Variant report

Variant	nsv882359
Chromosome Location	chr5:88710519-88785384
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:460)
CpG islands
(count:61)
Chromatin interactive
region (count:25)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:460 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

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	ATF1	chr5:88714293-88714771	K562	blood:	n/a	n/a
3	ATF1	chr5:88716866-88717066	K562	blood:	n/a	n/a
4	ATF2	chr5:88730620-88731813	GM12878	blood:	n/a	n/a
5	ATF2	chr5:88730926-88731620	GM12878	blood:	n/a	n/a
6	ATF2	chr5:88732128-88732729	GM12878	blood:	n/a	n/a
7	BATF	chr5:88731147-88731486	GM12878	blood:	n/a	n/a
8	BCL11A	chr5:88731140-88731577	GM12878	blood:	n/a	n/a
9	BCL11A	chr5:88731260-88731519	GM12878	blood:	n/a	n/a
10	BCLAF1	chr5:88730910-88731633	GM12878	blood:	n/a	n/a
11	BCLAF1	chr5:88730916-88731534	GM12878	blood:	n/a	n/a
12	BCLAF1	chr5:88732210-88732758	GM12878	blood:	n/a	n/a
13	BHLHE40	chr5:88730913-88731709	GM12878	blood:	n/a	n/a
14	BHLHE40	chr5:88741099-88741470	K562	blood:	n/a	n/a
15	BHLHE40	chr5:88714304-88714598	K562	blood:	n/a	n/a
16	BRCA1	chr5:88753787-88754226	Hela-S3	cervix:	n/a	n/a
17	CBX3	chr5:88713830-88714776	K562	blood:	n/a	n/a
18	CBX3	chr5:88753637-88754397	HCT-116	colon:	n/a	n/a
19	CBX3	chr5:88716768-88717192	HCT-116	colon:	n/a	n/a
20	CCNT2	chr5:88714151-88714592	K562	blood:	n/a	n/a
21	CEBPB	chr5:88740045-88740222	K562	blood:	n/a	chr5:88740088-88740099 chr5:88740090-88740101
22	CEBPB	chr5:88739924-88740262	IMR90	lung:	n/a	chr5:88740088-88740099 chr5:88740090-88740101
23	CEBPB	chr5:88739941-88740225	HepG2	liver:	n/a	chr5:88740088-88740099 chr5:88740090-88740101
24	CEBPB	chr5:88781938-88782238	HepG2	liver:	n/a	n/a
25	CEBPB	chr5:88739908-88740272	K562	blood:	n/a	chr5:88740088-88740099 chr5:88740090-88740101
26	CEBPB	chr5:88714066-88714644	K562	blood:	n/a	n/a
27	CEBPB	chr5:88739974-88740255	A549	lung:	n/a	chr5:88740088-88740099 chr5:88740090-88740101
28	CEBPB	chr5:88739924-88740310	K562	blood:	n/a	chr5:88740088-88740099 chr5:88740090-88740101
29	CEBPB	chr5:88749568-88749650	A549	lung:	n/a	chr5:88749608-88749619
30	CEBPB	chr5:88714222-88714602	K562	blood:	n/a	n/a
31	CEBPB	chr5:88749511-88749746	HepG2	liver:	n/a	chr5:88749608-88749619
32	CEBPB	chr5:88736883-88737045	K562	blood:	n/a	n/a
33	CEBPB	chr5:88753839-88754164	Hela-S3	cervix:	n/a	n/a
34	CEBPD	chr5:88714013-88714583	K562	blood:	n/a	n/a
