Variant report

Variant	nsv880796
Chromosome Location	chr5:40934832-40985604
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	BACH1	chr5:40957286-40957375	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr5:40973622-40973787	A549	lung:	n/a	n/a
3	CEBPB	chr5:40956045-40956290	HepG2	liver:	n/a	chr5:40956174-40956185
4	CEBPB	chr5:40974072-40974407	IMR90	lung:	n/a	chr5:40974236-40974247
5	CEBPB	chr5:40965401-40965585	HepG2	liver:	n/a	n/a
6	CEBPB	chr5:40938639-40938901	HepG2	liver:	n/a	chr5:40938772-40938783
7	CEBPB	chr5:40936932-40937135	HepG2	liver:	n/a	chr5:40936998-40937015
8	CEBPB	chr5:40974085-40974421	K562	blood:	n/a	chr5:40974236-40974247
9	CEBPB	chr5:40974125-40974378	HepG2	liver:	n/a	chr5:40974236-40974247
10	CHD2	chr5:40972729-40972811	HepG2	liver:	n/a	n/a
11	CTCF	chr5:40980640-40980790	HFF-Myc	foreskin:	n/a	n/a
12	CTCF	chr5:40962480-40962630	NB4	blood:	n/a	chr5:40962495-40962516
13	CTCF	chr5:40962500-40962650	RPTEC	kidney:	n/a	n/a
14	CTCF	chr5:40962400-40962550	A549	lung:	n/a	chr5:40962495-40962516
15	CTCF	chr5:40962440-40962581	Medullo	brain:	n/a	chr5:40962495-40962516
16	CTCF	chr5:40962414-40962624	MCF-7	breast:	n/a	chr5:40962495-40962516
17	CTCF	chr5:40962380-40962530	HMF	breast:	n/a	chr5:40962495-40962516
18	CTCF	chr5:40962440-40962590	WERI-Rb-1	eye:	n/a	chr5:40962495-40962516
19	CTCF	chr5:40962500-40962650	BE2_C	brain:	n/a	n/a
20	CTCF	chr5:40962460-40962610	HEEpiC	esophagus:	n/a	chr5:40962495-40962516
21	CTCF	chr5:40962460-40962610	BE2_C	brain:	n/a	chr5:40962495-40962516
22	CTCF	chr5:40962321-40962806	MCF-7	breast:	n/a	chr5:40962495-40962516
23	CTCF	chr5:40962320-40962470	RPTEC	kidney:	n/a	n/a
24	CTCF	chr5:40962420-40962570	K562	blood:	n/a	chr5:40962495-40962516
25	CTCF	chr5:40962440-40962640	GM12878	blood:	n/a	chr5:40962495-40962516
26	CTCF	chr5:40962310-40962721	MCF-7	breast:	n/a	chr5:40962495-40962516
27	CTCF	chr5:40950840-40950990	GM12867	blood:	n/a	n/a
28	CTCF	chr5:40965411-40965499	Spleen_OC	spleen:	n/a	n/a
29	CTCF	chr5:40962372-40962595	T-47D	breast:	n/a	chr5:40962495-40962516
30	CTCF	chr5:40962360-40962510	HBMEC	blood vessel:	n/a	n/a
31	CTCF	chr5:40962461-40962564	K562	blood:	n/a	chr5:40962495-40962516
32	CTCF	chr5:40962380-40962530	HMEC	breast:	n/a	chr5:40962495-40962516
33	CTCF	chr5:40962442-40962597	LNCaP	prostate:	n/a	chr5:40962495-40962516
34	CTCF	chr5:40962482-40962554	NHEK	skin:	n/a	chr5:40962495-40962516
35	CTCF	chr5:40962350-40962576	H1-hESC	embryonic stem cell:	n/a	chr5:40962495-40962516
36	CTCF	chr5:40962400-40962637	MCF-7	breast:	n/a	chr5:40962495-40962516
37	CTCF	chr5:40962490-40962567	HUVEC	blood vessel:	n/a	chr5:40962495-40962516
38	CTCF	chr5:40962448-40962593	LNCaP	prostate:	n/a	chr5:40962495-40962516
39	CTCF	chr5:40962428-40962612	Gliobla	brain:	n/a	chr5:40962495-40962516
40	CTCF	chr5:40962478-40962546	A549	lung:	n/a	chr5:40962495-40962516
41	CTCF	chr5:40962380-40962530	HPAF	blood vessel:	n/a	chr5:40962495-40962516
42	CTCF	chr5:40962480-40962630	HA-sp	spinal cord:	n/a	chr5:40962495-40962516
43	CTCF	chr5:40962426-40962603	Hela-S3	cervix:	n/a	chr5:40962495-40962516
44	CTCF	chr5:40962394-40962658	K562	blood:	n/a	chr5:40962495-40962516
45	CTCF	chr5:40962440-40962590	SK-N-SH_RA	brain:	n/a	chr5:40962495-40962516
46	CTCF	chr5:40962420-40962570	MCF-7	breast:	n/a	chr5:40962495-40962516
47	CTCF	chr5:40962440-40962590	HCM	heart:	n/a	chr5:40962495-40962516
48	CTCF	chr5:40962400-40962550	HPAF	blood vessel:	n/a	chr5:40962495-40962516
49	CTCF	chr5:40962460-40962610	HCPEpiC	choroid plexus:	n/a	chr5:40962495-40962516
50	CTCF	chr5:40962420-40962570	SK-N-SH_RA	brain:	n/a	chr5:40962495-40962516

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:40984654-40984704	Hepatocyte	liver:	n/a
2	chr5:40982092-40982142	HEK293	kidney:	embryo
3	chr5:40982092-40982142	ProgFib	skin:	n/a
4	chr5:40982092-40982142	HRE	kidney:	n/a
5	chr5:40982092-40982142	SAEC	small airway:	n/a
6	chr5:40982092-40982142	NH-A	brain:	n/a
7	chr5:40984654-40984704	HIPEpiC	eye:	n/a
8	chr5:40982092-40982142	BJ	skin:	n/a
9	chr5:40984654-40984704	ProgFib	skin:	n/a
