Variant report

Variant	nsv830546
Chromosome Location	chr5:167303135-167456271
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:167412514-167412754	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:167376502-167376530	HepG2	liver:	n/a	n/a
3	BACH1	chr5:167343857-167343875	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr5:167317090-167317307	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr5:167364567-167364935	K562	blood:	n/a	chr5:167364753-167364767
6	BACH1	chr5:167364570-167364945	H1-hESC	embryonic stem cell:	n/a	chr5:167364753-167364767
7	BATF	chr5:167397015-167397416	GM12878	blood:	n/a	chr5:167397202-167397210 chr5:167397231-167397242 chr5:167397232-167397242
8	BATF	chr5:167397014-167397318	GM12878	blood:	n/a	chr5:167397202-167397210 chr5:167397231-167397242 chr5:167397232-167397242
9	BHLHE40	chr5:167334953-167335055	GM12878	blood:	n/a	n/a
10	BHLHE40	chr5:167364649-167364839	GM12878	blood:	n/a	n/a
11	BRCA1	chr5:167372234-167373162	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr5:167371448-167371893	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr5:167426399-167426674	HepG2	liver:	n/a	chr5:167426660-167426673 chr5:167426660-167426673
14	CEBPB	chr5:167429191-167429528	A549	lung:	n/a	chr5:167429384-167429395 chr5:167429354-167429365
15	CEBPB	chr5:167362431-167362631	HepG2	liver:	n/a	n/a
16	CEBPB	chr5:167419398-167419511	HepG2	liver:	n/a	chr5:167419462-167419473
17	CEBPB	chr5:167372483-167373225	IMR90	lung:	n/a	n/a
18	CEBPB	chr5:167305352-167305552	Hela-S3	cervix:	n/a	chr5:167305432-167305445 chr5:167305434-167305443 chr5:167305434-167305443 chr5:167305434-167305443 chr5:167305433-167305444 chr5:167305432-167305443 chr5:167305434-167305443
19	CEBPB	chr5:167426411-167426636	IMR90	lung:	n/a	n/a
20	CEBPB	chr5:167330686-167331011	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr5:167305386-167305522	H1-hESC	embryonic stem cell:	n/a	chr5:167305432-167305445 chr5:167305434-167305443 chr5:167305434-167305443 chr5:167305434-167305443 chr5:167305433-167305444 chr5:167305432-167305443 chr5:167305434-167305443
22	CEBPB	chr5:167426419-167426677	A549	lung:	n/a	chr5:167426660-167426673 chr5:167426660-167426673
23	CEBPB	chr5:167331452-167331652	HepG2	liver:	n/a	chr5:167331500-167331511
24	CEBPB	chr5:167305255-167305579	IMR90	lung:	n/a	chr5:167305432-167305445 chr5:167305434-167305443 chr5:167305434-167305443 chr5:167305434-167305443 chr5:167305433-167305444 chr5:167305432-167305443 chr5:167305434-167305443
