Variant report

Variant	nsv462479
Chromosome Location	chr5:147648510-147688035
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:359)
CpG islands
(count:123)
Chromatin interactive
region (count:21)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:359 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr5:147656764-147656871	K562	blood:	n/a	n/a
2	CEBPB	chr5:147671442-147671605	K562	blood:	n/a	n/a
3	CEBPB	chr5:147670204-147670441	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr5:147669913-147670425	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr5:147648168-147648542	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr5:147677446-147677624	Hela-S3	cervix:	n/a	n/a
7	CHD2	chr5:147660593-147660796	GM12878	blood:	n/a	n/a
8	CTCF	chr5:147670220-147670370	HRE	kidney:	n/a	n/a
9	CTCF	chr5:147670220-147670370	GM12872	blood:	n/a	n/a
10	CTCF	chr5:147686160-147686310	NHEK	skin:	n/a	chr5:147686201-147686219
11	CTCF	chr5:147669993-147670049	Gliobla	brain:	n/a	n/a
12	CTCF	chr5:147686167-147686263	K562	blood:	n/a	chr5:147686201-147686219
13	CTCF	chr5:147686120-147686270	HVMF	connective:	n/a	chr5:147686201-147686219
14	CTCF	chr5:147670211-147670451	Medullo	brain:	n/a	n/a
15	CTCF	chr5:147670220-147670370	HepG2	liver:	n/a	n/a
16	CTCF	chr5:147669880-147670030	HPF	lung:	n/a	n/a
17	CTCF	chr5:147677410-147677587	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTCF	chr5:147686180-147686330	HAc	cerebellar:	n/a	chr5:147686201-147686219
19	CTCF	chr5:147670260-147670410	HRPEpiC	eye:	n/a	n/a
20	CTCF	chr5:147670280-147670430	HEK293	kidney:	n/a	n/a
21	CTCF	chr5:147670300-147670450	BJ	skin:	n/a	n/a
22	CTCF	chr5:147670240-147670390	HPF	lung:	n/a	n/a
23	CTCF	chr5:147670220-147670370	GM12870	blood:	n/a	n/a
24	CTCF	chr5:147677420-147677570	NHEK	skin:	n/a	n/a
25	CTCF	chr5:147686047-147686371	GM12878	blood:	n/a	chr5:147686201-147686219
26	CTCF	chr5:147670220-147670370	HEEpiC	esophagus:	n/a	n/a
27	CTCF	chr5:147670216-147670531	T-47D	breast:	n/a	n/a
28	CTCF	chr5:147670260-147670410	HA-sp	spinal cord:	n/a	n/a
29	CTCF	chr5:147677512-147677562	NHEK	skin:	n/a	n/a
30	CTCF	chr5:147670220-147670370	NHDF-neo	bronchial:	n/a	n/a
31	CTCF	chr5:147670086-147670608	MCF-7	breast:	n/a	n/a
32	CTCF	chr5:147670269-147670428	ProgFib	skin:	n/a	n/a
33	CTCF	chr5:147670340-147670490	HCPEpiC	choroid plexus:	n/a	n/a
34	CTCF	chr5:147669993-147670059	MCF-7	breast:	n/a	n/a
35	CTCF	chr5:147670194-147670562	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr5:147669971-147670091	ProgFib	skin:	n/a	n/a
37	CTCF	chr5:147670260-147670410	AoAF	blood vessel:	n/a	n/a
38	CTCF	chr5:147670167-147670511	K562	blood:	n/a	n/a
39	CTCF	chr5:147670140-147670290	GM12870	blood:	n/a	n/a
40	CTCF	chr5:147686078-147686326	MCF-7	breast:	n/a	chr5:147686201-147686219
41	CTCF	chr5:147686131-147686273	LNCaP	prostate:	n/a	chr5:147686201-147686219
42	CTCF	chr5:147669974-147670746	SK-N-SH	brain:	n/a	n/a
43	CTCF	chr5:147670160-147670310	HVMF	connective:	n/a	n/a
44	CTCF	chr5:147686100-147686250	HepG2	liver:	n/a	chr5:147686201-147686219
45	CTCF	chr5:147685780-147685930	GM12864	blood:	n/a	n/a
46	CTCF	chr5:147670240-147670390	HL-60	blood:	n/a	n/a
47	CTCF	chr5:147670240-147670390	HPAF	blood vessel:	n/a	n/a
48	CTCF	chr5:147670260-147670410	HBMEC	blood vessel:	n/a	n/a
49	CTCF	chr5:147686114-147686284	MCF-7	breast:	n/a	chr5:147686201-147686219
50	CTCF	chr5:147670240-147670390	GM12866	blood:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:147648492-147648542	HCF	heart:	n/a
2	chr5:147648492-147648542	HCF	heart:	n/a
3	chr5:147648492-147648542	HMEC	breast:	n/a
4	chr5:147648492-147648542	HCT-116	colon:	n/a
5	chr5:147651477-147651527	BJ	skin:	n/a
6	chr5:147651477-147651527	ovcar-3	ovarian:	n/a
7	chr5:147651477-147651527	HEEpiC	esophagus:	n/a
8	chr5:147651477-147651527	HIPEpiC	eye:	n/a
9	chr5:147648492-147648542	AG04449	skin:	fetal
10	chr5:147648492-147648542	AG09309	skin:	n/a
11	chr5:147648492-147648542	SK-N-SH_RA	brain:	n/a
12	chr5:147651477-147651527	AG09319	gingival:	n/a
13	chr5:147648492-147648542	GM12891	blood:	n/a
14	chr5:147648492-147648542	ECC-1	luminal epithelium:	n/a
15	chr5:147651477-147651527	HCPEpiC	choroid plexus:	n/a
16	chr5:147648492-147648542	HAEpiC	amniotic membrane:	n/a
