Variant report

Variant	nsv830416
Chromosome Location	chr5:96817328-96958233
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	chr5:96869893-96870174	HepG2	liver:	n/a	n/a
2	ATF1	chr5:96925354-96925372	K562	blood:	n/a	n/a
3	ATF2	chr5:96883703-96884520	GM12878	blood:	n/a	n/a
4	ATF2	chr5:96883636-96884569	GM12878	blood:	n/a	n/a
5	BACH1	chr5:96885956-96886136	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr5:96861461-96861877	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr5:96872429-96872695	GM12878	blood:	n/a	chr5:96872552-96872563
8	BATF	chr5:96883695-96884539	GM12878	blood:	n/a	chr5:96884341-96884350
9	BATF	chr5:96883741-96884022	GM12878	blood:	n/a	n/a
10	BATF	chr5:96884044-96884526	GM12878	blood:	n/a	chr5:96884341-96884350
11	BATF	chr5:96872418-96872668	GM12878	blood:	n/a	chr5:96872552-96872563
12	BCL11A	chr5:96884015-96884504	GM12878	blood:	n/a	n/a
13	BCL11A	chr5:96883801-96884003	GM12878	blood:	n/a	chr5:96883828-96883837
14	BCL11A	chr5:96884033-96884506	GM12878	blood:	n/a	n/a
15	BCL3	chr5:96928285-96928637	GM12878	blood:	n/a	n/a
16	BCL3	chr5:96831847-96832152	GM12878	blood:	n/a	n/a
17	BHLHE40	chr5:96830650-96830767	GM12878	blood:	n/a	n/a
18	BHLHE40	chr5:96883684-96884500	GM12878	blood:	n/a	n/a
19	BHLHE40	chr5:96869825-96870150	GM12878	blood:	n/a	n/a
20	CEBPB	chr5:96889560-96889890	A549	lung:	n/a	chr5:96889732-96889743 chr5:96889717-96889728
21	CEBPB	chr5:96835323-96835651	MCF-7	breast:	n/a	n/a
22	CEBPB	chr5:96869836-96870407	IMR90	lung:	n/a	chr5:96870105-96870116
23	CEBPB	chr5:96869872-96870368	A549	lung:	n/a	chr5:96870105-96870116
24	CEBPB	chr5:96827337-96827579	HepG2	liver:	n/a	chr5:96827480-96827491 chr5:96827469-96827480
25	CEBPB	chr5:96928194-96928475	HepG2	liver:	n/a	chr5:96928315-96928326
26	CEBPB	chr5:96869919-96870277	A549	lung:	n/a	chr5:96870105-96870116
27	CEBPB	chr5:96889557-96889904	HepG2	liver:	n/a	chr5:96889732-96889743 chr5:96889717-96889728
28	CEBPB	chr5:96889539-96889927	IMR90	lung:	n/a	chr5:96889732-96889743 chr5:96889717-96889728
29	CEBPB	chr5:96916250-96916433	HepG2	liver:	n/a	chr5:96916265-96916273
