Variant report

Variant	nsv877610
Chromosome Location	chr3:145465395-145653627
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	chr3:145485792-145485987	HepG2	liver:	n/a	chr3:145485811-145485827
2	BATF	chr3:145617884-145618161	GM12878	blood:	n/a	chr3:145617976-145617987
3	BATF	chr3:145617031-145617299	GM12878	blood:	n/a	chr3:145617167-145617178
4	BATF	chr3:145617922-145618098	GM12878	blood:	n/a	chr3:145617976-145617987
5	BATF	chr3:145617078-145617323	GM12878	blood:	n/a	chr3:145617167-145617178
6	BCL11A	chr3:145617942-145618090	GM12878	blood:	n/a	chr3:145617979-145617988 chr3:145617980-145617989
7	BCL11A	chr3:145617839-145618177	GM12878	blood:	n/a	chr3:145617979-145617988 chr3:145617980-145617989
8	BHLHE40	chr3:145494762-145494870	HepG2	liver:	n/a	n/a
9	BHLHE40	chr3:145535736-145536028	GM12878	blood:	n/a	n/a
10	BHLHE40	chr3:145616343-145617288	GM12878	blood:	n/a	n/a
11	BHLHE40	chr3:145617829-145618365	GM12878	blood:	n/a	n/a
12	BRCA1	chr3:145531712-145531727	Hela-S3	cervix:	n/a	n/a
13	BRCA1	chr3:145501013-145501017	Hela-S3	cervix:	n/a	n/a
14	BRCA1	chr3:145602167-145602271	Hela-S3	cervix:	n/a	n/a
15	BRCA1	chr3:145477935-145478012	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr3:145590915-145591265	HepG2	liver:	n/a	chr3:145591064-145591075
17	CEBPB	chr3:145578466-145578687	A549	lung:	n/a	chr3:145578531-145578542
18	CEBPB	chr3:145503531-145503790	ECC-1	luminal epithelium:	n/a	chr3:145503642-145503653 chr3:145503643-145503654 chr3:145503644-145503653
19	CEBPB	chr3:145564643-145564762	H1-hESC	embryonic stem cell:	n/a	chr3:145564643-145564654
20	CEBPB	chr3:145590926-145591356	IMR90	lung:	n/a	chr3:145591064-145591075
21	CEBPB	chr3:145627381-145627633	A549	lung:	n/a	chr3:145627469-145627480
22	CEBPB	chr3:145590904-145591245	K562	blood:	n/a	chr3:145591064-145591075
23	CEBPB	chr3:145518707-145518913	IMR90	lung:	n/a	chr3:145518841-145518854 chr3:145518841-145518854 chr3:145518841-145518852 chr3:145518841-145518854
24	CEBPB	chr3:145518696-145518945	Hela-S3	cervix:	n/a	chr3:145518841-145518854 chr3:145518841-145518854 chr3:145518841-145518852 chr3:145518841-145518854
25	CEBPB	chr3:145564493-145564795	HepG2	liver:	n/a	chr3:145564643-145564654
