Variant report

Variant	esv1840247
Chromosome Location	chr8:53353780-53381864
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:348)
CpG islands
(count:122)
Chromatin interactive
region (count:8)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:348 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:53379534-53379715	HepG2	liver:	n/a	n/a
2	ATF1	chr8:53359120-53359225	K562	blood:	n/a	n/a
3	ATF3	chr8:53380751-53380920	K562	blood:	n/a	n/a
4	BHLHE40	chr8:53379829-53380010	K562	blood:	n/a	n/a
5	BHLHE40	chr8:53379663-53380117	HepG2	liver:	n/a	n/a
6	BRCA1	chr8:53372746-53373386	Hela-S3	cervix:	n/a	n/a
7	BRCA1	chr8:53379588-53380167	Hela-S3	cervix:	n/a	chr8:53380042-53380051
8	BRCA1	chr8:53378991-53379357	Hela-S3	cervix:	n/a	n/a
9	CBX3	chr8:53379508-53380052	HCT-116	colon:	n/a	n/a
10	CEBPB	chr8:53379012-53380164	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr8:53380669-53381024	HepG2	liver:	n/a	chr8:53380846-53380857 chr8:53380675-53380688
12	CEBPB	chr8:53363255-53363417	K562	blood:	n/a	chr8:53363360-53363371
13	CEBPB	chr8:53380702-53380961	A549	lung:	n/a	chr8:53380846-53380857
14	CEBPB	chr8:53372721-53373146	MCF-7	breast:	n/a	n/a
15	CEBPB	chr8:53379757-53380001	HepG2	liver:	n/a	n/a
16	CEBPB	chr8:53380720-53380951	Hela-S3	cervix:	n/a	chr8:53380846-53380857
17	CEBPB	chr8:53363290-53363497	HepG2	liver:	n/a	chr8:53363360-53363371
18	CEBPB	chr8:53381863-53382286	MCF-7	breast:	n/a	n/a
19	CEBPB	chr8:53372293-53373280	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr8:53379594-53379970	ECC-1	luminal epithelium:	n/a	n/a
21	CEBPB	chr8:53372644-53373068	A549	lung:	n/a	n/a
22	CEBPB	chr8:53379510-53380065	MCF-7	breast:	n/a	n/a
23	CEBPB	chr8:53380703-53381035	K562	blood:	n/a	chr8:53380846-53380857
24	CEBPB	chr8:53380743-53381004	H1-hESC	embryonic stem cell:	n/a	chr8:53380846-53380857
25	CEBPB	chr8:53366024-53366229	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr8:53366626-53366812	HepG2	liver:	n/a	chr8:53366685-53366696
27	CEBPB	chr8:53379541-53380152	MCF-7	breast:	n/a	n/a
28	CEBPB	chr8:53380704-53380931	IMR90	lung:	n/a	chr8:53380846-53380857
29	CHD2	chr8:53379882-53380156	HepG2	liver:	n/a	chr8:53380042-53380051
30	CHD2	chr8:53379864-53380167	H1-hESC	embryonic stem cell:	n/a	chr8:53380042-53380051
31	CHD2	chr8:53372674-53373174	Hela-S3	cervix:	n/a	n/a
32	CHD2	chr8:53379613-53380244	Hela-S3	cervix:	n/a	chr8:53380042-53380051
33	CTBP2	chr8:53379690-53380087	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr8:53379802-53379975	A549	lung:	n/a	chr8:53379872-53379885
35	CTCF	chr8:53379780-53379930	HCM	heart:	n/a	chr8:53379872-53379885
36	CTCF	chr8:53379780-53379930	SAEC	small airway:	n/a	chr8:53379872-53379885
37	CTCF	chr8:53379780-53379930	GM12869	blood:	n/a	chr8:53379872-53379885
38	CTCF	chr8:53379740-53379890	HPAF	blood vessel:	n/a	chr8:53379872-53379885
39	CTCF	chr8:53379840-53379990	HPF	lung:	n/a	chr8:53379872-53379885
40	CTCF	chr8:53379820-53379970	GM12864	blood:	n/a	chr8:53379872-53379885
41	CTCF	chr8:53379874-53379963	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr8:53379860-53380010	HepG2	liver:	n/a	chr8:53379872-53379885
43	CTCF	chr8:53379700-53379850	BJ	skin:	n/a	n/a
44	CTCF	chr8:53379800-53379950	GM12875	blood:	n/a	chr8:53379872-53379885
45	CTCF	chr8:53379805-53379935	Gliobla	brain:	n/a	chr8:53379872-53379885
46	CTCF	chr8:53379837-53379890	NHEK	skin:	n/a	chr8:53379872-53379885
47	CTCF	chr8:53379766-53380014	MCF-7	breast:	n/a	chr8:53379872-53379885
48	CTCF	chr8:53379740-53379890	GM06990	blood:	n/a	chr8:53379872-53379885
49	CTCF	chr8:53373034-53373081	Hela-S3	cervix:	n/a	n/a
50	CTCF	chr8:53379760-53379910	HCPEpiC	choroid plexus:	n/a	chr8:53379872-53379885

