Variant report

Variant	nsv1022781
Chromosome Location	chr8:53358175-53398226
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:590)
CpG islands
(count:245)
Chromatin interactive
region (count:15)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:590 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

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	chr8:53381891-53381969	HepG2	liver:	n/a	n/a
6	BHLHE40	chr8:53379663-53380117	HepG2	liver:	n/a	n/a
7	BRCA1	chr8:53372746-53373386	Hela-S3	cervix:	n/a	n/a
8	BRCA1	chr8:53378991-53379357	Hela-S3	cervix:	n/a	n/a
9	BRCA1	chr8:53379588-53380167	Hela-S3	cervix:	n/a	chr8:53380042-53380051
10	BRCA1	chr8:53396527-53396846	Hela-S3	cervix:	n/a	n/a
11	CBX3	chr8:53379508-53380052	HCT-116	colon:	n/a	n/a
12	CEBPB	chr8:53396460-53396843	IMR90	lung:	n/a	chr8:53396637-53396650
13	CEBPB	chr8:53395946-53395953	A549	lung:	n/a	n/a
14	CEBPB	chr8:53380704-53380931	IMR90	lung:	n/a	chr8:53380846-53380857
15	CEBPB	chr8:53386645-53386969	HepG2	liver:	n/a	chr8:53386814-53386831
16	CEBPB	chr8:53380743-53381004	H1-hESC	embryonic stem cell:	n/a	chr8:53380846-53380857
17	CEBPB	chr8:53379541-53380152	MCF-7	breast:	n/a	n/a
18	CEBPB	chr8:53379012-53380164	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr8:53396522-53396810	H1-hESC	embryonic stem cell:	n/a	chr8:53396637-53396650
20	CEBPB	chr8:53381863-53382286	MCF-7	breast:	n/a	n/a
21	CEBPB	chr8:53396469-53396829	Hela-S3	cervix:	n/a	chr8:53396637-53396650
22	CEBPB	chr8:53396531-53396797	K562	blood:	n/a	chr8:53396637-53396650
23	CEBPB	chr8:53390859-53391231	A549	lung:	n/a	n/a
24	CEBPB	chr8:53379757-53380001	HepG2	liver:	n/a	n/a
25	CEBPB	chr8:53379510-53380065	MCF-7	breast:	n/a	n/a
26	CEBPB	chr8:53380720-53380951	Hela-S3	cervix:	n/a	chr8:53380846-53380857
27	CEBPB	chr8:53396438-53396902	MCF-7	breast:	n/a	chr8:53396452-53396464 chr8:53396637-53396650
28	CEBPB	chr8:53383928-53384094	A549	lung:	n/a	chr8:53384002-53384013
29	CEBPB	chr8:53396457-53396894	A549	lung:	n/a	chr8:53396637-53396650
30	CEBPB	chr8:53390956-53391156	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr8:53396464-53396816	A549	lung:	n/a	chr8:53396637-53396650
32	CEBPB	chr8:53390857-53391216	IMR90	lung:	n/a	n/a
33	CEBPB	chr8:53390896-53391184	K562	blood:	n/a	n/a
34	CEBPB	chr8:53363290-53363497	HepG2	liver:	n/a	chr8:53363360-53363371
35	CEBPB	chr8:53372721-53373146	MCF-7	breast:	n/a	n/a
36	CEBPB	chr8:53380703-53381035	K562	blood:	n/a	chr8:53380846-53380857
37	CEBPB	chr8:53366626-53366812	HepG2	liver:	n/a	chr8:53366685-53366696
38	CEBPB	chr8:53363255-53363417	K562	blood:	n/a	chr8:53363360-53363371
39	CEBPB	chr8:53366024-53366229	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr8:53372293-53373280	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr8:53396446-53396903	MCF-7	breast:	n/a	chr8:53396452-53396464 chr8:53396637-53396650
42	CEBPB	chr8:53379594-53379970	ECC-1	luminal epithelium:	n/a	n/a
43	CEBPB	chr8:53372644-53373068	A549	lung:	n/a	n/a
44	CEBPB	chr8:53383876-53384104	HepG2	liver:	n/a	chr8:53384002-53384013
45	CEBPB	chr8:53380702-53380961	A549	lung:	n/a	chr8:53380846-53380857
46	CEBPB	chr8:53390851-53391216	HepG2	liver:	n/a	n/a
47	CEBPB	chr8:53380669-53381024	HepG2	liver:	n/a	chr8:53380846-53380857 chr8:53380675-53380688
48	CHD2	chr8:53379613-53380244	Hela-S3	cervix:	n/a	chr8:53380042-53380051
49	CHD2	chr8:53379864-53380167	H1-hESC	embryonic stem cell:	n/a	chr8:53380042-53380051
50	CHD2	chr8:53379882-53380156	HepG2	liver:	n/a	chr8:53380042-53380051

