Variant report

Variant	nsv883018
Chromosome Location	chr5:147640718-147691470
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:423)
CpG islands
(count:367)
Chromatin interactive
region (count:25)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:423 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

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	ATF1	chr5:147645657-147645789	K562	blood:	n/a	n/a
3	CBX3	chr5:147688576-147688878	K562	blood:	n/a	n/a
4	CEBPB	chr5:147671442-147671605	K562	blood:	n/a	n/a
5	CEBPB	chr5:147648168-147648542	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr5:147644798-147644995	HepG2	liver:	n/a	chr5:147644893-147644904
7	CEBPB	chr5:147648219-147648441	HepG2	liver:	n/a	n/a
8	CEBPB	chr5:147690299-147690342	K562	blood:	n/a	chr5:147690303-147690316 chr5:147690303-147690316 chr5:147690303-147690314 chr5:147690303-147690316
9	CEBPB	chr5:147670204-147670441	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr5:147669913-147670425	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr5:147677446-147677624	Hela-S3	cervix:	n/a	n/a
12	CHD2	chr5:147660593-147660796	GM12878	blood:	n/a	n/a
13	CTCF	chr5:147670238-147670442	MCF-7	breast:	n/a	n/a
14	CTCF	chr5:147686183-147686230	A549	lung:	n/a	chr5:147686201-147686219
15	CTCF	chr5:147670007-147670025	GM19238	blood:	n/a	n/a
16	CTCF	chr5:147686100-147686250	A549	lung:	n/a	chr5:147686201-147686219
17	CTCF	chr5:147670151-147670512	GM12878	blood:	n/a	n/a
18	CTCF	chr5:147686160-147686310	NHEK	skin:	n/a	chr5:147686201-147686219
19	CTCF	chr5:147670142-147670473	A549	lung:	n/a	n/a
20	CTCF	chr5:147686060-147686210	RPTEC	kidney:	n/a	n/a
21	CTCF	chr5:147670233-147670436	K562	blood:	n/a	n/a
22	CTCF	chr5:147670213-147670419	SK-N-SH_RA	brain:	n/a	n/a
23	CTCF	chr5:147670232-147670430	HepG2	liver:	n/a	n/a
24	CTCF	chr5:147686047-147686371	GM12878	blood:	n/a	chr5:147686201-147686219
25	CTCF	chr5:147686100-147686250	MCF-7	breast:	n/a	chr5:147686201-147686219
26	CTCF	chr5:147686147-147686245	GM12892	blood:	n/a	chr5:147686201-147686219
27	CTCF	chr5:147670260-147670410	HEEpiC	esophagus:	n/a	n/a
28	CTCF	chr5:147670240-147670390	HAc	cerebellar:	n/a	n/a
29	CTCF	chr5:147686120-147686270	BE2_C	brain:	n/a	chr5:147686201-147686219
30	CTCF	chr5:147686120-147686270	HVMF	connective:	n/a	chr5:147686201-147686219
31	CTCF	chr5:147670320-147670470	BE2_C	brain:	n/a	n/a
32	CTCF	chr5:147670263-147670422	Kidney_OC	kidney:	n/a	n/a
33	CTCF	chr5:147670260-147670410	GM12873	blood:	n/a	n/a
34	CTCF	chr5:147686078-147686326	MCF-7	breast:	n/a	chr5:147686201-147686219
35	CTCF	chr5:147670227-147670416	GM10266	blood:	n/a	n/a
36	CTCF	chr5:147670280-147670430	GM12864	blood:	n/a	n/a
37	CTCF	chr5:147670300-147670450	BJ	skin:	n/a	n/a
38	CTCF	chr5:147685780-147685930	GM12864	blood:	n/a	n/a
39	CTCF	chr5:147670232-147670437	Pancreas_OC	pancreas:	n/a	n/a
40	CTCF	chr5:147670280-147670430	HRPEpiC	eye:	n/a	n/a
41	CTCF	chr5:147686150-147686159	Fibrobl	skin:	n/a	n/a
42	CTCF	chr5:147670280-147670570	HFF-Myc	foreskin:	n/a	n/a
43	CTCF	chr5:147670220-147670370	GM12864	blood:	n/a	n/a
44	CTCF	chr5:147648314-147648334	Gliobla	brain:	n/a	n/a
45	CTCF	chr5:147670201-147670463	A549	lung:	n/a	n/a
46	CTCF	chr5:147670280-147670430	HEK293	kidney:	n/a	n/a
47	CTCF	chr5:147686100-147686250	RPTEC	kidney:	n/a	chr5:147686201-147686219
48	CTCF	chr5:147670280-147670430	GM12874	blood:	n/a	n/a
49	CTCF	chr5:147670380-147670530	HFF-Myc	foreskin:	n/a	n/a
50	CTCF	chr5:147686200-147686350	SAEC	small airway:	n/a	chr5:147686201-147686219

