Variant report

Variant	nsv878140
Chromosome Location	chr3:195062395-195096625
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	chr3:195073888-195074208	K562	blood:	n/a	n/a
2	ATF1	chr3:195073832-195074099	K562	blood:	n/a	n/a
3	ATF3	chr3:195073748-195074155	K562	blood:	n/a	n/a
4	BRCA1	chr3:195073920-195073950	HepG2	liver:	n/a	n/a
5	CEBPB	chr3:195086924-195087310	MCF-7	breast:	n/a	chr3:195087145-195087156
6	CEBPB	chr3:195073856-195074333	HepG2	liver:	n/a	chr3:195074161-195074172
7	CEBPB	chr3:195073820-195074079	K562	blood:	n/a	n/a
8	CEBPB	chr3:195073740-195074319	K562	blood:	n/a	chr3:195074161-195074172
9	CEBPB	chr3:195073819-195074352	ECC-1	luminal epithelium:	n/a	chr3:195074161-195074172
10	CEBPB	chr3:195086978-195087308	IMR90	lung:	n/a	chr3:195087145-195087156
11	CEBPB	chr3:195086913-195087364	MCF-7	breast:	n/a	chr3:195087145-195087156
12	CEBPB	chr3:195086977-195087306	Hela-S3	cervix:	n/a	chr3:195087145-195087156
13	CEBPB	chr3:195073814-195074248	H1-hESC	embryonic stem cell:	n/a	chr3:195074161-195074172
14	CEBPB	chr3:195073641-195074396	HCT-116	colon:	n/a	chr3:195074161-195074172
15	CEBPB	chr3:195073769-195074348	IMR90	lung:	n/a	chr3:195074161-195074172
16	CEBPB	chr3:195073720-195074735	Hela-S3	cervix:	n/a	chr3:195074161-195074172
17	CEBPB	chr3:195073672-195074349	HCT-116	colon:	n/a	chr3:195074161-195074172
18	CEBPB	chr3:195073818-195074330	A549	lung:	n/a	chr3:195074161-195074172
19	CEBPB	chr3:195073775-195074333	K562	blood:	n/a	chr3:195074161-195074172
20	CEBPB	chr3:195086996-195087275	A549	lung:	n/a	chr3:195087145-195087156
21	CEBPB	chr3:195086963-195087317	HepG2	liver:	n/a	chr3:195087145-195087156
22	CHD1	chr3:195088318-195088426	GM12878	blood:	n/a	n/a
23	CHD2	chr3:195073778-195074278	Hela-S3	cervix:	n/a	n/a
24	CTCF	chr3:195073641-195073728	GM13976	blood:	n/a	n/a
25	CTCF	chr3:195077040-195077190	HBMEC	blood vessel:	n/a	n/a
26	CTCF	chr3:195072238-195072276	MCF-7	breast:	n/a	n/a
27	CTCF	chr3:195070420-195070570	HFF-Myc	foreskin:	n/a	n/a
28	E2F4	chr3:195092996-195093231	MCF10A-Er-Src	breast:	n/a	n/a
29	EP300	chr3:195073746-195074479	K562	blood:	n/a	n/a
30	EP300	chr3:195073748-195074691	Hela-S3	cervix:	n/a	chr3:195074541-195074555
31	FAM48A	chr3:195076606-195076738	GM12878	blood:	n/a	n/a
32	FAM48A	chr3:195067140-195067264	GM12878	blood:	n/a	n/a
33	FAM48A	chr3:195072671-195072834	GM12878	blood:	n/a	n/a
34	FOS	chr3:195094542-195094875	MCF10A-Er-Src	breast:	n/a	chr3:195094707-195094717 chr3:195094708-195094716 chr3:195094719-195094729 chr3:195094707-195094717 chr3:195094707-195094717 chr3:195094719-195094729 chr3:195094707-195094717 chr3:195094720-195094728
35	FOS	chr3:195086234-195086370	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr3:195086244-195086436	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr3:195094555-195094873	MCF10A-Er-Src	breast:	n/a	chr3:195094707-195094717 chr3:195094708-195094716 chr3:195094719-195094729 chr3:195094707-195094717 chr3:195094707-195094717 chr3:195094719-195094729 chr3:195094707-195094717 chr3:195094720-195094728
38	FOS	chr3:195073829-195074124	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr3:195094554-195094852	MCF10A-Er-Src	breast:	n/a	chr3:195094707-195094717 chr3:195094708-195094716 chr3:195094719-195094729 chr3:195094707-195094717 chr3:195094707-195094717 chr3:195094719-195094729 chr3:195094707-195094717 chr3:195094720-195094728
40	FOS	chr3:195073820-195074163	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr3:195073830-195074211	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr3:195092871-195093330	MCF10A-Er-Src	breast:	n/a	chr3:195093074-195093086
43	FOS	chr3:195092920-195093322	MCF10A-Er-Src	breast:	n/a	chr3:195093074-195093086
44	FOS	chr3:195092873-195093349	MCF10A-Er-Src	breast:	n/a	chr3:195093074-195093086
45	FOS	chr3:195073828-195074111	MCF10A-Er-Src	breast:	n/a	n/a
46	FOS	chr3:195092874-195093315	MCF10A-Er-Src	breast:	n/a	chr3:195093074-195093086
47	FOSL1	chr3:195073690-195074292	HCT-116	colon:	n/a	n/a
48	GATA3	chr3:195069568-195069715	SH-SY5Y	brain:	n/a	n/a
49	GATA3	chr3:195066318-195066898	SH-SY5Y	brain:	n/a	n/a
50	GTF2F1	chr3:195073749-195074234	Hela-S3	cervix:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:195077618-195077668	Caco-2	colon:	n/a
2	chr3:195077618-195077668	Caco-2	colon:	n/a
3	chr3:195087778-195087828	AG09319	gingival:	n/a
4	chr3:195077618-195077668	IMR90	lung:	fetal
5	chr3:195087778-195087828	A549	lung:	n/a
