Variant report

Variant	nsv525437
Chromosome Location	chr5:80876359-80964452
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	chr5:80922388-80922581	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:80922360-80922638	K562	blood:	n/a	n/a
3	ATF2	chr5:80926794-80927286	GM12878	blood:	n/a	n/a
4	BACH1	chr5:80902101-80902295	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCLAF1	chr5:80926895-80927254	GM12878	blood:	n/a	chr5:80927071-80927080
6	BHLHE40	chr5:80926952-80927319	GM12878	blood:	n/a	n/a
7	CBX3	chr5:80905521-80905970	K562	blood:	n/a	n/a
8	CCNT2	chr5:80898573-80898696	K562	blood:	n/a	n/a
9	CEBPB	chr5:80933203-80933458	HepG2	liver:	n/a	n/a
10	CEBPB	chr5:80896670-80896985	IMR90	lung:	n/a	chr5:80896765-80896776 chr5:80896949-80896961
11	CEBPB	chr5:80911151-80911470	HepG2	liver:	n/a	n/a
12	CEBPB	chr5:80894743-80894938	K562	blood:	n/a	chr5:80894817-80894828
13	CEBPB	chr5:80878335-80878599	K562	blood:	n/a	n/a
14	CEBPB	chr5:80922407-80922756	A549	lung:	n/a	n/a
15	CEBPB	chr5:80911147-80911374	IMR90	lung:	n/a	n/a
16	CEBPB	chr5:80934439-80934491	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr5:80894755-80894917	A549	lung:	n/a	chr5:80894817-80894828
18	CEBPB	chr5:80934362-80934557	K562	blood:	n/a	n/a
19	CEBPB	chr5:80896667-80896990	K562	blood:	n/a	chr5:80896765-80896776 chr5:80896949-80896961
20	CEBPB	chr5:80922304-80922846	A549	lung:	n/a	n/a
21	CEBPB	chr5:80911188-80911432	A549	lung:	n/a	n/a
22	CEBPB	chr5:80922245-80922799	IMR90	lung:	n/a	n/a
23	CEBPB	chr5:80896649-80896965	HepG2	liver:	n/a	chr5:80896765-80896776 chr5:80896949-80896961
24	CEBPB	chr5:80932774-80932778	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr5:80933278-80933515	A549	lung:	n/a	n/a
26	CEBPB	chr5:80894695-80894965	HepG2	liver:	n/a	chr5:80894817-80894828
27	CEBPB	chr5:80961277-80961422	K562	blood:	n/a	n/a
28	CEBPB	chr5:80896660-80896940	A549	lung:	n/a	chr5:80896765-80896776
29	CEBPB	chr5:80944805-80944897	K562	blood:	n/a	n/a
30	CEBPB	chr5:80905700-80905858	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD1	chr5:80935017-80935033	GM12878	blood:	n/a	n/a
32	CHD2	chr5:80902097-80902313	H1-hESC	embryonic stem cell:	n/a	n/a
33	CREB1	chr5:80902014-80902313	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr5:80928280-80928430	GM12875	blood:	n/a	n/a
35	CTCF	chr5:80909468-80909558	Hela-S3	cervix:	n/a	chr5:80909499-80909515 chr5:80909498-80909516 chr5:80909493-80909514 chr5:80909503-80909511
36	CTCF	chr5:80882720-80882870	BE2_C	brain:	n/a	n/a
37	CTCF	chr5:80925880-80926030	HPAF	blood vessel:	n/a	n/a
38	CTCF	chr5:80882540-80882690	AG10803	skin:	n/a	n/a
39	CTCF	chr5:80909420-80909570	MCF-7	breast:	n/a	chr5:80909499-80909515 chr5:80909498-80909516 chr5:80909493-80909514 chr5:80909503-80909511
40	CTCF	chr5:80909458-80909549	HUVEC	blood vessel:	n/a	chr5:80909499-80909515 chr5:80909498-80909516 chr5:80909493-80909514 chr5:80909503-80909511
41	CTCF	chr5:80948478-80948511	Pancreas_OC	pancreas:	n/a	n/a
42	CTCF	chr5:80909390-80909651	MCF-7	breast:	n/a	chr5:80909499-80909515 chr5:80909498-80909516 chr5:80909493-80909514 chr5:80909503-80909511
43	CTCF	chr5:80942620-80942770	NHLF	lung:	n/a	n/a
44	CTCF	chr5:80909460-80909610	BE2_C	brain:	n/a	chr5:80909499-80909515 chr5:80909498-80909516 chr5:80909493-80909514 chr5:80909503-80909511
45	CTCF	chr5:80909380-80909530	MCF-7	breast:	n/a	chr5:80909499-80909515 chr5:80909498-80909516 chr5:80909493-80909514 chr5:80909503-80909511
46	CTCF	chr5:80909480-80909630	RPTEC	kidney:	n/a	chr5:80909499-80909515 chr5:80909498-80909516 chr5:80909493-80909514 chr5:80909503-80909511
47	CTCF	chr5:80882560-80882710	HMF	breast:	n/a	n/a
48	CTCF	chr5:80909469-80909603	MCF-7	breast:	n/a	chr5:80909499-80909515 chr5:80909498-80909516 chr5:80909493-80909514 chr5:80909503-80909511
49	CTCF	chr5:80909380-80909530	HMEC	breast:	n/a	chr5:80909499-80909515 chr5:80909498-80909516 chr5:80909493-80909514 chr5:80909503-80909511
50	CTCF	chr5:80929560-80929710	HVMF	connective:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:80885936-80885986	AG04450	lung:	fetal
2	chr5:80922537-80922587	U87	brain:	n/a
3	chr5:80901358-80901408	HEK293	kidney:	embryo
4	chr5:80922537-80922587	BJ	skin:	n/a
5	chr5:80901358-80901408	CMK	blood:	n/a
6	chr5:80901358-80901408	BE2_C	brain:	n/a
