Variant report

Variant	nsv460869
Chromosome Location	chr3:140330108-140450655
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:505)
CpG islands
(count:734)
Chromatin interactive
region (count:26)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:505 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:140418329-140419193	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:140446760-140447646	HepG2	liver:	n/a	n/a
3	ATF1	chr3:140336242-140336250	K562	blood:	n/a	n/a
4	BACH1	chr3:140367452-140367456	K562	blood:	n/a	n/a
5	BATF	chr3:140435015-140435253	GM12878	blood:	n/a	n/a
6	BATF	chr3:140374547-140374771	GM12878	blood:	n/a	n/a
7	BATF	chr3:140444290-140444583	GM12878	blood:	n/a	chr3:140444440-140444451
8	BCL11A	chr3:140435034-140435158	GM12878	blood:	n/a	n/a
9	BHLHE40	chr3:140444451-140444496	HepG2	liver:	n/a	n/a
10	BHLHE40	chr3:140347642-140347676	GM12878	blood:	n/a	n/a
11	BHLHE40	chr3:140444050-140444669	GM12878	blood:	n/a	n/a
12	BHLHE40	chr3:140418726-140419133	HepG2	liver:	n/a	n/a
13	CEBPB	chr3:140398421-140398728	HepG2	liver:	n/a	chr3:140398565-140398578 chr3:140398567-140398576 chr3:140398566-140398577
14	CEBPB	chr3:140354064-140354201	HepG2	liver:	n/a	chr3:140354175-140354186
15	CEBPB	chr3:140348639-140349072	MCF-7	breast:	n/a	n/a
16	CEBPB	chr3:140418845-140419055	HepG2	liver:	n/a	n/a
17	CEBPB	chr3:140418802-140419142	HepG2	liver:	n/a	n/a
18	CEBPB	chr3:140446753-140447039	HepG2	liver:	n/a	n/a
19	CEBPB	chr3:140418669-140419087	HepG2	liver:	n/a	chr3:140418695-140418706
20	CEBPB	chr3:140396615-140396933	HepG2	liver:	n/a	chr3:140396722-140396733
21	CEBPB	chr3:140348665-140348999	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr3:140348716-140349002	HepG2	liver:	n/a	n/a
23	CEBPD	chr3:140418761-140419035	HepG2	liver:	n/a	n/a
24	CEBPZ	chr3:140418629-140419199	HepG2	liver:	n/a	n/a
25	CHD2	chr3:140450636-140450892	GM12878	blood:	n/a	n/a
26	CHD2	chr3:140418743-140419066	HepG2	liver:	n/a	n/a
27	CHD2	chr3:140447203-140447475	HepG2	liver:	n/a	n/a
28	CTCF	chr3:140354220-140354370	GM12873	blood:	n/a	n/a
29	CTCF	chr3:140405940-140406090	HBMEC	blood vessel:	n/a	n/a
30	CTCF	chr3:140405960-140406110	Caco-2	colon:	n/a	n/a
31	CTCF	chr3:140412924-140412955	GM13976	blood:	n/a	n/a
32	CTCF	chr3:140354140-140354290	GM12875	blood:	n/a	n/a
33	CTCF	chr3:140354160-140354310	GM06990	blood:	n/a	n/a
34	CTCF	chr3:140405980-140406130	GM12872	blood:	n/a	n/a
35	CTCF	chr3:140370548-140370617	Lung_OC	lung:	n/a	n/a
36	CTCF	chr3:140401863-140401929	GM13976	blood:	n/a	n/a
37	CTCF	chr3:140405960-140406110	GM12873	blood:	n/a	n/a
38	CTCF	chr3:140405880-140406030	RPTEC	kidney:	n/a	n/a
39	CTCF	chr3:140392234-140392277	Fibrobl	skin:	n/a	n/a
40	CTCF	chr3:140339469-140339560	LNCaP	prostate:	n/a	n/a
41	CTCF	chr3:140354240-140354390	GM12870	blood:	n/a	n/a
42	CTCF	chr3:140406000-140406150	HepG2	liver:	n/a	n/a
43	CTCF	chr3:140354238-140354382	GM12878	blood:	n/a	n/a
44	CTCF	chr3:140354164-140354432	GM12878	blood:	n/a	n/a
45	CTCF	chr3:140354200-140354350	HepG2	liver:	n/a	n/a
46	CTCF	chr3:140405976-140406017	HepG2	liver:	n/a	n/a
47	CTCF	chr3:140354288-140354348	MCF-7	breast:	n/a	n/a
48	CTCF	chr3:140405900-140406050	HEK293	kidney:	n/a	n/a
49	CTCF	chr3:140354180-140354330	GM12864	blood:	n/a	n/a
50	CTCF	chr3:140354248-140354396	MCF-7	breast:	n/a	n/a

