213-53854414	HepG2	liver:	n/a	n/a
22	BRCA1	chr8:53854261-53854544	H1-hESC	embryonic stem cell:	n/a	n/a
23	BRCA1	chr8:53853372-53853513	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr8:53917155-53917454	K562	blood:	n/a	n/a
25	CEBPB	chr8:53907958-53908021	K562	blood:	n/a	n/a
26	CEBPB	chr8:53830927-53831156	K562	blood:	n/a	chr8:53831113-53831124
27	CEBPB	chr8:53997677-53997687	A549	lung:	n/a	n/a
28	CEBPB	chr8:54032165-54032479	HepG2	liver:	n/a	chr8:54032340-54032351
29	CEBPB	chr8:53926310-53926522	HepG2	liver:	n/a	chr8:53926409-53926420 chr8:53926408-53926419
30	CEBPB	chr8:53827418-53827672	Hela-S3	cervix:	n/a	chr8:53827575-53827587
31	CEBPB	chr8:54032183-54032475	A549	lung:	n/a	chr8:54032340-54032351
32	CEBPB	chr8:53926371-53926521	K562	blood:	n/a	chr8:53926409-53926420 chr8:53926408-53926419
33	CEBPB	chr8:53830972-53831278	IMR90	lung:	n/a	chr8:53831113-53831124
34	CEBPB	chr8:53879899-53879925	A549	lung:	n/a	n/a
35	CEBPB	chr8:53910786-53911069	K562	blood:	n/a	chr8:53910933-53910944 chr8:53910931-53910944 chr8:53910931-53910944 chr8:53910933-53910944
36	CEBPB	chr8:53938166-53938448	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr8:53830968-53831268	HepG2	liver:	n/a	chr8:53831113-53831124
38	CEBPB	chr8:53854282-53854519	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr8:53834940-53834973	A549	lung:	n/a	n/a
40	CEBPB	chr8:54032178-54032458	IMR90	lung:	n/a	chr8:54032340-54032351
41	CEBPB	chr8:53916865-53917369	A549	lung:	n/a	n/a
42	CEBPB	chr8:54046555-54046759	HepG2	liver:	n/a	chr8:54046648-54046659 chr8:54046648-54046661
43	CEBPB	chr8:53850582-53850783	A549	lung:	n/a	n/a
44	CEBPB	chr8:54037433-54037565	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr8:53850499-53850779	K562	blood:	n/a	n/a
46	CEBPB	chr8:53831668-53832176	Hela-S3	cervix:	n/a	n/a
47	CHD1	chr8:53854039-53854723	IMR90	lung:	n/a	n/a
48	CHD1	chr8:53854213-53854389	GM12878	blood:	n/a	n/a
49	CHD1	chr8:53853898-53854325	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD1	chr8:53910064-53910138	GM12878	blood:	n/a	n/a

