Variant report

Variant	nsv462190
Chromosome Location	chr5:58936943-59023870
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	chr5:58969309-58969587	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:58957641-58958039	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:58960994-58961180	HepG2	liver:	n/a	n/a
4	ATF2	chr5:59005081-59005496	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr5:59005135-59005567	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr5:59009027-59009230	K562	blood:	n/a	n/a
7	BATF	chr5:58981051-58981275	GM12878	blood:	n/a	n/a
8	BCL11A	chr5:59005221-59005381	H1-hESC	embryonic stem cell:	n/a	n/a
9	BCL11A	chr5:59005117-59005450	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCL11A	chr5:58948417-58948651	GM12878	blood:	n/a	n/a
11	BHLHE40	chr5:58945013-58945327	K562	blood:	n/a	n/a
12	BHLHE40	chr5:58956285-58956315	GM12878	blood:	n/a	n/a
13	BRCA1	chr5:59017406-59017428	GM12878	blood:	n/a	n/a
14	CEBPB	chr5:59007143-59007476	A549	lung:	n/a	chr5:59007279-59007290 chr5:59007277-59007288
15	CEBPB	chr5:58957188-58957502	A549	lung:	n/a	n/a
16	CEBPB	chr5:59018686-59019146	Hela-S3	cervix:	n/a	chr5:59019061-59019074
17	CEBPB	chr5:59007127-59007493	Hela-S3	cervix:	n/a	chr5:59007279-59007290 chr5:59007277-59007288
18	CEBPB	chr5:58961256-58961683	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr5:58995910-58995921	HepG2	liver:	n/a	n/a
20	CEBPB	chr5:58999729-58999865	A549	lung:	n/a	n/a
21	CEBPB	chr5:58974823-58975077	IMR90	lung:	n/a	chr5:58974960-58974971 chr5:58974962-58974971 chr5:58975045-58975058
22	CEBPB	chr5:58974840-58975030	HepG2	liver:	n/a	chr5:58974960-58974971 chr5:58974962-58974971
23	CEBPB	chr5:58971573-58971599	A549	lung:	n/a	n/a
24	CEBPB	chr5:59007177-59007438	HepG2	liver:	n/a	chr5:59007279-59007290 chr5:59007277-59007288
25	CEBPB	chr5:58974841-58975128	Hela-S3	cervix:	n/a	chr5:58974960-58974971 chr5:58974962-58974971 chr5:58975045-58975058
26	CEBPB	chr5:59007060-59007575	A549	lung:	n/a	chr5:59007279-59007290 chr5:59007277-59007288
27	CEBPB	chr5:58957167-58957569	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr5:58945122-58945447	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr5:59020408-59020863	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr5:58957252-58957473	HepG2	liver:	n/a	n/a
31	CEBPB	chr5:58974871-58975073	A549	lung:	n/a	chr5:58974960-58974971 chr5:58974962-58974971 chr5:58975045-58975058
32	CEBPB	chr5:58949378-58949483	A549	lung:	n/a	n/a
33	CEBPB	chr5:59007192-59007371	H1-hESC	embryonic stem cell:	n/a	chr5:59007279-59007290 chr5:59007277-59007288
34	CEBPB	chr5:58948169-58948371	A549	lung:	n/a	n/a
35	CEBPB	chr5:58974742-58975231	A549	lung:	n/a	chr5:58974960-58974971 chr5:58974962-58974971 chr5:58975045-58975058
36	CEBPB	chr5:58961386-58961585	HepG2	liver:	n/a	n/a
37	CEBPB	chr5:58969329-58969533	A549	lung:	n/a	n/a
38	CEBPB	chr5:58944191-58944463	Hela-S3	cervix:	n/a	chr5:58944238-58944247 chr5:58944238-58944249
39	CEBPB	chr5:58974893-58975058	K562	blood:	n/a	chr5:58974960-58974971 chr5:58974962-58974971 chr5:58975045-58975058
40	CEBPB	chr5:58957816-58958074	HepG2	liver:	n/a	n/a
41	CTCF	chr5:59020400-59020550	HUVEC	blood vessel:	n/a	chr5:59020519-59020528 chr5:59020518-59020539 chr5:59020516-59020534
42	CTCF	chr5:59020500-59020650	GM12868	blood:	n/a	chr5:59020519-59020528 chr5:59020518-59020539 chr5:59020516-59020534
43	CTCF	chr5:59020460-59020610	HRPEpiC	eye:	n/a	chr5:59020519-59020528 chr5:59020518-59020539 chr5:59020516-59020534
44	CTCF	chr5:58956740-58956890	GM12864	blood:	n/a	chr5:58956770-58956791 chr5:58956775-58956793
45	CTCF	chr5:59020301-59020688	T-47D	breast:	n/a	chr5:59020519-59020528 chr5:59020518-59020539 chr5:59020516-59020534
46	CTCF	chr5:59020424-59020596	MCF-7	breast:	n/a	chr5:59020519-59020528 chr5:59020518-59020539 chr5:59020516-59020534
47	CTCF	chr5:58969360-58969510	GM12868	blood:	n/a	chr5:58969458-58969474 chr5:58969457-58969475 chr5:58969452-58969473 chr5:58969462-58969470
48	CTCF	chr5:58961780-58961868	GM12892	blood:	n/a	n/a
49	CTCF	chr5:58962640-58962790	HRPEpiC	eye:	n/a	n/a
50	CTCF	chr5:59020356-59020669	HUVEC	blood vessel:	n/a	chr5:59020519-59020528 chr5:59020518-59020539 chr5:59020516-59020534

