Variant report

Variant	nsv518575
Chromosome Location	chr5:96810447-96849023
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	BCL3	chr5:96831847-96832152	GM12878	blood:	n/a	n/a
2	BHLHE40	chr5:96830650-96830767	GM12878	blood:	n/a	n/a
3	CEBPB	chr5:96835323-96835651	MCF-7	breast:	n/a	n/a
4	CEBPB	chr5:96827337-96827579	HepG2	liver:	n/a	chr5:96827480-96827491 chr5:96827469-96827480
5	CTCF	chr5:96845160-96845310	BE2_C	brain:	n/a	n/a
6	CTCF	chr5:96845291-96845342	Spleen_OC	spleen:	n/a	n/a
7	CTCF	chr5:96831078-96831309	GM12878	blood:	n/a	n/a
8	CTCF	chr5:96811660-96811810	AG10803	skin:	n/a	n/a
9	CTCF	chr5:96823960-96824110	GM12866	blood:	n/a	n/a
10	CTCF	chr5:96825338-96825358	MCF-7	breast:	n/a	n/a
11	CTCF	chr5:96837780-96837930	GM12868	blood:	n/a	n/a
12	CUX1	chr5:96812711-96813224	GM12878	blood:	n/a	n/a
13	EBF1	chr5:96831746-96832129	GM12878	blood:	n/a	n/a
14	EP300	chr5:96812754-96812963	GM12878	blood:	n/a	chr5:96812779-96812793
15	EP300	chr5:96816475-96816487	GM12878	blood:	n/a	n/a
16	FAM48A	chr5:96839792-96839896	GM12878	blood:	n/a	n/a
17	FOS	chr5:96830507-96830677	MCF10A-Er-Src	breast:	n/a	n/a
18	FOS	chr5:96837032-96838034	MCF10A-Er-Src	breast:	n/a	chr5:96837845-96837853 chr5:96837845-96837854 chr5:96837843-96837855 chr5:96837845-96837852
19	FOS	chr5:96837018-96838030	MCF10A-Er-Src	breast:	n/a	chr5:96837845-96837853 chr5:96837845-96837854 chr5:96837843-96837855 chr5:96837845-96837852
20	FOS	chr5:96837055-96838037	MCF10A-Er-Src	breast:	n/a	chr5:96837845-96837853 chr5:96837845-96837854 chr5:96837843-96837855 chr5:96837845-96837852
21	FOS	chr5:96830515-96830751	MCF10A-Er-Src	breast:	n/a	n/a
22	FOS	chr5:96830471-96830806	MCF10A-Er-Src	breast:	n/a	n/a
23	FOS	chr5:96837020-96838028	MCF10A-Er-Src	breast:	n/a	chr5:96837845-96837853 chr5:96837845-96837854 chr5:96837843-96837855 chr5:96837845-96837852
24	FOS	chr5:96812093-96812102	MCF10A-Er-Src	breast:	n/a	n/a
25	FOXM1	chr5:96812514-96813035	GM12878	blood:	n/a	n/a
26	GATA3	chr5:96826108-96826235	SH-SY5Y	brain:	n/a	n/a
27	JUN	chr5:96817335-96817367	H1-hESC	embryonic stem cell:	n/a	n/a
28	JUN	chr5:96837800-96837955	HepG2	liver:	n/a	chr5:96837845-96837853 chr5:96837845-96837854 chr5:96837843-96837855 chr5:96837845-96837852
29	JUND	chr5:96837689-96838029	Hela-S3	cervix:	n/a	chr5:96837845-96837853 chr5:96837845-96837854 chr5:96837843-96837855 chr5:96837843-96837854 chr5:96837845-96837852
30	JUND	chr5:96823088-96823272	HepG2	liver:	n/a	n/a
31	JUND	chr5:96837506-96838204	SK-N-SH	brain:	n/a	chr5:96837845-96837853 chr5:96837845-96837854 chr5:96837843-96837855 chr5:96837843-96837854 chr5:96837845-96837852
32	JUND	chr5:96837746-96837940	H1-hESC	embryonic stem cell:	n/a	chr5:96837845-96837853 chr5:96837845-96837854 chr5:96837843-96837855 chr5:96837843-96837854 chr5:96837845-96837852
33	JUND	chr5:96837749-96838016	HepG2	liver:	n/a	chr5:96837845-96837853 chr5:96837845-96837854 chr5:96837843-96837855 chr5:96837843-96837854 chr5:96837845-96837852
34	MAFK	chr5:96831849-96832048	HepG2	liver:	n/a	chr5:96831987-96832002
35	MAFK	chr5:96812538-96812666	HepG2	liver:	n/a	n/a
36	MAX	chr5:96835314-96835684	MCF-7	breast:	n/a	chr5:96835542-96835553
37	MAZ	chr5:96848696-96848752	HepG2	liver:	n/a	n/a
38	MEF2A	chr5:96812475-96813098	GM12878	blood:	n/a	chr5:96812735-96812756 chr5:96812733-96812754
39	MEF2A	chr5:96812637-96813014	GM12878	blood:	n/a	chr5:96812735-96812756 chr5:96812733-96812754
40	MEF2C	chr5:96812539-96813022	GM12878	blood:	n/a	chr5:96812735-96812756 chr5:96812733-96812754
41	MYC	chr5:96835465-96835527	MCF-7	breast:	n/a	n/a
42	MYC	chr5:96837788-96837874	MCF10A-Er-Src	breast:	n/a	chr5:96837844-96837853 chr5:96837845-96837854
43	MYC	chr5:96823996-96824088	MCF-7	breast:	n/a	n/a
44	MYC	chr5:96835425-96835527	MCF-7	breast:	n/a	n/a
45	MYC	chr5:96836988-96837488	MCF10A-Er-Src	breast:	n/a	chr5:96837138-96837149
46	MYC	chr5:96830637-96830806	MCF10A-Er-Src	breast:	n/a	n/a
47	MYC	chr5:96836924-96837372	MCF10A-Er-Src	breast:	n/a	chr5:96837138-96837149
48	NFE2	chr5:96816577-96816581	GM12878	blood:	n/a	n/a
49	NFE2	chr5:96813062-96813078	GM12878	blood:	n/a	n/a
50	NFIC	chr5:96812310-96813324	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:96845117-96845167	IMR90	lung:	fetal
2	chr5:96845117-96845167	AG10803	skin:	n/a
3	chr5:96845117-96845167	HCF	heart:	n/a
4	chr5:96845117-96845167	AG04449	skin:	fetal
5	chr5:96845117-96845167	CMK	blood:	n/a
6	chr5:96845117-96845167	AoSMC	blood vessel:	n/a
7	chr5:96845117-96845167	Hepatocyte	liver:	n/a
8	chr5:96845117-96845167	HRE	kidney:	n/a
9	chr5:96845117-96845167	SK-N-SH_RA	brain:	n/a
10	chr5:96845117-96845167	AG09309	skin:	n/a
11	chr5:96845117-96845167	K562	blood:	n/a
12	chr5:96845117-96845167	BE2_C	brain:	n/a
13	chr5:96845117-96845167	U87	brain:	n/a
14	chr5:96845117-96845167	GM19239	blood:	n/a
15	chr5:96845117-96845167	SK-N-SH	brain:	n/a
16	chr5:96845117-96845167	HMEC	breast:	n/a
17	chr5:96845117-96845167	AG09319	gingival:	n/a
18	chr5:96845117-96845167	HRCEpiC	kidney:	n/a
19	chr5:96845117-96845167	GM12891	blood:	n/a
20	chr5:96845117-96845167	PrEC	prostate:	n/a
21	chr5:96845117-96845167	HEK293	kidney:	embryo
22	chr5:96845117-96845167	HIPEpiC	eye:	n/a
23	chr5:96845117-96845167	SAEC	small airway:	n/a
24	chr5:96845117-96845167	SK-N-MC	brain:	n/a
25	chr5:96845117-96845167	RPTEC	kidney:	n/a
26	chr5:96845117-96845167	AG04450	lung:	fetal
27	chr5:96845117-96845167	HCT-116	colon:	n/a
28	chr5:96845117-96845167	LNCaP	prostate:	n/a
29	chr5:96845117-96845167	HNPCEpiC	eye:	n/a
30	chr5:96845117-96845167	HL-60	blood:	n/a
31	chr5:96845117-96845167	H1-hESC	embryonic stem cell:	embryo
32	chr5:96845117-96845167	HRPEpiC	eye:	n/a
33	chr5:96845117-96845167	HCM	heart:	n/a
34	chr5:96845117-96845167	HEEpiC	esophagus:	n/a
35	chr5:96845117-96845167	HepG2	liver:	n/a
36	chr5:96845117-96845167	Caco-2	colon:	n/a
37	chr5:96845117-96845167	NT2-D1	testis:	n/a
38	chr5:96845117-96845167	SKMC	muscle:	n/a
39	chr5:96845117-96845167	ProgFib	skin:	n/a
40	chr5:96845117-96845167	MCF10A-Er-Src	breast:	n/a
41	chr5:96845117-96845167	NH-A	brain:	n/a
42	chr5:96845117-96845167	ovcar-3	ovarian:	n/a
43	chr5:96845117-96845167	PANC-1	pancreas:	n/a
44	chr5:96845117-96845167	GM12878	blood:	n/a
45	chr5:96845117-96845167	NHBE	bronchial:	n/a
46	chr5:96845117-96845167	ECC-1	luminal epithelium:	n/a
47	chr5:96845117-96845167	HCPEpiC	choroid plexus:	n/a
48	chr5:96845117-96845167	Jurkat	blood:	n/a
49	chr5:96845117-96845167	HAEpiC	amniotic membrane:	n/a
50	chr5:96845117-96845167	BJ	skin:	n/a