25	CEBPB	chr5:167343770-167344075	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr5:167377689-167377693	A549	lung:	n/a	n/a
27	CEBPB	chr5:167377712-167377724	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr5:167331420-167331614	IMR90	lung:	n/a	chr5:167331500-167331511
29	CEBPB	chr5:167305271-167305612	HepG2	liver:	n/a	chr5:167305432-167305445 chr5:167305434-167305443 chr5:167305434-167305443 chr5:167305434-167305443 chr5:167305433-167305444 chr5:167305432-167305443 chr5:167305434-167305443
30	CEBPB	chr5:167305274-167305556	A549	lung:	n/a	chr5:167305432-167305445 chr5:167305434-167305443 chr5:167305434-167305443 chr5:167305434-167305443 chr5:167305433-167305444 chr5:167305432-167305443 chr5:167305434-167305443
31	CEBPB	chr5:167305294-167305513	K562	blood:	n/a	chr5:167305432-167305445 chr5:167305434-167305443 chr5:167305434-167305443 chr5:167305434-167305443 chr5:167305433-167305444 chr5:167305432-167305443 chr5:167305434-167305443
32	CEBPB	chr5:167331467-167331612	A549	lung:	n/a	chr5:167331500-167331511
33	CEBPB	chr5:167429196-167429510	HepG2	liver:	n/a	chr5:167429384-167429395 chr5:167429354-167429365
34	CEBPB	chr5:167372317-167373342	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr5:167357922-167357942	A549	lung:	n/a	n/a
36	CHD2	chr5:167325751-167325949	H1-hESC	embryonic stem cell:	n/a	n/a
37	CHD2	chr5:167413424-167413430	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD2	chr5:167372531-167373241	Hela-S3	cervix:	n/a	n/a
39	CTCF	chr5:167338536-167338870	MCF-7	breast:	n/a	n/a
40	CTCF	chr5:167338500-167338650	RPTEC	kidney:	n/a	n/a
41	CTCF	chr5:167391680-167391830	K562	blood:	n/a	chr5:167391753-167391762
42	CTCF	chr5:167391649-167391850	Gliobla	brain:	n/a	chr5:167391753-167391762
43	CTCF	chr5:167394720-167394870	NHDF-neo	bronchial:	n/a	n/a
44	CTCF	chr5:167351620-167351770	NHEK	skin:	n/a	chr5:167351710-167351731 chr5:167351715-167351733
45	CTCF	chr5:167394680-167394830	HCM	heart:	n/a	n/a
46	CTCF	chr5:167397216-167397259	HepG2	liver:	n/a	n/a
47	CTCF	chr5:167448040-167448190	HEK293	kidney:	n/a	chr5:167448088-167448109 chr5:167448093-167448111
48	CTCF	chr5:167351492-167351591	MCF-7	breast:	n/a	chr5:167351537-167351555
49	CTCF	chr5:167315380-167315530	HRE	kidney:	n/a	n/a
50	CTCF	chr5:167391659-167391837	Medullo	brain:	n/a	chr5:167391753-167391762

