Variant report

Variant	nsv1033838
Chromosome Location	chr5:147360521-147484014
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:669)
CpG islands
(count:367)
Chromatin interactive
region (count:20)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:669 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr5:147391120-147391740	HCT-116	colon:	n/a	n/a
2	ATF3	chr5:147391110-147391690	HCT-116	colon:	n/a	n/a
3	BRCA1	chr5:147383611-147383682	Hela-S3	cervix:	n/a	n/a
4	BRCA1	chr5:147369749-147369877	Hela-S3	cervix:	n/a	n/a
5	BRCA1	chr5:147465542-147466030	Hela-S3	cervix:	n/a	n/a
6	BRCA1	chr5:147391272-147392099	Hela-S3	cervix:	n/a	n/a
7	BRCA1	chr5:147468993-147470890	Hela-S3	cervix:	n/a	n/a
8	CBX3	chr5:147391174-147391767	HCT-116	colon:	n/a	n/a
9	CBX3	chr5:147434864-147435069	K562	blood:	n/a	n/a
10	CCNT2	chr5:147414502-147414684	K562	blood:	n/a	n/a
11	CEBPB	chr5:147463872-147464201	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr5:147422501-147422663	H1-hESC	embryonic stem cell:	n/a	chr5:147422647-147422658 chr5:147422648-147422659
13	CEBPB	chr5:147391116-147391880	MCF-7	breast:	n/a	chr5:147391624-147391637
14	CEBPB	chr5:147391128-147391736	MCF-7	breast:	n/a	chr5:147391624-147391637
15	CEBPB	chr5:147464854-147465268	Hela-S3	cervix:	n/a	chr5:147464921-147464934 chr5:147464921-147464932 chr5:147464921-147464934 chr5:147465040-147465051 chr5:147464921-147464932
16	CEBPB	chr5:147369574-147369985	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr5:147418914-147418948	K562	blood:	n/a	chr5:147418926-147418937
18	CEBPB	chr5:147418802-147419070	HepG2	liver:	n/a	chr5:147418926-147418937
19	CEBPB	chr5:147382896-147383159	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr5:147443606-147443759	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr5:147390923-147392013	Hela-S3	cervix:	n/a	chr5:147391624-147391637
22	CEBPB	chr5:147471746-147472059	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr5:147399747-147400237	Hela-S3	cervix:	n/a	chr5:147400195-147400208
24	CEBPB	chr5:147412698-147412976	H1-hESC	embryonic stem cell:	n/a	chr5:147412825-147412838
25	CEBPB	chr5:147412654-147413105	Hela-S3	cervix:	n/a	chr5:147412825-147412838
26	CEBPB	chr5:147422543-147422729	HepG2	liver:	n/a	chr5:147422647-147422658 chr5:147422648-147422659
27	CEBPB	chr5:147469495-147470904	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr5:147391099-147391799	HCT-116	colon:	n/a	chr5:147391624-147391637
29	CEBPB	chr5:147418846-147418986	Hela-S3	cervix:	n/a	chr5:147418926-147418937
30	CEBPB	chr5:147463892-147464183	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr5:147465540-147465993	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr5:147418836-147419047	A549	lung:	n/a	chr5:147418926-147418937
33	CEBPB	chr5:147382025-147382370	MCF-7	breast:	n/a	n/a
34	CEBPB	chr5:147469045-147469285	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr5:147381845-147382414	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr5:147365708-147365959	HepG2	liver:	n/a	chr5:147365843-147365854 chr5:147365842-147365853 chr5:147365842-147365853
37	CEBPB	chr5:147464946-147465174	HepG2	liver:	n/a	chr5:147465040-147465051
38	CEBPB	chr5:147391069-147391801	HCT-116	colon:	n/a	chr5:147391624-147391637
39	CEBPB	chr5:147418757-147419079	IMR90	lung:	n/a	chr5:147418926-147418937
40	CEBPB	chr5:147391297-147391602	IMR90	lung:	n/a	n/a
41	CEBPB	chr5:147393467-147393635	Hela-S3	cervix:	n/a	n/a
42	CHD2	chr5:147399817-147400155	Hela-S3	cervix:	n/a	n/a
43	CHD2	chr5:147382081-147382376	Hela-S3	cervix:	n/a	n/a
44	CHD2	chr5:147391249-147391770	Hela-S3	cervix:	n/a	n/a
45	CHD2	chr5:147412774-147413110	Hela-S3	cervix:	n/a	n/a
46	CTCF	chr5:147385737-147385885	SK-N-SH_RA	brain:	n/a	n/a
47	CTCF	chr5:147385546-147385903	HCT-116	colon:	n/a	n/a
48	CTCF	chr5:147483005-147483114	Hela-S3	cervix:	n/a	n/a
49	CTCF	chr5:147482920-147483070	HMEC	breast:	n/a	n/a