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CTD-2215E18.1.1-2	chr5:96840400-96840496	XLOC_004483
2	lnc-CTD-2215E18.1.1-2	chr5:96840400-96840496	NR_105028
3	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: 1213 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:1213 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs531119398	chr5:96811816-96811817	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs370291829	chr5:96811830-96811831	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs182048295	chr5:96811852-96811853	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs549057498	chr5:96811939-96811940	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs150099661	chr5:96812014-96812015	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs547102094	chr5:96812015-96812016	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs376272483	chr5:96812028-96812029	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs546405636	chr5:96812029-96812030	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs138600828	chr5:96812037-96812038	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs532813418	chr5:96812048-96812049	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs568131317	chr5:96812060-96812061	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs370651034	chr5:96812091-96812092	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs551634062	chr5:96812128-96812129	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs569890528	chr5:96812166-96812167	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs537245594	chr5:96812180-96812181	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs1843330	chr5:96812218-96812219	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs76697313	chr5:96812231-96812232	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs34371656	chr5:96812232-96812233	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs62378487	chr5:96812233-96812234	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs116345377	chr5:96812260-96812261	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs62378488	chr5:96812262-96812263	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs77319833	chr5:96812324-96812325	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs115129658	chr5:96812448-96812449	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs553526218	chr5:96812449-96812450	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs12654477	chr5:96812450-96812451	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs538690983	chr5:96812509-96812510	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs557625556	chr5:96812520-96812521	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs6877080	chr5:96812542-96812543	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs138133570	chr5:96812588-96812589	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs143666085	chr5:96812590-96812591	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs144030140	chr5:96812598-96812599	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs115159334	chr5:96812599-96812600	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs148756255	chr5:96812697-96812698	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs187083776	chr5:96812713-96812714	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs116249504	chr5:96812718-96812719	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs141443667	chr5:96812725-96812726	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs563296047	chr5:96812741-96812742	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs377184389	chr5:96812781-96812782	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs71654381	chr5:96812833-96812834	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs549313514	chr5:96812878-96812879	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs78049804	chr5:96812888-96812889	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs192422964	chr5:96812903-96812904	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs114083257	chr5:96812940-96812941	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs547099589	chr5:96812946-96812947	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs547708644	chr5:96812950-96812951	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs182158221	chr5:96812982-96812983	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs539020287	chr5:96812994-96812995	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs557027504	chr5:96813013-96813014	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs150827807	chr5:96813057-96813058	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs536513527	chr5:96813129-96813130	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

