Variant report

Variant	esv2751980
Chromosome Location	chr3:145473020-145758194
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	chr3:145661502-145661720	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	BATF	chr3:145617031-145617299	GM12878	blood:	n/a	chr3:145617167-145617178
7	BCL11A	chr3:145617942-145618090	GM12878	blood:	n/a	chr3:145617979-145617988 chr3:145617980-145617989
8	BCL11A	chr3:145617839-145618177	GM12878	blood:	n/a	chr3:145617979-145617988 chr3:145617980-145617989
9	BHLHE40	chr3:145616343-145617288	GM12878	blood:	n/a	n/a
10	BHLHE40	chr3:145720051-145720159	A549	lung:	n/a	n/a
11	BHLHE40	chr3:145494762-145494870	HepG2	liver:	n/a	n/a
12	BHLHE40	chr3:145535736-145536028	GM12878	blood:	n/a	n/a
13	BHLHE40	chr3:145617829-145618365	GM12878	blood:	n/a	n/a
14	BRCA1	chr3:145724499-145724650	Hela-S3	cervix:	n/a	n/a
15	BRCA1	chr3:145531712-145531727	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr3:145501013-145501017	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr3:145602167-145602271	Hela-S3	cervix:	n/a	n/a
18	BRCA1	chr3:145477935-145478012	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr3:145654814-145655116	IMR90	lung:	n/a	chr3:145654981-145654992 chr3:145654981-145654990
20	CEBPB	chr3:145617170-145617502	HepG2	liver:	n/a	chr3:145617318-145617329
21	CEBPB	chr3:145581045-145581109	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr3:145578466-145578687	A549	lung:	n/a	chr3:145578531-145578542
23	CEBPB	chr3:145590953-145591270	Hela-S3	cervix:	n/a	chr3:145591064-145591075
24	CEBPB	chr3:145728394-145728794	A549	lung:	n/a	chr3:145728655-145728666
25	CEBPB	chr3:145525867-145526117	MCF-7	breast:	n/a	chr3:145525953-145525966
26	CEBPB	chr3:145615179-145615388	Hela-S3	cervix:	n/a	chr3:145615286-145615297
27	CEBPB	chr3:145753252-145753456	K562	blood:	n/a	chr3:145753339-145753350
28	CEBPB	chr3:145572327-145572667	Hela-S3	cervix:	n/a	chr3:145572530-145572543
29	CEBPB	chr3:145488644-145488837	A549	lung:	n/a	n/a
30	CEBPB	chr3:145575808-145576126	Hela-S3	cervix:	n/a	chr3:145575984-145575995
31	CEBPB	chr3:145566939-145567274	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr3:145496437-145496688	MCF-7	breast:	n/a	n/a
33	CEBPB	chr3:145752782-145753525	IMR90	lung:	n/a	chr3:145753339-145753350
34	CEBPB	chr3:145627345-145627605	IMR90	lung:	n/a	chr3:145627469-145627480
35	CEBPB	chr3:145752778-145753482	A549	lung:	n/a	chr3:145753339-145753350
36	CEBPB	chr3:145503493-145503794	A549	lung:	n/a	chr3:145503642-145503653 chr3:145503643-145503654 chr3:145503644-145503653
37	CEBPB	chr3:145566953-145567259	A549	lung:	n/a	n/a
38	CEBPB	chr3:145493724-145493841	HepG2	liver:	n/a	chr3:145493760-145493771 chr3:145493759-145493772
39	CEBPB	chr3:145590915-145591265	HepG2	liver:	n/a	chr3:145591064-145591075
40	CEBPB	chr3:145503430-145503866	MCF-7	breast:	n/a	chr3:145503642-145503653 chr3:145503643-145503654 chr3:145503644-145503653
41	CEBPB	chr3:145643100-145643364	HepG2	liver:	n/a	chr3:145643198-145643209 chr3:145643269-145643282 chr3:145643200-145643211 chr3:145643216-145643227
42	CEBPB	chr3:145479900-145479932	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr3:145753266-145753466	H1-hESC	embryonic stem cell:	n/a	chr3:145753339-145753350
44	CEBPB	chr3:145714310-145714590	A549	lung:	n/a	chr3:145714458-145714469
45	CEBPB	chr3:145617147-145617472	A549	lung:	n/a	chr3:145617318-145617329
46	CEBPB	chr3:145518738-145518905	K562	blood:	n/a	chr3:145518841-145518854 chr3:145518841-145518854 chr3:145518841-145518852 chr3:145518841-145518854
47	CEBPB	chr3:145503458-145503783	IMR90	lung:	n/a	chr3:145503642-145503653 chr3:145503643-145503654 chr3:145503644-145503653
48	CEBPB	chr3:145685646-145685950	IMR90	lung:	n/a	chr3:145685802-145685813
49	CEBPB	chr3:145503490-145503793	HepG2	liver:	n/a	chr3:145503642-145503653 chr3:145503643-145503654 chr3:145503644-145503653
50	CEBPB	chr3:145615167-145615415	HepG2	liver:	n/a	chr3:145615286-145615297

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:145517734-145517784	K562	blood:	n/a
2	chr3:145734655-145734705	GM12891	blood:	n/a
3	chr3:145517734-145517784	K562	blood:	n/a
4	chr3:145734655-145734705	GM12891	blood:	n/a
5	chr3:145735965-145736015	NHBE	bronchial:	n/a
