Variant report

Variant	nsv877546
Chromosome Location	chr3:140299603-140468370
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:845)
CpG islands
(count:795)
Chromatin interactive
region (count:37)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:845 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:140446760-140447646	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:140418329-140419193	HepG2	liver:	n/a	n/a
3	ATF1	chr3:140336242-140336250	K562	blood:	n/a	n/a
4	BACH1	chr3:140318453-140318653	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr3:140367452-140367456	K562	blood:	n/a	n/a
6	BATF	chr3:140374547-140374771	GM12878	blood:	n/a	n/a
7	BATF	chr3:140435015-140435253	GM12878	blood:	n/a	n/a
8	BATF	chr3:140444290-140444583	GM12878	blood:	n/a	chr3:140444440-140444451
9	BCL11A	chr3:140435034-140435158	GM12878	blood:	n/a	n/a
10	BHLHE40	chr3:140418726-140419133	HepG2	liver:	n/a	n/a
11	BHLHE40	chr3:140347642-140347676	GM12878	blood:	n/a	n/a
12	BHLHE40	chr3:140329685-140329713	K562	blood:	n/a	n/a
13	BHLHE40	chr3:140444451-140444496	HepG2	liver:	n/a	n/a
14	BHLHE40	chr3:140444050-140444669	GM12878	blood:	n/a	n/a
15	CCNT2	chr3:140314146-140314500	K562	blood:	n/a	chr3:140314351-140314371
16	CCNT2	chr3:140312647-140312920	K562	blood:	n/a	n/a
17	CEBPB	chr3:140418802-140419142	HepG2	liver:	n/a	n/a
18	CEBPB	chr3:140348639-140349072	MCF-7	breast:	n/a	n/a
19	CEBPB	chr3:140348665-140348999	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr3:140354064-140354201	HepG2	liver:	n/a	chr3:140354175-140354186
21	CEBPB	chr3:140418845-140419055	HepG2	liver:	n/a	n/a
22	CEBPB	chr3:140348716-140349002	HepG2	liver:	n/a	n/a
23	CEBPB	chr3:140396615-140396933	HepG2	liver:	n/a	chr3:140396722-140396733
24	CEBPB	chr3:140398421-140398728	HepG2	liver:	n/a	chr3:140398565-140398578 chr3:140398567-140398576 chr3:140398566-140398577
25	CEBPB	chr3:140418669-140419087	HepG2	liver:	n/a	chr3:140418695-140418706
26	CEBPB	chr3:140324409-140324596	HepG2	liver:	n/a	chr3:140324518-140324529
27	CEBPB	chr3:140446753-140447039	HepG2	liver:	n/a	n/a
28	CEBPD	chr3:140418761-140419035	HepG2	liver:	n/a	n/a
29	CEBPZ	chr3:140418629-140419199	HepG2	liver:	n/a	n/a
30	CHD2	chr3:140307456-140307691	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr3:140418743-140419066	HepG2	liver:	n/a	n/a
32	CHD2	chr3:140306728-140306917	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD2	chr3:140450636-140450892	GM12878	blood:	n/a	n/a
34	CHD2	chr3:140447203-140447475	HepG2	liver:	n/a	n/a
35	CTCF	chr3:140455959-140456216	Lung_OC	lung:	n/a	chr3:140456109-140456122 chr3:140456102-140456123 chr3:140456107-140456125
36	CTCF	chr3:140455920-140456227	K562	blood:	n/a	chr3:140456109-140456122 chr3:140456102-140456123 chr3:140456107-140456125
37	CTCF	chr3:140456039-140456185	SK-N-SH_RA	brain:	n/a	chr3:140456109-140456122 chr3:140456102-140456123 chr3:140456107-140456125
38	CTCF	chr3:140456000-140456150	HEK293	kidney:	n/a	chr3:140456109-140456122 chr3:140456102-140456123 chr3:140456107-140456125
39	CTCF	chr3:140456020-140456170	HPF	lung:	n/a	chr3:140456109-140456122 chr3:140456102-140456123 chr3:140456107-140456125
40	CTCF	chr3:140405976-140406017	HepG2	liver:	n/a	n/a
41	CTCF	chr3:140456000-140456150	GM12874	blood:	n/a	chr3:140456109-140456122 chr3:140456102-140456123 chr3:140456107-140456125
42	CTCF	chr3:140455988-140456234	Kidney_OC	kidney:	n/a	chr3:140456109-140456122 chr3:140456102-140456123 chr3:140456107-140456125
43	CTCF	chr3:140455978-140456235	Medullo	brain:	n/a	chr3:140456109-140456122 chr3:140456102-140456123 chr3:140456107-140456125
44	CTCF	chr3:140455924-140456239	HepG2	liver:	n/a	chr3:140456109-140456122 chr3:140456102-140456123 chr3:140456107-140456125
45	CTCF	chr3:140464240-140464390	GM12864	blood:	n/a	n/a
46	CTCF	chr3:140456040-140456190	HRE	kidney:	n/a	chr3:140456109-140456122 chr3:140456102-140456123 chr3:140456107-140456125
47	CTCF	chr3:140456020-140456186	H1-hESC	embryonic stem cell:	n/a	chr3:140456109-140456122 chr3:140456102-140456123 chr3:140456107-140456125
48	CTCF	chr3:140464180-140464330	HEK293	kidney:	n/a	n/a
49	CTCF	chr3:140354140-140354290	GM12875	blood:	n/a	n/a
50	CTCF	chr3:140456080-140456230	GM12872	blood:	n/a	chr3:140456109-140456122 chr3:140456102-140456123 chr3:140456107-140456125

