Variant report

Variant	nsv536757
Chromosome Location	chr3:145506353-145750883
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	BATF	chr3:145617031-145617299	GM12878	blood:	n/a	chr3:145617167-145617178
2	BATF	chr3:145661502-145661720	GM12878	blood:	n/a	chr3:145661650-145661660 chr3:145661649-145661660
3	BATF	chr3:145617078-145617323	GM12878	blood:	n/a	chr3:145617167-145617178
4	BATF	chr3:145617884-145618161	GM12878	blood:	n/a	chr3:145617976-145617987
5	BATF	chr3:145617922-145618098	GM12878	blood:	n/a	chr3:145617976-145617987
6	BCL11A	chr3:145617839-145618177	GM12878	blood:	n/a	chr3:145617979-145617988 chr3:145617980-145617989
7	BCL11A	chr3:145617942-145618090	GM12878	blood:	n/a	chr3:145617979-145617988 chr3:145617980-145617989
8	BHLHE40	chr3:145616343-145617288	GM12878	blood:	n/a	n/a
9	BHLHE40	chr3:145535736-145536028	GM12878	blood:	n/a	n/a
10	BHLHE40	chr3:145720051-145720159	A549	lung:	n/a	n/a
11	BHLHE40	chr3:145617829-145618365	GM12878	blood:	n/a	n/a
12	BRCA1	chr3:145602167-145602271	Hela-S3	cervix:	n/a	n/a
13	BRCA1	chr3:145724499-145724650	Hela-S3	cervix:	n/a	n/a
14	BRCA1	chr3:145531712-145531727	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr3:145575765-145576066	MCF-7	breast:	n/a	chr3:145575984-145575995
16	CEBPB	chr3:145627345-145627605	IMR90	lung:	n/a	chr3:145627469-145627480
17	CEBPB	chr3:145616337-145617569	Hela-S3	cervix:	n/a	chr3:145617318-145617329
18	CEBPB	chr3:145615201-145615448	IMR90	lung:	n/a	chr3:145615286-145615297
19	CEBPB	chr3:145566934-145567275	HepG2	liver:	n/a	n/a
20	CEBPB	chr3:145617031-145617489	IMR90	lung:	n/a	chr3:145617318-145617329
21	CEBPB	chr3:145654814-145655116	IMR90	lung:	n/a	chr3:145654981-145654992 chr3:145654981-145654990
22	CEBPB	chr3:145518696-145518945	Hela-S3	cervix:	n/a	chr3:145518841-145518854 chr3:145518841-145518854 chr3:145518841-145518852 chr3:145518841-145518854
23	CEBPB	chr3:145627345-145627654	HepG2	liver:	n/a	chr3:145627469-145627480
24	CEBPB	chr3:145718225-145718632	MCF-7	breast:	n/a	chr3:145718411-145718422
25	CEBPB	chr3:145654848-145655110	A549	lung:	n/a	chr3:145654981-145654992 chr3:145654981-145654990
26	CEBPB	chr3:145590915-145591265	HepG2	liver:	n/a	chr3:145591064-145591075
27	CEBPB	chr3:145643100-145643364	HepG2	liver:	n/a	chr3:145643198-145643209 chr3:145643269-145643282 chr3:145643200-145643211 chr3:145643216-145643227
28	CEBPB	chr3:145590953-145591270	Hela-S3	cervix:	n/a	chr3:145591064-145591075
29	CEBPB	chr3:145590915-145591255	A549	lung:	n/a	chr3:145591064-145591075
30	CEBPB	chr3:145728582-145728759	IMR90	lung:	n/a	chr3:145728655-145728666
31	CEBPB	chr3:145700948-145701207	HepG2	liver:	n/a	n/a
32	CEBPB	chr3:145668267-145668275	K562	blood:	n/a	n/a
33	CEBPB	chr3:145685675-145685947	HepG2	liver:	n/a	chr3:145685802-145685813
34	CEBPB	chr3:145581045-145581109	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr3:145590926-145591356	IMR90	lung:	n/a	chr3:145591064-145591075
36	CEBPB	chr3:145525914-145526064	H1-hESC	embryonic stem cell:	n/a	chr3:145525953-145525966
37	CEBPB	chr3:145566939-145567274	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr3:145728568-145728756	HepG2	liver:	n/a	chr3:145728655-145728666
39	CEBPB	chr3:145590904-145591245	K562	blood:	n/a	chr3:145591064-145591075
40	CEBPB	chr3:145518672-145518957	A549	lung:	n/a	chr3:145518841-145518854 chr3:145518841-145518854 chr3:145518841-145518852 chr3:145518841-145518854
41	CEBPB	chr3:145615167-145615415	HepG2	liver:	n/a	chr3:145615286-145615297
42	CEBPB	chr3:145575849-145576013	HepG2	liver:	n/a	chr3:145575984-145575995
43	CEBPB	chr3:145617147-145617472	A549	lung:	n/a	chr3:145617318-145617329
44	CEBPB	chr3:145578466-145578687	A549	lung:	n/a	chr3:145578531-145578542
45	CEBPB	chr3:145533471-145533784	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr3:145566953-145567259	A549	lung:	n/a	n/a
47	CEBPB	chr3:145654854-145655147	HepG2	liver:	n/a	chr3:145654981-145654992 chr3:145654981-145654990
48	CEBPB	chr3:145566939-145567262	IMR90	lung:	n/a	n/a
49	CEBPB	chr3:145575803-145576121	A549	lung:	n/a	chr3:145575984-145575995
50	CEBPB	chr3:145518738-145518905	K562	blood:	n/a	chr3:145518841-145518854 chr3:145518841-145518854 chr3:145518841-145518852 chr3:145518841-145518854

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:145735965-145736015	BJ	skin:	n/a
2	chr3:145517734-145517784	HCF	heart:	n/a
3	chr3:145736022-145736072	H1-hESC	embryonic stem cell:	embryo
4	chr3:145517734-145517784	HAEpiC	amniotic membrane:	n/a