7	chr5:80922537-80922587	HAEpiC	amniotic membrane:	n/a
8	chr5:80922537-80922587	PFSK-1	brain:	n/a
9	chr5:80901358-80901408	IMR90	lung:	fetal
10	chr5:80885936-80885986	Hela-S3	cervix:	n/a
11	chr5:80885936-80885986	GM06990	blood:	n/a
12	chr5:80922537-80922587	LNCaP	prostate:	n/a
13	chr5:80901358-80901408	HL-60	blood:	n/a
14	chr5:80885936-80885986	NHBE	bronchial:	n/a
15	chr5:80922537-80922587	HCM	heart:	n/a
16	chr5:80922537-80922587	ECC-1	luminal epithelium:	n/a
17	chr5:80885936-80885986	PrEC	prostate:	n/a
18	chr5:80885936-80885986	NHDF-neo	bronchial:	n/a
19	chr5:80922537-80922587	HCF	heart:	n/a
20	chr5:80901358-80901408	HCF	heart:	n/a
21	chr5:80885936-80885986	HNPCEpiC	eye:	n/a
22	chr5:80901358-80901408	Hepatocyte	liver:	n/a
23	chr5:80885936-80885986	AG09319	gingival:	n/a
24	chr5:80922537-80922587	HCPEpiC	choroid plexus:	n/a
25	chr5:80922537-80922587	AG04450	lung:	fetal
26	chr5:80922537-80922587	BE2_C	brain:	n/a
27	chr5:80885936-80885986	ECC-1	luminal epithelium:	n/a
28	chr5:80901358-80901408	GM12878	blood:	n/a
29	chr5:80922537-80922587	HCT-116	colon:	n/a
30	chr5:80901358-80901408	GM19239	blood:	n/a
31	chr5:80922537-80922587	CMK	blood:	n/a
32	chr5:80885936-80885986	HL-60	blood:	n/a
33	chr5:80901358-80901408	U87	brain:	n/a
34	chr5:80885936-80885986	HAEpiC	amniotic membrane:	n/a
35	chr5:80885936-80885986	HCPEpiC	choroid plexus:	n/a
36	chr5:80922537-80922587	HL-60	blood:	n/a
37	chr5:80885936-80885986	PANC-1	pancreas:	n/a
38	chr5:80901358-80901408	GM12892	blood:	n/a
39	chr5:80922537-80922587	NH-A	brain:	n/a
40	chr5:80901358-80901408	HepG2	liver:	n/a
41	chr5:80885936-80885986	HIPEpiC	eye:	n/a
42	chr5:80922537-80922587	Caco-2	colon:	n/a
43	chr5:80885936-80885986	HCT-116	colon:	n/a
44	chr5:80922537-80922587	HRPEpiC	eye:	n/a
45	chr5:80901358-80901408	AG09309	skin:	n/a
46	chr5:80885936-80885986	HRE	kidney:	n/a
47	chr5:80901358-80901408	PFSK-1	brain:	n/a
48	chr5:80922537-80922587	NB4	blood:	n/a
49	chr5:80901358-80901408	HRPEpiC	eye:	n/a
50	chr5:80922537-80922587	HRE	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:80940231..80942233-chr5:81040176..81042074,2	K562	blood:
2	chr5:80931196..80933943-chr5:80935625..80937292,2	K562	blood:
3	chr5:80937480..80940256-chr5:80940937..80944282,3	K562	blood:
4	chr5:80897320..80900374-chr5:80908175..80911251,3	K562	blood:
5	chr5:80937480..80940256-chr5:80940937..80944282,3	K562	blood:
6	chr5:80874625..80877374-chr5:81570400..81571959,2	K562	blood:
7	chr5:80934108..80935930-chr5:80938567..80940586,2	K562	blood:
8	chr5:80931139..80933943-chr5:80935605..80937292,2	K562	blood:
9	chr5:80961823..80964261-chr5:80965222..80967772,3	K562	blood:
10	chr5:80872758..80875728-chr5:80879949..80882376,2	K562	blood:
11	chr5:80897320..80900374-chr5:80908175..80911251,3	K562	blood:
12	chr5:80961632..80964415-chr5:80970591..80972149,2	MCF-7	breast:
13	chr5:80802649..80803453-chr5:80909108..80909743,2	MCF-7	breast:
14	chr5:80959308..80961024-chr5:81090290..81092398,2	K562	blood:
15	chr5:80895098..80897934-chr5:80899967..80903607,4	K562	blood:
16	chr5:80946322..80948172-chr5:80949841..80952303,2	K562	blood:
17	chr5:80900552..80902369-chr5:80906514..80908761,2	K562	blood:
18	chr5:80931139..80933943-chr5:80935605..80937292,2	K562	blood:
19	chr5:80870794..80873300-chr5:80875722..80877575,2	K562	blood:
20	chr5:80934108..80935930-chr5:80938567..80940586,2	K562	blood:
21	chr5:80931196..80933943-chr5:80935625..80937292,2	K562	blood:
22	chr5:80900552..80902369-chr5:80906514..80908761,2	K562	blood:
23	chr5:80895098..80897934-chr5:80899967..80903607,4	K562	blood:
24	chr5:80946322..80948172-chr5:80949841..80952303,2	K562	blood:

Variant related genes	Relation type
SSBP2	TF binding region
SSBP2	CpG island

Extended variants