(count:1466 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:53851156-53851206	HUVEC	blood vessel:	n/a
2	chr8:53852422-53852472	A549	lung:	n/a
3	chr8:53851156-53851206	HUVEC	blood vessel:	n/a
4	chr8:53852422-53852472	A549	lung:	n/a
5	chr8:53852101-53852151	GM06990	blood:	n/a
6	chr8:53866529-53866579	NH-A	brain:	n/a
7	chr8:53853444-53853494	AG04449	skin:	fetal
8	chr8:53854495-53854545	NHBE	bronchial:	n/a
9	chr8:53852184-53852234	GM12891	blood:	n/a
10	chr8:53851156-53851206	H1-hESC	embryonic stem cell:	embryo
11	chr8:53852101-53852151	HRE	kidney:	n/a
12	chr8:53864533-53864583	PrEC	prostate:	n/a
13	chr8:53854172-53854222	ovcar-3	ovarian:	n/a
14	chr8:53852661-53852711	HEEpiC	esophagus:	n/a
15	chr8:53852274-53852324	SK-N-SH	brain:	n/a
16	chr8:53851156-53851206	ECC-1	luminal epithelium:	n/a
17	chr8:53852101-53852151	PFSK-1	brain:	n/a
18	chr8:53853604-53853654	Hela-S3	cervix:	n/a
19	chr8:53854425-53854475	PrEC	prostate:	n/a
20	chr8:53852030-53852080	NB4	blood:	n/a
21	chr8:53851613-53851663	HCT-116	colon:	n/a
22	chr8:53849059-53849109	HMEC	breast:	n/a
23	chr8:53852443-53852493	AG04449	skin:	fetal
24	chr8:53851613-53851663	AG09309	skin:	n/a
25	chr8:53852274-53852324	NT2-D1	testis:	n/a
26	chr8:53866529-53866579	PrEC	prostate:	n/a
27	chr8:53857047-53857097	A549	lung:	n/a
28	chr8:53852446-53852496	AG04450	lung:	fetal
29	chr8:53854425-53854475	ovcar-3	ovarian:	n/a
30	chr8:53854425-53854475	HepG2	liver:	n/a
31	chr8:53851707-53851757	NT2-D1	testis:	n/a
32	chr8:53853659-53853709	HepG2	liver:	n/a
33	chr8:53849059-53849109	NB4	blood:	n/a
34	chr8:53852101-53852151	ECC-1	luminal epithelium:	n/a
35	chr8:53883763-53883813	HCM	heart:	n/a
36	chr8:53852446-53852496	LNCaP	prostate:	n/a
37	chr8:53852101-53852151	HCF	heart:	n/a
38	chr8:53852274-53852324	AG09309	skin:	n/a
39	chr8:53854495-53854545	HRPEpiC	eye:	n/a
40	chr8:53852030-53852080	HEEpiC	esophagus:	n/a
41	chr8:53854172-53854222	NH-A	brain:	n/a
42	chr8:53851156-53851206	HCT-116	colon:	n/a
43	chr8:53852101-53852151	AG04449	skin:	fetal
44	chr8:53853604-53853654	AoSMC	blood vessel:	n/a
45	chr8:53854172-53854222	Jurkat	blood:	n/a
46	chr8:53853112-53853162	AG09309	skin:	n/a
47	chr8:53852443-53852493	HRPEpiC	eye:	n/a
48	chr8:53852184-53852234	ProgFib	skin:	n/a
49	chr8:53883763-53883813	U87	brain:	n/a
50	chr8:53853444-53853494	SK-N-MC	brain:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:53824182..53826447-chr8:53833370..53835967,2	K562	blood:
2	chr8:53878134..53878972-chr8:54721059..54722142,3	K562	blood:
3	chr8:53490029..53490926-chr8:53861444..53862393,2	MCF-7	breast:
4	chr8:53939330..53941903-chr8:53942463..53944811,2	MCF-7	breast:
5	chr8:53818664..53820384-chr8:53824102..53826762,2	K562	blood:
6	chr8:53634696..53637064-chr8:53861267..53863053,2	MCF-7	breast:
7	chr8:53939330..53941903-chr8:53942463..53944811,2	MCF-7	breast:
8	chr8:53878008..53878947-chr8:55078471..55079402,3	K562	blood:
9	chr8:53649708..53650309-chr8:53861493..53862325,2	MCF-7	breast:
10	chr8:54031738..54034057-chr8:54034644..54036754,2	K562	blood:
11	chr8:53966830..53968334-chr8:53977318..53980118,2	K562	blood:
12	chr8:53636506..53637243-chr8:53861404..53862378,2	MCF-7	breast:
13	chr18:13291375..13292050-chr8:53976127..53977109,2	MCF-7	breast:
14	chr8:53824182..53826447-chr8:53833370..53835967,2	K562	blood:
15	chr8:53966830..53968334-chr8:53977318..53980118,2	K562	blood:
16	chr8:53649723..53650709-chr8:53861922..53862952,3	MCF-7	breast:
17	chr8:53878521..53879036-chr8:54398874..54399575,2	MCF-7	breast:
18	chr8:53649371..53650945-chr8:53853868..53854778,6	MCF-7	breast:
19	chr8:53878320..53879023-chr8:54317254..54317896,3	MCF-7	breast:
20	chr8:53963436..53966378-chr8:53966833..53968910,3	K562	blood:
21	chr8:53878057..53878612-chr8:54775599..54776413,2	K562	blood:
22	chr8:53649395..53650276-chr8:53853945..53854772,3	MCF-7	breast:
23	chr8:53627445..53629464-chr8:53852538..53854621,2	MCF-7	breast:
24	chr8:53711623..53712255-chr8:53854248..53854877,2	MCF-7	breast:
25	chr8:54031738..54034057-chr8:54034644..54036754,2	K562	blood:
26	chr8:53963436..53966378-chr8:53966833..53968910,3	K562	blood:

No data

Variant related genes	Relation type
ENSG00000265835	TF binding region
NPBWR1	TF binding region
ENSG00000251871	TF binding region
ENSG00000248911	TF binding region
ENSG00000265835	CpG island
NPBWR1	CpG island
ENSG00000251871	CpG island
ENSG00000248911	CpG island
ENSG00000271555	chromatin interactions

Extended variants
information (count: 4232 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:4232 , 50 per page) page: 1 2 3 4 5 6 7 ... 85

