Variant report

Variant	nsv882357
Chromosome Location	chr5:88677293-88774328
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:549)
CpG islands
(count:61)
Chromatin interactive
region (count:44)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:88714173-88714574	K562	blood:	n/a	n/a
2	ARID3A	chr5:88692310-88692798	K562	blood:	n/a	n/a
3	ATF1	chr5:88695469-88695597	K562	blood:	n/a	n/a
4	ATF1	chr5:88714293-88714771	K562	blood:	n/a	n/a
5	ATF1	chr5:88716866-88717066	K562	blood:	n/a	n/a
6	ATF1	chr5:88692448-88692733	K562	blood:	n/a	n/a
7	ATF1	chr5:88691926-88692160	K562	blood:	n/a	n/a
8	ATF2	chr5:88730926-88731620	GM12878	blood:	n/a	n/a
9	ATF2	chr5:88730620-88731813	GM12878	blood:	n/a	n/a
10	ATF2	chr5:88732128-88732729	GM12878	blood:	n/a	n/a
11	BATF	chr5:88695401-88695597	GM12878	blood:	n/a	n/a
12	BATF	chr5:88692957-88693208	GM12878	blood:	n/a	n/a
13	BATF	chr5:88692920-88693197	GM12878	blood:	n/a	n/a
14	BATF	chr5:88731147-88731486	GM12878	blood:	n/a	n/a
15	BCL11A	chr5:88731140-88731577	GM12878	blood:	n/a	n/a
16	BCL11A	chr5:88731260-88731519	GM12878	blood:	n/a	n/a
17	BCLAF1	chr5:88730910-88731633	GM12878	blood:	n/a	n/a
18	BCLAF1	chr5:88692020-88693049	GM12878	blood:	n/a	n/a
19	BCLAF1	chr5:88732210-88732758	GM12878	blood:	n/a	n/a
20	BCLAF1	chr5:88730916-88731534	GM12878	blood:	n/a	n/a
21	BHLHE40	chr5:88741099-88741470	K562	blood:	n/a	n/a
22	BHLHE40	chr5:88693055-88693246	GM12878	blood:	n/a	n/a
23	BHLHE40	chr5:88714304-88714598	K562	blood:	n/a	n/a
24	BHLHE40	chr5:88692508-88692720	GM12878	blood:	n/a	n/a
25	BHLHE40	chr5:88730913-88731709	GM12878	blood:	n/a	n/a
26	BRCA1	chr5:88753787-88754226	Hela-S3	cervix:	n/a	n/a
27	CBX3	chr5:88716768-88717192	HCT-116	colon:	n/a	n/a
28	CBX3	chr5:88692319-88692852	K562	blood:	n/a	n/a
29	CBX3	chr5:88713830-88714776	K562	blood:	n/a	n/a
30	CBX3	chr5:88753637-88754397	HCT-116	colon:	n/a	n/a
31	CCNT2	chr5:88714151-88714592	K562	blood:	n/a	n/a
32	CCNT2	chr5:88692477-88692745	K562	blood:	n/a	n/a
33	CEBPB	chr5:88749511-88749746	HepG2	liver:	n/a	chr5:88749608-88749619
34	CEBPB	chr5:88739924-88740262	IMR90	lung:	n/a	chr5:88740088-88740099 chr5:88740090-88740101
35	CEBPB	chr5:88692125-88692452	HepG2	liver:	n/a	chr5:88692273-88692284 chr5:88692272-88692285 chr5:88692274-88692283
36	CEBPB	chr5:88749568-88749650	A549	lung:	n/a	chr5:88749608-88749619
37	CEBPB	chr5:88736883-88737045	K562	blood:	n/a	n/a
38	CEBPB	chr5:88688333-88688463	A549	lung:	n/a	n/a
39	CEBPB	chr5:88714066-88714644	K562	blood:	n/a	n/a
40	CEBPB	chr5:88739908-88740272	K562	blood:	n/a	chr5:88740088-88740099 chr5:88740090-88740101
41	CEBPB	chr5:88739941-88740225	HepG2	liver:	n/a	chr5:88740088-88740099 chr5:88740090-88740101
42	CEBPB	chr5:88692079-88692825	K562	blood:	n/a	chr5:88692273-88692284 chr5:88692272-88692285 chr5:88692274-88692283
43	CEBPB	chr5:88753839-88754164	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr5:88714222-88714602	K562	blood:	n/a	n/a
45	CEBPB	chr5:88692088-88692470	IMR90	lung:	n/a	chr5:88692273-88692284 chr5:88692272-88692285 chr5:88692274-88692283
46	CEBPB	chr5:88692069-88692834	K562	blood:	n/a	chr5:88692273-88692284 chr5:88692272-88692285 chr5:88692274-88692283
47	CEBPB	chr5:88709695-88709705	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr5:88739974-88740255	A549	lung:	n/a	chr5:88740088-88740099 chr5:88740090-88740101
49	CEBPB	chr5:88740045-88740222	K562	blood:	n/a	chr5:88740088-88740099 chr5:88740090-88740101
50	CEBPB	chr5:88739924-88740310	K562	blood:	n/a	chr5:88740088-88740099 chr5:88740090-88740101