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:53361893-53361943	HRE	kidney:	n/a
2	chr8:53361936-53361986	HEEpiC	esophagus:	n/a
3	chr8:53361893-53361943	Caco-2	colon:	n/a
4	chr8:53361893-53361943	U87	brain:	n/a
5	chr8:53361893-53361943	AG09309	skin:	n/a
6	chr8:53361936-53361986	CMK	blood:	n/a
7	chr8:53361936-53361986	U87	brain:	n/a
8	chr8:53361936-53361986	PANC-1	pancreas:	n/a
9	chr8:53361936-53361986	Caco-2	colon:	n/a
10	chr8:53361893-53361943	SK-N-SH	brain:	n/a
11	chr8:53361893-53361943	CMK	blood:	n/a
12	chr8:53361936-53361986	AG04449	skin:	fetal
13	chr8:53361936-53361986	T-47D	breast:	n/a
14	chr8:53361893-53361943	HRCEpiC	kidney:	n/a
15	chr8:53361893-53361943	AG04450	lung:	fetal
16	chr8:53361936-53361986	GM12891	blood:	n/a
17	chr8:53361893-53361943	NHBE	bronchial:	n/a
18	chr8:53361893-53361943	HEK293	kidney:	embryo
19	chr8:53361936-53361986	NT2-D1	testis:	n/a
20	chr8:53361936-53361986	HAEpiC	amniotic membrane:	n/a
21	chr8:53361936-53361986	RPTEC	kidney:	n/a
22	chr8:53361936-53361986	GM12878	blood:	n/a
23	chr8:53361893-53361943	IMR90	lung:	fetal
24	chr8:53361893-53361943	NB4	blood:	n/a
25	chr8:53361893-53361943	BJ	skin:	n/a
26	chr8:53361893-53361943	GM06990	blood:	n/a
27	chr8:53361893-53361943	T-47D	breast:	n/a
28	chr8:53361936-53361986	NB4	blood:	n/a
29	chr8:53361936-53361986	BJ	skin:	n/a
30	chr8:53361936-53361986	SK-N-MC	brain:	n/a
31	chr8:53361893-53361943	HNPCEpiC	eye:	n/a
32	chr8:53361893-53361943	HUVEC	blood vessel:	n/a
33	chr8:53361936-53361986	SK-N-SH_RA	brain:	n/a
34	chr8:53361936-53361986	MCF-7	breast:	n/a
35	chr8:53361893-53361943	GM12891	blood:	n/a
36	chr8:53361893-53361943	ProgFib	skin:	n/a
37	chr8:53361936-53361986	HNPCEpiC	eye:	n/a
38	chr8:53361893-53361943	MCF10A-Er-Src	breast:	n/a
39	chr8:53361936-53361986	NH-A	brain:	n/a
40	chr8:53361893-53361943	PrEC	prostate:	n/a
41	chr8:53361893-53361943	HepG2	liver:	n/a
42	chr8:53361893-53361943	ovcar-3	ovarian:	n/a
43	chr8:53361893-53361943	HAEpiC	amniotic membrane:	n/a
44	chr8:53361936-53361986	AG10803	skin:	n/a
45	chr8:53361893-53361943	A549	lung:	n/a
46	chr8:53361893-53361943	GM12878	blood:	n/a
47	chr8:53361893-53361943	HCT-116	colon:	n/a
48	chr8:53361936-53361986	HMEC	breast:	n/a
49	chr8:53361893-53361943	HL-60	blood:	n/a
50	chr8:53361936-53361986	GM19239	blood:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:53377547..53380484-chr8:53382020..53384595,2	MCF-7	breast:
2	chr8:52810955..52812797-chr8:53371753..53374505,2	MCF-7	breast:
3	chr8:53354328..53356957-chr8:53358190..53360419,2	MCF-7	breast:
4	chr8:53379300..53382260-chr8:53389036..53391579,2	MCF-7	breast:
5	chr8:53372582..53373541-chr9:86594741..86595608,2	Hela-S3	cervix:
6	chr8:53372593..53375156-chr8:53377269..53381843,6	MCF-7	breast:
7	chr8:53379006..53383439-chr8:53384188..53388259,4	MCF-7	breast:
8	chr8:53354328..53356957-chr8:53358190..53360419,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PCMTD1-4	chr8:53373445-53373519	NONHSAT126569

No data

Variant related genes	Relation type
ST18	TF binding region
ST18	CpG island
ENSG00000147488	chromatin interactions
ENSG00000165119	chromatin interactions
ENSG00000228801	chromatin interactions
ENSG00000168300	chromatin interactions