6	chr3:195077618-195077668	Hela-S3	cervix:	n/a
7	chr3:195087778-195087828	H1-hESC	embryonic stem cell:	embryo
8	chr3:195077618-195077668	BJ	skin:	n/a
9	chr3:195077618-195077668	GM12892	blood:	n/a
10	chr3:195077618-195077668	HEK293	kidney:	embryo
11	chr3:195087778-195087828	SKMC	muscle:	n/a
12	chr3:195077618-195077668	CMK	blood:	n/a
13	chr3:195087778-195087828	Caco-2	colon:	n/a
14	chr3:195087778-195087828	NH-A	brain:	n/a
15	chr3:195087778-195087828	Hepatocyte	liver:	n/a
16	chr3:195077618-195077668	ovcar-3	ovarian:	n/a
17	chr3:195077618-195077668	HRPEpiC	eye:	n/a
18	chr3:195077618-195077668	H1-hESC	embryonic stem cell:	embryo
19	chr3:195077618-195077668	HEEpiC	esophagus:	n/a
20	chr3:195087778-195087828	GM12878	blood:	n/a
21	chr3:195087778-195087828	HIPEpiC	eye:	n/a
22	chr3:195087778-195087828	AoSMC	blood vessel:	n/a
23	chr3:195087778-195087828	HepG2	liver:	n/a
24	chr3:195087778-195087828	HRPEpiC	eye:	n/a
25	chr3:195077618-195077668	HRE	kidney:	n/a
26	chr3:195077618-195077668	LNCaP	prostate:	n/a
27	chr3:195077618-195077668	AG09319	gingival:	n/a
28	chr3:195077618-195077668	AG04450	lung:	fetal
29	chr3:195077618-195077668	NB4	blood:	n/a
30	chr3:195087778-195087828	CMK	blood:	n/a
31	chr3:195087778-195087828	GM12892	blood:	n/a
32	chr3:195077618-195077668	AG04449	skin:	fetal
33	chr3:195087778-195087828	NHBE	bronchial:	n/a
34	chr3:195077618-195077668	NT2-D1	testis:	n/a
35	chr3:195087778-195087828	HEEpiC	esophagus:	n/a
36	chr3:195087778-195087828	HCF	heart:	n/a
37	chr3:195087778-195087828	U87	brain:	n/a
38	chr3:195077618-195077668	HPAEpiC	pulmonary alveolar:	n/a
39	chr3:195077618-195077668	ProgFib	skin:	n/a
40	chr3:195077618-195077668	HepG2	liver:	n/a
41	chr3:195077618-195077668	HL-60	blood:	n/a
42	chr3:195077618-195077668	GM19239	blood:	n/a
43	chr3:195087778-195087828	NT2-D1	testis:	n/a
44	chr3:195077618-195077668	NHBE	bronchial:	n/a
45	chr3:195087778-195087828	HEK293	kidney:	embryo
46	chr3:195077618-195077668	PFSK-1	brain:	n/a
47	chr3:195077618-195077668	SK-N-SH_RA	brain:	n/a
48	chr3:195087778-195087828	PANC-1	pancreas:	n/a
49	chr3:195087778-195087828	BJ	skin:	n/a
50	chr3:195077618-195077668	HNPCEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:195073143..195075655-chr3:195078501..195080208,2	K562	blood:
2	chr3:195069594..195071491-chr3:195086274..195088422,2	K562	blood:
3	chr3:195081898..195084336-chr3:195160220..195162508,2	K562	blood:
4	chr3:195068888..195071135-chr3:195078131..195080514,2	MCF-7	breast:
5	chr3:195086495..195088641-chr3:195116660..195118594,2	K562	blood:
6	chr3:194991204..194993329-chr3:195059600..195062402,2	MCF-7	breast:
7	chr3:195073143..195075655-chr3:195078501..195080208,2	K562	blood:
8	chr3:195070745..195073123-chr3:195162194..195164615,2	K562	blood:
9	chr3:195078115..195080618-chr3:195098644..195100393,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MUC20-11	chr3:195070393-195070759	NONHSAT094153

Variant related genes	Relation type
ACAP2	TF binding region
ENSG00000227433	TF binding region
ACAP2	CpG island
ENSG00000227433	CpG island
ENSG00000227433	chromatin interactions
ENSG00000114331	chromatin interactions
ENSG00000173950	chromatin interactions

Extended variants
information (count: 1360 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:1360 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6437373	chr3:195062395-195062396	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs139290054	chr3:195062398-195062399	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs561139594	chr3:195062414-195062415	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs376631251	chr3:195062460-195062461	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs80278139	chr3:195062506-195062507	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs74918312	chr3:195062509-195062510	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs565359350	chr3:195062529-195062530	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs7630300	chr3:195062650-195062651	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs79026009	chr3:195062679-195062680	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs187771572	chr3:195062687-195062688	Weak transcription ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs530426384	chr3:195062692-195062693	Weak transcription ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs74288796	chr3:195062722-195062723	