Variant report

Variant	nsv890915
Chromosome Location	chr8:53842413-53885043
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	chr8:53851100-53851301	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr8:53854127-53854469	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr8:53853083-53853227	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr8:53852611-53852810	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	chr8:53883776-53883853	H1-hESC	embryonic stem cell:	n/a	n/a
12	BRCA1	chr8:53853372-53853513	H1-hESC	embryonic stem cell:	n/a	n/a
13	BRCA1	chr8:53854213-53854414	HepG2	liver:	n/a	n/a
14	BRCA1	chr8:53854261-53854544	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr8:53879899-53879925	A549	lung:	n/a	n/a
16	CEBPB	chr8:53850499-53850779	K562	blood:	n/a	n/a
17	CEBPB	chr8:53854282-53854519	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr8:53850582-53850783	A549	lung:	n/a	n/a
19	CHD1	chr8:53854039-53854723	IMR90	lung:	n/a	n/a
20	CHD1	chr8:53853898-53854325	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD1	chr8:53854213-53854389	GM12878	blood:	n/a	n/a
22	CHD2	chr8:53853125-53853738	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD2	chr8:53854239-53854481	HepG2	liver:	n/a	n/a
24	CHD2	chr8:53851260-53851279	H1-hESC	embryonic stem cell:	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	chr8:53854182-53854464	A549	lung:	n/a	n/a
28	CREB1	chr8:53853639-53854000	A549	lung:	n/a	n/a
29	CTBP2	chr8:53851626-53854473	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr8:53854213-53854489	GM12892	blood:	n/a	chr8:53854334-53854347 chr8:53854327-53854348 chr8:53854332-53854350 chr8:53854338-53854347 chr8:53854333-53854349 chr8:53854335-53854345
31	CTCF	chr8:53861800-53861950	HRE	kidney:	n/a	n/a
32	CTCF	chr8:53853080-53853230	HRE	kidney:	n/a	n/a
33	CTCF	chr8:53861877-53861970	SK-N-SH_RA	brain:	n/a	n/a
34	CTCF	chr8:53878458-53878670	MCF-7	breast:	n/a	chr8:53878564-53878573 chr8:53878563-53878584 chr8:53878561-53878579 chr8:53878562-53878578 chr8:53878564-53878577
35	CTCF	chr8:53861689-53862057	T-47D	breast:	n/a	n/a
36	CTCF	chr8:53853320-53853470	HRE	kidney:	n/a	n/a
37	CTCF	chr8:53878460-53878610	GM12867	blood:	n/a	chr8:53878564-53878573 chr8:53878563-53878584 chr8:53878561-53878579 chr8:53878562-53878578 chr8:53878564-53878577
38	CTCF	chr8:53883240-53883390	Hela-S3	cervix:	n/a	chr8:53883344-53883352 chr8:53883341-53883359 chr8:53883344-53883357
39	CTCF	chr8:53883060-53883210	GM06990	blood:	n/a	n/a
40	CTCF	chr8:53878460-53878610	AoAF	blood vessel:	n/a	chr8:53878564-53878573 chr8:53878563-53878584 chr8:53878561-53878579 chr8:53878562-53878578 chr8:53878564-53878577
41	CTCF	chr8:53878480-53878630	HRPEpiC	eye:	n/a	chr8:53878564-53878573 chr8:53878563-53878584 chr8:53878561-53878579 chr8:53878562-53878578 chr8:53878564-53878577
42	CTCF	chr8:53853760-53853910	HPAF	blood vessel:	n/a	chr8:53853894-53853907
43	CTCF	chr8:53878416-53878679	HepG2	liver:	n/a	chr8:53878564-53878573 chr8:53878563-53878584 chr8:53878561-53878579 chr8:53878562-53878578 chr8:53878564-53878577
