Variant report

Variant	esv3379945
Chromosome Location	chr3:145351163-145679850
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	ARID3A	chr3:145366991-145367605	HepG2	liver:	n/a	n/a
3	BATF	chr3:145617922-145618098	GM12878	blood:	n/a	chr3:145617976-145617987
4	BATF	chr3:145617031-145617299	GM12878	blood:	n/a	chr3:145617167-145617178
5	BATF	chr3:145617078-145617323	GM12878	blood:	n/a	chr3:145617167-145617178
6	BATF	chr3:145661502-145661720	GM12878	blood:	n/a	chr3:145661650-145661660 chr3:145661649-145661660
7	BATF	chr3:145617884-145618161	GM12878	blood:	n/a	chr3:145617976-145617987
8	BCL11A	chr3:145617839-145618177	GM12878	blood:	n/a	chr3:145617979-145617988 chr3:145617980-145617989
9	BCL11A	chr3:145617942-145618090	GM12878	blood:	n/a	chr3:145617979-145617988 chr3:145617980-145617989
10	BHLHE40	chr3:145367898-145368082	HepG2	liver:	n/a	n/a
11	BHLHE40	chr3:145367892-145368123	HepG2	liver:	n/a	n/a
12	BHLHE40	chr3:145616343-145617288	GM12878	blood:	n/a	n/a
13	BHLHE40	chr3:145494762-145494870	HepG2	liver:	n/a	n/a
14	BHLHE40	chr3:145367030-145367665	HepG2	liver:	n/a	n/a
15	BHLHE40	chr3:145617829-145618365	GM12878	blood:	n/a	n/a
16	BHLHE40	chr3:145535736-145536028	GM12878	blood:	n/a	n/a
17	BHLHE40	chr3:145367046-145367360	HepG2	liver:	n/a	n/a
18	BHLHE40	chr3:145367050-145367352	HepG2	liver:	n/a	n/a
19	BRCA1	chr3:145531712-145531727	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr3:145501013-145501017	Hela-S3	cervix:	n/a	n/a
21	BRCA1	chr3:145477935-145478012	Hela-S3	cervix:	n/a	n/a
22	BRCA1	chr3:145602167-145602271	Hela-S3	cervix:	n/a	n/a
23	CCNT2	chr3:145410614-145410809	K562	blood:	n/a	n/a
24	CEBPB	chr3:145455772-145456084	A549	lung:	n/a	chr3:145455933-145455946 chr3:145455933-145455944 chr3:145455933-145455946 chr3:145455935-145455946
25	CEBPB	chr3:145503485-145503780	H1-hESC	embryonic stem cell:	n/a	chr3:145503642-145503653 chr3:145503643-145503654 chr3:145503644-145503653
26	CEBPB	chr3:145492697-145492864	HepG2	liver:	n/a	chr3:145492742-145492753
27	CEBPB	chr3:145627345-145627605	IMR90	lung:	n/a	chr3:145627469-145627480
28	CEBPB	chr3:145617031-145617489	IMR90	lung:	n/a	chr3:145617318-145617329
29	CEBPB	chr3:145615167-145615415	HepG2	liver:	n/a	chr3:145615286-145615297
30	CEBPB	chr3:145368068-145368240	HepG2	liver:	n/a	chr3:145368173-145368184
31	CEBPB	chr3:145455799-145456091	K562	blood:	n/a	chr3:145455933-145455946 chr3:145455933-145455944 chr3:145455933-145455946 chr3:145455935-145455946
32	CEBPB	chr3:145572327-145572667	Hela-S3	cervix:	n/a	chr3:145572530-145572543
33	CEBPB	chr3:145654814-145655116	IMR90	lung:	n/a	chr3:145654981-145654992 chr3:145654981-145654990
34	CEBPB	chr3:145479900-145479932	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr3:145581045-145581109	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr3:145590953-145591270	Hela-S3	cervix:	n/a	chr3:145591064-145591075
37	CEBPB	chr3:145566939-145567274	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr3:145518738-145518905	K562	blood:	n/a	chr3:145518841-145518854 chr3:145518841-145518854 chr3:145518841-145518852 chr3:145518841-145518854
39	CEBPB	chr3:145367995-145368353	HepG2	liver:	n/a	chr3:145368173-145368184
40	CEBPB	chr3:145518672-145518957	A549	lung:	n/a	chr3:145518841-145518854 chr3:145518841-145518854 chr3:145518841-145518852 chr3:145518841-145518854
41	CEBPB	chr3:145503509-145503790	MCF-7	breast:	n/a	chr3:145503642-145503653 chr3:145503643-145503654 chr3:145503644-145503653
42	CEBPB	chr3:145493724-145493841	HepG2	liver:	n/a	chr3:145493760-145493771 chr3:145493759-145493772
43	CEBPB	chr3:145590915-145591265	HepG2	liver:	n/a	chr3:145591064-145591075
44	CEBPB	chr3:145453343-145453829	MCF-7	breast:	n/a	n/a
45	CEBPB	chr3:145368032-145368337	A549	lung:	n/a	chr3:145368173-145368184
46	CEBPB	chr3:145503474-145503830	Hela-S3	cervix:	n/a	chr3:145503642-145503653 chr3:145503643-145503654 chr3:145503644-145503653
47	CEBPB	chr3:145496437-145496688	MCF-7	breast:	n/a	n/a
48	CEBPB	chr3:145366989-145367692	HepG2	liver:	n/a	chr3:145367185-145367196
49	CEBPB	chr3:145518696-145518945	Hela-S3	cervix:	n/a	chr3:145518841-145518854 chr3:145518841-145518854 chr3:145518841-145518852 chr3:145518841-145518854