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs528436345	chr3:195062724-195062725	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs567096609	chr3:195062765-195062766	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs546798298	chr3:195062812-195062813	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs534117794	chr3:195062855-195062856	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs375515688	chr3:195062875-195062876	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs531942351	chr3:195062888-195062889	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs552677840	chr3:195062919-195062920	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs571031403	chr3:195062925-195062926	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs9844763	chr3:195062930-195062931	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs73206693	chr3:195062959-195062960	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs190948885	chr3:195062974-195062975	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs149964976	chr3:195062996-195062997	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs542954656	chr3:195063034-195063035	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs78369758	chr3:195063075-195063076	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs573028086	chr3:195063085-195063086	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs540404007	chr3:195063094-195063095	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs183142467	chr3:195063111-195063112	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs145089894	chr3:195063129-195063130	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs544675326	chr3:195063130-195063131	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs75198072	chr3:195063158-195063159	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs550742756	chr3:195063168-195063169	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs544134088	chr3:195063185-195063186	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs77149396	chr3:195063200-195063201	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs148058534	chr3:195063247-195063248	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs199909122	chr3:195063256-195063257	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs548901688	chr3:195063272-195063273	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs141814202	chr3:195063302-195063303	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs149035237	chr3:195063317-195063318	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs79748295	chr3:195063347-195063348	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs139935887	chr3:195063359-195063360	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs9862710	chr3:195063453-195063454	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs112958082	chr3:195063521-195063522	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs112488691	chr3:195063602-195063603	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs535855826	chr3:195063632-195063633	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs537660699	chr3:195063640-195063641	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs554873453	chr3:195063656-195063657	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs573073783	chr3:195063657-195063658	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs540496867	chr3:195063691-195063692	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	21115979	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	16608533	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Breast cancer	17133270	CNVD
Cancer	16751803	CNVD
abnormal development	18461090	CNVD
Autism	19653912	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Prostate cancer	18632612	CNVD
Cervical cancer	21062161	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Austim spectrum disorder	21302340	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	16397240	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
speech impairment	20736978	CNVD
Intracranial aneurysm	16715129	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Mental retardation	17124404	CNVD
Congenital anomalies of the kidney and urinary tract	20299530	CNVD
Developmental delay	21147756	CNVD
Breast cancer	21509527	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
Neurodevelopmental disorder	16760732	CNVD
Schizophrenia	22118685	CNVD