10	chr5:40984654-40984704	HL-60	blood:	n/a
11	chr5:40984654-40984704	AG04449	skin:	fetal
12	chr5:40982092-40982142	HPAEpiC	pulmonary alveolar:	n/a
13	chr5:40982092-40982142	AG09319	gingival:	n/a
14	chr5:40984654-40984704	GM19239	blood:	n/a
15	chr5:40984654-40984704	Caco-2	colon:	n/a
16	chr5:40982092-40982142	HRPEpiC	eye:	n/a
17	chr5:40984654-40984704	HRE	kidney:	n/a
18	chr5:40982092-40982142	Caco-2	colon:	n/a
19	chr5:40984654-40984704	T-47D	breast:	n/a
20	chr5:40984654-40984704	NT2-D1	testis:	n/a
21	chr5:40982092-40982142	GM12878	blood:	n/a
22	chr5:40984654-40984704	NB4	blood:	n/a
23	chr5:40982092-40982142	K562	blood:	n/a
24	chr5:40984654-40984704	HCT-116	colon:	n/a
25	chr5:40984654-40984704	PFSK-1	brain:	n/a
26	chr5:40982092-40982142	CMK	blood:	n/a
27	chr5:40982092-40982142	PrEC	prostate:	n/a
28	chr5:40982092-40982142	ECC-1	luminal epithelium:	n/a
29	chr5:40984654-40984704	HCPEpiC	choroid plexus:	n/a
30	chr5:40982092-40982142	HEEpiC	esophagus:	n/a
31	chr5:40982092-40982142	AG04450	lung:	fetal
32	chr5:40984654-40984704	HAEpiC	amniotic membrane:	n/a
33	chr5:40984654-40984704	SAEC	small airway:	n/a
34	chr5:40982092-40982142	MCF10A-Er-Src	breast:	n/a
35	chr5:40984654-40984704	GM12892	blood:	n/a
36	chr5:40982092-40982142	Hepatocyte	liver:	n/a
37	chr5:40982092-40982142	SK-N-SH	brain:	n/a
38	chr5:40982092-40982142	AG09309	skin:	n/a
39	chr5:40982092-40982142	U87	brain:	n/a
40	chr5:40982092-40982142	NHBE	bronchial:	n/a
41	chr5:40984654-40984704	NHBE	bronchial:	n/a
42	chr5:40982092-40982142	HCF	heart:	n/a
43	chr5:40982092-40982142	HepG2	liver:	n/a
44	chr5:40984654-40984704	SK-N-MC	brain:	n/a
45	chr5:40982092-40982142	PFSK-1	brain:	n/a
46	chr5:40982092-40982142	SK-N-SH_RA	brain:	n/a
47	chr5:40984654-40984704	PrEC	prostate:	n/a
48	chr5:40982092-40982142	HNPCEpiC	eye:	n/a
49	chr5:40984654-40984704	HEK293	kidney:	embryo
50	chr5:40984654-40984704	HRPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:40956867..40959314-chr5:40961623..40964279,2	K562	blood:
2	chr5:40973576..40975248-chr5:40975301..40976808,2	K562	blood:
3	chr5:40942973..40944757-chr5:40947112..40948755,2	K562	blood:
4	chr5:40966521..40968978-chr5:40972964..40975614,2	K562	blood:
5	chr5:40982776..40984808-chr5:40985903..40987745,2	MCF-7	breast:
6	chr5:40953904..40955665-chr5:40958137..40961291,3	K562	blood:
7	chr5:40956867..40959314-chr5:40961623..40964279,2	K562	blood:
8	chr5:40904493..40905461-chr5:40962028..40963060,5	MCF-7	breast:
9	chr5:40942973..40944757-chr5:40947112..40948755,2	K562	blood:
10	chr5:40976435..40978654-chr5:40981165..40983348,2	MCF-7	breast:
11	chr5:40953904..40955665-chr5:40958137..40961291,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HEATR7B2-2	chr5:40967607-40967865	NONHSAT101165

Variant related genes	Relation type
ENSG00000248120	TF binding region
C7	TF binding region
ENSG00000248120	CpG island
C7	CpG island
ENSG00000248120	chromatin interactions
ENSG00000112936	chromatin interactions

Extended variants
information (count: 2244 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:2244 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10512751	chr5:40934832-40934833	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs41271057	chr5:40934886-40934887	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs540416559	chr5:40934891-40934892	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs568112537	chr5:40934945-40934946	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs529290969	chr5:40934980-40934981	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs184162860	chr5:40935175-40935176	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs576431800	chr5:40935229-40935230	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs566061525	chr5:40935235-40935236	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs114504592	chr5:40935239-40935240	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs540142091	chr5:40935270-40935271	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs147205142	chr5:40935290-40935291	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs570240207	