44	CTCF	chr8:53878400-53878550	NHDF-neo	bronchial:	n/a	n/a
45	CTCF	chr8:53878431-53878680	K562	blood:	n/a	chr8:53878564-53878573 chr8:53878563-53878584 chr8:53878561-53878579 chr8:53878562-53878578 chr8:53878564-53878577
46	CTCF	chr8:53878460-53878610	HBMEC	blood vessel:	n/a	chr8:53878564-53878573 chr8:53878563-53878584 chr8:53878561-53878579 chr8:53878562-53878578 chr8:53878564-53878577
47	CTCF	chr8:53853832-53853898	GM12878	blood:	n/a	n/a
48	CTCF	chr8:53878500-53878650	HVMF	connective:	n/a	chr8:53878564-53878573 chr8:53878563-53878584 chr8:53878561-53878579 chr8:53878562-53878578 chr8:53878564-53878577
49	CTCF	chr8:53853340-53853490	GM12873	blood:	n/a	n/a
50	CTCF	chr8:53853838-53853842	HUVEC	blood vessel:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:53851613-53851663	ECC-1	luminal epithelium:	n/a
2	chr8:53883763-53883813	LNCaP	prostate:	n/a
3	chr8:53851613-53851663	ECC-1	luminal epithelium:	n/a
4	chr8:53883763-53883813	LNCaP	prostate:	n/a
5	chr8:53849059-53849109	CMK	blood:	n/a
6	chr8:53852443-53852493	PANC-1	pancreas:	n/a
7	chr8:53854425-53854475	HCM	heart:	n/a
8	chr8:53854495-53854545	HNPCEpiC	eye:	n/a
9	chr8:53853112-53853162	HRPEpiC	eye:	n/a
10	chr8:53854495-53854545	AG09309	skin:	n/a
11	chr8:53852101-53852151	GM12891	blood:	n/a
12	chr8:53866689-53866739	GM06990	blood:	n/a
13	chr8:53852422-53852472	AG04450	lung:	fetal
14	chr8:53857047-53857097	HRCEpiC	kidney:	n/a
15	chr8:53857047-53857097	RPTEC	kidney:	n/a
16	chr8:53854495-53854545	RPTEC	kidney:	n/a
17	chr8:53853444-53853494	HCF	heart:	n/a
18	chr8:53883763-53883813	HNPCEpiC	eye:	n/a
19	chr8:53866689-53866739	HIPEpiC	eye:	n/a
20	chr8:53853112-53853162	HRE	kidney:	n/a
21	chr8:53864533-53864583	NT2-D1	testis:	n/a
22	chr8:53883763-53883813	NHBE	bronchial:	n/a
23	chr8:53851156-53851206	HCM	heart:	n/a
24	chr8:53852101-53852151	HCPEpiC	choroid plexus:	n/a
25	chr8:53854425-53854475	AG09309	skin:	n/a
26	chr8:53852443-53852493	AG09319	gingival:	n/a
27	chr8:53857047-53857097	LNCaP	prostate:	n/a
28	chr8:53866529-53866579	HRPEpiC	eye:	n/a
29	chr8:53852422-53852472	HL-60	blood:	n/a
30	chr8:53853112-53853162	HEK293	kidney:	embryo
31	chr8:53866689-53866739	BE2_C	brain:	n/a
32	chr8:53851707-53851757	BE2_C	brain:	n/a
33	chr8:53853112-53853162	HUVEC	blood vessel:	n/a
34	chr8:53851707-53851757	K562	blood:	n/a
35	chr8:53854495-53854545	IMR90	lung:	fetal
36	chr8:53853112-53853162	NHDF-neo	bronchial:	n/a
37	chr8:53852030-53852080	Jurkat	blood:	n/a
38	chr8:53883763-53883813	HPAEpiC	pulmonary alveolar:	n/a
39	chr8:53853444-53853494	CMK	blood:	n/a
40	chr8:53853112-53853162	AoSMC	blood vessel:	n/a
41	chr8:53852422-53852472	HNPCEpiC	eye:	n/a
42	chr8:53854425-53854475	GM06990	blood:	n/a
43	chr8:53852274-53852324	Caco-2	colon:	n/a
44	chr8:53854172-53854222	NB4	blood:	n/a
45	chr8:53849059-53849109	AG04449	skin:	fetal
46	chr8:53854172-53854222	BJ	skin:	n/a
47	chr8:53852446-53852496	PrEC	prostate:	n/a
48	chr8:53883763-53883813	HRE	kidney:	n/a
49	chr8:53866689-53866739	AG09309	skin:	n/a
50	chr8:53852661-53852711	NH-A	brain:	n/a