17	chr5:147651477-147651527	NHBE	bronchial:	n/a
18	chr5:147651477-147651527	RPTEC	kidney:	n/a
19	chr5:147648492-147648542	RPTEC	kidney:	n/a
20	chr5:147651477-147651527	HCM	heart:	n/a
21	chr5:147648492-147648542	BE2_C	brain:	n/a
22	chr5:147651477-147651527	HMEC	breast:	n/a
23	chr5:147651477-147651527	H1-hESC	embryonic stem cell:	embryo
24	chr5:147648492-147648542	Jurkat	blood:	n/a
25	chr5:147648492-147648542	NT2-D1	testis:	n/a
26	chr5:147648492-147648542	A549	lung:	n/a
27	chr5:147648492-147648542	MCF-7	breast:	n/a
28	chr5:147648492-147648542	HRCEpiC	kidney:	n/a
29	chr5:147648492-147648542	SK-N-MC	brain:	n/a
30	chr5:147648492-147648542	HCM	heart:	n/a
31	chr5:147651477-147651527	HUVEC	blood vessel:	n/a
32	chr5:147651477-147651527	HepG2	liver:	n/a
33	chr5:147651477-147651527	BE2_C	brain:	n/a
34	chr5:147648492-147648542	ovcar-3	ovarian:	n/a
35	chr5:147648492-147648542	BJ	skin:	n/a
36	chr5:147651477-147651527	Jurkat	blood:	n/a
37	chr5:147648492-147648542	Caco-2	colon:	n/a
38	chr5:147651477-147651527	HRE	kidney:	n/a
39	chr5:147648492-147648542	AG09319	gingival:	n/a
40	chr5:147648492-147648542	GM19239	blood:	n/a
41	chr5:147648492-147648542	AG04450	lung:	fetal
42	chr5:147648492-147648542	Hela-S3	cervix:	n/a
43	chr5:147651477-147651527	Hela-S3	cervix:	n/a
44	chr5:147648492-147648542	HL-60	blood:	n/a
45	chr5:147648492-147648542	HIPEpiC	eye:	n/a
46	chr5:147648492-147648542	SKMC	muscle:	n/a
47	chr5:147651477-147651527	HL-60	blood:	n/a
48	chr5:147648492-147648542	GM12892	blood:	n/a
49	chr5:147648492-147648542	U87	brain:	n/a
50	chr5:147648492-147648542	GM12878	blood:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:147639756..147640340-chr5:147685294..147686119,2	MCF-7	breast:
2	chr5:147677424..147679473-chr5:147682301..147684884,2	K562	blood:
3	chr5:147669945..147670857-chr5:147754107..147754786,2	MCF-7	breast:
4	chr5:147575500..147576238-chr5:147685562..147686083,2	MCF-7	breast:
5	chr5:147661571..147663967-chr5:147664133..147665761,2	MCF-7	breast:
6	chr5:147677028..147678682-chr5:147715476..147717665,2	K562	blood:
7	chr5:147660137..147662912-chr5:147668622..147670237,2	MCF-7	breast:
8	chr5:147685104..147686094-chr5:147777956..147778480,2	MCF-7	breast:
9	chr5:147677424..147679473-chr5:147682301..147684884,2	K562	blood:
10	chr5:147662505..147664775-chr5:147666818..147669638,2	K562	blood:
11	chr5:147661571..147663967-chr5:147664133..147665761,2	MCF-7	breast:
12	chr5:147575500..147576422-chr5:147685184..147686083,4	MCF-7	breast:
13	chr5:147677196..147678915-chr5:147687992..147690676,2	K562	blood:
14	chr5:147670158..147670766-chr5:147685960..147686677,4	MCF-7	breast:
15	chr5:147660137..147662912-chr5:147668622..147670237,2	MCF-7	breast:
16	chr5:147677196..147678915-chr5:147687992..147690676,2	K562	blood:
17	chr5:147683748..147686752-chr5:147688766..147691110,3	MCF-7	breast:
18	chr5:147670158..147670766-chr5:147685960..147686677,4	MCF-7	breast:
19	chr5:147640461..147641294-chr5:147685206..147686032,5	MCF-7	breast:
20	chr5:147687739..147689963-chr5:147691402..147694032,2	K562	blood:
21	chr5:147662505..147664775-chr5:147666818..147669638,2	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HTR4-1	chr5:147687567-147687728	ENSG00000247199
2	lnc-HTR4-1	chr5:147647870-147648567	ENSG00000247199
3	lnc-HTR4-1	chr5:147687567-147687728	NR_105057
4	lnc-HTR4-1	chr5:147669815-147670558	ENSG00000247199
5	lnc-SPINK7-2	chr5:147686861-147686897	NONHSAT104442
6	lnc-SPINK7-2	chr5:147687278-147687821	NONHSAT104442
7	lnc-HTR4-1	chr5:147647870-147648567	NR_105057
8	lnc-HTR4-1	chr5:147669815-147670558	NR_105057

No data

Variant related genes	Relation type
SPINK7	TF binding region
PGBD4P3	TF binding region
SPINK7	CpG island
PGBD4P3	CpG island
ENSG00000145879	chromatin interactions
DLC1	miRNA target sites
FNDC3A	miRNA target sites
EIF2C2	miRNA target sites

Extended variants
information (count: 1458 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:1458 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7734352	chr5:147648510-147648511	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs140717841	chr5:147648534-147648535	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
3	rs574448190	chr5:147648553-147648554	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