chr5:40935376-40935377	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs536699368	chr5:40935423-40935424	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs558663384	chr5:40935461-40935462	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs555546857	chr5:40935493-40935494	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs189671709	chr5:40935510-40935511	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs6879251	chr5:40935520-40935521	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs546936897	chr5:40935577-40935578	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs553279658	chr5:40935602-40935603	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs577829532	chr5:40935604-40935605	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs192364587	chr5:40935607-40935608	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs545299445	chr5:40935614-40935615	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs372086195	chr5:40935627-40935628	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs540846341	chr5:40935629-40935630	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs563293876	chr5:40935648-40935649	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs530781458	chr5:40935680-40935681	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs543503483	chr5:40935702-40935703	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs140587978	chr5:40935712-40935713	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs184309039	chr5:40935735-40935736	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs529228049	chr5:40935745-40935746	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs529953450	chr5:40935764-40935765	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs563431586	chr5:40935767-40935768	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs190473436	chr5:40935769-40935770	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs371984547	chr5:40935795-40935796	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs566080606	chr5:40935800-40935801	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs533418193	chr5:40935819-40935820	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs552053173	chr5:40935910-40935911	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs567068435	chr5:40935940-40935941	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs570145709	chr5:40935968-40935969	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs537690028	chr5:40935969-40935970	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs115481644	chr5:40935977-40935978	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs567394059	chr5:40935992-40935993	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs534727273	chr5:40936002-40936003	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs552966813	chr5:40936018-40936019	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs577572164	chr5:40936030-40936031	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs544974569	chr5:40936035-40936036	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs35327290	chr5:40936060-40936061	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs138674554	chr5:40936083-40936084	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs557266162	chr5:40936182-40936183	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs528159556	chr5:40936183-40936184	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

Disease	PMID	Source
Cervical squamous cell carcinoma	21590768	CNVD
Non-small cell lung cancer	20864512	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	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
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Bladder cancer	21909424	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Cancer	16751803	CNVD
Breast cancer	16608533	CNVD
Autism	22495311	CNVD
Intellectual disability	22102821	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Non-small cell lung cancer	19010865	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	22286061	CNVD
Ovarian cancer	21720365	CNVD