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

Chromatin state (count:99 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:96811800-96812400	Enhancers	GM12878-XiMat	blood
2	chr5:96812200-96813000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr5:96812400-96812800	Enhancers	NHEK	skin
4	chr5:96812400-96813000	Flanking Active TSS	GM12878-XiMat	blood
5	chr5:96813000-96815600	Enhancers	GM12878-XiMat	blood
6	chr5:96814000-96814600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr5:96814200-96814600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr5:96814200-96814600	Enhancers	Fetal Lung	lung
9	chr5:96814200-96814600	Enhancers	Ovary	ovary
10	chr5:96814400-96815000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr5:96814600-96816200	Weak transcription	Ovary	ovary
12	chr5:96815600-96816600	Flanking Active TSS	GM12878-XiMat	blood
13	chr5:96816200-96816600	Enhancers	Ovary	ovary
14	chr5:96816600-96816800	Enhancers	GM12878-XiMat	blood
15	chr5:96816600-96818600	Weak transcription	Ovary	ovary
16	chr5:96817400-96817600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr5:96818400-96818600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr5:96818600-96819000	Enhancers	Ovary	ovary
19	chr5:96818800-96819000	Enhancers	Gastric	stomach
20	chr5:96821400-96821600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr5:96821600-96823800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr5:96822000-96824000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr5:96823800-96824000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr5:96823800-96824000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr5:96823800-96824200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr5:96823800-96824200	Enhancers	Breast Myoepithelial Primary Cells	Breast
27	chr5:96824000-96824200	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr5:96824000-96824200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr5:96824200-96824800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr5:96824800-96825200	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr5:96825000-96825200	Enhancers	Pancreas	Pancrea
32	chr5:96825200-96830200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr5:96829200-96831600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr5:96830200-96830400	Enhancers	Ovary	ovary
35	chr5:96830200-96831000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr5:96830200-96831200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr5:96830200-96831400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr5:96830200-96831400	Enhancers	Breast Myoepithelial Primary Cells	Breast
39	chr5:96830400-96831000	Weak transcription	Ovary	ovary
40	chr5:96830400-96832000	Enhancers	Cortex derived primary cultured neurospheres	brain
41	chr5:96831000-96831200	Enhancers	Ovary	ovary
42	chr5:96831200-96832000	Enhancers	Brain Hippocampus Middle	brain
43	chr5:96831200-96838400	Weak transcription	Ovary	ovary
44	chr5:96831400-96831800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
45	chr5:96831400-96832400	Enhancers	Dnd41	blood
46	chr5:96831800-96832000	Enhancers	Breast Myoepithelial Primary Cells	Breast
47	chr5:96832000-96835000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
48	chr5:96832000-96836600	Weak transcription	Cortex derived primary cultured neurospheres	brain
49	chr5:96835000-96835800	Enhancers	Breast Myoepithelial Primary Cells	Breast
50	chr5:96835200-96835400	Enhancers	Brain Substantia Nigra	brain

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