50	CEBPB	chr3:145488644-145488837	A549	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:145517734-145517784	HepG2	liver:	n/a
2	chr3:145517734-145517784	BE2_C	brain:	n/a
3	chr3:145517734-145517784	HL-60	blood:	n/a
4	chr3:145517734-145517784	HNPCEpiC	eye:	n/a
5	chr3:145517734-145517784	HRPEpiC	eye:	n/a
6	chr3:145517734-145517784	HCT-116	colon:	n/a
7	chr3:145517734-145517784	PFSK-1	brain:	n/a
8	chr3:145517734-145517784	HPAEpiC	pulmonary alveolar:	n/a
9	chr3:145517734-145517784	AoSMC	blood vessel:	n/a
10	chr3:145517734-145517784	SK-N-MC	brain:	n/a
11	chr3:145517734-145517784	AG09319	gingival:	n/a
12	chr3:145517734-145517784	U87	brain:	n/a
13	chr3:145517734-145517784	SK-N-SH	brain:	n/a
14	chr3:145517734-145517784	SAEC	small airway:	n/a
15	chr3:145517734-145517784	H1-hESC	embryonic stem cell:	embryo
16	chr3:145517734-145517784	SKMC	muscle:	n/a
17	chr3:145517734-145517784	Jurkat	blood:	n/a
18	chr3:145517734-145517784	AG10803	skin:	n/a
19	chr3:145517734-145517784	GM12892	blood:	n/a
20	chr3:145517734-145517784	AG09309	skin:	n/a
21	chr3:145517734-145517784	HEEpiC	esophagus:	n/a
22	chr3:145517734-145517784	GM12891	blood:	n/a
23	chr3:145517734-145517784	HCM	heart:	n/a
24	chr3:145517734-145517784	HRCEpiC	kidney:	n/a
25	chr3:145517734-145517784	K562	blood:	n/a
26	chr3:145517734-145517784	HMEC	breast:	n/a
27	chr3:145517734-145517784	T-47D	breast:	n/a
28	chr3:145517734-145517784	BJ	skin:	n/a
29	chr3:145517734-145517784	HCPEpiC	choroid plexus:	n/a
30	chr3:145517734-145517784	A549	lung:	n/a
31	chr3:145517734-145517784	MCF-7	breast:	n/a
32	chr3:145517734-145517784	HCF	heart:	n/a
33	chr3:145517734-145517784	SK-N-SH_RA	brain:	n/a
34	chr3:145517734-145517784	ProgFib	skin:	n/a
35	chr3:145517734-145517784	ECC-1	luminal epithelium:	n/a
36	chr3:145517734-145517784	HAEpiC	amniotic membrane:	n/a
37	chr3:145517734-145517784	NHDF-neo	bronchial:	n/a
38	chr3:145517734-145517784	RPTEC	kidney:	n/a
39	chr3:145517734-145517784	ovcar-3	ovarian:	n/a
40	chr3:145517734-145517784	GM12878	blood:	n/a
41	chr3:145517734-145517784	PANC-1	pancreas:	n/a
42	chr3:145517734-145517784	HRE	kidney:	n/a
43	chr3:145517734-145517784	AG04450	lung:	fetal
44	chr3:145517734-145517784	PrEC	prostate:	n/a
45	chr3:145517734-145517784	MCF10A-Er-Src	breast:	n/a
46	chr3:145517734-145517784	NHBE	bronchial:	n/a
47	chr3:145517734-145517784	Caco-2	colon:	n/a
48	chr3:145517734-145517784	Hela-S3	cervix:	n/a
49	chr3:145517734-145517784	GM19239	blood:	n/a
50	chr3:145517734-145517784	NH-A	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:144984029..144984834-chr3:145416240..145416755,2	MCF-7	breast:
2	chr3:145558279..145560976-chr3:145566285..145567836,2	MCF-7	breast:
3	chr3:145351605..145353581-chr3:145359076..145360606,2	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	chr3:144984069..144984806-chr3:145485343..145486312,4	MCF-7	breast:
7	chr3:145515573..145518093-chr3:145523034..145526059,3	MCF-7	breast:
8	chr3:145604775..145606383-chr3:145616815..145618517,2	MCF-7	breast:
9	chr3:145558279..145560976-chr3:145566285..145567836,2	MCF-7	breast:
10	chr3:144983996..144984506-chr3:145485486..145486139,2	MCF-7	breast:
11	chr3:145351605..145353581-chr3:145359076..145360606,2	MCF-7	breast:
12	chr3:145621110..145623041-chr3:145624593..145626157,2	K562	blood:
13	chr3:145501403..145502940-chr3:145505353..145507937,2	K562	blood:
14	chr3:145604775..145606383-chr3:145616815..145618517,2	MCF-7	breast:
15	chr3:144561413..144562304-chr3:145485449..145486072,2	MCF-7	breast:
16	chr3:145621110..145623041-chr3:145624593..145626157,2	K562	blood:
17	chr3:145494214..145495352-chr3:145744124..145745129,8	MCF-7	breast:

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

Variant related genes	Relation type
RPL21P39	TF binding region
ENSG00000244358	TF binding region
GM2AP1	TF binding region
ENSG00000240095	TF binding region
RPL21P39	CpG island
ENSG00000244358	CpG island
GM2AP1	CpG island
ENSG00000240095	CpG island
TWSG1	miRNA target sites
AP1M2	miRNA target sites

Extended variants
information (count: 7902 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:7902 , 50 per page) page: 1 2 3 4 5 6 7 ... 159