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:147648492-147648542	U87	brain:	n/a
2	chr5:147648492-147648542	U87	brain:	n/a
3	chr5:147647809-147647859	HPAEpiC	pulmonary alveolar:	n/a
4	chr5:147648312-147648362	H1-hESC	embryonic stem cell:	embryo
5	chr5:147648312-147648362	Hela-S3	cervix:	n/a
6	chr5:147648312-147648362	NHBE	bronchial:	n/a
7	chr5:147651477-147651527	AG09319	gingival:	n/a
8	chr5:147651477-147651527	HEEpiC	esophagus:	n/a
9	chr5:147647955-147648005	PrEC	prostate:	n/a
10	chr5:147647955-147648005	HCM	heart:	n/a
11	chr5:147648312-147648362	MCF-7	breast:	n/a
12	chr5:147651477-147651527	GM12892	blood:	n/a
13	chr5:147647809-147647859	HCF	heart:	n/a
14	chr5:147651477-147651527	MCF-7	breast:	n/a
15	chr5:147647955-147648005	NHBE	bronchial:	n/a
16	chr5:147648492-147648542	HEK293	kidney:	embryo
17	chr5:147647809-147647859	HL-60	blood:	n/a
18	chr5:147651477-147651527	HCM	heart:	n/a
19	chr5:147651477-147651527	GM12891	blood:	n/a
20	chr5:147647955-147648005	NB4	blood:	n/a
21	chr5:147647809-147647859	AG04449	skin:	fetal
22	chr5:147691248-147691298	H1-hESC	embryonic stem cell:	embryo
23	chr5:147648312-147648362	PANC-1	pancreas:	n/a
24	chr5:147648312-147648362	Hepatocyte	liver:	n/a
25	chr5:147691248-147691298	HUVEC	blood vessel:	n/a
26	chr5:147648492-147648542	HCT-116	colon:	n/a
27	chr5:147651477-147651527	K562	blood:	n/a
28	chr5:147648492-147648542	HCM	heart:	n/a
29	chr5:147691248-147691298	ovcar-3	ovarian:	n/a
30	chr5:147648492-147648542	SK-N-SH	brain:	n/a
31	chr5:147648492-147648542	T-47D	breast:	n/a
32	chr5:147648312-147648362	HIPEpiC	eye:	n/a
33	chr5:147691248-147691298	AG09309	skin:	n/a
34	chr5:147651477-147651527	GM19239	blood:	n/a
35	chr5:147648312-147648362	NH-A	brain:	n/a
36	chr5:147648492-147648542	ovcar-3	ovarian:	n/a
37	chr5:147651477-147651527	SK-N-SH_RA	brain:	n/a
38	chr5:147647955-147648005	NH-A	brain:	n/a
39	chr5:147647809-147647859	HRE	kidney:	n/a
40	chr5:147648312-147648362	T-47D	breast:	n/a
41	chr5:147691248-147691298	GM19239	blood:	n/a
42	chr5:147647955-147648005	HPAEpiC	pulmonary alveolar:	n/a
43	chr5:147647809-147647859	HNPCEpiC	eye:	n/a
44	chr5:147647809-147647859	AG04450	lung:	fetal
45	chr5:147651477-147651527	AG04450	lung:	fetal
46	chr5:147691248-147691298	A549	lung:	n/a
47	chr5:147647955-147648005	HEEpiC	esophagus:	n/a
