Variant report

Variant	nsv876608
Chromosome Location	chr3:21008710-21203048
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:509)
CpG islands
(count:61)
Chromatin interactive
region (count:38)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:509 , 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	chr3:21032828-21032835	K562	blood:	n/a	n/a
2	ATF1	chr3:21174936-21175053	K562	blood:	n/a	n/a
3	ATF1	chr3:21068871-21069019	K562	blood:	n/a	n/a
4	ATF2	chr3:21058567-21058914	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr3:21190793-21191040	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr3:21201055-21201284	GM12878	blood:	n/a	chr3:21201159-21201170
7	BATF	chr3:21194098-21194329	GM12878	blood:	n/a	n/a
8	BATF	chr3:21194072-21194305	GM12878	blood:	n/a	n/a
9	BHLHE40	chr3:21084924-21084951	K562	blood:	n/a	n/a
10	BHLHE40	chr3:21159378-21159417	K562	blood:	n/a	n/a
11	CCNT2	chr3:21073170-21073370	K562	blood:	n/a	n/a
12	CCNT2	chr3:21119156-21119258	K562	blood:	n/a	n/a
13	CEBPB	chr3:21108530-21108777	A549	lung:	n/a	n/a
14	CEBPB	chr3:21074999-21075313	K562	blood:	n/a	chr3:21075142-21075153
15	CEBPB	chr3:21075015-21075270	A549	lung:	n/a	chr3:21075142-21075153
16	CEBPB	chr3:21074993-21075295	HepG2	liver:	n/a	chr3:21075142-21075153
17	CEBPB	chr3:21183926-21184131	K562	blood:	n/a	chr3:21184052-21184063 chr3:21184051-21184064
18	CEBPB	chr3:21126029-21126290	K562	blood:	n/a	chr3:21126144-21126155
19	CEBPB	chr3:21019075-21019088	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr3:21183910-21184219	K562	blood:	n/a	chr3:21184052-21184063 chr3:21184051-21184064
21	CEBPB	chr3:21183980-21184119	A549	lung:	n/a	chr3:21184052-21184063 chr3:21184051-21184064
22	CEBPB	chr3:21075844-21075985	A549	lung:	n/a	n/a
23	CEBPB	chr3:21164447-21164713	A549	lung:	n/a	chr3:21164567-21164578 chr3:21164606-21164617
24	CEBPB	chr3:21164426-21164631	HepG2	liver:	n/a	chr3:21164567-21164578 chr3:21164606-21164617
25	CEBPB	chr3:21019780-21019956	K562	blood:	n/a	n/a
26	CEBPB	chr3:21125988-21126321	IMR90	lung:	n/a	chr3:21126144-21126155
27	CEBPB	chr3:21183929-21184180	HepG2	liver:	n/a	chr3:21184052-21184063 chr3:21184051-21184064
28	CEBPB	chr3:21063525-21063844	HepG2	liver:	n/a	chr3:21063672-21063683
29	CEBPB	chr3:21078426-21078702	HepG2	liver:	n/a	chr3:21078558-21078569
30	CEBPB	chr3:21083135-21083500	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr3:21183893-21184180	IMR90	lung:	n/a	chr3:21184052-21184063 chr3:21184051-21184064
32	CEBPB	chr3:21063705-21063713	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr3:21051088-21051274	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr3:21075107-21075111	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr3:21078417-21078675	K562	blood:	n/a	chr3:21078558-21078569
36	CEBPB	chr3:21125984-21126294	HepG2	liver:	n/a	chr3:21126144-21126155
37	CEBPB	chr3:21074983-21075302	IMR90	lung:	n/a	chr3:21075142-21075153
38	CEBPB	chr3:21126025-21126248	A549	lung:	n/a	chr3:21126144-21126155
39	CEBPB	chr3:21033936-21034166	K562	blood:	n/a	n/a
40	CEBPB	chr3:21061459-21061687	HepG2	liver:	n/a	chr3:21061538-21061549
41	CHD1	chr3:21187707-21187761	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD2	chr3:21058993-21059252	Hela-S3	cervix:	n/a	n/a
43	CHD2	chr3:21194221-21194308	GM12878	blood:	n/a	n/a