5	chr3:145735965-145736015	HEK293	kidney:	embryo
6	chr3:145734655-145734705	CMK	blood:	n/a
7	chr3:145517734-145517784	HRCEpiC	kidney:	n/a
8	chr3:145736001-145736051	HL-60	blood:	n/a
9	chr3:145735965-145736015	GM12892	blood:	n/a
10	chr3:145736001-145736051	HepG2	liver:	n/a
11	chr3:145735965-145736015	NHDF-neo	bronchial:	n/a
12	chr3:145517734-145517784	HPAEpiC	pulmonary alveolar:	n/a
13	chr3:145517734-145517784	SAEC	small airway:	n/a
14	chr3:145734655-145734705	IMR90	lung:	fetal
15	chr3:145736001-145736051	Caco-2	colon:	n/a
16	chr3:145734655-145734705	AG09319	gingival:	n/a
17	chr3:145734577-145734627	GM12891	blood:	n/a
18	chr3:145517734-145517784	AG04450	lung:	fetal
19	chr3:145736001-145736051	HRE	kidney:	n/a
20	chr3:145734577-145734627	PrEC	prostate:	n/a
21	chr3:145736022-145736072	PrEC	prostate:	n/a
22	chr3:145734577-145734627	MCF-7	breast:	n/a
23	chr3:145517734-145517784	HEEpiC	esophagus:	n/a
24	chr3:145736001-145736051	HNPCEpiC	eye:	n/a
25	chr3:145734655-145734705	NT2-D1	testis:	n/a
26	chr3:145734577-145734627	HCF	heart:	n/a
27	chr3:145736022-145736072	NHDF-neo	bronchial:	n/a
28	chr3:145735965-145736015	HepG2	liver:	n/a
29	chr3:145734577-145734627	HMEC	breast:	n/a
30	chr3:145517734-145517784	U87	brain:	n/a
31	chr3:145734655-145734705	HCT-116	colon:	n/a
32	chr3:145734577-145734627	SK-N-MC	brain:	n/a
33	chr3:145735965-145736015	HAEpiC	amniotic membrane:	n/a
34	chr3:145736001-145736051	HPAEpiC	pulmonary alveolar:	n/a
35	chr3:145734577-145734627	NB4	blood:	n/a
36	chr3:145517734-145517784	NH-A	brain:	n/a
37	chr3:145734577-145734627	SKMC	muscle:	n/a
38	chr3:145734577-145734627	SK-N-SH_RA	brain:	n/a
39	chr3:145734577-145734627	BE2_C	brain:	n/a
40	chr3:145734655-145734705	HAEpiC	amniotic membrane:	n/a
41	chr3:145517734-145517784	NB4	blood:	n/a
42	chr3:145735965-145736015	Caco-2	colon:	n/a
43	chr3:145734655-145734705	SKMC	muscle:	n/a
44	chr3:145734655-145734705	GM12892	blood:	n/a
45	chr3:145736001-145736051	HCM	heart:	n/a
46	chr3:145736022-145736072	HCM	heart:	n/a
47	chr3:145735965-145736015	MCF10A-Er-Src	breast:	n/a
48	chr3:145736001-145736051	GM19239	blood:	n/a
49	chr3:145735965-145736015	AG04450	lung:	fetal
50	chr3:145517734-145517784	HCM	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:145621110..145623041-chr3:145624593..145626157,2	K562	blood:
2	chr3:145558279..145560976-chr3:145566285..145567836,2	MCF-7	breast:
3	chr3:145736816..145738594-chr3:145881561..145884475,2	MCF-7	breast:
4	chr3:145735893..145737457-chr3:145739302..145741925,2	MCF-7	breast:
5	chr3:145688912..145689432-chr8:99049320..99049968,2	MCF-7	breast:
6	chr3:145621110..145623041-chr3:145624593..145626157,2	K562	blood:
7	chr3:145708427..145710747-chr3:145714607..145716482,2	MCF-7	breast:
8	chr3:145743585..145744532-chr3:145904873..145905604,2	MCF-7	breast:
9	chr3:145501403..145502940-chr3:145505353..145507937,2	K562	blood:
10	chr3:145558279..145560976-chr3:145566285..145567836,2	MCF-7	breast:
11	chr3:145515573..145518093-chr3:145523034..145526059,3	MCF-7	breast:
12	chr3:145604775..145606383-chr3:145616815..145618517,2	MCF-7	breast:
13	chr3:145738494..145739375-chr3:145904889..145905776,3	MCF-7	breast:
14	chr3:145494214..145495352-chr3:145744124..145745129,8	MCF-7	breast:
15	chr3:145515573..145518093-chr3:145523034..145526059,3	MCF-7	breast:
16	chr3:145735893..145737457-chr3:145739302..145741925,2	MCF-7	breast:
17	chr3:145604775..145606383-chr3:145616815..145618517,2	MCF-7	breast:
18	chr3:145708427..145710747-chr3:145714607..145716482,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC107021.1-2	chr3:145681308-145681410	XLOC_002853
2	lnc-PLOD2-6	chr3:145542044-145542526	NONHSAT092540
3	lnc-AC107021.1-3	chr3:145679104-145679323	XLOC_002852
4	lnc-AC107021.1-3	chr3:145657699-145657941	XLOC_002852
5	lnc-AC107021.1-3	chr3:145675182-145675618	XLOC_002852
6	lnc-AC107021.1-3	chr3:145664191-145664408	XLOC_002852
7	lnc-AC107021.1-3	chr3:145657755-145657941	XLOC_002852
8	lnc-AC107021.1-3	chr3:145675182-145675299	XLOC_002852
9	lnc-AC107021.1-2	chr3:145679542-145680007	XLOC_002853

Variant related genes	Relation type
RPL21P39	TF binding region
ENSG00000244358	TF binding region
ENSG00000240095	TF binding region
RPL21P39	CpG island
ENSG00000244358	CpG island
ENSG00000240095	CpG island
AP1M2	miRNA target sites
TWSG1	miRNA target sites

Extended variants
information (count: 7214 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:7214 , 50 per page) page: 1 2 3 4 5 6 7 ... 145

