Variant report

Variant	nsv1025259
Chromosome Location	chr5:99637293-99801104
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:580)
CpG islands
(count:490)
Chromatin interactive
region (count:5)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:580 , 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	BATF	chr5:99720609-99720839	GM12878	blood:	n/a	n/a
2	BATF	chr5:99684098-99684331	GM12878	blood:	n/a	n/a
3	BCLAF1	chr5:99765967-99766325	GM12878	blood:	n/a	n/a
4	BHLHE40	chr5:99766143-99766219	K562	blood:	n/a	n/a
5	CBX3	chr5:99722826-99723197	K562	blood:	n/a	n/a
6	CEBPB	chr5:99722893-99723094	K562	blood:	n/a	n/a
7	CEBPB	chr5:99725269-99725511	IMR90	lung:	n/a	chr5:99725330-99725341
8	CEBPB	chr5:99725233-99725508	A549	lung:	n/a	chr5:99725330-99725341
9	CEBPB	chr5:99784056-99784276	MCF-7	breast:	n/a	n/a
10	CEBPB	chr5:99725150-99725518	HepG2	liver:	n/a	chr5:99725330-99725341
11	CEBPB	chr5:99734563-99734858	K562	blood:	n/a	chr5:99734716-99734725 chr5:99734716-99734725 chr5:99734716-99734725 chr5:99734716-99734727 chr5:99734714-99734727 chr5:99734714-99734727 chr5:99734716-99734725
12	CEBPB	chr5:99784002-99784355	HepG2	liver:	n/a	n/a
13	CEBPB	chr5:99784028-99784357	ECC-1	luminal epithelium:	n/a	n/a
14	CEBPB	chr5:99784033-99784358	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr5:99725292-99725487	H1-hESC	embryonic stem cell:	n/a	chr5:99725330-99725341
16	CEBPB	chr5:99666989-99667301	IMR90	lung:	n/a	chr5:99667201-99667212 chr5:99667201-99667212
17	CEBPB	chr5:99722822-99723228	K562	blood:	n/a	n/a
18	CEBPD	chr5:99759761-99760095	K562	blood:	n/a	n/a
19	CREB1	chr5:99766039-99766253	A549	lung:	n/a	n/a
20	CTCF	chr5:99765990-99766372	K562	blood:	n/a	n/a
21	CTCF	chr5:99766120-99766270	GM12872	blood:	n/a	n/a
22	CTCF	chr5:99766100-99766250	HCT-116	colon:	n/a	n/a
23	CTCF	chr5:99766037-99766322	GM10266	blood:	n/a	n/a
24	CTCF	chr5:99766048-99766296	K562	blood:	n/a	n/a
25	CTCF	chr5:99766120-99766270	GM12878	blood:	n/a	n/a
26	CTCF	chr5:99766080-99766230	HVMF	connective:	n/a	n/a
27	CTCF	chr5:99766050-99766301	LNCaP	prostate:	n/a	n/a
28	CTCF	chr5:99706036-99706094	Spleen_OC	spleen:	n/a	n/a
29	CTCF	chr5:99697773-99697995	A549	lung:	n/a	n/a
30	CTCF	chr5:99691018-99691110	HepG2	liver:	n/a	n/a
31	CTCF	chr5:99766037-99766306	A549	lung:	n/a	n/a
32	CTCF	chr5:99647520-99647670	GM12872	blood:	n/a	n/a
33	CTCF	chr5:99715382-99715403	GM13976	blood:	n/a	n/a
34	CTCF	chr5:99647680-99647830	HCPEpiC	choroid plexus:	n/a	n/a
35	CTCF	chr5:99757340-99757490	HMEC	breast:	n/a	n/a
36	CTCF	chr5:99766100-99766250	SAEC	small airway:	n/a	n/a
37	CTCF	chr5:99741790-99741809	GM10248	blood:	n/a	n/a
38	CTCF	chr5:99766080-99766230	Caco-2	colon:	n/a	n/a
39	CTCF	chr5:99766046-99766290	MCF-7	breast:	n/a	n/a
40	CTCF	chr5:99647489-99648006	MCF-7	breast:	n/a	n/a
41	CTCF	chr5:99766068-99766264	SK-N-SH_RA	brain:	n/a	n/a
42	CTCF	chr5:99766057-99766351	HCT-116	colon:	n/a	n/a
43	CTCF	chr5:99766050-99766379	ECC-1	luminal epithelium:	n/a	n/a
44	CTCF	chr5:99695840-99695962	MCF-7	breast:	n/a	n/a
45	CTCF	chr5:99766026-99766332	Medullo	brain:	n/a	n/a
46	CTCF	chr5:99766120-99766270	HFF-Myc	foreskin:	n/a	n/a
47	CTCF	chr5:99698022-99698064	ProgFib	skin:	n/a	n/a
48	CTCF	chr5:99691016-99691115	Gliobla	brain:	n/a	n/a
49	CTCF	chr5:99765917-99766308	A549	lung:	n/a	n/a
50	CTCF	chr5:99647660-99647810	BE2_C	brain:	n/a	n/a