6	chr3:145736022-145736072	Caco-2	colon:	n/a
7	chr3:145735965-145736015	HAEpiC	amniotic membrane:	n/a
8	chr3:145736001-145736051	NB4	blood:	n/a
9	chr3:145735965-145736015	HCM	heart:	n/a
10	chr3:145734577-145734627	HRPEpiC	eye:	n/a
11	chr3:145736022-145736072	GM12892	blood:	n/a
12	chr3:145734655-145734705	HMEC	breast:	n/a
13	chr3:145734655-145734705	K562	blood:	n/a
14	chr3:145734577-145734627	LNCaP	prostate:	n/a
15	chr3:145735965-145736015	MCF-7	breast:	n/a
16	chr3:145736022-145736072	Hela-S3	cervix:	n/a
17	chr3:145736022-145736072	HAEpiC	amniotic membrane:	n/a
18	chr3:145735965-145736015	T-47D	breast:	n/a
19	chr3:145517734-145517784	NHBE	bronchial:	n/a
20	chr3:145734655-145734705	Jurkat	blood:	n/a
21	chr3:145734655-145734705	AG09309	skin:	n/a
22	chr3:145735965-145736015	A549	lung:	n/a
23	chr3:145736001-145736051	HRPEpiC	eye:	n/a
24	chr3:145736001-145736051	HepG2	liver:	n/a
25	chr3:145736001-145736051	HEK293	kidney:	embryo
26	chr3:145517734-145517784	HCF	heart:	n/a
27	chr3:145736001-145736051	Caco-2	colon:	n/a
28	chr3:145734655-145734705	AG10803	skin:	n/a
29	chr3:145735965-145736015	AG09309	skin:	n/a
30	chr3:145736022-145736072	HEEpiC	esophagus:	n/a
31	chr3:145734577-145734627	ECC-1	luminal epithelium:	n/a
32	chr3:145517734-145517784	Jurkat	blood:	n/a
33	chr3:145736022-145736072	HMEC	breast:	n/a
34	chr3:145736022-145736072	PFSK-1	brain:	n/a
35	chr3:145517734-145517784	CMK	blood:	n/a
36	chr3:145736001-145736051	HCPEpiC	choroid plexus:	n/a
37	chr3:145736022-145736072	AG09319	gingival:	n/a
38	chr3:145734577-145734627	SKMC	muscle:	n/a
39	chr3:145736001-145736051	GM12892	blood:	n/a
40	chr3:145736001-145736051	GM06990	blood:	n/a
41	chr3:145736001-145736051	A549	lung:	n/a
42	chr3:145734577-145734627	A549	lung:	n/a
43	chr3:145734577-145734627	CMK	blood:	n/a
44	chr3:145735965-145736015	NH-A	brain:	n/a
45	chr3:145734655-145734705	HRCEpiC	kidney:	n/a
46	chr3:145735965-145736015	SKMC	muscle:	n/a
47	chr3:145735965-145736015	HCPEpiC	choroid plexus:	n/a
48	chr3:145517734-145517784	Hepatocyte	liver:	n/a
49	chr3:145736001-145736051	AG04449	skin:	fetal
50	chr3:145735965-145736015	GM19239	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:145558279..145560976-chr3:145566285..145567836,2	MCF-7	breast:
2	chr3:145708427..145710747-chr3:145714607..145716482,2	MCF-7	breast:
3	chr3:144984069..144984806-chr3:145485343..145486312,4	MCF-7	breast:
4	chr3:145501403..145502940-chr3:145505353..145507937,2	K562	blood:
5	chr3:145515573..145518093-chr3:145523034..145526059,3	MCF-7	breast:
6	chr3:145688912..145689432-chr8:99049320..99049968,2	MCF-7	breast:
7	chr3:145515573..145518093-chr3:145523034..145526059,3	MCF-7	breast:
8	chr3:145743585..145744532-chr3:145904873..145905604,2	MCF-7	breast:
9	chr3:144561413..144562304-chr3:145485449..145486072,2	MCF-7	breast:
10	chr3:145501403..145502940-chr3:145505353..145507937,2	K562	blood:
11	chr3:145621110..145623041-chr3:145624593..145626157,2	K562	blood:
12	chr3:145736816..145738594-chr3:145881561..145884475,2	MCF-7	breast:
13	chr3:144983996..144984506-chr3:145485486..145486139,2	MCF-7	breast:
14	chr3:145604775..145606383-chr3:145616815..145618517,2	MCF-7	breast:
15	chr3:145621110..145623041-chr3:145624593..145626157,2	K562	blood:
16	chr3:145494214..145495352-chr3:145744124..145745129,8	MCF-7	breast:
17	chr3:145735893..145737457-chr3:145739302..145741925,2	MCF-7	breast:
18	chr3:145738494..145739375-chr3:145904889..145905776,3	MCF-7	breast:
19	chr3:145735893..145737457-chr3:145739302..145741925,2	MCF-7	breast:
20	chr3:145604775..145606383-chr3:145616815..145618517,2	MCF-7	breast:
21	chr3:145494214..145495352-chr3:145744124..145745129,8	MCF-7	breast:
22	chr3:145708427..145710747-chr3:145714607..145716482,2	MCF-7	breast:
23	chr3:145558279..145560976-chr3:145566285..145567836,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC107021.1-2	chr3:145681308-145681410	XLOC_002853
2	lnc-AC107021.1-3	chr3:145679104-145679323	XLOC_002852
3	lnc-AC107021.1-3	chr3:145664191-145664408	XLOC_002852
4	lnc-AC107021.1-3	chr3:145657755-145657941	XLOC_002852
5	lnc-AC107021.1-3	chr3:145675182-145675618	XLOC_002852
6	lnc-AC107021.1-3	chr3:145657699-145657941	XLOC_002852
7	lnc-AC107021.1-3	chr3:145675182-145675299	XLOC_002852