Schizophrenia	22958593	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	20970697	CNVD
Mental retardation	19951919	CNVD
Autism	20970697	CNVD
Developmental delay	18471269	CNVD
Intellectual disability	22045946	CNVD
Breast cancer	21045282	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Ovarian cancer	20844748	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Uveal melanoma	20484589	CNVD
3q29 microdeletion syndrome	20500065	CNVD
Biliary cancer	20453639	CNVD
3q29 microdeletion syndrome	22283845	CNVD
3q29 microdeletion syndrome	21626679	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD

Chromatin state (count:731 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:194992600-195090000	Weak transcription	Aorta	Aorta
2	chr3:194993000-195076000	Weak transcription	Fetal Heart	heart
3	chr3:195004000-195066600	Weak transcription	Small Intestine	intestine
4	chr3:195010000-195076400	Weak transcription	Brain Angular Gyrus	brain
5	chr3:195022600-195073400	Weak transcription	HMEC	breast
6	chr3:195022800-195073400	Weak transcription	NHEK	skin
7	chr3:195034800-195076800	Weak transcription	Psoas Muscle	Psoas
8	chr3:195040400-195062600	Weak transcription	Skeletal Muscle Male	skeletal muscle
9	chr3:195040400-195064800	Weak transcription	Placenta Amnion	Placenta Amnion
10	chr3:195040400-195066000	Strong transcription	Primary neutrophils fromperipheralblood	blood
11	chr3:195040400-195076400	Weak transcription	Brain Cingulate Gyrus	brain
12	chr3:195040400-195076600	Weak transcription	Brain Anterior Caudate	brain
13	chr3:195040400-195079400	Strong transcription	Monocytes-CD14+_RO01746	blood
14	chr3:195040400-195108400	Weak transcription	Colonic Mucosa	Colon
15	chr3:195040600-195111200	Weak transcription	Fetal Brain Male	brain
16	chr3:195040800-195071200	Strong transcription	Primary monocytes fromperipheralblood	blood
17	chr3:195040800-195072800	Weak transcription	K562	blood
18	chr3:195040800-195073200	Weak transcription	Pancreas	Pancrea
19	chr3:195040800-195076400	Weak transcription	Brain Hippocampus Middle	brain
20	chr3:195041000-195062600	Weak transcription	Brain Germinal Matrix	brain
21	chr3:195041000-195065400	Weak transcription	H1 Cell Line	embryonic stem cell
22	chr3:195041000-195066400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
23	chr3:195041000-195067200	Weak transcription	Brain Substantia Nigra	brain
24	chr3:195041000-195077000	Weak transcription	H9 Cell Line	embryonic stem cell
25	chr3:195041000-195131200	Weak transcription	Gastric	stomach
26	chr3:195041200-195077200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr3:195041400-195064800	Strong transcription	Primary B cells from cord blood	blood
28	chr3:195041400-195076800	Weak transcription	Rectal Smooth Muscle	rectum
29	chr3:195041600-195071600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
30	chr3:195041600-195073600	Weak transcription	NHLF	lung
31	chr3:195041600-195077800	Weak transcription	Fetal Brain Female	brain
32	chr3:195042200-195062400	Weak transcription	HUES6 Cell Line	embryonic stem cell
33	chr3:195045800-195065200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr3:195048800-195076800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
35	chr3:195049600-195106000	Weak transcription	HUVEC	blood vessel
36	chr3:195050400-195062600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
37	chr3:195051800-195073800	Weak transcription	Skeletal Muscle Female	skeletal muscle
38	chr3:195051800-195077000	Weak transcription	HUES48 Cell Line	embryonic stem cell
39	chr3:195052000-195062400	Weak transcription	Muscle Satellite Cultured Cells	--
40	chr3:195052000-195071400	Weak transcription	HepG2	liver
41	chr3:195052000-195076400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr3:195052200-195070000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr3:195052200-195076200	Weak transcription	Colon Smooth Muscle	Colon
44	chr3:195052200-195076800	Weak transcription	Spleen	Spleen
45	chr3:195052200-195077000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr3:195052200-195102800	Weak transcription	Cortex derived primary cultured neurospheres	brain
47	chr3:195052400-195062600	Weak transcription	NH-A	brain
48	chr3:195052400-195064200	Weak transcription	Esophagus	oesophagus
49	chr3:195052400-195064200	Weak transcription	Left Ventricle	heart
50	chr3:195052400-195073400	Weak transcription	HSMMtube	muscle

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