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:58957910-58957960	SAEC	small airway:	n/a
2	chr5:58957910-58957960	GM12891	blood:	n/a
3	chr5:58957910-58957960	ovcar-3	ovarian:	n/a
4	chr5:58957910-58957960	HPAEpiC	pulmonary alveolar:	n/a
5	chr5:58957910-58957960	SKMC	muscle:	n/a
6	chr5:58957910-58957960	MCF10A-Er-Src	breast:	n/a
7	chr5:58957910-58957960	SK-N-SH_RA	brain:	n/a
8	chr5:58957910-58957960	Hela-S3	cervix:	n/a
9	chr5:58957910-58957960	AG10803	skin:	n/a
10	chr5:58957910-58957960	AG09319	gingival:	n/a
11	chr5:58957910-58957960	GM12878	blood:	n/a
12	chr5:58957910-58957960	Hepatocyte	liver:	n/a
13	chr5:58957910-58957960	RPTEC	kidney:	n/a
14	chr5:58957910-58957960	HRCEpiC	kidney:	n/a
15	chr5:58957910-58957960	NHDF-neo	bronchial:	n/a
16	chr5:58957910-58957960	PFSK-1	brain:	n/a
17	chr5:58957910-58957960	BJ	skin:	n/a
18	chr5:58957910-58957960	HepG2	liver:	n/a
19	chr5:58957910-58957960	HAEpiC	amniotic membrane:	n/a
20	chr5:58957910-58957960	ProgFib	skin:	n/a
21	chr5:58957910-58957960	IMR90	lung:	fetal
22	chr5:58957910-58957960	Caco-2	colon:	n/a
23	chr5:58957910-58957960	HEK293	kidney:	embryo
24	chr5:58957910-58957960	HCF	heart:	n/a
25	chr5:58957910-58957960	CMK	blood:	n/a
26	chr5:58957910-58957960	LNCaP	prostate:	n/a
27	chr5:58957910-58957960	GM06990	blood:	n/a
28	chr5:58957910-58957960	Jurkat	blood:	n/a
29	chr5:58957910-58957960	PrEC	prostate:	n/a
30	chr5:58957910-58957960	HEEpiC	esophagus:	n/a
31	chr5:58957910-58957960	NH-A	brain:	n/a
32	chr5:58957910-58957960	U87	brain:	n/a
33	chr5:58957910-58957960	HL-60	blood:	n/a
34	chr5:58957910-58957960	A549	lung:	n/a
35	chr5:58957910-58957960	HNPCEpiC	eye:	n/a
36	chr5:58957910-58957960	T-47D	breast:	n/a
37	chr5:58957910-58957960	HCT-116	colon:	n/a
38	chr5:58957910-58957960	NB4	blood:	n/a
39	chr5:58957910-58957960	H1-hESC	embryonic stem cell:	embryo
40	chr5:58957910-58957960	HCM	heart:	n/a
41	chr5:58957910-58957960	ECC-1	luminal epithelium:	n/a
42	chr5:58957910-58957960	AG04450	lung:	fetal
43	chr5:58957910-58957960	HCPEpiC	choroid plexus:	n/a
44	chr5:58957910-58957960	NT2-D1	testis:	n/a
45	chr5:58957910-58957960	SK-N-MC	brain:	n/a
46	chr5:58957910-58957960	MCF-7	breast:	n/a
47	chr5:58957910-58957960	HMEC	breast:	n/a
48	chr5:58957910-58957960	SK-N-SH	brain:	n/a
49	chr5:58957910-58957960	NHBE	bronchial:	n/a
50	chr5:58957910-58957960	AoSMC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:58921699..58924088-chr5:58961415..58963109,2	MCF-7	breast:
2	chr5:58801703..58803307-chr5:58968055..58970489,2	MCF-7	breast:
3	chr5:58968638..58970043-chr5:59019689..59021106,4	MCF-7	breast:
4	chr5:58956441..58957361-chr5:58968943..58969531,2	MCF-7	breast:
5	chr5:58803367..58805536-chr5:58956722..58959458,2	MCF-7	breast:
6	chr12:53139319..53140001-chr5:58956637..58957236,2	MCF-7	breast:
7	chr5:58685998..58686505-chr5:58956311..58957192,2	MCF-7	breast:
8	chr5:59022602..59025084-chr5:59040662..59042603,2	MCF-7	breast:
9	chr5:59002219..59005898-chr5:59006477..59009673,3	K562	blood:
10	chr5:59002219..59005898-chr5:59006477..59009673,3	K562	blood:
11	chr12:17875088..17875599-chr5:58957118..58957618,2	Hela-S3	cervix:
12	chr5:58968638..58970043-chr5:59019689..59021106,4	MCF-7	breast:
13	chr5:58938220..58940371-chr5:58941651..58943411,2	MCF-7	breast:
14	chr5:58803075..58803840-chr5:58956390..58957074,2	MCF-7	breast:
15	chr5:58956441..58957361-chr5:58968943..58969531,2	MCF-7	breast:
16	chr5:58938220..58940371-chr5:58941651..58943411,2	MCF-7	breast:
17	chr5:58801867..58802786-chr5:58968976..58969858,3	MCF-7	breast:
18	chr5:58801872..58802902-chr5:58956210..58957251,7	MCF-7	breast:
19	chr5:58821597..58822483-chr5:58956197..58956887,3	MCF-7	breast:
20	chr5:58969044..58969563-chr5:59095719..59096533,2	MCF-7	breast:
21	chr5:58802090..58802764-chr5:58956093..58957045,3	MCF-7	breast:
22	chr5:58801963..58802644-chr5:58962690..58963296,2	MCF-7	breast:
23	chr5:58801995..58802802-chr5:58968998..58969985,2	MCF-7	breast:

miRNA name	Chromosome Location	mirBase accession
hsa-miR-582-5p	chr5:58999492-58999514	MIMAT0003247
hsa-miR-582-3p	chr5:58999456-58999477	MIMAT0004797

Variant related genes	Relation type
MIR582	TF binding region
MIR582	CpG island
MCL1	Mature miRNA region

Extended variants
information (count: 3101 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:3101 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs298034	chr5:58936943-58936944	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs186148086	chr5:58936970-58936971	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs540639549	chr5:58936971-58936972	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs115274038	chr5:58936998-58936999	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs574079358	chr5:58937036-58937037	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs151099797	chr5:58937069-58937070	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs373340878	chr5:58937087-58937088	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs202183082	chr5:58937090-58937091	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs562936887	chr5:58937198-58937199	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs377013475	chr5:58937201-58937202	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs531833910	chr5:58937217-58937218	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs192207518	chr5:58937225-58937226	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs183696308	chr5:58937267-58937268	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs75890032	chr5:58937286-58937287	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs140979640	chr5:58937294-58937295	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs547679010	chr5:58937296-58937297	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs298033	chr5:58937328-58937329	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs535069785	chr5:58937449-58937450	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs548687546	chr5:58937467-58937468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs568907734	chr5:58937486-58937487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs576258788	chr5:58937504-58937505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs150211956	chr5:58937626-58937627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs565876184	chr5:58937631-58937632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs539680198	chr5:58937691-58937692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs138821537	chr5:58937725-58937726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs141502399	chr5:58937739-58937740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs533505395	chr5:58937763-58937764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs534128492	chr5:58937796-58937797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs554086919	chr5:58937836-58937837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs574097932	chr5:58937873-58937874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs189136614	chr5:58937939-58937940	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs562843180	chr5:58937944-58937945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs298032	chr5:58937978-58937979	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs34213521	chr5:58937983-58937984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs190444546	chr5:58937993-58937994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs575739385	chr5:58938077-58938078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs565518967	chr5:58938118-58938119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs527855615	chr5:58938207-58938208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs147036795	chr5:58938261-58938262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs561215339	chr5:58938262-58938263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs528882292	chr5:58938290-58938291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs576493715	chr5:58938309-58938310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs183058772	chr5:58938326-58938327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs142935527	chr5:58938338-58938339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs551185875	chr5:58938359-58938360	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs298031	chr5:58938411-58938412	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs187122896	chr5:58938415-58938416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs148040957	chr5:58938418-58938419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs201694275	chr5:58938419-58938420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs191938767	chr5:58938444-58938445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Cancer	16751803	CNVD
Autism	22495311	CNVD
Intellectual disability	22102821	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Prostate cancer	21965145	CNVD
Esophageal cancer	20955586	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
adenomatous polyposis	22470819	CNVD
Acute myeloid leukemia	20729466	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Hepatocellular carcinoma	16750200	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	21251322	CNVD
Oral cancer	21386901	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17133270	CNVD
Breast cancer	19602461	CNVD
Renal cell carcinoma	18194544	CNVD
abnormal development	18461090	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	20164920	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Lung adenocarcinoma	17982442	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Neuroticism	17667963	CNVD