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372239085	chr3:145351176-145351177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs553072364	chr3:145351181-145351182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs141886346	chr3:145351182-145351183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs76846502	chr3:145351197-145351198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs111389494	chr3:145351207-145351208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs556918906	chr3:145351250-145351251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs575395506	chr3:145351266-145351267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs67152956	chr3:145351284-145351285	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs6808739	chr3:145351299-145351300	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs572889158	chr3:145351307-145351308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs540204511	chr3:145351313-145351314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs564874452	chr3:145351335-145351336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs78503843	chr3:145351373-145351374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs575118750	chr3:145351379-145351380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs550639838	chr3:145351431-145351432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs368096061	chr3:145351444-145351445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs142313695	chr3:145351477-145351478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs563775921	chr3:145351478-145351479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs530963754	chr3:145351517-145351518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs77625463	chr3:145351522-145351523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs36007331	chr3:145351531-145351532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs184505781	chr3:145351537-145351538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs73875308	chr3:145351564-145351565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs546625191	chr3:145351569-145351570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs367994839	chr3:145351612-145351613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs536299671	chr3:145351622-145351623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs538805547	chr3:145351650-145351651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs557382184	chr3:145351680-145351681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs116593917	chr3:145351702-145351703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs536420664	chr3:145351823-145351824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs554777823	chr3:145351875-145351876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs73875309	chr3:145351929-145351930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs573200028	chr3:145351943-145351944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs200947900	chr3:145351948-145351949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs397754350	chr3:145351949-145351950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs369283167	chr3:145351950-145351951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs551877572	chr3:145352006-145352007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs191718416	chr3:145352076-145352077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs540515463	chr3:145352091-145352092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs540267359	chr3:145352191-145352192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs558308222	chr3:145352277-145352278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs576768741	chr3:145352288-145352289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs543974326	chr3:145352310-145352311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs74393744	chr3:145352325-145352326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs184736852	chr3:145352326-145352327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs189658750	chr3:145352345-145352346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs565311386	chr3:145352362-145352363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs2375843	chr3:145352404-145352405	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs528801196	chr3:145352491-145352492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs544935298	chr3:145352525-145352526	Weak transcription	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
