Variant report

Variant	nsv829731
Chromosome Location	chr3:134711713-134885064
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	ATF2	chr3:134737365-134737784	GM12878	blood:	n/a	n/a
2	ATF3	chr3:134874140-134874328	K562	blood:	n/a	n/a
3	BACH1	chr3:134786215-134786398	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr3:134864563-134864763	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL11A	chr3:134737385-134737727	GM12878	blood:	n/a	n/a
6	BHLHE40	chr3:134737060-134737736	GM12878	blood:	n/a	n/a
7	BHLHE40	chr3:134877438-134877473	GM12878	blood:	n/a	n/a
8	BHLHE40	chr3:134742787-134743472	GM12878	blood:	n/a	n/a
9	BRCA1	chr3:134736236-134736333	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr3:134772757-134772802	HepG2	liver:	n/a	chr3:134772784-134772795
11	CEBPB	chr3:134874226-134874422	K562	blood:	n/a	n/a
12	CEBPB	chr3:134719386-134719664	IMR90	lung:	n/a	chr3:134719522-134719531 chr3:134719520-134719533 chr3:134719520-134719531 chr3:134719521-134719532 chr3:134719522-134719531 chr3:134719522-134719531 chr3:134719522-134719531
13	CEBPB	chr3:134719404-134719632	A549	lung:	n/a	chr3:134719522-134719531 chr3:134719520-134719533 chr3:134719520-134719531 chr3:134719521-134719532 chr3:134719522-134719531 chr3:134719522-134719531 chr3:134719522-134719531
14	CEBPB	chr3:134719376-134719636	Hela-S3	cervix:	n/a	chr3:134719522-134719531 chr3:134719520-134719533 chr3:134719520-134719531 chr3:134719521-134719532 chr3:134719522-134719531 chr3:134719522-134719531 chr3:134719522-134719531
15	CEBPB	chr3:134879622-134879734	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr3:134719324-134719734	ECC-1	luminal epithelium:	n/a	chr3:134719522-134719531 chr3:134719520-134719533 chr3:134719520-134719531 chr3:134719521-134719532 chr3:134719522-134719531 chr3:134719522-134719531 chr3:134719522-134719531
17	CEBPB	chr3:134739094-134739293	K562	blood:	n/a	chr3:134739181-134739192
18	CEBPB	chr3:134719355-134719684	HepG2	liver:	n/a	chr3:134719522-134719531 chr3:134719520-134719533 chr3:134719520-134719531 chr3:134719521-134719532 chr3:134719522-134719531 chr3:134719522-134719531 chr3:134719522-134719531
19	CEBPB	chr3:134739116-134739316	HepG2	liver:	n/a	chr3:134739181-134739192
20	CEBPB	chr3:134719348-134719620	K562	blood:	n/a	chr3:134719522-134719531 chr3:134719520-134719533 chr3:134719520-134719531 chr3:134719521-134719532 chr3:134719522-134719531 chr3:134719522-134719531 chr3:134719522-134719531
21	CEBPB	chr3:134719337-134719724	ECC-1	luminal epithelium:	n/a	chr3:134719522-134719531 chr3:134719520-134719533 chr3:134719520-134719531 chr3:134719521-134719532 chr3:134719522-134719531 chr3:134719522-134719531 chr3:134719522-134719531
22	CHD1	chr3:134742803-134743033	GM12878	blood:	n/a	n/a
23	CHD2	chr3:134786193-134786329	GM12878	blood:	n/a	n/a
24	CHD2	chr3:134742841-134743502	GM12878	blood:	n/a	n/a
25	CHD2	chr3:134737429-134737855	GM12878	blood:	n/a	n/a
26	CTCF	chr3:134797220-134797370	GM12866	blood:	n/a	chr3:134797316-134797324
27	CTCF	chr3:134797233-134797433	H1-hESC	embryonic stem cell:	n/a	chr3:134797316-134797324
28	CTCF	chr3:134713491-134713526	ProgFib	skin:	n/a	n/a
29	CTCF	chr3:134797273-134797404	GM19239	blood:	n/a	chr3:134797316-134797324
30	CTCF	chr3:134719978-134720058	MCF-7	breast:	n/a	n/a
31	CTCF	chr3:134734311-134734361	LNCaP	prostate:	n/a	n/a
32	CTCF	chr3:134717840-134717990	GM12873	blood:	n/a	n/a
33	CTCF	chr3:134797260-134797410	Caco-2	colon:	n/a	chr3:134797316-134797324
34	CTCF	chr3:134797220-134797370	GM12869	blood:	n/a	chr3:134797316-134797324
35	CTCF	chr3:134797240-134797390	HepG2	liver:	n/a	chr3:134797316-134797324
36	CTCF	chr3:134797220-134797370	MCF-7	breast:	n/a	chr3:134797316-134797324
37	CTCF	chr3:134880460-134880610	GM12871	blood:	n/a	n/a
38	CTCF	chr3:134797280-134797414	GM19240	blood:	n/a	chr3:134797316-134797324
39	CTCF	chr3:134717839-134717902	MCF-7	breast:	n/a	n/a
40	CTCF	chr3:134797280-134797430	GM12874	blood:	n/a	chr3:134797316-134797324
41	CTCF	chr3:134797278-134797424	MCF-7	breast:	n/a	chr3:134797316-134797324
42	CTCF	chr3:134797160-134797310	RPTEC	kidney:	n/a	n/a
43	CTCF	chr3:134797220-134797370	RPTEC	kidney:	n/a	chr3:134797316-134797324
44	CTCF	chr3:134797160-134797310	WERI-Rb-1	eye:	n/a	n/a
45	CTCF	chr3:134857765-134857855	MCF-7	breast:	n/a	chr3:134857770-134857788 chr3:134857771-134857787
46	CTCF	chr3:134880420-134880570	GM12873	blood:	n/a	n/a
47	CTCF	chr3:134797300-134797450	HepG2	liver:	n/a	chr3:134797316-134797324
48	CTCF	chr3:134797320-134797470	GM12873	blood:	n/a	n/a