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs529695444	chr3:145506354-145506355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs548175949	chr3:145506360-145506361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs144166818	chr3:145506370-145506371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs7636688	chr3:145506378-145506379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs550638590	chr3:145506380-145506381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs148447383	chr3:145506431-145506432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs185393186	chr3:145506441-145506442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs141794297	chr3:145506461-145506462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs79830534	chr3:145506486-145506487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs115366215	chr3:145506488-145506489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs536507335	chr3:145506505-145506506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs554952254	chr3:145506535-145506536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs573128763	chr3:145506543-145506544	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs534043140	chr3:145506576-145506577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs9866001	chr3:145506580-145506581	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs576673099	chr3:145506583-145506584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs543992735	chr3:145506620-145506621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs562502478	chr3:145506663-145506664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs6440371	chr3:145506681-145506682	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs541727996	chr3:145506688-145506689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs560107983	chr3:145506738-145506739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs147214314	chr3:145506742-145506743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs541676182	chr3:145506767-145506768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs200099176	chr3:145506768-145506769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs6794778	chr3:145506807-145506808	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs372959701	chr3:145506841-145506842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs35597300	chr3:145506843-145506844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs564170821	chr3:145506844-145506845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs6770379	chr3:145506849-145506850	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs551207937	chr3:145506866-145506867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs140740155	chr3:145506933-145506934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs558449442	chr3:145506944-145506945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs369091201	chr3:145506956-145506957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs189554505	chr3:145506962-145506963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs192834852	chr3:145506963-145506964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs533928236	chr3:145506979-145506980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs9850729	chr3:145506991-145506992	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs58303051	chr3:145506993-145506994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs10935584	chr3:145507007-145507008	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs373362105	chr3:145507032-145507033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs556343469	chr3:145507061-145507062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs556249059	chr3:145507064-145507065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs184784018	chr3:145507065-145507066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs542137967	chr3:145507074-145507075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs80342409	chr3:145507098-145507099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs6783698	chr3:145507173-145507174	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs564272943	chr3:145507186-145507187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs188177804	chr3:145507198-145507199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs6795250	chr3:145507247-145507248	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs560176986	chr3:145507261-145507262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