information (count: 2922 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:2922 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2973347	chr5:80876359-80876360	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs11738820	chr5:80876411-80876412	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs561435429	chr5:80876431-80876432	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs192033541	chr5:80876485-80876486	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs184223156	chr5:80876486-80876487	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs57028565	chr5:80876503-80876504	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs34164327	chr5:80876551-80876552	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs10651788	chr5:80876569-80876570	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs35014014	chr5:80876570-80876571	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs397709936	chr5:80876583-80876584	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs201828490	chr5:80876585-80876586	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs539168082	chr5:80876608-80876609	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs73135614	chr5:80876623-80876624	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs569319396	chr5:80876651-80876652	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs538601489	chr5:80876726-80876727	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs537853250	chr5:80876760-80876761	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs201034872	chr5:80876768-80876769	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs190327342	chr5:80876829-80876830	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs75965742	chr5:80876859-80876860	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs181102404	chr5:80876867-80876868	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs534072997	chr5:80876872-80876873	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs553585319	chr5:80876980-80876981	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs576620741	chr5:80877077-80877078	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs545543645	chr5:80877092-80877093	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs115975383	chr5:80877103-80877104	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs114865043	chr5:80877104-80877105	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs74333930	chr5:80877116-80877117	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs79264116	chr5:80877138-80877139	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs540910361	chr5:80877142-80877143	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs184934910	chr5:80877184-80877185	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs141071982	chr5:80877187-80877188	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs146959021	chr5:80877217-80877218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs569261005	chr5:80877226-80877227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs531805140	chr5:80877253-80877254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs114836877	chr5:80877288-80877289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs189145237	chr5:80877289-80877290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs181075214	chr5:80877309-80877310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs553649271	chr5:80877334-80877335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs369715926	chr5:80877347-80877348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs186373341	chr5:80877374-80877375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs539259527	chr5:80877381-80877382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs190890406	chr5:80877465-80877466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs576075872	chr5:80877603-80877604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs181981241	chr5:80877613-80877614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs555100668	chr5:80877635-80877636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs186539032	chr5:80877716-80877717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs551850577	chr5:80877729-80877730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs540973723	chr5:80877759-80877760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs370342265	chr5:80877859-80877860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs191898124	chr5:80877895-80877896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

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
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	22032731	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Prostate cancer	21965145	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	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