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:88743831-88743881	H1-hESC	embryonic stem cell:	embryo
2	chr5:88743831-88743881	LNCaP	prostate:	n/a
3	chr5:88743831-88743881	SAEC	small airway:	n/a
4	chr5:88743831-88743881	HPAEpiC	pulmonary alveolar:	n/a
5	chr5:88743831-88743881	SKMC	muscle:	n/a
6	chr5:88743831-88743881	Caco-2	colon:	n/a
7	chr5:88743831-88743881	ProgFib	skin:	n/a
8	chr5:88743831-88743881	BJ	skin:	n/a
9	chr5:88743831-88743881	NHDF-neo	bronchial:	n/a
10	chr5:88743831-88743881	NB4	blood:	n/a
11	chr5:88743831-88743881	NHBE	bronchial:	n/a
12	chr5:88743831-88743881	HNPCEpiC	eye:	n/a
13	chr5:88743831-88743881	HEK293	kidney:	embryo
14	chr5:88743831-88743881	AG10803	skin:	n/a
15	chr5:88743831-88743881	K562	blood:	n/a
16	chr5:88743831-88743881	AoSMC	blood vessel:	n/a
17	chr5:88743831-88743881	AG04450	lung:	fetal
18	chr5:88743831-88743881	Hela-S3	cervix:	n/a
19	chr5:88743831-88743881	PrEC	prostate:	n/a
20	chr5:88743831-88743881	SK-N-SH_RA	brain:	n/a
21	chr5:88743831-88743881	ECC-1	luminal epithelium:	n/a
22	chr5:88743831-88743881	MCF-7	breast:	n/a
23	chr5:88743831-88743881	Hepatocyte	liver:	n/a
24	chr5:88743831-88743881	HAEpiC	amniotic membrane:	n/a
25	chr5:88743831-88743881	HRCEpiC	kidney:	n/a
26	chr5:88743831-88743881	PFSK-1	brain:	n/a
27	chr5:88743831-88743881	AG09319	gingival:	n/a
28	chr5:88743831-88743881	HCF	heart:	n/a
29	chr5:88743831-88743881	GM12892	blood:	n/a
30	chr5:88743831-88743881	GM12878	blood:	n/a
31	chr5:88743831-88743881	RPTEC	kidney:	n/a
32	chr5:88743831-88743881	PANC-1	pancreas:	n/a
33	chr5:88743831-88743881	GM12891	blood:	n/a
34	chr5:88743831-88743881	GM19239	blood:	n/a
35	chr5:88743831-88743881	HCPEpiC	choroid plexus:	n/a
36	chr5:88743831-88743881	U87	brain:	n/a
37	chr5:88743831-88743881	HUVEC	blood vessel:	n/a
38	chr5:88743831-88743881	HRE	kidney:	n/a
39	chr5:88743831-88743881	HCT-116	colon:	n/a
40	chr5:88743831-88743881	HL-60	blood:	n/a
41	chr5:88743831-88743881	SK-N-SH	brain:	n/a
42	chr5:88743831-88743881	NH-A	brain:	n/a
43	chr5:88743831-88743881	ovcar-3	ovarian:	n/a
44	chr5:88743831-88743881	HCM	heart:	n/a
45	chr5:88743831-88743881	AG04449	skin:	fetal
46	chr5:88743831-88743881	GM06990	blood:	n/a
47	chr5:88743831-88743881	NT2-D1	testis:	n/a
48	chr5:88743831-88743881	MCF10A-Er-Src	breast:	n/a
49	chr5:88743831-88743881	T-47D	breast:	n/a
50	chr5:88743831-88743881	HepG2	liver:	n/a