26	CEBPB	chr3:145575849-145576013	HepG2	liver:	n/a	chr3:145575984-145575995
27	CEBPB	chr3:145575808-145576126	Hela-S3	cervix:	n/a	chr3:145575984-145575995
28	CEBPB	chr3:145590915-145591255	A549	lung:	n/a	chr3:145591064-145591075
29	CEBPB	chr3:145518738-145518905	K562	blood:	n/a	chr3:145518841-145518854 chr3:145518841-145518854 chr3:145518841-145518852 chr3:145518841-145518854
30	CEBPB	chr3:145525867-145526117	MCF-7	breast:	n/a	chr3:145525953-145525966
31	CEBPB	chr3:145590953-145591270	Hela-S3	cervix:	n/a	chr3:145591064-145591075
32	CEBPB	chr3:145627344-145627617	Hela-S3	cervix:	n/a	chr3:145627469-145627480
33	CEBPB	chr3:145575803-145576121	A549	lung:	n/a	chr3:145575984-145575995
34	CEBPB	chr3:145566972-145567248	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr3:145525914-145526064	H1-hESC	embryonic stem cell:	n/a	chr3:145525953-145525966
36	CEBPB	chr3:145616337-145617569	Hela-S3	cervix:	n/a	chr3:145617318-145617329
37	CEBPB	chr3:145581045-145581109	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr3:145643100-145643364	HepG2	liver:	n/a	chr3:145643198-145643209 chr3:145643269-145643282 chr3:145643200-145643211 chr3:145643216-145643227
39	CEBPB	chr3:145617147-145617472	A549	lung:	n/a	chr3:145617318-145617329
40	CEBPB	chr3:145578393-145578651	HepG2	liver:	n/a	chr3:145578531-145578542
41	CEBPB	chr3:145566934-145567275	HepG2	liver:	n/a	n/a
42	CEBPB	chr3:145566939-145567274	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr3:145533471-145533784	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr3:145503490-145503793	HepG2	liver:	n/a	chr3:145503642-145503653 chr3:145503643-145503654 chr3:145503644-145503653
45	CEBPB	chr3:145575765-145576066	MCF-7	breast:	n/a	chr3:145575984-145575995
46	CEBPB	chr3:145479861-145479895	HepG2	liver:	n/a	n/a
47	CEBPB	chr3:145566939-145567262	IMR90	lung:	n/a	n/a
48	CEBPB	chr3:145615167-145615415	HepG2	liver:	n/a	chr3:145615286-145615297
49	CEBPB	chr3:145518672-145518957	A549	lung:	n/a	chr3:145518841-145518854 chr3:145518841-145518854 chr3:145518841-145518852 chr3:145518841-145518854
50	CEBPB	chr3:145503493-145503794	A549	lung:	n/a	chr3:145503642-145503653 chr3:145503643-145503654 chr3:145503644-145503653