(count:490 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:99690406-99690456	BE2_C	brain:	n/a
2	chr5:99725277-99725327	AG10803	skin:	n/a
3	chr5:99690406-99690456	BE2_C	brain:	n/a
4	chr5:99725277-99725327	AG10803	skin:	n/a
5	chr5:99725058-99725108	HEEpiC	esophagus:	n/a
6	chr5:99690406-99690456	HNPCEpiC	eye:	n/a
7	chr5:99690406-99690456	Jurkat	blood:	n/a
8	chr5:99715943-99715993	BJ	skin:	n/a
9	chr5:99690406-99690456	LNCaP	prostate:	n/a
10	chr5:99725277-99725327	SKMC	muscle:	n/a
11	chr5:99690406-99690456	HCM	heart:	n/a
12	chr5:99725277-99725327	PrEC	prostate:	n/a
13	chr5:99690406-99690456	SKMC	muscle:	n/a
14	chr5:99723951-99724001	LNCaP	prostate:	n/a
15	chr5:99725376-99725426	Hela-S3	cervix:	n/a
16	chr5:99723987-99724037	PANC-1	pancreas:	n/a
17	chr5:99715943-99715993	HL-60	blood:	n/a
18	chr5:99715943-99715993	RPTEC	kidney:	n/a
19	chr5:99715943-99715993	Hepatocyte	liver:	n/a
20	chr5:99723987-99724037	NT2-D1	testis:	n/a
21	chr5:99723951-99724001	NB4	blood:	n/a
22	chr5:99723951-99724001	GM12878	blood:	n/a
23	chr5:99723951-99724001	A549	lung:	n/a
24	chr5:99723987-99724037	NHDF-neo	bronchial:	n/a
25	chr5:99726346-99726396	SK-N-SH	brain:	n/a
26	chr5:99725376-99725426	NH-A	brain:	n/a
27	chr5:99715943-99715993	SK-N-SH	brain:	n/a
28	chr5:99725277-99725327	SK-N-SH	brain:	n/a
29	chr5:99725376-99725426	ProgFib	skin:	n/a
30	chr5:99726346-99726396	HCT-116	colon:	n/a
31	chr5:99715943-99715993	MCF-7	breast:	n/a
32	chr5:99715943-99715993	ovcar-3	ovarian:	n/a
33	chr5:99725376-99725426	GM12891	blood:	n/a
34	chr5:99726346-99726396	T-47D	breast:	n/a
35	chr5:99726346-99726396	Jurkat	blood:	n/a
36	chr5:99723951-99724001	GM12891	blood:	n/a
37	chr5:99723951-99724001	HNPCEpiC	eye:	n/a
38	chr5:99723951-99724001	RPTEC	kidney:	n/a
39	chr5:99690406-99690456	HCF	heart:	n/a
40	chr5:99725058-99725108	BE2_C	brain:	n/a
41	chr5:99725376-99725426	HEEpiC	esophagus:	n/a
42	chr5:99725058-99725108	T-47D	breast:	n/a
43	chr5:99725058-99725108	MCF-7	breast:	n/a
44	chr5:99725058-99725108	NB4	blood:	n/a
45	chr5:99726346-99726396	SKMC	muscle:	n/a
46	chr5:99723987-99724037	NB4	blood:	n/a
47	chr5:99725277-99725327	AG09319	gingival:	n/a
48	chr5:99715943-99715993	HEEpiC	esophagus:	n/a
49	chr5:99726346-99726396	NB4	blood:	n/a
50	chr5:99725058-99725108	HCT-116	colon:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:99763910..99766552-chr5:99768110..99770337,2	MCF-7	breast:
2	chr4:32147186..32148048-chr5:99775915..99776706,2	MCF-7	breast:
3	chr5:99763910..99766552-chr5:99768110..99770337,2	MCF-7	breast:
4	chr5:98656230..98656989-chr5:99647221..99648200,3	MCF-7	breast:
5	chr5:98440068..98440810-chr5:99647288..99647935,2	MCF-7	breast:

(count:16 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ST8SIA4-3	chr5:99785458-99786801	NONHSAT103002
2	lnc-ST8SIA4-3	chr5:99792761-99792828	ENSG00000247877
3	lnc-FAM174A-1	chr5:99742959-99743077	XLOC_004490
4	lnc-FAM174A-1	chr5:99737145-99737487	XLOC_004490
5	lnc-FAM174A-1	chr5:99759095-99759158	NONHSAT103000
6	lnc-ST8SIA4-3	chr5:99786639-99786801	ENSG00000247877
7	lnc-FAM174A-1	chr5:99744503-99744603	XLOC_004490
8	lnc-FAM174A-1	chr5:99742959-99743077	XLOC_004490
9	lnc-FAM174A-1	chr5:99737164-99737487	XLOC_004490
10	lnc-FAM174A-1	chr5:99755954-99756452	XLOC_004490
11	lnc-ST8SIA4-3	chr5:99785458-99786801	ENSG00000247877
12	lnc-FAM174A-1	chr5:99755149-99755217	XLOC_004490
13	lnc-FAM174A-1	chr5:99742959-99743077	NONHSAT103000
14	lnc-FAM174A-1	chr5:99755149-99755217	NONHSAT103000
15	lnc-FAM174A-1	chr5:99755954-99756151	NONHSAT103000
16	lnc-FAM174A-1	chr5:99737280-99737487	NONHSAT103000

No data

Variant related genes	Relation type
ENSG00000249787	TF binding region
ENSG00000249787	CpG island
FAM81A	miRNA target sites
KIAA0430	miRNA target sites
RLF	miRNA target sites
DMD	miRNA target sites
TJAP1	miRNA target sites
EIF2B1	miRNA target sites
RTN4	miRNA target sites
PDPK1	miRNA target sites
FAM190B	miRNA target sites

Extended variants
information (count: 1817 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:1817 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs5869904	chr5:99637404-99637405	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs35187986	chr5:99637405-99637406	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs554782271	chr5:99637406-99637407	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs557954126	chr5:99637407-99637408	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs576209787	chr5:99637410-99637411	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs183794434	chr5:99637411-99637412	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs397881790	chr5:99637412-99637413	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs555776508	chr5:99637490-99637491	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs190297668	chr5:99637495-99637496	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs182523850	chr5:99637510-99637511	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs369391114	chr5:99637576-99637577	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs373066853	chr5:99637607-99637608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs559350965	chr5:99637615-99637616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs537520585	chr5:99637652-99637653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs1841982	chr5:99637690-99637691	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs150309342	chr5:99637725-99637726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs563500775	chr5:99637754-99637755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs568397064	chr5:99637763-99637764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs111747279	chr5:99637827-99637828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs560015589	chr5:99637829-99637830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs527257244	chr5:99637862-99637863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs1973172	chr5:99637888-99637889	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs372947591	chr5:99637913-99637914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs560628151	chr5:99637922-99637923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs185031942	chr5:99637934-99637935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs531346257	chr5:99637949-99637950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs201128085	chr5:99637999-99638000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs539998476	chr5:99638005-99638006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs543073120	chr5:99638008-99638009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs547405727	chr5:99638025-99638026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs1125289	chr5:99638041-99638042	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs557816690	chr5:99638088-99638089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs190320848	chr5:99638103-99638104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs115833	chr5:99638125-99638126	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs571309984	chr5:99638279-99638280	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs115380383	chr5:99638323-99638324	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs386690486	chr5:99638332-99638333	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs17146499	chr5:99638333-99638334	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs370446411	chr5:99638367-99638368	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs181082095	chr5:99638371-99638372	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs553025965	chr5:99638486-99638487	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs562725714	chr5:99638494-99638495	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs545157242	chr5:99638503-99638504	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs563361912	chr5:99638524-99638525	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs373779853	chr5:99638537-99638538	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs1820146	chr5:99638560-99638561	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs542458150	chr5:99638570-99638571	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs566001138	chr5:99638583-99638584	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs545170068	chr5:99638585-99638586	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs561093521	chr5:99638622-99638623	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