(count:734 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:140401955-140402005	HUVEC	blood vessel:	n/a
2	chr3:140401925-140401975	HRCEpiC	kidney:	n/a
3	chr3:140401955-140402005	HUVEC	blood vessel:	n/a
4	chr3:140401925-140401975	HRCEpiC	kidney:	n/a
5	chr3:140401543-140401593	ovcar-3	ovarian:	n/a
6	chr3:140405436-140405486	AG04450	lung:	fetal
7	chr3:140401955-140402005	HIPEpiC	eye:	n/a
8	chr3:140402167-140402217	HMEC	breast:	n/a
9	chr3:140395898-140395948	AG09309	skin:	n/a
10	chr3:140401765-140401815	ovcar-3	ovarian:	n/a
11	chr3:140402167-140402217	HRE	kidney:	n/a
12	chr3:140395771-140395821	SKMC	muscle:	n/a
13	chr3:140402167-140402217	HCF	heart:	n/a
14	chr3:140396803-140396853	CMK	blood:	n/a
15	chr3:140401543-140401593	AG09319	gingival:	n/a
16	chr3:140395898-140395948	CMK	blood:	n/a
17	chr3:140405436-140405486	MCF10A-Er-Src	breast:	n/a
18	chr3:140401955-140402005	AG09309	skin:	n/a
19	chr3:140395771-140395821	AG10803	skin:	n/a
20	chr3:140395898-140395948	GM12892	blood:	n/a
21	chr3:140400911-140400961	GM12891	blood:	n/a
22	chr3:140396963-140397013	NHBE	bronchial:	n/a
23	chr3:140395771-140395821	U87	brain:	n/a
24	chr3:140401955-140402005	AoSMC	blood vessel:	n/a
25	chr3:140395771-140395821	AoSMC	blood vessel:	n/a
26	chr3:140396803-140396853	GM12891	blood:	n/a
27	chr3:140401925-140401975	IMR90	lung:	fetal
28	chr3:140401765-140401815	HL-60	blood:	n/a
29	chr3:140401925-140401975	BE2_C	brain:	n/a
30	chr3:140405436-140405486	HUVEC	blood vessel:	n/a
31	chr3:140396963-140397013	HepG2	liver:	n/a
32	chr3:140402167-140402217	HCT-116	colon:	n/a
33	chr3:140396803-140396853	AG09319	gingival:	n/a
34	chr3:140396963-140397013	NHDF-neo	bronchial:	n/a
35	chr3:140395898-140395948	NT2-D1	testis:	n/a
36	chr3:140401765-140401815	HEK293	kidney:	embryo
37	chr3:140397089-140397139	AG09319	gingival:	n/a
38	chr3:140402167-140402217	HPAEpiC	pulmonary alveolar:	n/a
39	chr3:140401543-140401593	PANC-1	pancreas:	n/a
40	chr3:140401925-140401975	HCPEpiC	choroid plexus:	n/a
41	chr3:140397089-140397139	BJ	skin:	n/a
42	chr3:140397089-140397139	SK-N-SH	brain:	n/a
43	chr3:140401765-140401815	SK-N-MC	brain:	n/a
44	chr3:140395898-140395948	GM19239	blood:	n/a
45	chr3:140401543-140401593	HMEC	breast:	n/a
46	chr3:140395898-140395948	HUVEC	blood vessel:	n/a
47	chr3:140402167-140402217	GM12878	blood:	n/a
48	chr3:140401765-140401815	U87	brain:	n/a
49	chr3:140400911-140400961	HIPEpiC	eye:	n/a
50	chr3:140401765-140401815	HPAEpiC	pulmonary alveolar:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:140442579..140445613-chr3:140449550..140453378,3	K562	blood:
2	chr3:140328498..140333077-chr3:140333423..140336140,4	MCF-7	breast:
3	chr3:140425316..140427124-chr3:140431791..140433516,2	MCF-7	breast:
4	chr3:140435248..140437189-chr3:140439215..140440913,2	K562	blood:
5	chr3:140402179..140404321-chr3:140405178..140407110,2	K562	blood:
6	chr3:140398849..140401533-chr3:140405253..140408358,3	K562	blood:
7	chr3:140438664..140441463-chr3:140446085..140448524,2	MCF-7	breast:
8	chr17:41400537..41402663-chr3:140426790..140428290,2	K562	blood:
9	chr3:140418901..140421597-chr3:140424922..140429163,3	K562	blood:
10	chr3:140442579..140445613-chr3:140449550..140453378,3	K562	blood:
11	chr3:140395530..140397595-chr3:140401305..140403330,2	K562	blood:
12	chr3:140399760..140401307-chr3:140404568..140407227,2	MCF-7	breast:
13	chr3:140399760..140401307-chr3:140404568..140407227,2	MCF-7	breast:
14	chr3:140418901..140421597-chr3:140424922..140429163,3	K562	blood:
15	chr3:140404247..140407194-chr3:140408344..140410912,4	K562	blood:
16	chr3:140354121..140354796-chr3:140455695..140456494,2	MCF-7	breast:
17	chr3:140425316..140427124-chr3:140431791..140433516,2	MCF-7	breast:
18	chr17:41462273..41463839-chr3:140426790..140428290,2	K562	blood:
19	chr3:140398849..140401533-chr3:140405253..140408358,3	K562	blood:
20	chr3:140438664..140441463-chr3:140446085..140448524,2	MCF-7	breast:
21	chr3:140433649..140435909-chr3:140440994..140443307,2	K562	blood:
22	chr3:140433649..140435909-chr3:140440994..140443307,2	K562	blood:
23	chr3:140402179..140404321-chr3:140405178..140407110,2	K562	blood:
24	chr3:140404247..140407194-chr3:140408344..140410912,4	K562	blood:
25	chr3:140435248..140437189-chr3:140439215..140440913,2	K562	blood:
26	chr3:140328498..140333077-chr3:140333423..140336140,4	MCF-7	breast:

(count:1 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NMNAT3-10	chr3:140434525-140435054	refGeneNc_2651_NR_027070

No data

Variant related genes	Relation type
TRIM42	TF binding region
ENSG00000249305	TF binding region
TRIM42	CpG island
ENSG00000249305	CpG island
ENSG00000155890	chromatin interactions

Extended variants
information (count: 3068 )
Associated
traits (count: 52 )

Variant overlapped rSNPs/rCNVs (count:3068 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9830840	chr3:140330108-140330109	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs564998825	chr3:140330144-140330145	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs532546411	chr3:140330148-140330149	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs550653481	chr3:140330164-140330165	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs563043942	chr3:140330172-140330173	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs530123116	chr3:140330240-140330241	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs548407030	chr3:140330257-140330258	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs374121433	chr3:140330288-140330289	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs566699141	chr3:140330293-140330294	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs73231288	chr3:140330314-140330315	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs141200573	chr3:140330363-140330364	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs552853348	chr3:140330382-140330383	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs568574746	chr3:140330387-140330388	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs571019388	chr3:140330401-140330402	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs538633468	chr3:140330414-140330415	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs556681791	chr3:140330426-140330427	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs537610098	chr3:140330430-140330431	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs536338043	chr3:140330440-140330441	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs554833367	chr3:140330565-140330566	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs573096621	chr3:140330578-140330579	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs553619267	chr3:140330610-140330611	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs9869402	chr3:140330617-140330618	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs577058179	chr3:140330653-140330654	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs181439048	chr3:140330687-140330688	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs9289605	chr3:140330763-140330764	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs1499876	chr3:140330785-140330786	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs6790926	chr3:140330804-140330805	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs6803694	chr3:140330879-140330880	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs6766452	chr3:140330888-140330889	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs11927646	chr3:140330894-140330895	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs148279941	chr3:140330906-140330907	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs370006804	chr3:140330911-140330912	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs531903655	chr3:140330946-140330947	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs1512042	chr3:140330964-140330965	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs373374146	chr3:140330980-140330981	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs185975399	chr3:140330986-140330987	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs566611101	chr3:140331603-140331604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs1874146	chr3:140331746-140331747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs138037448	chr3:140331802-140331803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs570574693	chr3:140331849-140331850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs573465725	chr3:140331852-140331853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs182638773	chr3:140331854-140331855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs187071242	chr3:140331880-140331881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs542156375	chr3:140331924-140331925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs371273747	chr3:140331942-140331943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs369582853	chr3:140331951-140331952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs553743080	chr3:140331953-140331954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs572538690	chr3:140331973-140331974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs545960246	chr3:140331997-140331998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs561957600	chr3:140331999-140332000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:52)