48	chr5:147651477-147651527	Caco-2	colon:	n/a
49	chr5:147691248-147691298	AG10803	skin:	n/a
50	chr5:147651477-147651527	HRE	kidney:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr5:147677028..147678682-chr5:147715476..147717665,2	K562	blood:
2	chr5:147685104..147686094-chr5:147777956..147778480,2	MCF-7	breast:
3	chr5:147575494..147576358-chr5:147640450..147641242,3	MCF-7	breast:
4	chr5:147683748..147686752-chr5:147688766..147691110,3	MCF-7	breast:
5	chr5:147677196..147678915-chr5:147687992..147690676,2	K562	blood:
6	chr5:147662505..147664775-chr5:147666818..147669638,2	K562	blood:
7	chr5:147640461..147641294-chr5:147685206..147686032,5	MCF-7	breast:
8	chr5:147661571..147663967-chr5:147664133..147665761,2	MCF-7	breast:
9	chr5:147669945..147670857-chr5:147754107..147754786,2	MCF-7	breast:
10	chr5:147661571..147663967-chr5:147664133..147665761,2	MCF-7	breast:
11	chr5:147662505..147664775-chr5:147666818..147669638,2	K562	blood:
12	chr5:147670158..147670766-chr5:147685960..147686677,4	MCF-7	breast:
13	chr5:147660137..147662912-chr5:147668622..147670237,2	MCF-7	breast:
14	chr5:147639756..147640340-chr5:147685294..147686119,2	MCF-7	breast:
15	chr5:147575500..147576422-chr5:147685184..147686083,4	MCF-7	breast:
16	chr5:147670158..147670766-chr5:147685960..147686677,4	MCF-7	breast:
17	chr5:147677196..147678915-chr5:147687992..147690676,2	K562	blood:
18	chr5:147677424..147679473-chr5:147682301..147684884,2	K562	blood:
19	chr5:147660137..147662912-chr5:147668622..147670237,2	MCF-7	breast:
20	chr5:147640461..147641294-chr5:147685206..147686032,5	MCF-7	breast:
21	chr5:147575500..147576238-chr5:147685562..147686083,2	MCF-7	breast:
22	chr5:147575494..147576358-chr5:147640450..147641333,4	MCF-7	breast:
23	chr5:147683748..147686752-chr5:147688766..147691110,3	MCF-7	breast:
24	chr5:147677424..147679473-chr5:147682301..147684884,2	K562	blood:
25	chr5:147687739..147689963-chr5:147691402..147694032,2	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	NR_105057
3	lnc-HTR4-1	chr5:147669815-147670558	ENSG00000247199
4	lnc-HTR4-1	chr5:147687567-147687728	NR_105057
5	lnc-HTR4-1	chr5:147669815-147670558	NR_105057
6	lnc-SPINK7-2	chr5:147686861-147686897	NONHSAT104442
7	lnc-HTR4-1	chr5:147647870-147648567	ENSG00000247199
8	lnc-SPINK7-2	chr5:147687278-147687821	NONHSAT104442

