Variant report

Variant	nsv1008123
Chromosome Location	chr3:140328825-140464786
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:738)
CpG islands
(count:733)
Chromatin interactive
region (count:31)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:738 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

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	chr3:140444290-140444583	GM12878	blood:	n/a	chr3:140444440-140444451
6	BATF	chr3:140374547-140374771	GM12878	blood:	n/a	n/a
7	BATF	chr3:140435015-140435253	GM12878	blood:	n/a	n/a
8	BCL11A	chr3:140435034-140435158	GM12878	blood:	n/a	n/a
9	BHLHE40	chr3:140444050-140444669	GM12878	blood:	n/a	n/a
10	BHLHE40	chr3:140444451-140444496	HepG2	liver:	n/a	n/a
11	BHLHE40	chr3:140347642-140347676	GM12878	blood:	n/a	n/a
12	BHLHE40	chr3:140418726-140419133	HepG2	liver:	n/a	n/a
13	BHLHE40	chr3:140329685-140329713	K562	blood:	n/a	n/a
14	CEBPB	chr3:140446753-140447039	HepG2	liver:	n/a	n/a
15	CEBPB	chr3:140348716-140349002	HepG2	liver:	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	chr3:140396615-140396933	HepG2	liver:	n/a	chr3:140396722-140396733
19	CEBPB	chr3:140348639-140349072	MCF-7	breast:	n/a	n/a
20	CEBPB	chr3:140418669-140419087	HepG2	liver:	n/a	chr3:140418695-140418706
21	CEBPB	chr3:140398421-140398728	HepG2	liver:	n/a	chr3:140398565-140398578 chr3:140398567-140398576 chr3:140398566-140398577
22	CEBPB	chr3:140348665-140348999	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr3:140354064-140354201	HepG2	liver:	n/a	chr3:140354175-140354186
24	CEBPD	chr3:140418761-140419035	HepG2	liver:	n/a	n/a
25	CEBPZ	chr3:140418629-140419199	HepG2	liver:	n/a	n/a
26	CHD2	chr3:140450636-140450892	GM12878	blood:	n/a	n/a
27	CHD2	chr3:140418743-140419066	HepG2	liver:	n/a	n/a
28	CHD2	chr3:140447203-140447475	HepG2	liver:	n/a	n/a
29	CTCF	chr3:140456100-140456250	A549	lung:	n/a	chr3:140456109-140456122 chr3:140456102-140456123 chr3:140456107-140456125
30	CTCF	chr3:140405980-140406130	GM12872	blood:	n/a	n/a
31	CTCF	chr3:140455860-140456010	A549	lung:	n/a	n/a
32	CTCF	chr3:140456019-140456219	HUVEC	blood vessel:	n/a	chr3:140456109-140456122 chr3:140456102-140456123 chr3:140456107-140456125
33	CTCF	chr3:140455960-140456110	HFF-Myc	foreskin:	n/a	n/a
34	CTCF	chr3:140354248-140354396	MCF-7	breast:	n/a	n/a
35	CTCF	chr3:140456020-140456170	HRPEpiC	eye:	n/a	chr3:140456109-140456122 chr3:140456102-140456123 chr3:140456107-140456125
36	CTCF	chr3:140455880-140456030	HCM	heart:	n/a	n/a
37	CTCF	chr3:140456060-140456210	HA-sp	spinal cord:	n/a	chr3:140456109-140456122 chr3:140456102-140456123 chr3:140456107-140456125
38	CTCF	chr3:140455946-140456188	ECC-1	luminal epithelium:	n/a	chr3:140456109-140456122 chr3:140456102-140456123 chr3:140456107-140456125
39	CTCF	chr3:140392234-140392277	Fibrobl	skin:	n/a	n/a
40	CTCF	chr3:140354200-140354350	HepG2	liver:	n/a	n/a
41	CTCF	chr3:140455957-140456187	A549	lung:	n/a	chr3:140456109-140456122 chr3:140456102-140456123 chr3:140456107-140456125
42	CTCF	chr3:140455880-140456030	HCT-116	colon:	n/a	n/a
43	CTCF	chr3:140456020-140456170	SK-N-SH_RA	brain:	n/a	chr3:140456109-140456122 chr3:140456102-140456123 chr3:140456107-140456125
44	CTCF	chr3:140456040-140456190	HEK293	kidney:	n/a	chr3:140456109-140456122 chr3:140456102-140456123 chr3:140456107-140456125
45	CTCF	chr3:140456100-140456250	HAc	cerebellar:	n/a	chr3:140456109-140456122 chr3:140456102-140456123 chr3:140456107-140456125
46	CTCF	chr3:140456020-140456170	GM12869	blood:	n/a	chr3:140456109-140456122 chr3:140456102-140456123 chr3:140456107-140456125
47	CTCF	chr3:140456040-140456190	GM12871	blood:	n/a	chr3:140456109-140456122 chr3:140456102-140456123 chr3:140456107-140456125
48	CTCF	chr3:140455940-140456090	NHLF	lung:	n/a	n/a
49	CTCF	chr3:140456040-140456190	WERI-Rb-1	eye:	n/a	chr3:140456109-140456122 chr3:140456102-140456123 chr3:140456107-140456125
50	CTCF	chr3:140456032-140456202	GM20000	blood:	n/a	chr3:140456109-140456122 chr3:140456102-140456123 chr3:140456107-140456125

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:140395771-140395821	NT2-D1	testis:	n/a
2	chr3:140395771-140395821	NT2-D1	testis:	n/a
3	chr3:140395898-140395948	HL-60	blood:	n/a
4	chr3:140405436-140405486	BE2_C	brain:	n/a