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs564265808	chr8:53825201-53825202	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs531650886	chr8:53825243-53825244	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs563612272	chr8:53825269-53825270	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs185051031	chr8:53825272-53825273	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs12156149	chr8:53825288-53825289	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs537081985	chr8:53825294-53825295	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs72614660	chr8:53825296-53825297	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs547551121	chr8:53825337-53825338	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs565747912	chr8:53825412-53825413	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs539106575	chr8:53825422-53825423	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs559185969	chr8:53825424-53825425	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs557723753	chr8:53825440-53825441	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs575905430	chr8:53825451-53825452	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs528048614	chr8:53825459-53825460	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs376180201	chr8:53825468-53825469	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs72640828	chr8:53825474-53825475	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs556412309	chr8:53825504-53825505	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs375178391	chr8:53825531-53825532	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs73681244	chr8:53825537-53825538	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs78992134	chr8:53825558-53825559	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs572493812	chr8:53825559-53825560	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs142392778	chr8:53825575-53825576	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs114516721	chr8:53825646-53825647	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs3895796	chr8:53825655-53825656	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs191329835	chr8:53825667-53825668	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs528632075	chr8:53825715-53825716	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs550117945	chr8:53825718-53825719	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs369721089	chr8:53825777-53825778	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs561950214	chr8:53825802-53825803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs529132150	chr8:53825862-53825863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs547564685	chr8:53825869-53825870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs565676079	chr8:53825924-53825925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs181226632	chr8:53825953-53825954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs551140874	chr8:53825976-53825977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs569332196	chr8:53826030-53826031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs536615213	chr8:53826034-53826035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs556472797	chr8:53826036-53826037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs4873231	chr8:53826049-53826050	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs146585615	chr8:53826060-53826061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs554354398	chr8:53826067-53826068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs551183248	chr8:53826110-53826111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs139006642	chr8:53826111-53826112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs546300075	chr8:53826112-53826113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs567902187	chr8:53826148-53826149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs4873232	chr8:53826337-53826338	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs576543766	chr8:53826359-53826360	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs554082217	chr8:53826377-53826378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs543819406	chr8:53826409-53826410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs368143003	chr8:53826412-53826413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs186241163	chr8:53826420-53826421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:773 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:53825200-53825600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr8:53825200-53825600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr8:53825200-53825800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr8:53825200-53825800	Enhancers	HMEC	breast
5	chr8:53825400-53825600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
6	chr8:53825400-53825600	Enhancers	Hela-S3	cervix
7	chr8:53825400-53825600	Enhancers	HSMMtube	muscle
8	chr8:53825400-53825800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr8:53825800-53831200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr8:53826000-53831000	Weak transcription	Hela-S3	cervix
11	chr8:53831000-53832400	Enhancers	Hela-S3	cervix
12	chr8:53831000-53832400	Enhancers	HSMMtube	muscle
13	chr8:53831200-53832000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr8:53831200-53832000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr8:53831200-53832200	Enhancers	HSMM	muscle
16	chr8:53831200-53832600	Enhancers	Liver	Liver
17	chr8:53831400-53831800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr8:53831600-53832200	Enhancers	Dnd41	blood
19	chr8:53832000-53836600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr8:53832200-53834600	Weak transcription	HSMM	muscle
21	chr8:53832400-53834800	Weak transcription	HSMMtube	muscle
22	chr8:53834600-53835000	Enhancers	HSMM	muscle
23	chr8:53834600-53836000	Enhancers	Muscle Satellite Cultured Cells	--
24	chr8:53834800-53835200	Bivalent Enhancer	A549	lung
25	chr8:53834800-53836000	Enhancers	HSMMtube	muscle
26	chr8:53835000-53835600	Flanking Active TSS	HSMM	muscle
27	chr8:53835600-53836200	Enhancers	HSMM	muscle
28	chr8:53836600-53836800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr8:53836600-53836800	Enhancers	Brain Germinal Matrix	brain
30	chr8:53850600-53850800	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
31	chr8:53850600-53851000	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
32	chr8:53850600-53851000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr8:53850600-53851000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr8:53850600-53851200	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
35	chr8:53850600-53851400	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
36	chr8:53850800-53851200	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
37	chr8:53850800-53853400	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
38	chr8:53850800-53854400	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
39	chr8:53851000-53851200	Bivalent Enhancer	Primary T cells from cord blood	blood
40	chr8:53851000-53851200	Bivalent/Poised TSS	Primary hematopoietic stem cells	blood
41	chr8:53851000-53851200	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells short term culture	blood
42	chr8:53851000-53851400	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
43	chr8:53851000-53851600	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
44	chr8:53851000-53851800	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
45	chr8:53851000-53851800	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
46	chr8:53851000-53852000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
47	chr8:53851000-53852200	Bivalent Enhancer	Brain Anterior Caudate	brain
48	chr8:53851000-53852200	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
49	chr8:53851000-53854400	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr8:53851000-53854400	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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