35	CEBPD	chr5:88714043-88714621	K562	blood:	n/a	n/a
36	CHD1	chr5:88733655-88733656	GM12878	blood:	n/a	n/a
37	CHD2	chr5:88731138-88731580	GM12878	blood:	n/a	n/a
38	CHD2	chr5:88729725-88729727	GM12878	blood:	n/a	n/a
39	CHD2	chr5:88753889-88754125	Hela-S3	cervix:	n/a	n/a
40	CREB1	chr5:88714108-88714606	K562	blood:	n/a	n/a
41	CTCF	chr5:88728840-88728990	GM12873	blood:	n/a	n/a
42	CTCF	chr5:88713967-88714074	ProgFib	skin:	n/a	n/a
43	CTCF	chr5:88713895-88714085	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr5:88713940-88714090	SK-N-SH_RA	brain:	n/a	n/a
45	CTCF	chr5:88713752-88714143	K562	blood:	n/a	n/a
46	CTCF	chr5:88713920-88714070	HCPEpiC	choroid plexus:	n/a	n/a
47	CTCF	chr5:88785217-88785237	GM20000	blood:	n/a	n/a
48	CTCF	chr5:88713940-88714090	HMEC	breast:	n/a	n/a
49	CTCF	chr5:88713900-88714050	MCF-7	breast:	n/a	n/a
50	CTCF	chr5:88713920-88714070	WERI-Rb-1	eye:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:88743831-88743881	HRPEpiC	eye:	n/a
2	chr5:88743831-88743881	H1-hESC	embryonic stem cell:	embryo
3	chr5:88743831-88743881	BJ	skin:	n/a
4	chr5:88743831-88743881	HCM	heart:	n/a
5	chr5:88743831-88743881	HRE	kidney:	n/a
6	chr5:88743831-88743881	SK-N-SH	brain:	n/a
7	chr5:88743831-88743881	HCF	heart:	n/a
8	chr5:88743831-88743881	ProgFib	skin:	n/a
9	chr5:88743831-88743881	GM12891	blood:	n/a
10	chr5:88743831-88743881	Hepatocyte	liver:	n/a
11	chr5:88743831-88743881	Caco-2	colon:	n/a
12	chr5:88743831-88743881	ovcar-3	ovarian:	n/a
13	chr5:88743831-88743881	NT2-D1	testis:	n/a
14	chr5:88743831-88743881	AG04449	skin:	fetal
15	chr5:88743831-88743881	HPAEpiC	pulmonary alveolar:	n/a
16	chr5:88743831-88743881	AoSMC	blood vessel:	n/a
17	chr5:88743831-88743881	PrEC	prostate:	n/a
18	chr5:88743831-88743881	SK-N-SH_RA	brain:	n/a
19	chr5:88743831-88743881	HMEC	breast:	n/a
20	chr5:88743831-88743881	NH-A	brain:	n/a
21	chr5:88743831-88743881	NHDF-neo	bronchial:	n/a
22	chr5:88743831-88743881	AG09309	skin:	n/a
23	chr5:88743831-88743881	MCF-7	breast:	n/a
24	chr5:88743831-88743881	LNCaP	prostate:	n/a
25	chr5:88743831-88743881	MCF10A-Er-Src	breast:	n/a
26	chr5:88743831-88743881	CMK	blood:	n/a
27	chr5:88743831-88743881	K562	blood:	n/a
28	chr5:88743831-88743881	PANC-1	pancreas:	n/a
29	chr5:88743831-88743881	SK-N-MC	brain:	n/a
30	chr5:88743831-88743881	RPTEC	kidney:	n/a
31	chr5:88743831-88743881	T-47D	breast:	n/a
32	chr5:88743831-88743881	AG09319	gingival:	n/a
33	chr5:88743831-88743881	A549	lung:	n/a
34	chr5:88743831-88743881	HL-60	blood:	n/a