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

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

Extended variants
information (count: 1436 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:1436 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs544155664	chr8:53845994-53845995	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs562365933	chr8:53846072-53846073	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs57777727	chr8:53846094-53846095	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs187318279	chr8:53846110-53846111	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs61269045	chr8:53846128-53846129	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs533486613	chr8:53846183-53846184	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs566868329	chr8:53847414-53847415	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs566440191	chr8:53847450-53847451	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs562642590	chr8:53847939-53847940	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs554719642	chr8:53847955-53847956	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs545849360	chr8:53849059-53849060	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
12	rs565566762	chr8:53849063-53849064	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
13	rs563962321	chr8:53849077-53849078	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
14	rs531203144	chr8:53849092-53849093	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
15	rs550902278	chr8:53849094-53849095	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
16	rs531161408	chr8:53849119-53849120	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs181346401	chr8:53849130-53849131	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs569217130	chr8:53849155-53849156	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs530283438	chr8:53849168-53849169	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs548392967	chr8:53849169-53849170	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs567017424	chr8:53849176-53849177	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs77819189	chr8:53849478-53849479	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs574790649	chr8:53849484-53849485	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs546979265	chr8:53849542-53849543	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs566058569	chr8:53849554-53849555	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs80336434	chr8:53849566-53849567	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs72643590	chr8:53849595-53849596	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs186357165	chr8:53849633-53849634	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs563311841	chr8:53849661-53849662	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs191606483	chr8:53849662-53849663	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs138315324	chr8:53849668-53849669	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs543015443	chr8:53849673-53849674	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs201034797	chr8:53849676-53849677	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs28514829	chr8:53849682-53849683	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs142353936	chr8:53849685-53849686	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs186589034	chr8:53849689-53849690	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs571187877	chr8:53849690-53849691	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs548846907	chr8:53849695-53849696	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs376374939	chr8:53849697-53849698	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs190997964	chr8:53849711-53849712	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs538679289	chr8:53849717-53849718	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs557004198	chr8:53849720-53849721	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs202130579	chr8:53849722-53849723	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs143936496	chr8:53849737-53849738	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs62638828	chr8:53849751-53849752	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs575263552	chr8:53849767-53849768	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs552432796	chr8:53849814-53849815	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs556843506	chr8:53849828-53849829	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs76783670	chr8:53849839-53849840	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs553028874	chr8:53849840-53849841	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:557 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:53850600-53850800	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
2	chr8:53850600-53851000	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
3	chr8:53850600-53851000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr8:53850600-53851000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr8:53850600-53851200	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
6	chr8:53850600-53851400	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
7	chr8:53850800-53851200	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
8	chr8:53850800-53853400	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
9	chr8:53850800-53854400	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
10	chr8:53851000-53851200	Bivalent Enhancer	Primary T cells from cord blood	blood
11	chr8:53851000-53851200	Bivalent/Poised TSS	Primary hematopoietic stem cells	blood
12	chr8:53851000-53851200	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells short term culture	blood
13	chr8:53851000-53851400	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
14	chr8:53851000-53851600	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
15	chr8:53851000-53851800	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
16	chr8:53851000-53851800	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
17	chr8:53851000-53852000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
18	chr8:53851000-53852200	Bivalent Enhancer	Brain Anterior Caudate	brain
19	chr8:53851000-53852200	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
20	chr8:53851000-53854400	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr8:53851000-53854400	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr8:53851000-53854600	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
23	chr8:53851000-53854800	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
24	chr8:53851200-53851400	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
25	chr8:53851200-53851400	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
26	chr8:53851200-53851400	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
27	chr8:53851200-53851400	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
28	chr8:53851200-53851400	Bivalent/Poised TSS	Primary hematopoietic stem cells short term culture	blood
29	chr8:53851200-53851600	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
30	chr8:53851200-53851600	Flanking Bivalent TSS/Enh	Primary T cells from cord blood	blood
31	chr8:53851200-53852600	Bivalent Enhancer	Primary T helper 17 cells PMA-I stimulated	--
32	chr8:53851200-53854400	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells	blood
33	chr8:53851200-53854800	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
34	chr8:53851200-53854800	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
35	chr8:53851400-53851600	Flanking Bivalent TSS/Enh	Primary monocytes fromperipheralblood	blood
36	chr8:53851400-53851600	Bivalent Enhancer	Duodenum Mucosa	Duodenum
37	chr8:53851400-53851800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
38	chr8:53851400-53851800	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
39	chr8:53851400-53852000	Bivalent Enhancer	Primary B cells from cord blood	blood
40	chr8:53851400-53852000	Bivalent Enhancer	Primary T helper naive cells from peripheral blood	blood
41	chr8:53851400-53852000	Bivalent Enhancer	Primary T killer naive cells fromperipheralblood	blood
42	chr8:53851400-53852000	Enhancers	Primary T killer memory cells from peripheral blood	blood
43	chr8:53851400-53852000	Bivalent Enhancer	Fetal Brain Male	brain
44	chr8:53851400-53852200	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
45	chr8:53851400-53852200	Flanking Bivalent TSS/Enh	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr8:53851400-53852200	Bivalent Enhancer	Liver	Liver
47	chr8:53851400-53852400	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr8:53851400-53852600	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
49	chr8:53851400-53852600	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
50	chr8:53851400-53853000	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived

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