8	lnc-PLOD2-6	chr3:145542044-145542526	NONHSAT092540
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
TWSG1	miRNA target sites
AP1M2	miRNA target sites

Extended variants
information (count: 7864 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:7864 , 50 per page) page: 1 2 3 4 5 6 7 ... 158

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2673884	chr3:145473020-145473021	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs377043432	chr3:145473128-145473129	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs574226734	chr3:145473145-145473146	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs552372210	chr3:145473163-145473164	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs137979478	chr3:145473209-145473210	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs559788909	chr3:145473215-145473216	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs149520822	chr3:145473281-145473282	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs115893565	chr3:145473282-145473283	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs565483456	chr3:145473446-145473447	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs111579407	chr3:145473474-145473475	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs74493397	chr3:145473496-145473497	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs373687314	chr3:145473504-145473505	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs374711462	chr3:145473505-145473506	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs144048448	chr3:145473521-145473522	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs113409043	chr3:145473549-145473550	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs75223668	chr3:145473551-145473552	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs193300161	chr3:145473583-145473584	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs548703521	chr3:145473618-145473619	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs566916429	chr3:145473619-145473620	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs148651683	chr3:145473648-145473649	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs552130571	chr3:145473674-145473675	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs577092456	chr3:145473676-145473677	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs144538009	chr3:145473754-145473755	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs556005949	chr3:145473855-145473856	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs183399674	chr3:145473858-145473859	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs188505302	chr3:145473879-145473880	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs560002769	chr3:145473928-145473929	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs572099892	chr3:145473962-145473963	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs368897635	chr3:145473992-145473993	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs4493385	chr3:145474032-145474033	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs368054101	chr3:145474040-145474041	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs147422353	chr3:145474041-145474042	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs371501767	chr3:145474073-145474074	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs532560644	chr3:145474090-145474091	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs551316211	chr3:145474173-145474174	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs530423369	chr3:145474240-145474241	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs79176168	chr3:145474295-145474296	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs2459127	chr3:145474304-145474305	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs548592975	chr3:145474386-145474387	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs2459128	chr3:145474407-145474408	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs534278863	chr3:145474479-145474480	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs139909430	chr3:145474509-145474510	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs13325978	chr3:145474562-145474563	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs142088712	