Extended variants
information (count: 1183 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:1183 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2613243	chr8:53353780-53353781	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs555621231	chr8:53353793-53353794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs541564880	chr8:53353802-53353803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs111358008	chr8:53353803-53353804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs574214556	chr8:53353826-53353827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs541731157	chr8:53353859-53353860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs16917843	chr8:53353878-53353879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs78924818	chr8:53353884-53353885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs545515700	chr8:53353945-53353946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs189363887	chr8:53353953-53353954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs530912884	chr8:53353956-53353957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs527341850	chr8:53353971-53353972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs561358928	chr8:53353976-53353977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs113606776	chr8:53353987-53353988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs528330233	chr8:53354006-53354007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs7824826	chr8:53354039-53354040	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs181771522	chr8:53354081-53354082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs185162768	chr8:53354082-53354083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs371750037	chr8:53354111-53354112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs13275665	chr8:53354121-53354122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs13275918	chr8:53354153-53354154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs550237594	chr8:53354181-53354182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs13275947	chr8:53354198-53354199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs564474978	chr8:53354205-53354206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs549284192	chr8:53354209-53354210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs535954762	chr8:53354214-53354215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs11780238	chr8:53354222-53354223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs566465553	chr8:53354235-53354236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs534965227	chr8:53354263-53354264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs189564736	chr8:53354274-53354275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs200027785	chr8:53354287-53354288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs148407173	chr8:53354288-53354289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs578202324	chr8:53354303-53354304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs539271267	chr8:53354329-53354330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs369158004	chr8:53354334-53354335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs201188459	chr8:53354336-53354337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs61062375	chr8:53354378-53354379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs557603842	chr8:53354379-53354380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs138541526	chr8:53354395-53354396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs375292943	chr8:53354406-53354407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs147361060	chr8:53354407-53354408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs570149975	chr8:53354443-53354444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs561087909	chr8:53354453-53354454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs373450106	chr8:53354469-53354470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs375782040	chr8:53354475-53354476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs369992077	chr8:53354477-53354478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs373836585	chr8:53354486-53354487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs200568071	chr8:53354494-53354495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs200472102	chr8:53354497-53354498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs201734191	chr8:53354516-53354517	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
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
Colorectal cancer	21645411	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:277 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:53352800-53360000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
2	chr8:53360000-53360400	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
3	chr8:53360400-53371200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr8:53361200-53363800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr8:53361800-53362200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr8:53361800-53362400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr8:53361800-53362600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr8:53365600-53366400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr8:53366000-53366400	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr8:53366000-53366400	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr8:53366000-53366400	Enhancers	iPS-20b Cell Line	embryonic stem cell
12	chr8:53366000-53366600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr8:53366000-53366800	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr8:53371200-53371600	Enhancers	Primary hematopoietic stem cells short term culture	blood
15	chr8:53371600-53371800	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
16	chr8:53371600-53372000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr8:53371800-53372000	Active TSS	Primary hematopoietic stem cells short term culture	blood
18	chr8:53371800-53372800	Enhancers	Primary hematopoietic stem cells	blood
19	chr8:53372000-53372200	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
20	chr8:53372000-53372400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr8:53372000-53374800	Enhancers	Hela-S3	cervix
22	chr8:53372200-53372400	Active TSS	Primary hematopoietic stem cells short term culture	blood
23	chr8:53372200-53373000	Enhancers	HMEC	breast
24	chr8:53372400-53372600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr8:53372400-53373000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
26	chr8:53372600-53372800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr8:53372600-53372800	Active TSS	Monocytes-CD14+_RO01746	blood
28	chr8:53372600-53373800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr8:53372600-53374200	Enhancers	Primary monocytes fromperipheralblood	blood
30	chr8:53372800-53373400	Flanking Active TSS	Primary hematopoietic stem cells	blood
31	chr8:53372800-53373400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr8:53372800-53373400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
33	chr8:53373000-53373200	Active TSS	Primary hematopoietic stem cells short term culture	blood
34	chr8:53373000-53373800	Enhancers	Placenta Amnion	Placenta Amnion
35	chr8:53373200-53373600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
36	chr8:53373400-53374200	Enhancers	Primary hematopoietic stem cells	blood
37	chr8:53373400-53374200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr8:53373400-53374200	Enhancers	Monocytes-CD14+_RO01746	blood
39	chr8:53373600-53374200	Enhancers	Primary hematopoietic stem cells short term culture	blood
40	chr8:53373800-53374000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr8:53374000-53379000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr8:53374200-53376200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
43	chr8:53374200-53376400	Weak transcription	Primary monocytes fromperipheralblood	blood
44	chr8:53374200-53376400	Weak transcription	Monocytes-CD14+_RO01746	blood
45	chr8:53374200-53379400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr8:53374200-53379600	Weak transcription	Primary hematopoietic stem cells	blood
47	chr8:53374600-53379600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr8:53374800-53377000	Weak transcription	Hela-S3	cervix
49	chr8:53375400-53375600	Enhancers	Fetal Intestine Small	intestine
50	chr8:53376200-53376400	Enhancers	Placenta	Placenta

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