(count:44 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:88735614..88737189-chr5:88739533..88741408,2	K562	blood:
2	chr5:88767316..88769071-chr5:88771619..88773249,2	K562	blood:
3	chr5:88674571..88676699-chr5:88688418..88689981,2	K562	blood:
4	chr5:88719926..88723053-chr5:88724997..88727412,3	K562	blood:
5	chr5:88735614..88737189-chr5:88739533..88741408,2	K562	blood:
6	chr5:88737623..88740179-chr5:88745152..88747035,3	K562	blood:
7	chr5:88682123..88685115-chr5:88685986..88688180,3	K562	blood:
8	chr5:88712499..88714282-chr5:88718036..88720039,2	K562	blood:
9	chr5:88694571..88697294-chr5:88699493..88701753,2	K562	blood:
10	chr5:88737623..88740179-chr5:88745152..88747035,3	K562	blood:
11	chr5:88719926..88723053-chr5:88724997..88727412,3	K562	blood:
12	chr5:88729730..88731957-chr5:88733593..88736207,3	K562	blood:
13	chr5:88241583..88243119-chr5:88682861..88684655,2	K562	blood:
14	chr5:88730457..88733389-chr5:88733593..88735953,2	K562	blood:
15	chr5:88756505..88760313-chr5:88761840..88765543,4	K562	blood:
16	chr5:88729730..88731957-chr5:88733593..88736207,3	K562	blood:
17	chr5:88682123..88685115-chr5:88685986..88688180,3	K562	blood:
18	chr5:88666552..88668277-chr5:88674891..88677318,2	K562	blood:
19	chr5:88689648..88692385-chr5:88695321..88697768,2	MCF-7	breast:
20	chr5:88689648..88692385-chr5:88695321..88697768,2	MCF-7	breast:
21	chr5:88678895..88681771-chr5:88690608..88693401,2	K562	blood:
22	chr5:88745543..88747237-chr5:88748817..88750936,2	K562	blood:
23	chr5:88685101..88686656-chr5:88688204..88690615,2	K562	blood:
24	chr5:88712499..88714282-chr5:88718036..88720039,2	K562	blood:
25	chr5:88745543..88747237-chr5:88748817..88750936,2	K562	blood:
26	chr5:88735614..88738275-chr5:88739232..88742098,4	K562	blood:
27	chr5:88718329..88721031-chr5:88729691..88731199,2	K562	blood:
28	chr5:88690770..88693915-chr5:88701829..88704519,3	K562	blood:
29	chr5:88682304..88683982-chr5:88687712..88689947,2	MCF-7	breast:
30	chr5:88756505..88760313-chr5:88761840..88765543,4	K562	blood:
31	chr5:88767316..88769071-chr5:88771619..88773249,2	K562	blood:
32	chr5:88678895..88681771-chr5:88690608..88693401,2	K562	blood:
33	chr5:88685101..88686656-chr5:88688204..88690615,2	K562	blood:
34	chr5:88682304..88683982-chr5:88687712..88689947,2	MCF-7	breast:
35	chr5:88742180..88743903-chr5:88752684..88754964,2	K562	blood:
36	chr5:88690770..88693915-chr5:88701829..88704519,3	K562	blood:
37	chr5:88718329..88721031-chr5:88729691..88731199,2	K562	blood:
38	chr5:88694571..88697294-chr5:88699493..88701753,2	K562	blood:
39	chr5:88687703..88689475-chr5:88693463..88695074,2	MCF-7	breast:
40	chr5:88730457..88733389-chr5:88733593..88735953,2	K562	blood:
41	chr5:88742180..88743903-chr5:88752684..88754964,2	K562	blood:
42	chr5:88735614..88738275-chr5:88739232..88742098,4	K562	blood:
43	chr5:88687703..88689475-chr5:88693463..88695074,2	MCF-7	breast:
44	chr5:88703848..88705592-chr5:88713136..88714824,2	K562	blood:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RASA1-7	chr5:88761733-88761799	ENSG00000248309
2	lnc-RASA1-7	chr5:88751921-88751947	NONHSAT102714
3	lnc-RASA1-7	chr5:88761483-88761592	ENSG00000248309
4	lnc-RASA1-7	chr5:88708856-88708935	l_2966_chr5:88236262-88274788_thyroid
5	lnc-RASA1-7	chr5:88761733-88761925	NONHSAT102714
6	lnc-RASA1-7	chr5:88761733-88762215	ENSG00000248309
7	lnc-RASA1-7	chr5:88761483-88761592	NONHSAT102714
8	lnc-MEF2C-4	chr5:88762354-88762488	XLOC_004920
9	lnc-MEF2C-4	chr5:88765739-88765856	XLOC_004920
10	lnc-RASA1-7	chr5:88761483-88761592	ENSG00000248309
11	lnc-RASA1-7	chr5:88714624-88714709	ENSG00000248309