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:53397932-53397982	HNPCEpiC	eye:	n/a
2	chr8:53397932-53397982	HNPCEpiC	eye:	n/a
3	chr8:53361936-53361986	HIPEpiC	eye:	n/a
4	chr8:53361893-53361943	HRE	kidney:	n/a
5	chr8:53392286-53392336	Hela-S3	cervix:	n/a
6	chr8:53361936-53361986	HCPEpiC	choroid plexus:	n/a
7	chr8:53361936-53361986	HRE	kidney:	n/a
8	chr8:53392286-53392336	HCPEpiC	choroid plexus:	n/a
9	chr8:53397932-53397982	GM12891	blood:	n/a
10	chr8:53361893-53361943	HepG2	liver:	n/a
11	chr8:53392286-53392336	AG09309	skin:	n/a
12	chr8:53361893-53361943	MCF10A-Er-Src	breast:	n/a
13	chr8:53361893-53361943	Hela-S3	cervix:	n/a
14	chr8:53361936-53361986	BJ	skin:	n/a
15	chr8:53361936-53361986	NB4	blood:	n/a
16	chr8:53397932-53397982	HUVEC	blood vessel:	n/a
17	chr8:53361936-53361986	AG09309	skin:	n/a
18	chr8:53392286-53392336	GM12878	blood:	n/a
19	chr8:53361936-53361986	HPAEpiC	pulmonary alveolar:	n/a
20	chr8:53361893-53361943	CMK	blood:	n/a
21	chr8:53392286-53392336	NT2-D1	testis:	n/a
22	chr8:53397932-53397982	RPTEC	kidney:	n/a
23	chr8:53397932-53397982	GM19239	blood:	n/a
24	chr8:53397932-53397982	ECC-1	luminal epithelium:	n/a
25	chr8:53361893-53361943	ProgFib	skin:	n/a
26	chr8:53361936-53361986	SK-N-SH	brain:	n/a
27	chr8:53392286-53392336	PFSK-1	brain:	n/a
28	chr8:53361893-53361943	LNCaP	prostate:	n/a
29	chr8:53361936-53361986	CMK	blood:	n/a
30	chr8:53397932-53397982	ProgFib	skin:	n/a
31	chr8:53397932-53397982	AG09319	gingival:	n/a
32	chr8:53392286-53392336	Caco-2	colon:	n/a
33	chr8:53392286-53392336	NB4	blood:	n/a
34	chr8:53397932-53397982	AoSMC	blood vessel:	n/a
35	chr8:53392286-53392336	HRCEpiC	kidney:	n/a
36	chr8:53392286-53392336	U87	brain:	n/a
37	chr8:53361893-53361943	PrEC	prostate:	n/a
38	chr8:53361893-53361943	HCPEpiC	choroid plexus:	n/a
39	chr8:53361936-53361986	GM19239	blood:	n/a
40	chr8:53397932-53397982	SK-N-SH_RA	brain:	n/a
41	chr8:53361936-53361986	GM12878	blood:	n/a
42	chr8:53392286-53392336	HIPEpiC	eye:	n/a
43	chr8:53361936-53361986	AG09319	gingival:	n/a
44	chr8:53361893-53361943	HEK293	kidney:	embryo
45	chr8:53397932-53397982	NHBE	bronchial:	n/a
46	chr8:53397932-53397982	ovcar-3	ovarian:	n/a
47	chr8:53361936-53361986	GM12892	blood:	n/a
48	chr8:53361893-53361943	HMEC	breast:	n/a
49	chr8:53361893-53361943	GM19239	blood:	n/a
50	chr8:53361936-53361986	H1-hESC	embryonic stem cell:	embryo