49	CTCF	chr3:134797200-134797350	GM12878	blood:	n/a	chr3:134797316-134797324
50	CTCF	chr3:134880340-134880490	WERI-Rb-1	eye:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:134758333-134758383	HCM	heart:	n/a
2	chr3:134758333-134758383	HCM	heart:	n/a
3	chr3:134819027-134819077	ECC-1	luminal epithelium:	n/a
4	chr3:134819027-134819077	GM12892	blood:	n/a
5	chr3:134798947-134798997	HCM	heart:	n/a
6	chr3:134758333-134758383	HAEpiC	amniotic membrane:	n/a
7	chr3:134801915-134801965	GM12878	blood:	n/a
8	chr3:134798947-134798997	RPTEC	kidney:	n/a
9	chr3:134758333-134758383	AG09319	gingival:	n/a
10	chr3:134758333-134758383	LNCaP	prostate:	n/a
11	chr3:134798947-134798997	HL-60	blood:	n/a
12	chr3:134801915-134801965	ECC-1	luminal epithelium:	n/a
13	chr3:134819027-134819077	HRPEpiC	eye:	n/a
14	chr3:134801915-134801965	HEEpiC	esophagus:	n/a
15	chr3:134798947-134798997	HCPEpiC	choroid plexus:	n/a
16	chr3:134819027-134819077	SK-N-SH	brain:	n/a
17	chr3:134878739-134878789	IMR90	lung:	fetal
18	chr3:134878739-134878789	Hela-S3	cervix:	n/a
19	chr3:134819027-134819077	AG04450	lung:	fetal
20	chr3:134798947-134798997	U87	brain:	n/a
21	chr3:134819027-134819077	HRE	kidney:	n/a
22	chr3:134878739-134878789	Hepatocyte	liver:	n/a
23	chr3:134819027-134819077	ovcar-3	ovarian:	n/a
24	chr3:134819027-134819077	AG09309	skin:	n/a
25	chr3:134798947-134798997	GM12878	blood:	n/a
26	chr3:134819027-134819077	Jurkat	blood:	n/a
27	chr3:134758333-134758383	H1-hESC	embryonic stem cell:	embryo
28	chr3:134798947-134798997	SK-N-SH_RA	brain:	n/a
29	chr3:134801915-134801965	NHDF-neo	bronchial:	n/a
30	chr3:134801915-134801965	AG10803	skin:	n/a
31	chr3:134878739-134878789	HRE	kidney:	n/a
32	chr3:134798947-134798997	HRCEpiC	kidney:	n/a
33	chr3:134801915-134801965	PFSK-1	brain:	n/a
34	chr3:134798947-134798997	SK-N-MC	brain:	n/a
35	chr3:134878739-134878789	BJ	skin:	n/a
36	chr3:134819027-134819077	GM12878	blood:	n/a
37	chr3:134819027-134819077	AoSMC	blood vessel:	n/a
38	chr3:134801915-134801965	CMK	blood:	n/a
39	chr3:134801915-134801965	LNCaP	prostate:	n/a
40	chr3:134819027-134819077	MCF10A-Er-Src	breast:	n/a
41	chr3:134801915-134801965	NH-A	brain:	n/a
42	chr3:134801915-134801965	SAEC	small airway:	n/a
43	chr3:134878739-134878789	HIPEpiC	eye:	n/a
44	chr3:134801915-134801965	A549	lung:	n/a
45	chr3:134798947-134798997	SKMC	muscle:	n/a
46	chr3:134801915-134801965	AG09309	skin:	n/a
47	chr3:134798947-134798997	PrEC	prostate:	n/a
48	chr3:134819027-134819077	NH-A	brain:	n/a
49	chr3:134878739-134878789	HL-60	blood:	n/a
50	chr3:134801915-134801965	NHBE	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:134853213..134856024-chr3:134858094..134860828,2	K562	blood:
2	chr3:134795759..134797342-chr3:134802255..134804359,2	MCF-7	breast:
3	chr3:134711495..134714035-chr3:134895700..134897544,2	K562	blood:
4	chr3:134853213..134856667-chr3:134858094..134860828,3	K562	blood:
5	chr3:134725899..134728503-chr3:134730689..134733347,3	MCF-7	breast:
6	chr3:134880013..134880813-chr3:135222472..135223108,2	MCF-7	breast:
7	chr3:134814726..134816547-chr3:134832650..134834181,2	K562	blood:
8	chr3:134853213..134856667-chr3:134858094..134860828,3	K562	blood:
9	chr3:134725899..134728503-chr3:134730689..134733347,3	MCF-7	breast:
10	chr3:134769674..134771857-chr3:134772148..134774562,2	K562	blood:
11	chr3:134513827..134514378-chr3:134719808..134720327,2	MCF-7	breast:
12	chr3:134857366..134857914-chr3:135222828..135223498,2	MCF-7	breast:
13	chr3:134866815..134868422-chr3:134868696..134870926,2	MCF-7	breast:
14	chr3:134769674..134771857-chr3:134772148..134774562,2	K562	blood:
15	chr3:134795759..134797342-chr3:134802255..134804359,2	MCF-7	breast:
16	chr3:134870327..134872584-chr3:134875480..134877102,2	K562	blood:
17	chr3:134814726..134816547-chr3:134832650..134834181,2	K562	blood:
18	chr3:134866815..134868422-chr3:134868696..134870926,2	MCF-7	breast:
19	chr3:134870327..134872584-chr3:134875480..134877102,2	K562	blood:
20	chr3:134853213..134856024-chr3:134858094..134860828,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KY-8	chr3:134857998-134859247	NONHSAT092261
2	lnc-KY-7	chr3:134839473-134839667	NONHSAT092259
3	lnc-KY-7	chr3:134843996-134844075	NONHSAT092259
4	lnc-KY-8	chr3:134866043-134866126	NONHSAT092262
5	lnc-KY-8	chr3:134871178-134872255	NONHSAT092261
6	lnc-KY-8	chr3:134857998-134859247	NONHSAT092260
7	lnc-KY-7	chr3:134828502-134828524	NONHSAT092259
8	lnc-KY-8	chr3:134874330-134874706	NONHSAT092260
9	lnc-KY-8	chr3:134866048-134866121	NONHSAT092261
10	lnc-KY-8	chr3:134857998-134859247	NONHSAT092262