5	chr3:140396803-140396853	HL-60	blood:	n/a
6	chr3:140401543-140401593	HUVEC	blood vessel:	n/a
7	chr3:140395898-140395948	AG09309	skin:	n/a
8	chr3:140396963-140397013	MCF10A-Er-Src	breast:	n/a
9	chr3:140395771-140395821	AG09319	gingival:	n/a
10	chr3:140402167-140402217	HAEpiC	amniotic membrane:	n/a
11	chr3:140395771-140395821	HEEpiC	esophagus:	n/a
12	chr3:140396963-140397013	SK-N-SH_RA	brain:	n/a
13	chr3:140401543-140401593	RPTEC	kidney:	n/a
14	chr3:140401925-140401975	AG10803	skin:	n/a
15	chr3:140395898-140395948	H1-hESC	embryonic stem cell:	embryo
16	chr3:140396963-140397013	T-47D	breast:	n/a
17	chr3:140402167-140402217	SK-N-SH_RA	brain:	n/a
18	chr3:140397089-140397139	HRPEpiC	eye:	n/a
19	chr3:140400911-140400961	AG09319	gingival:	n/a
20	chr3:140401925-140401975	HepG2	liver:	n/a
21	chr3:140395771-140395821	A549	lung:	n/a
22	chr3:140396803-140396853	HEK293	kidney:	embryo
23	chr3:140400911-140400961	AG09309	skin:	n/a
24	chr3:140401955-140402005	HIPEpiC	eye:	n/a
25	chr3:140395898-140395948	MCF10A-Er-Src	breast:	n/a
26	chr3:140400911-140400961	HL-60	blood:	n/a
27	chr3:140401765-140401815	HPAEpiC	pulmonary alveolar:	n/a
28	chr3:140397089-140397139	HUVEC	blood vessel:	n/a
29	chr3:140401543-140401593	ECC-1	luminal epithelium:	n/a
30	chr3:140400911-140400961	GM12878	blood:	n/a
31	chr3:140395771-140395821	LNCaP	prostate:	n/a
32	chr3:140396963-140397013	HPAEpiC	pulmonary alveolar:	n/a
33	chr3:140400911-140400961	GM12892	blood:	n/a
34	chr3:140396803-140396853	NHDF-neo	bronchial:	n/a
35	chr3:140397089-140397139	HepG2	liver:	n/a
36	chr3:140400911-140400961	CMK	blood:	n/a
37	chr3:140396803-140396853	HPAEpiC	pulmonary alveolar:	n/a
38	chr3:140401955-140402005	ECC-1	luminal epithelium:	n/a
39	chr3:140400911-140400961	HRPEpiC	eye:	n/a
40	chr3:140401955-140402005	CMK	blood:	n/a
41	chr3:140395898-140395948	AG09319	gingival:	n/a
42	chr3:140401543-140401593	HCF	heart:	n/a
43	chr3:140401765-140401815	ECC-1	luminal epithelium:	n/a
44	chr3:140401925-140401975	HRPEpiC	eye:	n/a
45	chr3:140397089-140397139	T-47D	breast:	n/a
46	chr3:140396803-140396853	NT2-D1	testis:	n/a
47	chr3:140396803-140396853	ECC-1	luminal epithelium:	n/a
48	chr3:140397089-140397139	HIPEpiC	eye:	n/a
49	chr3:140402167-140402217	GM12891	blood:	n/a
50	chr3:140405436-140405486	HCF	heart:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:140435248..140437189-chr3:140439215..140440913,2	K562	blood:
2	chr3:140328498..140333077-chr3:140333423..140336140,4	MCF-7	breast:
3	chr3:140442579..140445613-chr3:140449550..140453378,3	K562	blood:
4	chr3:140398849..140401533-chr3:140405253..140408358,3	K562	blood:
5	chr3:140455659..140456657-chr3:140582285..140583107,3	MCF-7	breast:
6	chr3:139847350..139848064-chr3:140455872..140456504,2	MCF-7	breast:
7	chr3:140425316..140427124-chr3:140431791..140433516,2	MCF-7	breast:
8	chr3:140404247..140407194-chr3:140408344..140410912,4	K562	blood:
9	chr3:140418901..140421597-chr3:140424922..140429163,3	K562	blood:
10	chr17:41400537..41402663-chr3:140426790..140428290,2	K562	blood:
11	chr3:140398849..140401533-chr3:140405253..140408358,3	K562	blood:
12	chr3:140442579..140445613-chr3:140449550..140453378,3	K562	blood:
13	chr3:140399760..140401307-chr3:140404568..140407227,2	MCF-7	breast:
14	chr17:41462273..41463839-chr3:140426790..140428290,2	K562	blood:
15	chr3:140399760..140401307-chr3:140404568..140407227,2	MCF-7	breast:
16	chr3:140435248..140437189-chr3:140439215..140440913,2	K562	blood:
17	chr3:140402179..140404321-chr3:140405178..140407110,2	K562	blood:
18	chr3:140438664..140441463-chr3:140446085..140448524,2	MCF-7	breast:
19	chr3:140433649..140435909-chr3:140440994..140443307,2	K562	blood:
20	chr3:140433649..140435909-chr3:140440994..140443307,2	K562	blood:
21	chr3:140354121..140354796-chr3:140455695..140456494,2	MCF-7	breast:
22	chr3:140418901..140421597-chr3:140424922..140429163,3	K562	blood:
23	chr3:140328498..140333077-chr3:140333423..140336140,4	MCF-7	breast:
24	chr3:140395530..140397595-chr3:140401305..140403330,2	K562	blood:
25	chr3:140425316..140427124-chr3:140431791..140433516,2	MCF-7	breast:
26	chr3:140402179..140404321-chr3:140405178..140407110,2	K562	blood:
27	chr3:140404247..140407194-chr3:140408344..140410912,4	K562	blood:
28	chr3:140457040..140458949-chr3:140465410..140467161,2	MCF-7	breast:
29	chr3:140354121..140354796-chr3:140455695..140456494,2	MCF-7	breast:
30	chr3:140438664..140441463-chr3:140446085..140448524,2	MCF-7	breast:
31	chr3:140271350..140272024-chr3:140455669..140456272,2	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: 3355 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:3355 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs193287525	chr3:140329211-140329212	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs530701763	chr3:140329217-140329218	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs142646340	chr3:140329234-140329235	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs543982466	chr3:140329256-140329257	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs536413687	chr3:140329278-140329279	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs184316113	chr3:140329313-140329314	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs573155870	chr3:140329336-140329337	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs564162927	chr3:140329346-140329347	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs540674214	chr3:140329355-140329356	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs139965989	chr3:140329426-140329427	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs116974678	chr3:140329429-140329430	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs532883886	chr3:140329430-140329431	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs28569452	chr3:140329435-140329436	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs563205940	chr3:140329493-140329494	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs530745972	chr3:140329553-140329554	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs149838153	chr3:140329600-140329601	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs372271944	chr3:140329603-140329604	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs16850639	chr3:140329618-140329619	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs528393022	chr3:140329704-140329705	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs566118425	chr3:140329722-140329723	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs547058945	chr3:140329725-140329726	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs571601346	chr3:140329749-140329750	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs145807621	chr3:140329753-140329754	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs141706697	chr3:140329765-140329766	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs189648418	chr3:140329781-140329782	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs536450244	chr3:140329808-140329809	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs9868284	chr3:140329923-140329924	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs145448369	chr3:140329957-140329958	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs534204264	chr3:140329973-140329974	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs369312425	chr3:140329978-140329979	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs180876242	chr3:140329980-140329981	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs1494521	chr3:140329994-140329995	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs538225359	chr3:140330000-140330001	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs557030804	chr3:140330015-140330016	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs9830692	chr3:140330040-140330041	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs147685510	chr3:140330064-140330065	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs142350304	chr3:140330071-140330072	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs185302397	chr3:140330078-140330079	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs9830840	chr3:140330108-140330109	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs564998825	chr3:140330144-140330145	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs532546411	chr3:140330148-140330149	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs550653481	chr3:140330164-140330165	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs563043942	