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	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
Lung cancer	18438408	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
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16774939	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	22286061	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Ovarian cancer	21720365	CNVD
Prostate cancer	16461572	CNVD
Neurocytoma	17123091	CNVD
Salivary gland tumor	18059337	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Bipolar disorder	19114987	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:109 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:99637400-99637600	Enhancers	Brain Germinal Matrix	brain
2	chr5:99637600-99638200	Weak transcription	Brain Germinal Matrix	brain
3	chr5:99638200-99639000	Enhancers	Brain Germinal Matrix	brain
4	chr5:99639000-99639400	Weak transcription	Brain Germinal Matrix	brain
5	chr5:99639400-99640800	Enhancers	Brain Germinal Matrix	brain
6	chr5:99641400-99642400	Enhancers	HUVEC	blood vessel
7	chr5:99641600-99642200	Enhancers	NHEK	skin
8	chr5:99641800-99642200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr5:99649000-99649800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr5:99649200-99649800	Enhancers	Monocytes-CD14+_RO01746	blood
11	chr5:99649200-99650000	Enhancers	Primary hematopoietic stem cells short term culture	blood
12	chr5:99649200-99650000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr5:99687600-99688000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr5:99696400-99696600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr5:99699800-99700000	Enhancers	Muscle Satellite Cultured Cells	--
16	chr5:99699800-99700400	Enhancers	A549	lung
17	chr5:99699800-99700400	Enhancers	NH-A	brain
18	chr5:99699800-99702000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr5:99700000-99700200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr5:99700000-99700200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
21	chr5:99700000-99700600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr5:99700200-99700400	Enhancers	Muscle Satellite Cultured Cells	--
23	chr5:99700200-99701000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr5:99700200-99701400	Enhancers	Osteobl	bone
25	chr5:99700400-99700600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
26	chr5:99700400-99700600	Flanking Active TSS	NH-A	brain
27	chr5:99700400-99701000	Enhancers	Fetal Lung	lung
28	chr5:99700400-99701200	Active TSS	A549	lung
29	chr5:99700600-99700800	Enhancers	Muscle Satellite Cultured Cells	--
30	chr5:99700600-99700800	Enhancers	NH-A	brain
31	chr5:99700800-99701000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
32	chr5:99700800-99701000	Flanking Active TSS	NH-A	brain
33	chr5:99701000-99701400	Enhancers	NH-A	brain
34	chr5:99701000-99702000	Enhancers	Muscle Satellite Cultured Cells	--
35	chr5:99701000-99702200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr5:99701200-99701400	Flanking Active TSS	A549	lung
37	chr5:99701800-99702200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr5:99734400-99734800	Active TSS	Monocytes-CD14+_RO01746	blood
39	chr5:99734400-99735400	Enhancers	Primary monocytes fromperipheralblood	blood
40	chr5:99736800-99738200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr5:99737000-99738000	Enhancers	Fetal Lung	lung
42	chr5:99737200-99738200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr5:99737400-99738000	Active TSS	Fetal Brain Male	brain
44	chr5:99738000-99738800	Weak transcription	Fetal Brain Male	brain
45	chr5:99738000-99740000	Weak transcription	Fetal Lung	lung
46	chr5:99738200-99739200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr5:99739200-99739400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr5:99740000-99740600	Enhancers	Fetal Lung	lung
49	chr5:99740200-99740800	Enhancers	Muscle Satellite Cultured Cells	--
50	chr5:99740400-99742200	Weak transcription	Fetal Brain Male	brain

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