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:167315790-167315840	HEEpiC	esophagus:	n/a
2	chr5:167394019-167394069	HUVEC	blood vessel:	n/a
3	chr5:167315790-167315840	CMK	blood:	n/a
4	chr5:167343339-167343389	CMK	blood:	n/a
5	chr5:167378696-167378746	Jurkat	blood:	n/a
6	chr5:167332342-167332392	HMEC	breast:	n/a
7	chr5:167332342-167332392	AG10803	skin:	n/a
8	chr5:167332342-167332392	LNCaP	prostate:	n/a
9	chr5:167332342-167332392	Hela-S3	cervix:	n/a
10	chr5:167343339-167343389	GM06990	blood:	n/a
11	chr5:167315790-167315840	Hepatocyte	liver:	n/a
12	chr5:167394019-167394069	HCPEpiC	choroid plexus:	n/a
13	chr5:167378696-167378746	HEEpiC	esophagus:	n/a
14	chr5:167343339-167343389	ECC-1	luminal epithelium:	n/a
15	chr5:167332342-167332392	RPTEC	kidney:	n/a
16	chr5:167378696-167378746	Caco-2	colon:	n/a
17	chr5:167315790-167315840	BE2_C	brain:	n/a
18	chr5:167343339-167343389	AG04449	skin:	fetal
19	chr5:167315790-167315840	HCM	heart:	n/a
20	chr5:167332342-167332392	AG09319	gingival:	n/a
21	chr5:167332342-167332392	GM06990	blood:	n/a
22	chr5:167332342-167332392	HCT-116	colon:	n/a
23	chr5:167394019-167394069	HCM	heart:	n/a
24	chr5:167315790-167315840	HNPCEpiC	eye:	n/a
25	chr5:167343339-167343389	AG04450	lung:	fetal
26	chr5:167378696-167378746	T-47D	breast:	n/a
27	chr5:167315790-167315840	GM06990	blood:	n/a
28	chr5:167332342-167332392	AG04450	lung:	fetal
29	chr5:167332342-167332392	HCM	heart:	n/a
30	chr5:167394019-167394069	SK-N-MC	brain:	n/a
31	chr5:167315790-167315840	GM12892	blood:	n/a
32	chr5:167343339-167343389	RPTEC	kidney:	n/a
33	chr5:167394019-167394069	RPTEC	kidney:	n/a
34	chr5:167394019-167394069	AG09319	gingival:	n/a
35	chr5:167315790-167315840	T-47D	breast:	n/a
36	chr5:167332342-167332392	MCF10A-Er-Src	breast:	n/a
37	chr5:167315790-167315840	HMEC	breast:	n/a
38	chr5:167394019-167394069	HMEC	breast:	n/a
39	chr5:167378696-167378746	HCT-116	colon:	n/a
40	chr5:167378696-167378746	ECC-1	luminal epithelium:	n/a
41	chr5:167343339-167343389	PANC-1	pancreas:	n/a
42	chr5:167332342-167332392	HRE	kidney:	n/a
43	chr5:167332342-167332392	IMR90	lung:	fetal
44	chr5:167315790-167315840	Caco-2	colon:	n/a
45	chr5:167378696-167378746	BJ	skin:	n/a
46	chr5:167378696-167378746	HPAEpiC	pulmonary alveolar:	n/a
47	chr5:167332342-167332392	ProgFib	skin:	n/a
48	chr5:167343339-167343389	LNCaP	prostate:	n/a
49	chr5:167332342-167332392	Jurkat	blood:	n/a
50	chr5:167315790-167315840	GM12878	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:167335263..167337677-chr5:167338618..167340951,2	K562	blood:
2	chr5:167150041..167150634-chr5:167447492..167448418,3	MCF-7	breast:
3	chr5:167426744..167429532-chr5:167429967..167431982,2	MCF-7	breast:
4	chr5:167335263..167337677-chr5:167338618..167340951,2	K562	blood:
5	chr5:167433427..167437109-chr5:167443043..167445741,3	K562	blood:
6	chr5:167351075..167351891-chr5:167646939..167647556,2	MCF-7	breast:
7	chr5:167433427..167437109-chr5:167443043..167445741,3	K562	blood:
8	chr5:167361443..167363556-chr5:167372770..167374605,2	MCF-7	breast:
9	chr5:167439208..167441791-chr5:167445435..167448219,2	K562	blood:
10	chr5:167439208..167441791-chr5:167445435..167448219,2	K562	blood:
11	chr5:167426744..167429532-chr5:167429967..167431982,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PANK3-4	chr5:167392192-167392583	ENSG00000253947.1
2	lnc-PANK3-16	chr5:167444912-167445128	ucscGeneNc_uc003lzs_1
3	lnc-PANK3-4	chr5:167393995-167394091	ENSG00000253947.1
4	lnc-PANK3-16	chr5:167447806-167447891	ucscGeneNc_uc003lzs_1
5	lnc-PANK3-5	chr5:167380397-167380474	ENSG00000253660.1
6	lnc-PANK3-5	chr5:167375821-167375923	ENSG00000253660.1
7	lnc-PANK3-5	chr5:167365530-167365636	ENSG00000253660.1
8	lnc-PANK3-5	chr5:167364722-167365096	ENSG00000253660.1
9	lnc-PANK3-16	chr5:167446862-167447023	ucscGeneNc_uc003lzs_1