11	lnc-KY-8	chr3:134866572-134866665	NONHSAT092262
12	lnc-KY-8	chr3:134866043-134866126	NONHSAT092260
13	lnc-KY-8	chr3:134871178-134871302	NONHSAT092260

Variant related genes	Relation type
EPHB1	TF binding region
EPHB1	CpG island
ENSG00000154928	chromatin interactions

Extended variants
information (count: 6375 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:6375 , 50 per page) page: 1 2 3 4 5 6 7 ... 128

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs40618	chr3:134711722-134711723	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs137973193	chr3:134711730-134711731	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs147460304	chr3:134711828-134711829	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs34788895	chr3:134711858-134711859	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs62273061	chr3:134711928-134711929	Enhancers Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs143495310	chr3:134711976-134711977	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs553037788	chr3:134712003-134712004	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs188667290	chr3:134712006-134712007	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs566513679	chr3:134712007-134712008	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs535511963	chr3:134712033-134712034	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs191626186	chr3:134712178-134712179	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs147511918	chr3:134712205-134712206	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs538343848	chr3:134712239-134712240	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs557142948	chr3:134712248-134712249	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs184215297	chr3:134712258-134712259	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs377446531	chr3:134712284-134712285	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs36093	chr3:134712304-134712305	Strong transcription Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs553336796	chr3:134712330-134712331	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs572774364	chr3:134712339-134712340	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs541432203	chr3:134712394-134712395	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs561738897	chr3:134712395-134712396	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs188157258	chr3:134712407-134712408	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs572751767	chr3:134712414-134712415	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs575203450	chr3:134712460-134712461	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs180996638	chr3:134712474-134712475	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs564332005	chr3:134712548-134712549	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs75073161	chr3:134712567-134712568	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs546870094	chr3:134712582-134712583	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs560388143	chr3:134712590-134712591	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs529609608	chr3:134712602-134712603	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs541768706	chr3:134712627-134712628	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs549063538	chr3:134712711-134712712	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs569235519	chr3:134712724-134712725	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs370482587	chr3:134712780-134712781	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs187117433	chr3:134712820-134712821	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs570643747	chr3:134712863-134712864	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs140043009	chr3:134712877-134712878	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs376196544	chr3:134712892-134712893	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs114935390	chr3:134712911-134712912	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs190784252	chr3:134712962-134712963	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs535744112	chr3:134713006-134713007	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs555065934	chr3:134713090-134713091	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs575236801	chr3:134713096-134713097	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs543980714	chr3:134713115-134713116	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs145707982	chr3:134713124-134713125	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs76678996	chr3:134713134-134713135	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs181703400	chr3:134713199-134713200	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs58259247	chr3:134713204-134713205	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs111686583	chr3:134713218-134713219	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs532488910	chr3:134713234-134713235	Strong transcription 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