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:145517734-145517784	U87	brain:	n/a
2	chr3:145517734-145517784	HNPCEpiC	eye:	n/a
3	chr3:145517734-145517784	U87	brain:	n/a
4	chr3:145517734-145517784	HNPCEpiC	eye:	n/a
5	chr3:145517734-145517784	SK-N-MC	brain:	n/a
6	chr3:145517734-145517784	GM19239	blood:	n/a
7	chr3:145517734-145517784	HCF	heart:	n/a
8	chr3:145517734-145517784	HCM	heart:	n/a
9	chr3:145517734-145517784	SKMC	muscle:	n/a
10	chr3:145517734-145517784	NH-A	brain:	n/a
11	chr3:145517734-145517784	HUVEC	blood vessel:	n/a
12	chr3:145517734-145517784	ECC-1	luminal epithelium:	n/a
13	chr3:145517734-145517784	HRE	kidney:	n/a
14	chr3:145517734-145517784	PrEC	prostate:	n/a
15	chr3:145517734-145517784	GM12892	blood:	n/a
16	chr3:145517734-145517784	IMR90	lung:	fetal
17	chr3:145517734-145517784	HMEC	breast:	n/a
18	chr3:145517734-145517784	Jurkat	blood:	n/a
19	chr3:145517734-145517784	ovcar-3	ovarian:	n/a
20	chr3:145517734-145517784	AG10803	skin:	n/a
21	chr3:145517734-145517784	BE2_C	brain:	n/a
22	chr3:145517734-145517784	H1-hESC	embryonic stem cell:	embryo
23	chr3:145517734-145517784	NT2-D1	testis:	n/a
24	chr3:145517734-145517784	A549	lung:	n/a
25	chr3:145517734-145517784	HepG2	liver:	n/a
26	chr3:145517734-145517784	NB4	blood:	n/a
27	chr3:145517734-145517784	HPAEpiC	pulmonary alveolar:	n/a
28	chr3:145517734-145517784	RPTEC	kidney:	n/a
29	chr3:145517734-145517784	HAEpiC	amniotic membrane:	n/a
30	chr3:145517734-145517784	AG04449	skin:	fetal
31	chr3:145517734-145517784	AoSMC	blood vessel:	n/a
32	chr3:145517734-145517784	HIPEpiC	eye:	n/a
33	chr3:145517734-145517784	MCF-7	breast:	n/a
34	chr3:145517734-145517784	HRCEpiC	kidney:	n/a
35	chr3:145517734-145517784	GM12878	blood:	n/a
36	chr3:145517734-145517784	SK-N-SH	brain:	n/a
37	chr3:145517734-145517784	T-47D	breast:	n/a
38	chr3:145517734-145517784	HRPEpiC	eye:	n/a
39	chr3:145517734-145517784	PANC-1	pancreas:	n/a
40	chr3:145517734-145517784	SAEC	small airway:	n/a
41	chr3:145517734-145517784	AG09309	skin:	n/a
42	chr3:145517734-145517784	BJ	skin:	n/a
43	chr3:145517734-145517784	Hepatocyte	liver:	n/a
44	chr3:145517734-145517784	AG09319	gingival:	n/a
45	chr3:145517734-145517784	NHDF-neo	bronchial:	n/a
46	chr3:145517734-145517784	LNCaP	prostate:	n/a
47	chr3:145517734-145517784	GM12891	blood:	n/a
48	chr3:145517734-145517784	HL-60	blood:	n/a
49	chr3:145517734-145517784	HCPEpiC	choroid plexus:	n/a
50	chr3:145517734-145517784	PFSK-1	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:145604775..145606383-chr3:145616815..145618517,2	MCF-7	breast:
2	chr3:145501403..145502940-chr3:145505353..145507937,2	K562	blood:
3	chr3:145621110..145623041-chr3:145624593..145626157,2	K562	blood:
4	chr3:145515573..145518093-chr3:145523034..145526059,3	MCF-7	breast:
5	chr3:144984069..144984806-chr3:145485343..145486312,4	MCF-7	breast:
6	chr3:145494214..145495352-chr3:145744124..145745129,8	MCF-7	breast:
7	chr3:145604775..145606383-chr3:145616815..145618517,2	MCF-7	breast:
8	chr3:144983996..144984506-chr3:145485486..145486139,2	MCF-7	breast:
9	chr3:145621110..145623041-chr3:145624593..145626157,2	K562	blood:
10	chr3:144561413..144562304-chr3:145485449..145486072,2	MCF-7	breast:
11	chr3:145515573..145518093-chr3:145523034..145526059,3	MCF-7	breast:
12	chr3:145558279..145560976-chr3:145566285..145567836,2	MCF-7	breast:
13	chr3:145558279..145560976-chr3:145566285..145567836,2	MCF-7	breast:
14	chr3:145501403..145502940-chr3:145505353..145507937,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PLOD2-6	chr3:145542044-145542526	NONHSAT092540