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
Oral cancer	21386901	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	19602461	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	21251322	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Myelofibrosis	22110671	CNVD
craniofacial dysmorphism	21918468	CNVD
lymphocytic leukemia	21291569	CNVD
Lung cancer	16773561	CNVD
Multiple myeloma	16616336	CNVD
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Tetralogy of Fallot	22912587	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1297 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:80840800-80883400	Weak transcription	HSMM	muscle
2	chr5:80840800-80884600	Weak transcription	Ovary	ovary
3	chr5:80844200-80884600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr5:80846200-80880600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr5:80849000-80885600	Weak transcription	Left Ventricle	heart
6	chr5:80860200-80878800	Weak transcription	Esophagus	oesophagus
7	chr5:80862800-80878800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
8	chr5:80864200-80886400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr5:80864200-80894200	Weak transcription	Fetal Lung	lung
10	chr5:80864600-80894200	Weak transcription	Primary T helper cells fromperipheralblood	blood
11	chr5:80869400-80887600	Weak transcription	Fetal Stomach	stomach
12	chr5:80869800-80886400	Weak transcription	Thymus	Thymus
13	chr5:80870000-80887600	Weak transcription	Aorta	Aorta
14	chr5:80870600-80883000	Weak transcription	Fetal Thymus	thymus
15	chr5:80870600-80886600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
16	chr5:80870800-80894200	Weak transcription	Primary B cells from cord blood	blood
17	chr5:80871200-80876600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr5:80871400-80876400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr5:80875200-80876400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
20	chr5:80875400-80877200	Genic enhancers	Dnd41	blood
21	chr5:80875400-80880000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr5:80875600-80877000	Enhancers	Pancreatic Islets	Pancreatic Islet
23	chr5:80875600-80886800	Weak transcription	Brain Anterior Caudate	brain
24	chr5:80875600-80894000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr5:80875600-80894200	Weak transcription	GM12878-XiMat	blood
26	chr5:80876000-80877000	Weak transcription	Fetal Brain Female	brain
27	chr5:80876000-80878800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
28	chr5:80876000-80880200	Weak transcription	HUVEC	blood vessel
29	chr5:80876000-80880400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr5:80876000-80885600	Weak transcription	Primary T cells from cord blood	blood
31	chr5:80876000-80894200	Weak transcription	Cortex derived primary cultured neurospheres	brain
32	chr5:80876200-80876600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr5:80876200-80880200	Weak transcription	Primary hematopoietic stem cells	blood
34	chr5:80876400-80878800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr5:80876600-80877200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr5:80876600-80877200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr5:80876800-80877000	Enhancers	Primary T helper naive cells from peripheral blood	blood
38	chr5:80876800-80877200	Enhancers	Rectal Smooth Muscle	rectum
39	chr5:80877000-80877200	Enhancers	Fetal Brain Female	brain
40	chr5:80877000-80882600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
41	chr5:80877000-80884800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr5:80877200-80880000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr5:80877200-80881600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr5:80877200-80885800	Weak transcription	Dnd41	blood
45	chr5:80877400-80878000	Weak transcription	Rectal Smooth Muscle	rectum
46	chr5:80878800-80879000	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
47	chr5:80878800-80879000	ZNF genes & repeats	Esophagus	oesophagus
48	chr5:80878800-80879200	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr5:80879000-80887600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
50	chr5:80879200-80883200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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