4	rs145855103	chr5:147648556-147648557	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
5	rs576321054	chr5:147648577-147648578	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs115597309	chr5:147648675-147648676	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs555867581	chr5:147648694-147648695	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs560255036	chr5:147648698-147648699	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs181014495	chr5:147648705-147648706	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs541577154	chr5:147648711-147648712	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs138321621	chr5:147648734-147648735	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs7733564	chr5:147648750-147648751	Weak transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs527488250	chr5:147648761-147648762	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs79126418	chr5:147648832-147648833	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs149626126	chr5:147648901-147648902	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs531613715	chr5:147648911-147648912	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs200767838	chr5:147648942-147648943	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs531412846	chr5:147648946-147648947	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs186423074	chr5:147648950-147648951	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs529257480	chr5:147648952-147648953	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs200316981	chr5:147648960-147648961	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs545639741	chr5:147648961-147648962	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs564030956	chr5:147648986-147648987	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs1347115	chr5:147649030-147649031	Weak transcription Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs565797223	chr5:147649055-147649056	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs539687406	chr5:147649118-147649119	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs561657159	chr5:147649145-147649146	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs557929633	chr5:147649147-147649148	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs192045675	chr5:147649152-147649153	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs17108103	chr5:147649181-147649182	Weak transcription Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs371032900	chr5:147649193-147649194	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs547775592	chr5:147649273-147649274	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs181756939	chr5:147649274-147649275	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs541763666	chr5:147649352-147649353	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs367672291	chr5:147649365-147649366	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs553948628	chr5:147649385-147649386	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs572167545	chr5:147649395-147649396	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs11435083	chr5:147649398-147649399	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs537672268	chr5:147649399-147649400	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs568382771	chr5:147649404-147649405	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs574314014	chr5:147649408-147649409	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs546048424	chr5:147649412-147649413	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs564257785	chr5:147649475-147649476	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs531496848	chr5:147649480-147649481	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs552465998	chr5:147649491-147649492	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs561969193	chr5:147649500-147649501	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs370523345	chr5:147649503-147649504	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs56306866	chr5:147649509-147649510	Weak transcription Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs186617788	chr5:147649520-147649521	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs547763255	chr5:147649539-147649540	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	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