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:53372582..53373541-chr9:86594741..86595608,2	Hela-S3	cervix:
2	chr8:52810955..52812797-chr8:53371753..53374505,2	MCF-7	breast:
3	chr8:53379300..53382260-chr8:53389036..53391579,2	MCF-7	breast:
4	chr8:53372593..53375156-chr8:53377269..53381843,6	MCF-7	breast:
5	chr8:53354328..53356957-chr8:53358190..53360419,2	MCF-7	breast:
6	chr8:53384050..53386139-chr8:53390786..53392939,2	MCF-7	breast:
7	chr8:53333225..53333725-chr8:53388714..53389585,2	MCF-7	breast:
8	chr8:53379006..53383439-chr8:53384188..53388259,4	MCF-7	breast:
9	chr8:53379300..53382260-chr8:53389036..53391579,2	MCF-7	breast:
10	chr8:53377547..53380484-chr8:53382020..53384595,2	MCF-7	breast:
11	chr8:53379006..53383439-chr8:53384188..53388259,4	MCF-7	breast:
12	chr8:53396327..53397778-chr8:53408319..53409731,6	MCF-7	breast:
13	chr8:53395676..53397810-chr8:53399596..53402225,2	MCF-7	breast:
14	chr8:53377547..53380484-chr8:53382020..53384595,2	MCF-7	breast:
15	chr8:53384050..53386139-chr8:53390786..53392939,2	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
ENSG00000228801	chromatin interactions
ENSG00000165119	chromatin interactions
ENSG00000147488	chromatin interactions
ENSG00000168300	chromatin interactions

Extended variants
information (count: 1248 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:1248 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs111869821	chr8:53358178-53358179	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs529407263	chr8:53358211-53358212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs547444847	chr8:53358214-53358215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs189871700	chr8:53358218-53358219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs533221070	chr8:53358229-53358230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs551738919	chr8:53358253-53358254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs1660544	chr8:53358275-53358276	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs537270816	chr8:53358329-53358330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs533888724	chr8:53358339-53358340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs117307536	chr8:53358411-53358412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs76254566	chr8:53358416-53358417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs57285453	chr8:53358435-53358436	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs141245409	chr8:53358442-53358443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs551917070	chr8:53358479-53358480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs76679212	chr8:53358531-53358532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs552655405	chr8:53358564-53358565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs372396115	chr8:53358568-53358569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs181171175	chr8:53358573-53358574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs546086307	chr8:53358585-53358586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs558060320	chr8:53358602-53358603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs576215936	chr8:53358605-53358606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs543622034	chr8:53358606-53358607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs562331996	chr8:53358663-53358664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs529320655	chr8:53358684-53358685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs375784171	chr8:53358704-53358705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs571661595	chr8:53358706-53358707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs530954630	chr8:53358723-53358724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs146923776	chr8:53358771-53358772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs559772608	chr8:53358777-53358778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs533411275	chr8:53358796-53358797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs137911337	chr8:53358861-53358862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs185630127	chr8:53358865-53358866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs530849533	chr8:53358868-53358869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs113455763	chr8:53358887-53358888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs569813557	chr8:53358889-53358890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs12114093	chr8:53358895-53358896	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs369122562	chr8:53358941-53358942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs190779132	chr8:53358982-53358983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs570890287	chr8:53358993-53358994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs143692100	chr8:53359058-53359059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs556556811	chr8:53359070-53359071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs535760787	chr8:53359109-53359110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs576302896	chr8:53359124-53359125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs72645520	chr8:53359166-53359167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs565547563	chr8:53359194-53359195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs555637904	chr8:53359200-53359201	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs183016262	chr8:53359235-53359236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs541162527	chr8:53359259-53359260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs559913704	chr8:53359263-53359264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs578058429	chr8:53359290-53359291	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:289 , 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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