Variant related genes	Relation type
RPL21P39	TF binding region
ENSG00000244358	TF binding region
RPL21P39	CpG island
ENSG00000244358	CpG island

Extended variants
information (count: 4075 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:4075 , 50 per page) page: 1 2 3 4 5 6 7 ... 82

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs560396928	chr3:145467437-145467438	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs150280120	chr3:145467460-145467461	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs138932912	chr3:145467466-145467467	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs78488532	chr3:145467471-145467472	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs200924638	chr3:145467483-145467484	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs558807025	chr3:145467518-145467519	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs570878691	chr3:145467530-145467531	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs537654739	chr3:145467549-145467550	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs556316983	chr3:145467570-145467571	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs574441767	chr3:145467583-145467584	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs57856744	chr3:145467630-145467631	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs576043775	chr3:145467642-145467643	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs114451931	chr3:145467673-145467674	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs571729076	chr3:145467702-145467703	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs2399948	chr3:145467720-145467721	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs573531756	chr3:145467735-145467736	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs564032300	chr3:145467742-145467743	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs373545573	chr3:145467760-145467761	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs575365286	chr3:145467765-145467766	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs540657977	chr3:145467793-145467794	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs544525233	chr3:145467807-145467808	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs563051326	chr3:145467840-145467841	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs71313864	chr3:145467853-145467854	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs114498615	chr3:145467875-145467876	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs559185364	chr3:145467881-145467882	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs150111840	chr3:145467887-145467888	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs140824405	chr3:145467893-145467894	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs142404261	chr3:145467969-145467970	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs564862334	chr3:145467985-145467986	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs560739804	chr3:145468056-145468057	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs115163027	chr3:145468085-145468086	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs552503879	chr3:145468139-145468140	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs76221341	chr3:145468156-145468157	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs539898248	chr3:145468169-145468170	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs538336019	chr3:145468236-145468237	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs549740129	chr3:145468281-145468282	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs567900710	chr3:145468310-145468311	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs145937612	chr3:145468325-145468326	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs553651262	chr3:145468335-145468336	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs544756170	chr3:145468359-145468360	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs369765974	chr3:145468409-145468410	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs201993251	chr3:145468413-145468414	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs377055170	chr3:145468420-145468421	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs56876939	chr3:145468423-145468424	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs58092180	chr3:145468435-145468436	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs13073247	chr3:145468439-145468440	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs57801578	chr3:145468441-145468442	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs71621121	chr3:145468443-145468444	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs13073394	chr3:145468447-145468448	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs368450818	chr3:145468458-145468459	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

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

Chromatin state (count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:145467400-145469600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr3:145467800-145468200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr3:145468200-145468600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr3:145468600-145468800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr3:145468800-145471800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr3:145469600-145471400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr3:145470400-145471000	Enhancers	Fetal Stomach	stomach
8	chr3:145470800-145474200	Enhancers	Cortex derived primary cultured neurospheres	brain
9	chr3:145471400-145474600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr3:145471800-145472800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr3:145471800-145474000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr3:145472000-145473000	Enhancers	Brain Anterior Caudate	brain
13	chr3:145474200-145474600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr3:145492800-145493800	Enhancers	Fetal Heart	heart
15	chr3:145493000-145493800	Enhancers	HSMMtube	muscle
16	chr3:145493200-145493800	Enhancers	HSMM	muscle
17	chr3:145493200-145494400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
18	chr3:145493800-145498200	Weak transcription	HSMMtube	muscle
19	chr3:145498200-145498400	Enhancers	HSMMtube	muscle
20	chr3:145503400-145504600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr3:145504600-145508000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr3:145507600-145507800	Enhancers	Gastric	stomach
23	chr3:145507800-145508200	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr3:145507800-145508600	Weak transcription	Gastric	stomach
25	chr3:145508000-145508800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr3:145508600-145509400	Enhancers	Gastric	stomach
27	chr3:145508600-145509400	Enhancers	Pancreas	Pancrea
28	chr3:145508800-145509600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr3:145509600-145509800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr3:145509800-145510200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr3:145510200-145514800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr3:145514800-145515400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr3:145515400-145517200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr3:145515800-145516400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr3:145515800-145517800	Enhancers	Cortex derived primary cultured neurospheres	brain
36	chr3:145515800-145517800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr3:145516000-145516400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr3:145516000-145516600	Enhancers	Brain Hippocampus Middle	brain
39	chr3:145516000-145516600	Enhancers	Gastric	stomach
40	chr3:145516000-145516600	Enhancers	Pancreas	Pancrea
41	chr3:145516000-145517600	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr3:145516000-145518000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr3:145516200-145516600	Enhancers	Brain Inferior Temporal Lobe	brain
44	chr3:145516200-145516600	Bivalent Enhancer	HSMMtube	muscle
45	chr3:145516200-145516800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr3:145516200-145516800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr3:145516200-145516800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr3:145516200-145516800	Enhancers	Brain Cingulate Gyrus	brain
49	chr3:145516200-145516800	Enhancers	Esophagus	oesophagus
50	chr3:145516200-145517000	Enhancers	Fetal Muscle Leg	muscle

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