30	CEBPB	chr5:96869919-96870296	Hela-S3	cervix:	n/a	chr5:96870105-96870116
31	CEBPB	chr5:96869837-96870355	MCF-7	breast:	n/a	chr5:96870105-96870116
32	CEBPB	chr5:96889795-96889802	K562	blood:	n/a	n/a
33	CEBPB	chr5:96869955-96870234	K562	blood:	n/a	chr5:96870105-96870116
34	CEBPB	chr5:96889595-96889861	Hela-S3	cervix:	n/a	chr5:96889732-96889743 chr5:96889717-96889728
35	CEBPB	chr5:96869838-96870259	MCF-7	breast:	n/a	chr5:96870105-96870116
36	CEBPB	chr5:96930445-96930679	IMR90	lung:	n/a	n/a
37	CEBPB	chr5:96869858-96870217	H1-hESC	embryonic stem cell:	n/a	chr5:96870105-96870116
38	CEBPB	chr5:96869911-96870297	HepG2	liver:	n/a	chr5:96870105-96870116
39	CHD2	chr5:96869836-96870045	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD2	chr5:96883728-96884432	GM12878	blood:	n/a	n/a
41	CTCF	chr5:96893511-96893533	Fibrobl	skin:	n/a	n/a
42	CTCF	chr5:96869900-96870050	AG10803	skin:	n/a	chr5:96869980-96869998 chr5:96869975-96869996 chr5:96869981-96869997 chr5:96869986-96869995
43	CTCF	chr5:96869894-96870113	Hela-S3	cervix:	n/a	chr5:96869980-96869998 chr5:96869975-96869996 chr5:96869981-96869997 chr5:96869986-96869995
44	CTCF	chr5:96869880-96870030	HVMF	connective:	n/a	chr5:96869980-96869998 chr5:96869975-96869996 chr5:96869981-96869997 chr5:96869986-96869995
45	CTCF	chr5:96869884-96870057	A549	lung:	n/a	chr5:96869980-96869998 chr5:96869975-96869996 chr5:96869981-96869997 chr5:96869986-96869995
46	CTCF	chr5:96869900-96870050	HBMEC	blood vessel:	n/a	chr5:96869980-96869998 chr5:96869975-96869996 chr5:96869981-96869997 chr5:96869986-96869995
47	CTCF	chr5:96869920-96870070	NHDF-neo	bronchial:	n/a	chr5:96869980-96869998 chr5:96869975-96869996 chr5:96869981-96869997 chr5:96869986-96869995
48	CTCF	chr5:96869880-96870030	AG04450	lung:	n/a	chr5:96869980-96869998 chr5:96869975-96869996 chr5:96869981-96869997 chr5:96869986-96869995
49	CTCF	chr5:96869900-96870050	GM12869	blood:	n/a	chr5:96869980-96869998 chr5:96869975-96869996 chr5:96869981-96869997 chr5:96869986-96869995
50	CTCF	chr5:96869930-96870052	MCF-7	breast:	n/a	chr5:96869980-96869998 chr5:96869975-96869996 chr5:96869981-96869997 chr5:96869986-96869995