chr3:140330172-140330173	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs530123116	chr3:140330240-140330241	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs548407030	chr3:140330257-140330258	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs374121433	chr3:140330288-140330289	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs566699141	chr3:140330293-140330294	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs73231288	chr3:140330314-140330315	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs141200573	chr3:140330363-140330364	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs552853348	chr3:140330382-140330383	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:53)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:334 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:140329200-140330000	Enhancers	NH-A	brain
2	chr3:140329200-140331000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr3:140329400-140329800	Enhancers	Osteobl	bone
4	chr3:140329400-140330000	Enhancers	Muscle Satellite Cultured Cells	--
5	chr3:140329600-140329800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr3:140331600-140332200	Weak transcription	Psoas Muscle	Psoas
7	chr3:140332400-140332600	Enhancers	Psoas Muscle	Psoas
8	chr3:140336000-140346800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr3:140344400-140348200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr3:140345600-140346200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr3:140346200-140346400	Enhancers	Placenta	Placenta
12	chr3:140346200-140349000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr3:140346200-140349600	Enhancers	HSMM	muscle
14	chr3:140346200-140352800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr3:140346400-140346600	Enhancers	HSMMtube	muscle
16	chr3:140346400-140348200	Enhancers	Muscle Satellite Cultured Cells	--
17	chr3:140346400-140350000	Enhancers	Osteobl	bone
18	chr3:140346400-140350200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr3:140346400-140350200	Enhancers	NHDF-Ad	bronchial
20	chr3:140346400-140350200	Enhancers	NHEK	skin
21	chr3:140346600-140347600	Weak transcription	HSMMtube	muscle
22	chr3:140346600-140350000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr3:140346600-140350200	Enhancers	HMEC	breast
24	chr3:140346600-140352000	Enhancers	Placenta Amnion	Placenta Amnion
25	chr3:140346800-140350000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr3:140346800-140350000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr3:140346800-140350200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr3:140346800-140350200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr3:140346800-140350400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr3:140347000-140348400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr3:140347400-140349400	Enhancers	NHLF	lung
32	chr3:140347400-140350200	Enhancers	NH-A	brain
33	chr3:140347600-140349800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr3:140347600-140350000	Enhancers	HSMMtube	muscle
35	chr3:140348200-140348600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
36	chr3:140348200-140349200	Enhancers	Adipose Nuclei	Adipose
37	chr3:140348200-140349400	Enhancers	HUVEC	blood vessel
38	chr3:140348200-140350400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr3:140348200-140352000	Enhancers	Placenta	Placenta
40	chr3:140348400-140348600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr3:140348400-140348800	Enhancers	Pancreas	Pancrea
42	chr3:140348400-140349000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr3:140348400-140349000	Enhancers	Brain Substantia Nigra	brain
44	chr3:140348400-140349400	Enhancers	Brain Hippocampus Middle	brain
45	chr3:140348600-140349000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr3:140348600-140349000	Enhancers	Brain Cingulate Gyrus	brain
47	chr3:140348600-140349600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr3:140348600-140350200	Enhancers	Muscle Satellite Cultured Cells	--
49	chr3:140349000-140349400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr3:140349000-140349600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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