(count:795 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:140396803-140396853	NHBE	bronchial:	n/a
2	chr3:140402167-140402217	SK-N-MC	brain:	n/a
3	chr3:140396803-140396853	NHBE	bronchial:	n/a
4	chr3:140402167-140402217	SK-N-MC	brain:	n/a
5	chr3:140401543-140401593	AG09309	skin:	n/a
6	chr3:140400911-140400961	LNCaP	prostate:	n/a
7	chr3:140405436-140405486	T-47D	breast:	n/a
8	chr3:140395898-140395948	NHDF-neo	bronchial:	n/a
9	chr3:140401765-140401815	LNCaP	prostate:	n/a
10	chr3:140402167-140402217	ovcar-3	ovarian:	n/a
11	chr3:140400911-140400961	AG04449	skin:	fetal
12	chr3:140306730-140306780	HL-60	blood:	n/a
13	chr3:140396803-140396853	AG04450	lung:	fetal
14	chr3:140401955-140402005	HL-60	blood:	n/a
15	chr3:140401765-140401815	Hela-S3	cervix:	n/a
16	chr3:140397089-140397139	AoSMC	blood vessel:	n/a
17	chr3:140405436-140405486	GM19239	blood:	n/a
18	chr3:140306730-140306780	GM12892	blood:	n/a
19	chr3:140396963-140397013	BJ	skin:	n/a
20	chr3:140402167-140402217	IMR90	lung:	fetal
21	chr3:140401955-140402005	Caco-2	colon:	n/a
22	chr3:140395898-140395948	ProgFib	skin:	n/a
23	chr3:140401955-140402005	AG09319	gingival:	n/a
24	chr3:140401955-140402005	HRCEpiC	kidney:	n/a
25	chr3:140400911-140400961	NT2-D1	testis:	n/a
26	chr3:140401543-140401593	IMR90	lung:	fetal
27	chr3:140395898-140395948	T-47D	breast:	n/a
28	chr3:140401765-140401815	U87	brain:	n/a
29	chr3:140306730-140306780	ECC-1	luminal epithelium:	n/a
30	chr3:140405436-140405486	AG09319	gingival:	n/a
31	chr3:140405436-140405486	HCT-116	colon:	n/a
32	chr3:140395898-140395948	Caco-2	colon:	n/a
33	chr3:140401955-140402005	Hepatocyte	liver:	n/a
34	chr3:140395898-140395948	HepG2	liver:	n/a
35	chr3:140401925-140401975	A549	lung:	n/a
36	chr3:140395771-140395821	SKMC	muscle:	n/a
37	chr3:140396963-140397013	SK-N-MC	brain:	n/a
38	chr3:140400911-140400961	A549	lung:	n/a
39	chr3:140395771-140395821	HUVEC	blood vessel:	n/a
40	chr3:140401925-140401975	HEK293	kidney:	embryo
41	chr3:140401765-140401815	HNPCEpiC	eye:	n/a
42	chr3:140401955-140402005	AG10803	skin:	n/a
43	chr3:140402167-140402217	HIPEpiC	eye:	n/a
44	chr3:140400911-140400961	GM06990	blood:	n/a
45	chr3:140397089-140397139	BJ	skin:	n/a
46	chr3:140397089-140397139	HCF	heart:	n/a
47	chr3:140401925-140401975	Hela-S3	cervix:	n/a
48	chr3:140397089-140397139	AG09309	skin:	n/a
49	chr3:140401955-140402005	GM06990	blood:	n/a
50	chr3:140400911-140400961	HEEpiC	esophagus:	n/a