No data

Variant related genes	Relation type
SPINK7	TF binding region
SPINK13	TF binding region
PGBD4P3	TF binding region
SPINK7	CpG island
SPINK13	CpG island
PGBD4P3	CpG island
ENSG00000145879	chromatin interactions
EIF2C2	miRNA target sites
FNDC3A	miRNA target sites
DLC1	miRNA target sites

Extended variants
information (count: 1888 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:1888 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10477367	chr5:147640718-147640719	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs35456640	chr5:147640729-147640730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs397705510	chr5:147640734-147640735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs183444954	chr5:147640805-147640806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs568563389	chr5:147640875-147640876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs536054703	chr5:147640895-147640896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs116090315	chr5:147640963-147640964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs55716930	chr5:147640980-147640981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs534073320	chr5:147640981-147640982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs77621704	chr5:147641074-147641075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs143458205	chr5:147641093-147641094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs544589572	chr5:147641124-147641125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs375201374	chr5:147641129-147641130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs528092451	chr5:147641149-147641150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs574977041	chr5:147641221-147641222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs187417008	chr5:147641237-147641238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs560714449	chr5:147641243-147641244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs1368311	chr5:147641248-147641249	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs535999475	chr5:147641266-147641267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs564594130	chr5:147641268-147641269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs73278510	chr5:147641270-147641271	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs550123182	chr5:147641278-147641279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs192161834	chr5:147641366-147641367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs115726777	chr5:147641368-147641369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs183099152	chr5:147641378-147641379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs566645646	chr5:147641416-147641417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs571354859	chr5:147641467-147641468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs73278512	chr5:147641485-147641486	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs142014230	chr5:147641492-147641493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs570712497	chr5:147641544-147641545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs150703516	chr5:147641546-147641547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs547881424	chr5:147641552-147641553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs556593928	chr5:147641556-147641557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs575013951	chr5:147641575-147641576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs1368312	chr5:147641587-147641588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs1368313	chr5:147641639-147641640	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs115930044	chr5:147641666-147641667	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs546031660	chr5:147641689-147641690	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs75778105	chr5:147641722-147641723	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs531876955	chr5:147641755-147641756	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs543854040	chr5:147641853-147641854	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs188132903	chr5:147641884-147641885	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs10066740	chr5:147641903-147641904	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs1368314	chr5:147641928-147641929	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs34857050	chr5:147641949-147641950	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs150826172	chr5:147641968-147641969	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs192703330	chr5:147642066-147642067	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs140180040	chr5:147642090-147642091	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs142174913	chr5:147642093-147642094	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs566703998	chr5:147642095-147642096	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

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
Autism	21865298	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:88 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:147618800-147647600	Weak transcription	Hela-S3	cervix
2	chr5:147635000-147647800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr5:147641600-147642800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
4	chr5:147647400-147648200	Enhancers	Stomach Mucosa	stomach
5	chr5:147647400-147650600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
6	chr5:147647600-147648600	Enhancers	Hela-S3	cervix
7	chr5:147647800-147648600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr5:147647800-147648600	Enhancers	HMEC	breast
9	chr5:147648000-147648400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr5:147648000-147648400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr5:147648000-147648600	Enhancers	Muscle Satellite Cultured Cells	--
12	chr5:147648000-147648600	Enhancers	NH-A	brain
13	chr5:147648000-147648800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr5:147648200-147648400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr5:147648200-147648600	Enhancers	Pancreas	Pancrea
16	chr5:147648200-147648600	Enhancers	NHLF	lung
17	chr5:147648400-147648600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr5:147648400-147660200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr5:147648600-147649800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr5:147648600-147661400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr5:147658000-147658200	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
22	chr5:147658200-147659800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
23	chr5:147658800-147663200	Weak transcription	Hela-S3	cervix
24	chr5:147659800-147660000	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
25	chr5:147659800-147661200	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chr5:147660000-147660200	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr5:147660000-147660200	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr5:147660000-147661200	Enhancers	H1 Cell Line	embryonic stem cell
29	chr5:147660000-147661200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr5:147660200-147660400	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
31	chr5:147660200-147660400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
32	chr5:147660200-147660400	Enhancers	Gastric	stomach
33	chr5:147660200-147661200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr5:147660200-147661200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr5:147660200-147661600	Enhancers	Stomach Mucosa	stomach
36	chr5:147660200-147669400	Weak transcription	Skeletal Muscle Female	skeletal muscle
37	chr5:147660400-147660800	Active TSS	HUES6 Cell Line	embryonic stem cell
38	chr5:147660400-147661000	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr5:147660400-147661200	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr5:147660600-147661200	Enhancers	Lung	lung
41	chr5:147660600-147661600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
42	chr5:147660800-147661000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
43	chr5:147660800-147661200	Enhancers	HUES64 Cell Line	embryonic stem cell
44	chr5:147660800-147661200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr5:147661000-147661200	Enhancers	HUES6 Cell Line	embryonic stem cell
46	chr5:147661000-147661200	Enhancers	Gastric	stomach
47	chr5:147661200-147664800	Weak transcription	Right Ventricle	heart
48	chr5:147661400-147668200	Weak transcription	Skeletal Muscle Male	skeletal muscle
49	chr5:147661600-147666200	Weak transcription	Stomach Mucosa	stomach
50	chr5:147661600-147670400	Weak transcription	Brain Hippocampus Middle	brain

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