No data

Variant related genes	Relation type
MEF2C-AS1	TF binding region
ENSG00000250831	TF binding region
MEF2C-AS1	CpG island
ENSG00000250831	CpG island
ENSG00000248309	chromatin interactions
TRPC3	miRNA target sites
MAPK1	miRNA target sites
CD276	miRNA target sites
CDKN1C	miRNA target sites
CDKN1A	miRNA target sites

Extended variants
information (count: 2265 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:2265 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs539461653	chr5:88678209-88678210	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs576479641	chr5:88678230-88678231	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs116486915	chr5:88678279-88678280	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs150574221	chr5:88678307-88678308	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs572976270	chr5:88678320-88678321	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs113212322	chr5:88678323-88678324	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs561877573	chr5:88678357-88678358	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs247585	chr5:88678420-88678421	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs192479755	chr5:88678440-88678441	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs183900577	chr5:88678474-88678475	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs139609562	chr5:88678493-88678494	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs149753971	chr5:88678495-88678496	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs560075074	chr5:88678500-88678501	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs529363562	chr5:88678507-88678508	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs549038198	chr5:88678557-88678558	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs186790650	chr5:88678579-88678580	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs180675082	chr5:88679804-88679805	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs71629716	chr5:88679825-88679826	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs562494750	chr5:88679832-88679833	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs552037555	chr5:88679838-88679839	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs568840185	chr5:88679886-88679887	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs531840145	chr5:88679889-88679890	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs141322362	chr5:88679946-88679947	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs565494404	chr5:88679961-88679962	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs537773728	chr5:88679975-88679976	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs527907461	chr5:88680004-88680005	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs374806918	chr5:88680013-88680014	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs369629208	chr5:88680034-88680035	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs547993945	chr5:88680035-88680036	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs142392416	chr5:88680081-88680082	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs367826088	chr5:88680095-88680096	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs530412404	chr5:88680127-88680128	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs549009357	chr5:88680163-88680164	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs151309503	chr5:88680165-88680166	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs537968393	chr5:88680214-88680215	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs35242886	chr5:88680230-88680231	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs186450287	chr5:88680236-88680237	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs372343599	chr5:88680265-88680266	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs568172797	chr5:88680283-88680284	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs372052558	chr5:88680295-88680296	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs571307280	chr5:88680300-88680301	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs398065017	chr5:88680303-88680304	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs533789252	chr5:88680313-88680314	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs542890628	chr5:88680314-88680315	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs553550241	chr5:88680326-88680327	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs34735489	chr5:88680332-88680333	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs191277813	chr5:88680391-88680392	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs536099768	chr5:88680393-88680394	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs183568211	chr5:88680411-88680412	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs576327674	chr5:88680447-88680448	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