chr3:145492836-145492837	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs533532789	chr3:145492859-145492860	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs6806150	chr3:145492901-145492902	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs62270970	chr3:145492951-145492952	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs151201100	chr3:145492959-145492960	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs557280074	chr3:145492973-145492974	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs575860434	chr3:145493009-145493010	Enhancers	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:448 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:145470800-145474200	Enhancers	Cortex derived primary cultured neurospheres	brain
2	chr3:145471400-145474600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr3:145471800-145474000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr3:145474200-145474600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr3:145492800-145493800	Enhancers	Fetal Heart	heart
6	chr3:145493000-145493800	Enhancers	HSMMtube	muscle
7	chr3:145493200-145493800	Enhancers	HSMM	muscle
8	chr3:145493200-145494400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
9	chr3:145493800-145498200	Weak transcription	HSMMtube	muscle
10	chr3:145498200-145498400	Enhancers	HSMMtube	muscle
11	chr3:145503400-145504600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr3:145504600-145508000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr3:145507600-145507800	Enhancers	Gastric	stomach
14	chr3:145507800-145508200	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr3:145507800-145508600	Weak transcription	Gastric	stomach
16	chr3:145508000-145508800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr3:145508600-145509400	Enhancers	Gastric	stomach
18	chr3:145508600-145509400	Enhancers	Pancreas	Pancrea
19	chr3:145508800-145509600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr3:145509600-145509800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr3:145509800-145510200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr3:145510200-145514800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr3:145514800-145515400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr3:145515400-145517200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr3:145515800-145516400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr3:145515800-145517800	Enhancers	Cortex derived primary cultured neurospheres	brain
27	chr3:145515800-145517800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr3:145516000-145516400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr3:145516000-145516600	Enhancers	Brain Hippocampus Middle	brain
30	chr3:145516000-145516600	Enhancers	Gastric	stomach
31	chr3:145516000-145516600	Enhancers	Pancreas	Pancrea
32	chr3:145516000-145517600	Enhancers	iPS-15b Cell Line	embryonic stem cell
33	chr3:145516000-145518000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr3:145516200-145516600	Enhancers	Brain Inferior Temporal Lobe	brain
35	chr3:145516200-145516600	Bivalent Enhancer	HSMMtube	muscle
36	chr3:145516200-145516800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr3:145516200-145516800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr3:145516200-145516800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr3:145516200-145516800	Enhancers	Brain Cingulate Gyrus	brain
40	chr3:145516200-145516800	Enhancers	Esophagus	oesophagus
41	chr3:145516200-145517000	Enhancers	Fetal Muscle Leg	muscle
42	chr3:145516200-145517200	Enhancers	H1 Cell Line	embryonic stem cell
43	chr3:145516200-145517200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr3:145516200-145517200	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr3:145516200-145517800	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr3:145516200-145518000	Enhancers	iPS-18 Cell Line	embryonic stem cell
47	chr3:145516200-145518800	Enhancers	Fetal Lung	lung
48	chr3:145516400-145516800	Enhancers	Brain Angular Gyrus	brain
49	chr3:145516400-145516800	Enhancers	Fetal Muscle Trunk	muscle
50	chr3:145516400-145516800	Enhancers	Fetal Stomach	stomach

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