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
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	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
microdeletion syndrome	22180640	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Multiple myeloma	17550852	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	18645599	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Hepatocellular carcinoma	16750200	CNVD
Lung cancer	16740712	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
Myelofibrosis	22110671	CNVD
abnormal development	18461090	CNVD
Schizophrenia	17989066	CNVD
Ovarian cancer	23621864	CNVD

Chromatin state (count:318 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:140329200-140331000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr3:140331600-140332200	Weak transcription	Psoas Muscle	Psoas
3	chr3:140332400-140332600	Enhancers	Psoas Muscle	Psoas
4	chr3:140336000-140346800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr3:140344400-140348200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr3:140345600-140346200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr3:140346200-140346400	Enhancers	Placenta	Placenta
8	chr3:140346200-140349000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr3:140346200-140349600	Enhancers	HSMM	muscle
10	chr3:140346200-140352800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr3:140346400-140346600	Enhancers	HSMMtube	muscle
12	chr3:140346400-140348200	Enhancers	Muscle Satellite Cultured Cells	--
13	chr3:140346400-140350000	Enhancers	Osteobl	bone
14	chr3:140346400-140350200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr3:140346400-140350200	Enhancers	NHDF-Ad	bronchial
16	chr3:140346400-140350200	Enhancers	NHEK	skin
17	chr3:140346600-140347600	Weak transcription	HSMMtube	muscle
18	chr3:140346600-140350000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr3:140346600-140350200	Enhancers	HMEC	breast
20	chr3:140346600-140352000	Enhancers	Placenta Amnion	Placenta Amnion
21	chr3:140346800-140350000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr3:140346800-140350000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr3:140346800-140350200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr3:140346800-140350200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr3:140346800-140350400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr3:140347000-140348400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr3:140347400-140349400	Enhancers	NHLF	lung
28	chr3:140347400-140350200	Enhancers	NH-A	brain
29	chr3:140347600-140349800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr3:140347600-140350000	Enhancers	HSMMtube	muscle
31	chr3:140348200-140348600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
32	chr3:140348200-140349200	Enhancers	Adipose Nuclei	Adipose
33	chr3:140348200-140349400	Enhancers	HUVEC	blood vessel
34	chr3:140348200-140350400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr3:140348200-140352000	Enhancers	Placenta	Placenta
36	chr3:140348400-140348600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr3:140348400-140348800	Enhancers	Pancreas	Pancrea
38	chr3:140348400-140349000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr3:140348400-140349000	Enhancers	Brain Substantia Nigra	brain
40	chr3:140348400-140349400	Enhancers	Brain Hippocampus Middle	brain
41	chr3:140348600-140349000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr3:140348600-140349000	Enhancers	Brain Cingulate Gyrus	brain
43	chr3:140348600-140349600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr3:140348600-140350200	Enhancers	Muscle Satellite Cultured Cells	--
45	chr3:140349000-140349400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr3:140349000-140349600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr3:140349400-140349800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr3:140349600-140350000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr3:140349800-140350000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr3:140350000-140350200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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