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
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	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
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	17053054	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	19592390	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Mental retardation	19471318	CNVD
Colorectal cancer	16774939	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	21339820	CNVD

Chromatin state (count:457 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:88678200-88678600	Enhancers	HUVEC	blood vessel
2	chr5:88679800-88680600	Enhancers	Monocytes-CD14+_RO01746	blood
3	chr5:88680000-88680600	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr5:88680200-88680800	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr5:88684800-88685200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr5:88687000-88692400	Weak transcription	Aorta	Aorta
7	chr5:88689800-88691600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr5:88689800-88691800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr5:88689800-88692000	Enhancers	Primary neutrophils fromperipheralblood	blood
10	chr5:88689800-88692400	Enhancers	Primary hematopoietic stem cells	blood
11	chr5:88689800-88693600	Enhancers	Primary monocytes fromperipheralblood	blood
12	chr5:88690000-88690800	Enhancers	Monocytes-CD14+_RO01746	blood
13	chr5:88690000-88691800	Enhancers	Primary T cells from cord blood	blood
14	chr5:88690000-88691800	Enhancers	Primary hematopoietic stem cells short term culture	blood
15	chr5:88690000-88693600	Enhancers	Primary B cells from peripheral blood	blood
16	chr5:88690400-88692000	Enhancers	Primary B cells from cord blood	blood
17	chr5:88690800-88693600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
18	chr5:88691600-88692000	Enhancers	GM12878-XiMat	blood
19	chr5:88691600-88692400	Enhancers	K562	blood
20	chr5:88691600-88693000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr5:88691600-88693600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr5:88691800-88692000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr5:88691800-88692400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr5:88691800-88692400	Enhancers	NHDF-Ad	bronchial
25	chr5:88691800-88692600	Flanking Active TSS	Primary T cells from cord blood	blood
26	chr5:88691800-88692800	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
27	chr5:88691800-88693200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr5:88692000-88692400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr5:88692000-88692400	Enhancers	Osteobl	bone
30	chr5:88692000-88692600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
31	chr5:88692000-88692600	Enhancers	Adipose Nuclei	Adipose
32	chr5:88692000-88692600	Enhancers	Liver	Liver
33	chr5:88692000-88692800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr5:88692000-88692800	Flanking Active TSS	Primary B cells from cord blood	blood
35	chr5:88692000-88693200	Flanking Active TSS	GM12878-XiMat	blood
36	chr5:88692200-88692600	Enhancers	HUES6 Cell Line	embryonic stem cell
37	chr5:88692200-88692600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr5:88692200-88692800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr5:88692200-88693200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr5:88692200-88693200	Enhancers	Muscle Satellite Cultured Cells	--
41	chr5:88692200-88693400	Enhancers	Sigmoid Colon	Sigmoid Colon
42	chr5:88692400-88692600	Enhancers	Aorta	Aorta
43	chr5:88692400-88692600	Flanking Active TSS	K562	blood
44	chr5:88692400-88692800	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr5:88692400-88692800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr5:88692400-88692800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr5:88692400-88692800	Enhancers	Fetal Intestine Large	intestine
48	chr5:88692400-88692800	Enhancers	Right Atrium	heart
49	chr5:88692400-88692800	Active TSS	Stomach Smooth Muscle	stomach
50	chr5:88692400-88692800	Flanking Active TSS	NHDF-Ad	bronchial

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