50	CTCF	chr5:147376120-147376270	WERI-Rb-1	eye:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:147473666-147473716	HCF	heart:	n/a
2	chr5:147473666-147473716	HCF	heart:	n/a
3	chr5:147443284-147443334	HEK293	kidney:	embryo
4	chr5:147443252-147443302	ProgFib	skin:	n/a
5	chr5:147443252-147443302	SK-N-MC	brain:	n/a
6	chr5:147443536-147443586	NHDF-neo	bronchial:	n/a
7	chr5:147443347-147443397	GM06990	blood:	n/a
8	chr5:147443536-147443586	NB4	blood:	n/a
9	chr5:147443536-147443586	AG04449	skin:	fetal
10	chr5:147443536-147443586	HIPEpiC	eye:	n/a
11	chr5:147443347-147443397	CMK	blood:	n/a
12	chr5:147443067-147443117	GM19239	blood:	n/a
13	chr5:147443067-147443117	AG04450	lung:	fetal
14	chr5:147443284-147443334	HRPEpiC	eye:	n/a
15	chr5:147443252-147443302	BJ	skin:	n/a
16	chr5:147443252-147443302	Caco-2	colon:	n/a
17	chr5:147443536-147443586	ProgFib	skin:	n/a
18	chr5:147443347-147443397	IMR90	lung:	fetal
19	chr5:147443252-147443302	SK-N-SH	brain:	n/a
20	chr5:147443347-147443397	GM19239	blood:	n/a
21	chr5:147443536-147443586	AG04450	lung:	fetal
22	chr5:147473666-147473716	MCF10A-Er-Src	breast:	n/a
23	chr5:147473666-147473716	U87	brain:	n/a
24	chr5:147443067-147443117	AG09319	gingival:	n/a
25	chr5:147443284-147443334	NB4	blood:	n/a
26	chr5:147443347-147443397	A549	lung:	n/a
27	chr5:147443536-147443586	HCF	heart:	n/a
28	chr5:147443252-147443302	HRE	kidney:	n/a
29	chr5:147443067-147443117	HRPEpiC	eye:	n/a
30	chr5:147443252-147443302	GM19239	blood:	n/a
31	chr5:147443347-147443397	Hela-S3	cervix:	n/a
32	chr5:147443067-147443117	A549	lung:	n/a
33	chr5:147443284-147443334	NT2-D1	testis:	n/a
34	chr5:147443067-147443117	HCF	heart:	n/a
35	chr5:147443347-147443397	HRE	kidney:	n/a
36	chr5:147443284-147443334	HepG2	liver:	n/a
37	chr5:147473666-147473716	HAEpiC	amniotic membrane:	n/a
38	chr5:147443067-147443117	NHDF-neo	bronchial:	n/a
39	chr5:147443347-147443397	PANC-1	pancreas:	n/a
40	chr5:147443067-147443117	HEEpiC	esophagus:	n/a
41	chr5:147443067-147443117	MCF-7	breast:	n/a
42	chr5:147443252-147443302	U87	brain:	n/a
43	chr5:147443536-147443586	T-47D	breast:	n/a
44	chr5:147443536-147443586	NT2-D1	testis:	n/a
45	chr5:147443347-147443397	T-47D	breast:	n/a
46	chr5:147443347-147443397	AG09319	gingival:	n/a
47	chr5:147443067-147443117	HEK293	kidney:	embryo
48	chr5:147443536-147443586	GM06990	blood:	n/a
49	chr5:147443252-147443302	RPTEC	kidney:	n/a
50	chr5:147473666-147473716	GM06990	blood:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:147360976..147363272-chr5:147364853..147367805,2	MCF-7	breast:
2	chr5:147369292..147371929-chr5:147395160..147396738,2	K562	blood:
3	chr5:147362057..147364652-chr5:147367228..147369017,2	K562	blood:
4	chr5:147424525..147426952-chr5:147437496..147439638,2	K562	blood:
5	chr17:74638250..74639918-chr5:147391748..147393250,2	K562	blood:
6	chr5:147362057..147364652-chr5:147367228..147369017,2	K562	blood:
7	chr5:147424525..147426952-chr5:147437496..147439638,2	K562	blood:
8	chr5:147374166..147375846-chr5:147383379..147385077,2	K562	blood:
9	chr5:147374166..147375846-chr5:147383379..147385077,2	K562	blood:
10	chr15:84049266..84049996-chr5:147385383..147386056,2	MCF-7	breast:
11	chr5:147388872..147389373-chrX:84273269..84273769,2	Hela-S3	cervix:
12	chr5:147369292..147371929-chr5:147395160..147396738,2	K562	blood:
13	chr5:147476011..147478506-chr5:147489825..147491357,2	K562	blood:
14	chr16:60919408..60919976-chr5:147395742..147396497,2	MCF-7	breast:
15	chr5:147377762..147382319-chr5:147386529..147391595,4	MCF-7	breast:
16	chr5:147439149..147441922-chr5:147442667..147445001,2	K562	blood:
17	chr5:147377762..147382319-chr5:147386529..147391595,4	MCF-7	breast:
18	chr5:147449509..147451055-chr5:147462616..147464573,2	K562	blood:
19	chr5:147449509..147451055-chr5:147462616..147464573,2	K562	blood:
20	chr5:147360976..147363272-chr5:147364853..147367805,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SPINK5-1	chr5:147391170-147391287	NONHSAT104436
2	lnc-SPINK5-1	chr5:147366249-147366668	NONHSAT104436