Lung cancer	18438408	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Esophageal cancer	20955586	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	19553991	CNVD
Lung cancer	19553991	CNVD
Melanoma	19553991	CNVD
Ovarian cancer	19553991	CNVD
Prostate cancer	19553991	CNVD
Non-small cell lung cancer	17156491	CNVD
Breast cancer	17133270	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Breast cancer	17393978	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Hepatocellular carcinoma	18929564	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:146 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:40926600-40936600	Weak transcription	Left Ventricle	heart
2	chr5:40931200-40992200	Weak transcription	Stomach Smooth Muscle	stomach
3	chr5:40931800-40991000	Weak transcription	Duodenum Mucosa	Duodenum
4	chr5:40932600-40935000	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr5:40932800-40942000	Strong transcription	Fetal Lung	lung
6	chr5:40933000-40935200	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr5:40933000-40937000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
8	chr5:40933000-40937800	Strong transcription	Ovary	ovary
9	chr5:40933400-40956400	Weak transcription	Fetal Brain Male	brain
10	chr5:40934800-40935000	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr5:40935800-40936400	Weak transcription	Pancreatic Islets	Pancreatic Islet
12	chr5:40936400-40936600	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
13	chr5:40936600-40937000	ZNF genes & repeats	Left Ventricle	heart
14	chr5:40937000-40938800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
15	chr5:40937000-40959600	Weak transcription	Left Ventricle	heart
16	chr5:40937800-40938600	Weak transcription	Ovary	ovary
17	chr5:40938600-40939200	Strong transcription	Ovary	ovary
18	chr5:40938800-40943400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
19	chr5:40939200-40941800	Weak transcription	Ovary	ovary
20	chr5:40941800-40942400	Strong transcription	Ovary	ovary
21	chr5:40942000-40944000	Weak transcription	Fetal Lung	lung
22	chr5:40942400-40947600	Weak transcription	Ovary	ovary
23	chr5:40943400-40949600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
24	chr5:40944000-40945800	Strong transcription	Fetal Lung	lung
25	chr5:40944600-40945000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr5:40945200-40958200	Weak transcription	Duodenum Smooth Muscle	Duodenum
27	chr5:40945800-40947200	Weak transcription	Fetal Lung	lung
28	chr5:40947200-40953400	Strong transcription	Fetal Lung	lung
29	chr5:40947600-40948600	Strong transcription	Ovary	ovary
30	chr5:40948600-40948800	Genic enhancers	Ovary	ovary
31	chr5:40948800-40951400	Weak transcription	Ovary	ovary
32	chr5:40949600-40953600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
33	chr5:40951200-40959600	Weak transcription	Pancreas	Pancrea
34	chr5:40951400-40952000	Enhancers	Fetal Heart	heart
35	chr5:40951400-40953400	Strong transcription	Ovary	ovary
36	chr5:40953400-40954800	Weak transcription	Ovary	ovary
37	chr5:40953400-40955200	Weak transcription	Fetal Lung	lung
38	chr5:40953600-40956800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
39	chr5:40954800-40968000	Strong transcription	Ovary	ovary
40	chr5:40955200-40967600	Strong transcription	Fetal Lung	lung
41	chr5:40955400-40955800	Enhancers	HUES64 Cell Line	embryonic stem cell
42	chr5:40956400-40956600	ZNF genes & repeats	Fetal Brain Male	brain
43	chr5:40956600-40958600	Weak transcription	Fetal Brain Male	brain
44	chr5:40956800-40957000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
45	chr5:40957000-40957200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
46	chr5:40957200-40957400	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
47	chr5:40957200-40959200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr5:40957400-40958200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
49	chr5:40958000-40958600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr5:40958200-40958400	Enhancers	Right Ventricle	heart

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