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:96915770-96915820	NB4	blood:	n/a
2	chr5:96890257-96890307	HEEpiC	esophagus:	n/a
3	chr5:96876834-96876884	LNCaP	prostate:	n/a
4	chr5:96876834-96876884	HAEpiC	amniotic membrane:	n/a
5	chr5:96876834-96876884	HCF	heart:	n/a
6	chr5:96881859-96881909	NH-A	brain:	n/a
7	chr5:96876834-96876884	GM19239	blood:	n/a
8	chr5:96890257-96890307	HCF	heart:	n/a
9	chr5:96845117-96845167	AG04450	lung:	fetal
10	chr5:96881859-96881909	BJ	skin:	n/a
11	chr5:96876834-96876884	NB4	blood:	n/a
12	chr5:96915770-96915820	GM06990	blood:	n/a
13	chr5:96881859-96881909	Hepatocyte	liver:	n/a
14	chr5:96915770-96915820	SK-N-SH_RA	brain:	n/a
15	chr5:96890257-96890307	GM06990	blood:	n/a
16	chr5:96881859-96881909	CMK	blood:	n/a
17	chr5:96845117-96845167	HUVEC	blood vessel:	n/a
18	chr5:96881859-96881909	HNPCEpiC	eye:	n/a
19	chr5:96890257-96890307	H1-hESC	embryonic stem cell:	embryo
20	chr5:96845117-96845167	Jurkat	blood:	n/a
21	chr5:96915770-96915820	A549	lung:	n/a
22	chr5:96855476-96855526	LNCaP	prostate:	n/a
23	chr5:96881859-96881909	HPAEpiC	pulmonary alveolar:	n/a
24	chr5:96876834-96876884	PrEC	prostate:	n/a
25	chr5:96845117-96845167	HAEpiC	amniotic membrane:	n/a
26	chr5:96855476-96855526	ovcar-3	ovarian:	n/a
27	chr5:96890257-96890307	MCF10A-Er-Src	breast:	n/a
28	chr5:96855476-96855526	HIPEpiC	eye:	n/a
29	chr5:96845117-96845167	SK-N-MC	brain:	n/a
30	chr5:96915770-96915820	U87	brain:	n/a
31	chr5:96890257-96890307	GM12891	blood:	n/a
32	chr5:96876834-96876884	CMK	blood:	n/a
33	chr5:96881859-96881909	AG10803	skin:	n/a
34	chr5:96890257-96890307	AG04450	lung:	fetal
35	chr5:96915770-96915820	GM12878	blood:	n/a
36	chr5:96890257-96890307	ProgFib	skin:	n/a
37	chr5:96855476-96855526	GM06990	blood:	n/a
38	chr5:96881859-96881909	AG04449	skin:	fetal
39	chr5:96876834-96876884	AoSMC	blood vessel:	n/a
40	chr5:96876834-96876884	SK-N-SH	brain:	n/a
41	chr5:96855476-96855526	HEK293	kidney:	embryo
42	chr5:96881859-96881909	HRPEpiC	eye:	n/a
43	chr5:96845117-96845167	GM12892	blood:	n/a
44	chr5:96855476-96855526	GM12892	blood:	n/a
45	chr5:96890257-96890307	PANC-1	pancreas:	n/a
46	chr5:96915770-96915820	MCF10A-Er-Src	breast:	n/a
47	chr5:96915770-96915820	SKMC	muscle:	n/a
48	chr5:96915770-96915820	CMK	blood:	n/a
49	chr5:96881859-96881909	ProgFib	skin:	n/a
50	chr5:96845117-96845167	GM19239	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:96865281..96867677-chr5:96867921..96869530,2	K562	blood:
2	chr5:96566460..96567205-chr5:96869494..96870442,2	MCF-7	breast:
3	chr5:96902855..96905560-chr5:96907320..96909656,2	K562	blood:
4	chr5:96898495..96900851-chr5:96905056..96906917,2	K562	blood:
5	chr5:96865281..96867677-chr5:96867921..96869530,2	K562	blood:
6	chr5:96902855..96905560-chr5:96907320..96909656,2	K562	blood:
7	chr5:96898495..96900851-chr5:96905056..96906917,2	K562	blood:
8	chr5:96869180..96869850-chr5:98103055..98104021,2	MCF-7	breast:
9	chr5:96632616..96633407-chr5:96869853..96870506,3	MCF-7	breast:
10	chr5:96632479..96633406-chr5:96869339..96870359,6	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CTD-2215E18.1.1-2	chr5:96856933-96856994	XLOC_004483
2	lnc-CTD-2215E18.1.1-2	chr5:96840400-96840496	XLOC_004483
3	lnc-CTD-2215E18.1.1-2	chr5:96840400-96840496	NR_105028
4	lnc-CTD-2215E18.1.1-2	chr5:96856933-96856994	NR_105028
5	lnc-CTD-2215E18.1.1-2	chr5:96856932-96856994	NONHSAT102931
6	lnc-CTD-2215E18.1.1-2	chr5:96840399-96840496	NONHSAT102931