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
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	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
Colorectal cancer	18645599	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Hepatocellular carcinoma	16750200	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
abnormal development	18461090	CNVD
Breast cancer	21364760	CNVD
Mental retardation	17847001	CNVD
Basal cell lymphoma	17170743	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Autism	18923514	CNVD
Autism	22241247	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Autism	21956041	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Breast cancer	16608533	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	21509527	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	23813976	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:425 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:145504600-145508000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr3:145507600-145507800	Enhancers	Gastric	stomach
3	chr3:145507800-145508200	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr3:145507800-145508600	Weak transcription	Gastric	stomach
5	chr3:145508000-145508800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr3:145508600-145509400	Enhancers	Gastric	stomach
7	chr3:145508600-145509400	Enhancers	Pancreas	Pancrea
8	chr3:145508800-145509600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr3:145509600-145509800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr3:145509800-145510200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr3:145510200-145514800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr3:145514800-145515400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr3:145515400-145517200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr3:145515800-145516400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr3:145515800-145517800	Enhancers	Cortex derived primary cultured neurospheres	brain
16	chr3:145515800-145517800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr3:145516000-145516400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr3:145516000-145516600	Enhancers	Brain Hippocampus Middle	brain
19	chr3:145516000-145516600	Enhancers	Gastric	stomach
20	chr3:145516000-145516600	Enhancers	Pancreas	Pancrea
21	chr3:145516000-145517600	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr3:145516000-145518000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr3:145516200-145516600	Enhancers	Brain Inferior Temporal Lobe	brain
24	chr3:145516200-145516600	Bivalent Enhancer	HSMMtube	muscle
25	chr3:145516200-145516800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr3:145516200-145516800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr3:145516200-145516800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr3:145516200-145516800	Enhancers	Brain Cingulate Gyrus	brain
29	chr3:145516200-145516800	Enhancers	Esophagus	oesophagus
30	chr3:145516200-145517000	Enhancers	Fetal Muscle Leg	muscle
31	chr3:145516200-145517200	Enhancers	H1 Cell Line	embryonic stem cell
32	chr3:145516200-145517200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr3:145516200-145517200	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr3:145516200-145517800	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr3:145516200-145518000	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr3:145516200-145518800	Enhancers	Fetal Lung	lung
37	chr3:145516400-145516800	Enhancers	Brain Angular Gyrus	brain
38	chr3:145516400-145516800	Enhancers	Fetal Muscle Trunk	muscle
39	chr3:145516400-145516800	Enhancers	Fetal Stomach	stomach
40	chr3:145516400-145517000	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr3:145516400-145517000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr3:145516400-145517200	Enhancers	H9 Cell Line	embryonic stem cell
43	chr3:145516400-145517200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr3:145516400-145517200	Enhancers	Brain Anterior Caudate	brain
45	chr3:145516400-145517200	Enhancers	Brain Substantia Nigra	brain
46	chr3:145516400-145517600	Enhancers	iPS-20b Cell Line	embryonic stem cell
47	chr3:145516600-145517200	Enhancers	HUES64 Cell Line	embryonic stem cell
48	chr3:145516600-145517200	Enhancers	HSMMtube	muscle
49	chr3:145516600-145517800	Enhancers	NHDF-Ad	bronchial
50	chr3:145516600-145518000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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