No data

Variant related genes	Relation type
SPINK5	TF binding region
SPINK5	CpG island
ENSG00000133710	chromatin interactions
ENSG00000070526	chromatin interactions

Extended variants
information (count: 4301 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:4301 , 50 per page) page: 1 2 3 4 5 6 7 ... 87

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11168014	chr5:147360521-147360522	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs11168015	chr5:147360532-147360533	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs193091137	chr5:147360543-147360544	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs371974623	chr5:147360592-147360593	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs549273029	chr5:147360607-147360608	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs567681803	chr5:147360636-147360637	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs528454678	chr5:147360728-147360729	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs546781948	chr5:147360730-147360731	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs2098249	chr5:147360731-147360732	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs185856926	chr5:147360859-147360860	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs113358651	chr5:147360897-147360898	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs550477390	chr5:147360898-147360899	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs373025971	chr5:147360899-147360900	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs538750110	chr5:147360900-147360901	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs2080085	chr5:147360904-147360905	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs137901756	chr5:147360952-147360953	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs536569091	chr5:147360979-147360980	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs549934309	chr5:147361003-147361004	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs573309053	chr5:147361006-147361007	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs534271128	chr5:147361120-147361121	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs188320211	chr5:147361133-147361134	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs552688515	chr5:147361207-147361208	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs374432639	chr5:147361240-147361241	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs577706460	chr5:147361285-147361286	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs372256093	chr5:147361301-147361302	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs544757677	chr5:147361324-147361325	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs144139366	chr5:147361416-147361417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs534058349	chr5:147361428-147361429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs79824185	chr5:147361434-147361435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs367802540	chr5:147361437-147361438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs553122656	chr5:147361438-147361439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs377192875	chr5:147361445-147361446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs566506027	chr5:147361451-147361452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs147321428	chr5:147361452-147361453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs535545864	chr5:147361459-147361460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs528392882	chr5:147361535-147361536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs547013829	chr5:147361550-147361551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs565118719	chr5:147361629-147361630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs368110172	chr5:147361744-147361745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs139272058	chr5:147361818-147361819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs74709377	chr5:147361848-147361849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs536405160	chr5:147361861-147361862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs555471939	chr5:147361882-147361883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs575325660	chr5:147361913-147361914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs141503920	chr5:147361923-147361924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs192224522	chr5:147361932-147361933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs570054208	chr5:147361935-147361936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs371657628	chr5:147361971-147361972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs535538485	chr5:147362025-147362026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs538744658	chr5:147362044-147362045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:79)

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
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:378 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:147344400-147363000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr5:147359600-147361000	Weak transcription	Hela-S3	cervix
3	chr5:147360400-147361200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr5:147361000-147361400	Enhancers	Hela-S3	cervix
5	chr5:147364600-147367400	Enhancers	Liver	Liver
6	chr5:147365200-147365400	Enhancers	Esophagus	oesophagus
7	chr5:147365400-147365800	Enhancers	Fetal Intestine Small	intestine
8	chr5:147365400-147379400	Weak transcription	Esophagus	oesophagus
9	chr5:147368400-147368800	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr5:147368400-147369800	Enhancers	HUVEC	blood vessel
11	chr5:147368400-147370000	Enhancers	Hela-S3	cervix
12	chr5:147368600-147369800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr5:147371600-147371800	Enhancers	H9 Cell Line	embryonic stem cell
14	chr5:147371800-147378400	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr5:147376000-147377800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr5:147376600-147376800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr5:147376600-147377000	Enhancers	Fetal Stomach	stomach
18	chr5:147376600-147378600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr5:147376800-147378600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr5:147377200-147380200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr5:147377800-147379800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr5:147378000-147378200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr5:147378200-147378800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr5:147378400-147378600	Enhancers	H9 Cell Line	embryonic stem cell
25	chr5:147378600-147379800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr5:147378800-147379200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr5:147379200-147382400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr5:147379800-147382000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr5:147379800-147382400	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr5:147380200-147380600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr5:147380200-147381800	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
32	chr5:147380200-147381800	ZNF genes & repeats	Adipose Nuclei	Adipose
33	chr5:147380400-147382400	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr5:147380600-147381000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr5:147380800-147381400	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
36	chr5:147380800-147381800	ZNF genes & repeats	Brain Hippocampus Middle	brain
37	chr5:147381000-147381800	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
38	chr5:147381000-147382000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
39	chr5:147381000-147382200	ZNF genes & repeats	Liver	Liver
40	chr5:147381200-147382000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr5:147381200-147382400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
42	chr5:147381600-147381800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
43	chr5:147381600-147385000	Enhancers	Hela-S3	cervix
44	chr5:147382000-147387200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr5:147382000-147391000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr5:147382200-147382800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
47	chr5:147382400-147386000	Weak transcription	HUES6 Cell Line	embryonic stem cell
48	chr5:147382400-147390600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr5:147382400-147391200	Weak transcription	HUES64 Cell Line	embryonic stem cell
50	chr5:147384800-147391000	Weak transcription	H9 Cell Line	embryonic stem cell

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