(count:37 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:140425316..140427124-chr3:140431791..140433516,2	MCF-7	breast:
2	chr3:140442579..140445613-chr3:140449550..140453378,3	K562	blood:
3	chr3:140314929..140317518-chr3:140320988..140323953,2	K562	blood:
4	chr3:140425316..140427124-chr3:140431791..140433516,2	MCF-7	breast:
5	chr3:139847350..139848064-chr3:140455872..140456504,2	MCF-7	breast:
6	chr3:140418901..140421597-chr3:140424922..140429163,3	K562	blood:
7	chr3:140404247..140407194-chr3:140408344..140410912,4	K562	blood:
8	chr3:140435248..140437189-chr3:140439215..140440913,2	K562	blood:
9	chr3:140395530..140397595-chr3:140401305..140403330,2	K562	blood:
10	chr3:140457040..140458949-chr3:140465410..140467161,2	MCF-7	breast:
11	chr3:140438664..140441463-chr3:140446085..140448524,2	MCF-7	breast:
12	chr3:140328498..140333077-chr3:140333423..140336140,4	MCF-7	breast:
13	chr3:140313745..140316717-chr3:140320885..140322798,2	K562	blood:
14	chr3:140418901..140421597-chr3:140424922..140429163,3	K562	blood:
15	chr3:140433649..140435909-chr3:140440994..140443307,2	K562	blood:
16	chr3:140354121..140354796-chr3:140455695..140456494,2	MCF-7	breast:
17	chr3:140271350..140272024-chr3:140455669..140456272,2	MCF-7	breast:
18	chr3:140433649..140435909-chr3:140440994..140443307,2	K562	blood:
19	chr3:140435248..140437189-chr3:140439215..140440913,2	K562	blood:
20	chr17:41462273..41463839-chr3:140426790..140428290,2	K562	blood:
21	chr3:140328498..140333077-chr3:140333423..140336140,4	MCF-7	breast:
22	chr3:140402179..140404321-chr3:140405178..140407110,2	K562	blood:
23	chr3:140399760..140401307-chr3:140404568..140407227,2	MCF-7	breast:
24	chr3:140294766..140296496-chr3:140304376..140305951,2	MCF-7	breast:
25	chr3:140354121..140354796-chr3:140455695..140456494,2	MCF-7	breast:
26	chr3:140398849..140401533-chr3:140405253..140408358,3	K562	blood:
27	chr3:140313745..140316717-chr3:140320885..140322798,2	K562	blood:
28	chr3:140438664..140441463-chr3:140446085..140448524,2	MCF-7	breast:
29	chr17:41400537..41402663-chr3:140426790..140428290,2	K562	blood:
30	chr3:140404247..140407194-chr3:140408344..140410912,4	K562	blood:
31	chr3:140399760..140401307-chr3:140404568..140407227,2	MCF-7	breast:
32	chr3:140402179..140404321-chr3:140405178..140407110,2	K562	blood:
33	chr3:140398849..140401533-chr3:140405253..140408358,3	K562	blood:
34	chr3:140457040..140458949-chr3:140465410..140467161,2	MCF-7	breast:
35	chr3:140314929..140317518-chr3:140320988..140323953,2	K562	blood:
36	chr3:140442579..140445613-chr3:140449550..140453378,3	K562	blood:
37	chr3:140455659..140456657-chr3:140582285..140583107,3	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NMNAT3-10	chr3:140434525-140435054	refGeneNc_2651_NR_027070
2	lnc-CLSTN2-3	chr3:140310744-140310837	l_2484_NR_026783
3	lnc-CLSTN2-3	chr3:140325513-140326693	l_2484_NR_026783
4	lnc-CLSTN2-3	chr3:140305717-140307953	l_2484_NR_026783

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: 4396 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:4396 , 50 per page) page: 1 2 3 4 5 6 7 ... 88