Variant related genes	Relation type
ENSG00000250331	TF binding region
ENSG00000250331	CpG island

Extended variants
information (count: 3063 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:3063 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561882544	chr5:96817460-96817461	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs528995046	chr5:96817481-96817482	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs529568475	chr5:96817506-96817507	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs541758168	chr5:96817516-96817517	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs1485469	chr5:96817528-96817529	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs533386498	chr5:96817558-96817559	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs6861329	chr5:96817568-96817569	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs531714362	chr5:96817593-96817594	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs72766307	chr5:96817653-96817654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs531332781	chr5:96817674-96817675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs549318469	chr5:96817719-96817720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs201188311	chr5:96817729-96817730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs146633374	chr5:96817730-96817731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs376827784	chr5:96817732-96817733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs10658948	chr5:96817735-96817736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs375160350	chr5:96817736-96817737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs369809698	chr5:96817737-96817738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs371857905	chr5:96817738-96817739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs77407473	chr5:96817748-96817749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs371977661	chr5:96817759-96817760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs553673419	chr5:96817856-96817857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs144719724	chr5:96817863-96817864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs34543687	chr5:96817867-96817868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs565847487	chr5:96817879-96817880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs539291366	chr5:96817927-96817928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs189545532	chr5:96818033-96818034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs75518307	chr5:96818040-96818041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs543940406	chr5:96818042-96818043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs112670193	chr5:96818096-96818097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs377520891	chr5:96818098-96818099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs574101933	chr5:96818102-96818103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs541721298	chr5:96818198-96818199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs548375822	chr5:96818250-96818251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs180891072	chr5:96818292-96818293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs186231283	chr5:96818311-96818312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs114938742	chr5:96818398-96818399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs191531470	chr5:96818467-96818468	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs111425962	chr5:96818529-96818530	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs529409883	chr5:96818590-96818591	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs531265556	chr5:96818647-96818648	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs111264866	chr5:96818653-96818654	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs534769388	chr5:96818656-96818657	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs558099064	chr5:96818657-96818658	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs370453875	chr5:96818875-96818876	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs374434972	chr5:96818916-96818917	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs528885998	chr5:96818926-96818927	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs571210233	chr5:96818935-96818936	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs146056481	chr5:96818999-96819000	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs11741545	chr5:96821463-96821464	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs534365767	chr5:96821483-96821484	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

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
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Mental retardation	19471318	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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	19036926	CNVD

Chromatin state (count:503 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:96816600-96818600	Weak transcription	Ovary	ovary
2	chr5:96817400-96817600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr5:96818400-96818600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr5:96818600-96819000	Enhancers	Ovary	ovary
5	chr5:96818800-96819000	Enhancers	Gastric	stomach
6	chr5:96821400-96821600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr5:96821600-96823800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr5:96822000-96824000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr5:96823800-96824000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr5:96823800-96824000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr5:96823800-96824200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr5:96823800-96824200	Enhancers	Breast Myoepithelial Primary Cells	Breast
13	chr5:96824000-96824200	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr5:96824000-96824200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr5:96824200-96824800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr5:96824800-96825200	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr5:96825000-96825200	Enhancers	Pancreas	Pancrea
18	chr5:96825200-96830200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr5:96829200-96831600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr5:96830200-96830400	Enhancers	Ovary	ovary
21	chr5:96830200-96831000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr5:96830200-96831200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr5:96830200-96831400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr5:96830200-96831400	Enhancers	Breast Myoepithelial Primary Cells	Breast
25	chr5:96830400-96831000	Weak transcription	Ovary	ovary
26	chr5:96830400-96832000	Enhancers	Cortex derived primary cultured neurospheres	brain
27	chr5:96831000-96831200	Enhancers	Ovary	ovary
28	chr5:96831200-96832000	Enhancers	Brain Hippocampus Middle	brain
29	chr5:96831200-96838400	Weak transcription	Ovary	ovary
30	chr5:96831400-96831800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
31	chr5:96831400-96832400	Enhancers	Dnd41	blood
32	chr5:96831800-96832000	Enhancers	Breast Myoepithelial Primary Cells	Breast
33	chr5:96832000-96835000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
34	chr5:96832000-96836600	Weak transcription	Cortex derived primary cultured neurospheres	brain
35	chr5:96835000-96835800	Enhancers	Breast Myoepithelial Primary Cells	Breast
36	chr5:96835200-96835400	Enhancers	Brain Substantia Nigra	brain
37	chr5:96835200-96835600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr5:96835400-96835600	Enhancers	Brain Anterior Caudate	brain
39	chr5:96835400-96835600	Enhancers	Brain Cingulate Gyrus	brain
40	chr5:96835400-96835600	Enhancers	Right Atrium	heart
41	chr5:96835400-96837000	Weak transcription	Brain Substantia Nigra	brain
42	chr5:96835600-96835800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr5:96835600-96837000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr5:96835800-96837000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
45	chr5:96835800-96837000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr5:96836600-96837800	Enhancers	Cortex derived primary cultured neurospheres	brain
47	chr5:96836600-96837800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr5:96837000-96837200	Enhancers	Aorta	Aorta
49	chr5:96837000-96837800	Enhancers	Breast Myoepithelial Primary Cells	Breast
50	chr5:96837000-96837800	Enhancers	Brain Substantia Nigra	brain

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