Chromatin state (count:906 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:58923600-58957200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr5:58923800-58945000	Weak transcription	Aorta	Aorta
3	chr5:58927000-58939800	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr5:58928600-58938800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr5:58934800-58943800	Weak transcription	HUVEC	blood vessel
6	chr5:58935400-58938800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
7	chr5:58935800-58937400	Enhancers	Hela-S3	cervix
8	chr5:58936600-58937400	Enhancers	A549	lung
9	chr5:58936600-58949200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr5:58937400-58940200	Weak transcription	Hela-S3	cervix
11	chr5:58937400-58940800	Weak transcription	A549	lung
12	chr5:58938800-58940000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr5:58938800-58940800	Enhancers	Primary hematopoietic stem cells short term culture	blood
14	chr5:58939600-58940400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr5:58939600-58940600	Enhancers	Primary hematopoietic stem cells	blood
16	chr5:58939600-58941000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr5:58939800-58941600	Enhancers	Pancreatic Islets	Pancreatic Islet
18	chr5:58940000-58940600	Enhancers	Stomach Mucosa	stomach
19	chr5:58940000-58941000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr5:58940200-58940600	Enhancers	Hela-S3	cervix
21	chr5:58940400-58941600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr5:58940600-58940800	Flanking Active TSS	Primary hematopoietic stem cells	blood
23	chr5:58940600-58941000	Weak transcription	Stomach Mucosa	stomach
24	chr5:58940600-58941000	Weak transcription	Hela-S3	cervix
25	chr5:58940800-58941000	Enhancers	Primary hematopoietic stem cells	blood
26	chr5:58940800-58941600	Enhancers	Primary neutrophils fromperipheralblood	blood
27	chr5:58940800-58941600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
28	chr5:58940800-58941800	Genic enhancers	A549	lung
29	chr5:58941000-58941200	Strong transcription	Hela-S3	cervix
30	chr5:58941000-58941400	Flanking Active TSS	Primary hematopoietic stem cells	blood
31	chr5:58941000-58941400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr5:58941000-58941400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr5:58941000-58941400	Enhancers	Fetal Thymus	thymus
34	chr5:58941000-58941600	Enhancers	Primary B cells from peripheral blood	blood
35	chr5:58941000-58941600	Enhancers	Stomach Mucosa	stomach
36	chr5:58941200-58941400	Genic enhancers	Hela-S3	cervix
37	chr5:58941400-58941600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr5:58941400-58941800	Enhancers	Primary hematopoietic stem cells	blood
39	chr5:58941400-58942600	Strong transcription	Hela-S3	cervix
40	chr5:58941400-58944800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr5:58941600-58941800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr5:58941600-58943800	Weak transcription	Stomach Mucosa	stomach
43	chr5:58941600-58944400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr5:58941600-58944400	Weak transcription	Pancreatic Islets	Pancreatic Islet
45	chr5:58941600-58946400	Enhancers	Primary hematopoietic stem cells short term culture	blood
46	chr5:58941600-58951600	Weak transcription	Primary B cells from peripheral blood	blood
47	chr5:58941800-58943800	Weak transcription	A549	lung
48	chr5:58941800-58944000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr5:58941800-58944400	Weak transcription	Primary hematopoietic stem cells	blood
50	chr5:58942600-58944400	Weak transcription	Hela-S3	cervix

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