Breast cancer	22522925	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:526 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:145349400-145359600	Weak transcription	Aorta	Aorta
2	chr3:145354000-145354400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr3:145356600-145358400	Enhancers	Fetal Heart	heart
4	chr3:145357200-145358400	Enhancers	Fetal Intestine Large	intestine
5	chr3:145357400-145358400	Enhancers	HepG2	liver
6	chr3:145358400-145363200	Weak transcription	Fetal Intestine Large	intestine
7	chr3:145359600-145359800	Enhancers	Aorta	Aorta
8	chr3:145363200-145363800	Enhancers	Fetal Intestine Large	intestine
9	chr3:145363800-145366200	Weak transcription	Fetal Intestine Large	intestine
10	chr3:145366200-145366600	Enhancers	Fetal Intestine Large	intestine
11	chr3:145366200-145368000	Enhancers	HepG2	liver
12	chr3:145366600-145367400	Weak transcription	Fetal Intestine Large	intestine
13	chr3:145367400-145367600	Enhancers	Fetal Intestine Large	intestine
14	chr3:145367400-145367600	Enhancers	Fetal Intestine Small	intestine
15	chr3:145368000-145369400	Weak transcription	Fetal Intestine Large	intestine
16	chr3:145369400-145370000	Enhancers	Fetal Intestine Large	intestine
17	chr3:145378400-145378600	Enhancers	Fetal Intestine Large	intestine
18	chr3:145378600-145380800	Weak transcription	Fetal Intestine Large	intestine
19	chr3:145380800-145381000	Enhancers	Fetal Intestine Large	intestine
20	chr3:145381000-145381800	Weak transcription	Fetal Intestine Large	intestine
21	chr3:145381800-145382400	Enhancers	Fetal Intestine Large	intestine
22	chr3:145382400-145383600	Weak transcription	Fetal Intestine Large	intestine
23	chr3:145383800-145384000	Enhancers	Fetal Intestine Large	intestine
24	chr3:145385800-145386600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr3:145385800-145386800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr3:145386600-145390400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr3:145386800-145390800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr3:145390400-145390800	Enhancers	HUVEC	blood vessel
29	chr3:145390400-145391600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr3:145390800-145392000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr3:145391600-145392000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr3:145391600-145392000	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr3:145391600-145392000	Enhancers	Fetal Brain Male	brain
34	chr3:145392000-145396000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr3:145392000-145396200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr3:145394800-145398400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr3:145396000-145396400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr3:145396200-145396600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr3:145396400-145398400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr3:145396600-145397600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr3:145397600-145398000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr3:145398000-145399000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr3:145398400-145399400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr3:145398600-145399400	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr3:145399000-145399400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr3:145399000-145399400	Enhancers	Cortex derived primary cultured neurospheres	brain
47	chr3:145399200-145399600	Enhancers	HUES64 Cell Line	embryonic stem cell
48	chr3:145402200-145404800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr3:145404800-145405600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr3:145404800-145405600	Enhancers	Stomach Mucosa	stomach

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