Variant related genes	Relation type
ENSG00000253660	TF binding region
TENM2	TF binding region
ENSG00000253947	TF binding region
ENSG00000253660	CpG island
TENM2	CpG island
ENSG00000253947	CpG island
ENSG00000145934	chromatin interactions

Extended variants
information (count: 5819 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:5819 , 50 per page) page: 1 2 3 4 5 6 7 ... 117

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549348179	chr5:167303210-167303211	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs1592800	chr5:167303239-167303240	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs192958776	chr5:167303253-167303254	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs557962311	chr5:167303260-167303261	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs577778594	chr5:167303266-167303267	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs1862198	chr5:167303317-167303318	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs140450711	chr5:167303343-167303344	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs554132499	chr5:167303344-167303345	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs574268096	chr5:167303360-167303361	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs541509809	chr5:167303362-167303363	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs182359485	chr5:167303398-167303399	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs575447589	chr5:167303417-167303418	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs574163459	chr5:167303463-167303464	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs186689247	chr5:167303497-167303498	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs577275999	chr5:167303498-167303499	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs144089918	chr5:167303601-167303602	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs546230155	chr5:167303611-167303612	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs142975417	chr5:167303614-167303615	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs562762138	chr5:167303622-167303623	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs372754502	chr5:167303633-167303634	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs541269514	chr5:167303645-167303646	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs114415202	chr5:167303646-167303647	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs560227770	chr5:167303686-167303687	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs374598791	chr5:167303706-167303707	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs2193981	chr5:167303747-167303748	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs549136731	chr5:167303759-167303760	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs568894481	chr5:167303788-167303789	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs146494772	chr5:167303848-167303849	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs571442996	chr5:167304022-167304023	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs551430475	chr5:167304027-167304028	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs571507822	chr5:167304035-167304036	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs371082965	chr5:167304040-167304041	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs534171700	chr5:167304062-167304063	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs369664685	chr5:167304102-167304103	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs536991718	chr5:167304147-167304148	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs567895125	chr5:167304162-167304163	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs536937848	chr5:167304172-167304173	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs1421988	chr5:167304210-167304211	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs1421987	chr5:167304230-167304231	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs544327564	chr5:167304238-167304239	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs192480253	chr5:167304276-167304277	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs184797786	chr5:167304298-167304299	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs188875959	chr5:167304334-167304335	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs75314766	chr5:167304345-167304346	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs560271685	chr5:167304365-167304366	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs529206735	chr5:167304396-167304397	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs542477430	chr5:167304415-167304416	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs7443761	chr5:167304434-167304435	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs531549032	chr5:167304462-167304463	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs551354805	chr5:167304464-167304465	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

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
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
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Acute myeloid leukemia	21251322	CNVD
Salivary gland tumor	18059337	CNVD
Renal cell carcinoma	19377443	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Renal cell carcinoma	18592004	CNVD
Hodgkin''s lymphoma	17606441	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
Embryonal rhabdomyosarcoma	16790082	CNVD
Breast cancer	17603634	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	21720365	CNVD
Myelofibrosis	22110671	CNVD
severe myoclonic epilepsy of infancy	18294202	CNVD
Olfactory neuroblastoma	18408657	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Mental retardation	17124404	CNVD
epilepsy	18472482	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	16865294	CNVD
Sotos syndrome	21572526	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Sotos syndrome	17561922	CNVD
Sotos syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Sotos syndrome	22470819	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD

Chromatin state (count:1478 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:167266600-167326200	Weak transcription	HMEC	breast
2	chr5:167285600-167325600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr5:167296800-167303600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr5:167298000-167311000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr5:167299200-167310600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr5:167300000-167311000	Weak transcription	Fetal Lung	lung
7	chr5:167300200-167303800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr5:167300200-167308600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr5:167300800-167310600	Strong transcription	NHEK	skin
10	chr5:167301800-167306000	Weak transcription	HSMM	muscle
11	chr5:167302000-167303400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
12	chr5:167302000-167308400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr5:167303000-167303200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr5:167303400-167303600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
15	chr5:167303600-167303800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr5:167303600-167308600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
17	chr5:167303800-167305800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr5:167305800-167323600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr5:167306000-167306400	Strong transcription	HSMM	muscle
20	chr5:167306400-167326600	Weak transcription	HSMM	muscle
21	chr5:167308400-167311200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr5:167308600-167309200	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr5:167308600-167310800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
24	chr5:167309200-167310000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr5:167310000-167310600	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr5:167310600-167315400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr5:167310600-167317600	Weak transcription	NHEK	skin
28	chr5:167310600-167323000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr5:167310800-167314000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
30	chr5:167311000-167314000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr5:167311200-167316400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr5:167312200-167312800	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr5:167312400-167312600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
34	chr5:167312400-167312600	Enhancers	H9 Cell Line	embryonic stem cell
35	chr5:167312400-167312800	Enhancers	H1 Cell Line	embryonic stem cell
36	chr5:167312600-167325400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
37	chr5:167312800-167316000	Weak transcription	H1 Cell Line	embryonic stem cell
38	chr5:167312800-167316200	Weak transcription	HUES64 Cell Line	embryonic stem cell
39	chr5:167313800-167314400	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr5:167314000-167315000	Enhancers	Breast Myoepithelial Primary Cells	Breast
41	chr5:167314000-167316600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr5:167314400-167315200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
43	chr5:167315200-167316400	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chr5:167315200-167317000	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr5:167315400-167316400	Enhancers	Liver	Liver
46	chr5:167315400-167316800	Enhancers	H9 Cell Line	embryonic stem cell
47	chr5:167315400-167316800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr5:167315400-167317200	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr5:167315600-167316800	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr5:167316000-167317200	Enhancers	H1 Cell Line	embryonic stem cell

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