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18194544	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Renal cell carcinoma	18592004	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	17053054	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Hyperekplexia	16941485	CNVD
Myelofibrosis	22110671	CNVD
Crohn''s disease	20877625	CNVD
T-cell lymphomas	19863542	CNVD
Breast cancer	17603634	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:79 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:147647400-147650600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
2	chr5:147647600-147648600	Enhancers	Hela-S3	cervix
3	chr5:147647800-147648600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr5:147647800-147648600	Enhancers	HMEC	breast
5	chr5:147648000-147648600	Enhancers	Muscle Satellite Cultured Cells	--
6	chr5:147648000-147648600	Enhancers	NH-A	brain
7	chr5:147648000-147648800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr5:147648200-147648600	Enhancers	Pancreas	Pancrea
9	chr5:147648200-147648600	Enhancers	NHLF	lung
10	chr5:147648400-147648600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr5:147648400-147660200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr5:147648600-147649800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr5:147648600-147661400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr5:147658000-147658200	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
15	chr5:147658200-147659800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr5:147658800-147663200	Weak transcription	Hela-S3	cervix
17	chr5:147659800-147660000	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
18	chr5:147659800-147661200	Enhancers	iPS-15b Cell Line	embryonic stem cell
19	chr5:147660000-147660200	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr5:147660000-147660200	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr5:147660000-147661200	Enhancers	H1 Cell Line	embryonic stem cell
22	chr5:147660000-147661200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr5:147660200-147660400	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
24	chr5:147660200-147660400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
25	chr5:147660200-147660400	Enhancers	Gastric	stomach
26	chr5:147660200-147661200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr5:147660200-147661200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr5:147660200-147661600	Enhancers	Stomach Mucosa	stomach
29	chr5:147660200-147669400	Weak transcription	Skeletal Muscle Female	skeletal muscle
30	chr5:147660400-147660800	Active TSS	HUES6 Cell Line	embryonic stem cell
31	chr5:147660400-147661000	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr5:147660400-147661200	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chr5:147660600-147661200	Enhancers	Lung	lung
34	chr5:147660600-147661600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
35	chr5:147660800-147661000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
36	chr5:147660800-147661200	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr5:147660800-147661200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
38	chr5:147661000-147661200	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr5:147661000-147661200	Enhancers	Gastric	stomach
40	chr5:147661200-147664800	Weak transcription	Right Ventricle	heart
41	chr5:147661400-147668200	Weak transcription	Skeletal Muscle Male	skeletal muscle
42	chr5:147661600-147666200	Weak transcription	Stomach Mucosa	stomach
43	chr5:147661600-147670400	Weak transcription	Brain Hippocampus Middle	brain
44	chr5:147661600-147670400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
45	chr5:147662600-147662800	Enhancers	Ovary	ovary
46	chr5:147662800-147663000	ZNF genes & repeats	Aorta	Aorta
47	chr5:147662800-147664600	Weak transcription	Ovary	ovary
48	chr5:147663000-147667600	Weak transcription	Aorta	Aorta
49	chr5:147664600-147664800	Enhancers	Ovary	ovary
50	chr5:147666200-147666800	Enhancers	Stomach Mucosa	stomach

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