35	chr5:88743831-88743881	ECC-1	luminal epithelium:	n/a
36	chr5:88743831-88743881	GM06990	blood:	n/a
37	chr5:88743831-88743881	NHBE	bronchial:	n/a
38	chr5:88743831-88743881	IMR90	lung:	fetal
39	chr5:88743831-88743881	HepG2	liver:	n/a
40	chr5:88743831-88743881	GM12878	blood:	n/a
41	chr5:88743831-88743881	AG04450	lung:	fetal
42	chr5:88743831-88743881	HCT-116	colon:	n/a
43	chr5:88743831-88743881	HNPCEpiC	eye:	n/a
44	chr5:88743831-88743881	AG10803	skin:	n/a
45	chr5:88743831-88743881	HAEpiC	amniotic membrane:	n/a
46	chr5:88743831-88743881	U87	brain:	n/a
47	chr5:88743831-88743881	HIPEpiC	eye:	n/a
48	chr5:88743831-88743881	HUVEC	blood vessel:	n/a
49	chr5:88743831-88743881	GM12892	blood:	n/a
50	chr5:88743831-88743881	HCPEpiC	choroid plexus:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:88730457..88733389-chr5:88733593..88735953,2	K562	blood:
2	chr5:88745543..88747237-chr5:88748817..88750936,2	K562	blood:
3	chr5:88756505..88760313-chr5:88761840..88765543,4	K562	blood:
4	chr5:88745543..88747237-chr5:88748817..88750936,2	K562	blood:
5	chr5:88735614..88737189-chr5:88739533..88741408,2	K562	blood:
6	chr5:88718329..88721031-chr5:88729691..88731199,2	K562	blood:
7	chr5:88719926..88723053-chr5:88724997..88727412,3	K562	blood:
8	chr5:88735614..88738275-chr5:88739232..88742098,4	K562	blood:
9	chr5:88767316..88769071-chr5:88771619..88773249,2	K562	blood:
10	chr5:88729730..88731957-chr5:88733593..88736207,3	K562	blood:
11	chr5:88742180..88743903-chr5:88752684..88754964,2	K562	blood:
12	chr5:88742180..88743903-chr5:88752684..88754964,2	K562	blood:
13	chr5:88729730..88731957-chr5:88733593..88736207,3	K562	blood:
14	chr5:88781201..88784356-chr5:88786376..88788302,3	K562	blood:
15	chr5:88737623..88740179-chr5:88745152..88747035,3	K562	blood:
16	chr5:88737623..88740179-chr5:88745152..88747035,3	K562	blood:
17	chr5:88712499..88714282-chr5:88718036..88720039,2	K562	blood:
18	chr5:88756505..88760313-chr5:88761840..88765543,4	K562	blood:
19	chr5:88767316..88769071-chr5:88771619..88773249,2	K562	blood:
20	chr5:88730457..88733389-chr5:88733593..88735953,2	K562	blood:
21	chr5:88718329..88721031-chr5:88729691..88731199,2	K562	blood:
22	chr5:88719926..88723053-chr5:88724997..88727412,3	K562	blood:
23	chr5:88712499..88714282-chr5:88718036..88720039,2	K562	blood:
24	chr5:88735614..88738275-chr5:88739232..88742098,4	K562	blood:
25	chr5:88735614..88737189-chr5:88739533..88741408,2	K562	blood:

(count:10 , 50 per page) page: 1

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

No data

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

Extended variants
information (count: 1978 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:1978 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs529042127	chr5:88710710-88710711	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs548909428	chr5:88710800-88710801	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs560790683	chr5:88710908-88710909	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs247558	chr5:88710913-88710914	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs112475875	chr5:88710981-88710982	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs247559	chr5:88711071-88711072	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs571732037	chr5:88711108-88711109	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs186845456	chr5:88711151-88711152	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs139796798	chr5:88711154-88711155	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs149245195	chr5:88711188-88711189	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs144472650	chr5:88711197-88711198	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs556897927	chr5:88711233-88711234	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs374395869	chr5:88711259-88711260	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs114902980	chr5:88713423-88713424	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs374652425	chr5:88713459-88713460	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs200762497	chr5:88713489-88713490	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs555988389	chr5:88713519-88713520	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs247554	chr5:88713564-88713565	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs538470630	chr5:88713586-88713587	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs529818813	chr5:88713588-88713589	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs546154101	chr5:88713629-88713630	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs149172924	chr5:88713657-88713658	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs541371436	chr5:88713723-88713724	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs539147810	chr5:88713777-88713778	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs566141044	chr5:88713791-88713792	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs574936607	chr5:88713858-88713859	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs543756065	chr5:88713869-88713870	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs375787311	chr5:88713878-88713879	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs553965066	chr5:88713895-88713896	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs563642755	chr5:88713902-88713903	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs116669396	chr5:88713903-88713904	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs207466223	chr5:88713931-88713932	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs79503690	chr5:88713933-88713934	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs552100424	chr5:88713939-88713940	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs145101866	chr5:88713957-88713958	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs569025420	chr5:88713980-88713981	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs528649077	chr5:88714038-88714039	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs548515814	chr5:88714045-88714046	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs568366918	chr5:88714046-88714047	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs535878233	chr5:88714075-88714076	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs370330015	chr5:88714095-88714096	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs185999935	chr5:88714117-88714118	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs569671537	chr5:88714143-88714144	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs538755029	chr5:88714144-88714145	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs558671225	chr5:88714145-88714146	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs537681331	chr5:88714149-88714150	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs375110000	chr5:88714158-88714159	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs138934638	chr5:88714175-88714176	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs367992123	chr5:88714191-88714192	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs140674347	chr5:88714214-88714215	Enhancers	TF binding region	1 gene(s)	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:359 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:88713400-88717600	Enhancers	Primary neutrophils fromperipheralblood	blood
2	chr5:88713600-88715000	Enhancers	K562	blood
3	chr5:88713800-88714800	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr5:88714400-88715200	Enhancers	Monocytes-CD14+_RO01746	blood
5	chr5:88714600-88714800	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr5:88714600-88714800	Enhancers	Fetal Intestine Large	intestine
7	chr5:88714800-88715000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr5:88714800-88715000	Enhancers	Hela-S3	cervix
9	chr5:88714800-88715800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
10	chr5:88714800-88715800	Weak transcription	Fetal Intestine Large	intestine
11	chr5:88714800-88716400	Weak transcription	Primary monocytes fromperipheralblood	blood
12	chr5:88715000-88715800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr5:88715000-88717000	Weak transcription	K562	blood
14	chr5:88715200-88716400	Weak transcription	Hela-S3	cervix
15	chr5:88715200-88716400	Weak transcription	Monocytes-CD14+_RO01746	blood
16	chr5:88715400-88717600	Enhancers	Breast Myoepithelial Primary Cells	Breast
17	chr5:88715600-88717200	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr5:88715800-88716600	Enhancers	Fetal Intestine Large	intestine
19	chr5:88715800-88717200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr5:88715800-88717200	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr5:88715800-88717200	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr5:88716200-88716600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr5:88716200-88716800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
24	chr5:88716400-88716600	Enhancers	Monocytes-CD14+_RO01746	blood
25	chr5:88716400-88717000	Enhancers	iPS-20b Cell Line	embryonic stem cell
26	chr5:88716400-88717400	Enhancers	Primary B cells from cord blood	blood
27	chr5:88716400-88717400	Enhancers	HUVEC	blood vessel
28	chr5:88716400-88717600	Enhancers	Primary monocytes fromperipheralblood	blood
29	chr5:88716400-88717600	Enhancers	Fetal Intestine Small	intestine
30	chr5:88716400-88717600	Enhancers	Hela-S3	cervix
31	chr5:88716600-88717200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr5:88716600-88717400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr5:88716600-88717400	Weak transcription	Fetal Intestine Large	intestine
34	chr5:88716600-88717400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
35	chr5:88716800-88717200	Enhancers	Muscle Satellite Cultured Cells	--
36	chr5:88716800-88717200	Enhancers	NH-A	brain
37	chr5:88716800-88717200	Enhancers	NHDF-Ad	bronchial
38	chr5:88716800-88717400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr5:88716800-88717400	Enhancers	Pancreatic Islets	Pancreatic Islet
40	chr5:88716800-88717600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr5:88716800-88717600	Enhancers	Rectal Mucosa Donor 31	rectum
42	chr5:88717000-88717200	Enhancers	Primary hematopoietic stem cells	blood
43	chr5:88717000-88717400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr5:88717000-88717400	Enhancers	Duodenum Mucosa	Duodenum
45	chr5:88717000-88717600	Enhancers	Primary B cells from peripheral blood	blood
46	chr5:88717000-88717600	Enhancers	Primary hematopoietic stem cells short term culture	blood
47	chr5:88717400-88717600	Enhancers	Fetal Intestine Large	intestine
48	chr5:88717400-88717600	Enhancers	Monocytes-CD14+_RO01746	blood
49	chr5:88720200-88721600	Enhancers	Primary T cells from cord blood	blood
50	chr5:88723200-88730000	Weak transcription	Primary B cells from cord blood	blood

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