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1845476	chr3:140299603-140299604	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs533227597	chr3:140299618-140299619	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs368785322	chr3:140299619-140299620	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs540942605	chr3:140299642-140299643	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs191240659	chr3:140299683-140299684	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs144854346	chr3:140299726-140299727	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs545108579	chr3:140299751-140299752	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs376269544	chr3:140299804-140299805	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs376653292	chr3:140299920-140299921	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs369044759	chr3:140299922-140299923	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs530956999	chr3:140299929-140299930	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs74697051	chr3:140299952-140299953	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs567871620	chr3:140299979-140299980	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs371745963	chr3:140299980-140299981	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs75061883	chr3:140300035-140300036	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs545433582	chr3:140300063-140300064	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs547191539	chr3:140300102-140300103	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs147510297	chr3:140300107-140300108	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs539329062	chr3:140300153-140300154	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs557513363	chr3:140300162-140300163	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs569586718	chr3:140300169-140300170	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs557311568	chr3:140300250-140300251	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs372506457	chr3:140300251-140300252	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs80352824	chr3:140300261-140300262	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs183550124	chr3:140300305-140300306	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs347958	chr3:140300308-140300309	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs187492883	chr3:140300358-140300359	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs540856613	chr3:140300370-140300371	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs190862228	chr3:140300403-140300404	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs164345	chr3:140300418-140300419	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs10541037	chr3:140300445-140300446	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs36093241	chr3:140300446-140300447	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs4046204	chr3:140300458-140300459	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs151050945	chr3:140300524-140300525	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs347959	chr3:140300525-140300526	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs530897578	chr3:140300588-140300589	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs140949005	chr3:140300635-140300636	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs201367728	chr3:140300651-140300652	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs561393258	chr3:140300758-140300759	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs183453766	chr3:140300760-140300761	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs547254651	chr3:140300766-140300767	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs79279975	chr3:140300770-140300771	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs370521511	chr3:140300791-140300792	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs571865576	chr3:140300801-140300802	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs532697307	chr3:140300813-140300814	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs562062953	chr3:140300888-140300889	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs347960	chr3:140300897-140300898	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs118070229	chr3:140300912-140300913	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs374123936	chr3:140300942-140300943	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs537023035	chr3:140300943-140300944	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:55)

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
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Ovarian cancer	23621864	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:490 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:140296800-140299800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr3:140297200-140299800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr3:140298400-140300000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr3:140299200-140299800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr3:140299200-140300000	Enhancers	NHEK	skin
6	chr3:140299200-140300200	Enhancers	NH-A	brain
7	chr3:140299200-140300400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr3:140299200-140300400	Enhancers	HMEC	breast
9	chr3:140299200-140301200	Enhancers	HSMM	muscle
10	chr3:140299400-140300200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr3:140299400-140300200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr3:140299400-140300400	Enhancers	Muscle Satellite Cultured Cells	--
13	chr3:140299400-140300400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr3:140299400-140300400	Enhancers	HSMMtube	muscle
15	chr3:140299800-140300000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr3:140299800-140300200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr3:140300000-140305200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr3:140300200-140303600	Weak transcription	NH-A	brain
19	chr3:140300200-140304600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr3:140300200-140304600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr3:140300400-140303000	Weak transcription	HSMMtube	muscle
22	chr3:140300400-140303800	Weak transcription	HMEC	breast
23	chr3:140300400-140304200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr3:140300400-140304200	Weak transcription	Muscle Satellite Cultured Cells	--
25	chr3:140301200-140303400	Weak transcription	HSMM	muscle
26	chr3:140301600-140302000	Active TSS	Small Intestine	intestine
27	chr3:140303000-140305200	Enhancers	HSMMtube	muscle
28	chr3:140303400-140306000	Enhancers	HSMM	muscle
29	chr3:140303600-140304400	Enhancers	NH-A	brain
30	chr3:140303800-140305800	Enhancers	HMEC	breast
31	chr3:140304200-140305800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr3:140304200-140305800	Enhancers	Osteobl	bone
33	chr3:140304200-140306000	Enhancers	Muscle Satellite Cultured Cells	--
34	chr3:140304400-140304800	Flanking Active TSS	NH-A	brain
35	chr3:140304400-140305400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr3:140304600-140304800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr3:140304600-140305000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr3:140304600-140305400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr3:140304800-140305200	Enhancers	NH-A	brain
40	chr3:140305000-140306800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr3:140305200-140305400	Flanking Active TSS	NH-A	brain
42	chr3:140305200-140305800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr3:140305200-140305800	Flanking Active TSS	HSMMtube	muscle
44	chr3:140305400-140305800	Enhancers	NH-A	brain
45	chr3:140305800-140306000	Enhancers	HSMMtube	muscle
46	chr3:140305800-140306800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr3:140305800-140307600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr3:140305800-140307600	Weak transcription	NH-A	brain
49	chr3:140306000-140307400	Weak transcription	HSMMtube	muscle
50	chr3:140306000-140318200	Weak transcription	HSMM	muscle

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