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
Intracranial aneurysm	16715129	CNVD
Lung cancer	16740712	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Myelofibrosis	22110671	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Developmental delay	21147756	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Cancer	20164919	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Autism	21865298	CNVD

Chromatin state (count:628 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:134708000-134717800	Weak transcription	Psoas Muscle	Psoas
2	chr3:134709600-134711800	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr3:134709600-134712000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr3:134709600-134712800	Enhancers	GM12878-XiMat	blood
5	chr3:134710000-134712000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr3:134710000-134712400	Enhancers	Brain Anterior Caudate	brain
7	chr3:134711000-134712200	Enhancers	Fetal Brain Female	brain
8	chr3:134711000-134713400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
9	chr3:134711200-134712000	Enhancers	Brain Germinal Matrix	brain
10	chr3:134711200-134712000	Enhancers	Dnd41	blood
11	chr3:134711200-134712200	Enhancers	Adipose Nuclei	Adipose
12	chr3:134711400-134712200	Enhancers	Brain Hippocampus Middle	brain
13	chr3:134711600-134712200	Enhancers	Fetal Brain Male	brain
14	chr3:134712000-134716800	Weak transcription	Dnd41	blood
15	chr3:134712800-134716800	Weak transcription	GM12878-XiMat	blood
16	chr3:134713400-134718400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
17	chr3:134716800-134717200	Enhancers	Dnd41	blood
18	chr3:134716800-134717800	Enhancers	GM12878-XiMat	blood
19	chr3:134717800-134718400	Enhancers	Psoas Muscle	Psoas
20	chr3:134718400-134720800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
21	chr3:134719200-134720200	Enhancers	Brain Hippocampus Middle	brain
22	chr3:134719400-134719600	Enhancers	Stomach Smooth Muscle	stomach
23	chr3:134719400-134720000	Enhancers	Brain Substantia Nigra	brain
24	chr3:134720800-134727600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
25	chr3:134727600-134727800	Enhancers	Breast Myoepithelial Primary Cells	Breast
26	chr3:134727800-134728000	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
27	chr3:134728000-134742000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
28	chr3:134729000-134735200	Weak transcription	Fetal Brain Female	brain
29	chr3:134730800-134735400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr3:134731000-134731200	Enhancers	Skeletal Muscle Female	skeletal muscle
31	chr3:134732000-134732400	Active TSS	Gastric	stomach
32	chr3:134732800-134733400	Weak transcription	Skeletal Muscle Female	skeletal muscle
33	chr3:134733400-134733600	Enhancers	Skeletal Muscle Female	skeletal muscle
34	chr3:134733600-134737000	Weak transcription	Skeletal Muscle Female	skeletal muscle
35	chr3:134733800-134734000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr3:134734000-134735000	Enhancers	Liver	Liver
37	chr3:134734200-134737200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
38	chr3:134734400-134734600	Enhancers	Esophagus	oesophagus
39	chr3:134735200-134736200	Enhancers	Fetal Brain Female	brain
40	chr3:134735400-134735600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr3:134735400-134736200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr3:134735600-134736400	Enhancers	Brain Germinal Matrix	brain
43	chr3:134736000-134738200	Enhancers	GM12878-XiMat	blood
44	chr3:134736200-134737800	Enhancers	iPS-18 Cell Line	embryonic stem cell
45	chr3:134736400-134738200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr3:134736800-134737600	Weak transcription	Spleen	Spleen
47	chr3:134736800-134737800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr3:134737000-134737200	Enhancers	Psoas Muscle	Psoas
49	chr3:134737000-134737800	Enhancers	Skeletal Muscle Female	skeletal muscle
50	chr3:134737000-134738000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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