44	CTCF	chr3:21058620-21058770	GM12874	blood:	n/a	n/a
45	CTCF	chr3:21058540-21058690	HEEpiC	esophagus:	n/a	n/a
46	CTCF	chr3:21058560-21058710	HL-60	blood:	n/a	n/a
47	CTCF	chr3:21058639-21058750	GM10248	blood:	n/a	n/a
48	CTCF	chr3:21058568-21058700	GM20000	blood:	n/a	n/a
49	CTCF	chr3:21058640-21058790	BJ	skin:	n/a	n/a
50	CTCF	chr3:21058780-21058930	AG09309	skin:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:21038502-21038552	HIPEpiC	eye:	n/a
2	chr3:21038502-21038552	SAEC	small airway:	n/a
3	chr3:21038502-21038552	HCPEpiC	choroid plexus:	n/a
4	chr3:21038502-21038552	HepG2	liver:	n/a
5	chr3:21038502-21038552	Jurkat	blood:	n/a
6	chr3:21038502-21038552	AG09309	skin:	n/a
7	chr3:21038502-21038552	U87	brain:	n/a
8	chr3:21038502-21038552	PrEC	prostate:	n/a
9	chr3:21038502-21038552	NHDF-neo	bronchial:	n/a
10	chr3:21038502-21038552	HUVEC	blood vessel:	n/a
11	chr3:21038502-21038552	ECC-1	luminal epithelium:	n/a
12	chr3:21038502-21038552	IMR90	lung:	fetal
13	chr3:21038502-21038552	T-47D	breast:	n/a
14	chr3:21038502-21038552	HL-60	blood:	n/a
15	chr3:21038502-21038552	HNPCEpiC	eye:	n/a
16	chr3:21038502-21038552	Hepatocyte	liver:	n/a
17	chr3:21038502-21038552	BJ	skin:	n/a
18	chr3:21038502-21038552	HCF	heart:	n/a
19	chr3:21038502-21038552	ovcar-3	ovarian:	n/a
20	chr3:21038502-21038552	SK-N-SH_RA	brain:	n/a
21	chr3:21038502-21038552	RPTEC	kidney:	n/a
22	chr3:21038502-21038552	GM12878	blood:	n/a
23	chr3:21038502-21038552	MCF10A-Er-Src	breast:	n/a
24	chr3:21038502-21038552	HCM	heart:	n/a
25	chr3:21038502-21038552	HPAEpiC	pulmonary alveolar:	n/a
26	chr3:21038502-21038552	Hela-S3	cervix:	n/a
27	chr3:21038502-21038552	HCT-116	colon:	n/a
28	chr3:21038502-21038552	AG04450	lung:	fetal
29	chr3:21038502-21038552	SK-N-MC	brain:	n/a
30	chr3:21038502-21038552	NHBE	bronchial:	n/a
31	chr3:21038502-21038552	LNCaP	prostate:	n/a
32	chr3:21038502-21038552	AG04449	skin:	fetal
33	chr3:21038502-21038552	H1-hESC	embryonic stem cell:	embryo
34	chr3:21038502-21038552	A549	lung:	n/a
35	chr3:21038502-21038552	AG09319	gingival:	n/a
36	chr3:21038502-21038552	HRPEpiC	eye:	n/a
37	chr3:21038502-21038552	ProgFib	skin:	n/a
38	chr3:21038502-21038552	PANC-1	pancreas:	n/a
39	chr3:21038502-21038552	GM12891	blood:	n/a
40	chr3:21038502-21038552	GM06990	blood:	n/a
41	chr3:21038502-21038552	K562	blood:	n/a
42	chr3:21038502-21038552	Caco-2	colon:	n/a
43	chr3:21038502-21038552	AG10803	skin:	n/a
44	chr3:21038502-21038552	HAEpiC	amniotic membrane:	n/a
45	chr3:21038502-21038552	GM12892	blood:	n/a
46	chr3:21038502-21038552	NT2-D1	testis:	n/a
47	chr3:21038502-21038552	BE2_C	brain:	n/a
48	chr3:21038502-21038552	AoSMC	blood vessel:	n/a
49	chr3:21038502-21038552	SK-N-SH	brain:	n/a
50	chr3:21038502-21038552	HEK293	kidney:	embryo

(count:38 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:21020852..21022735-chr3:21071640..21073973,2	K562	blood:
2	chr3:21067350..21069805-chr3:21070647..21072179,2	K562	blood:
3	chr3:21087665..21089357-chr3:21090092..21092558,2	MCF-7	breast:
4	chr3:21020852..21022735-chr3:21071640..21073973,2	K562	blood:
5	chr3:21062603..21065448-chr3:21079335..21081512,2	K562	blood:
6	chr3:21086967..21088509-chr3:21091717..21094188,2	K562	blood:
7	chr3:21086967..21088509-chr3:21091717..21094188,2	K562	blood:
8	chr3:21027317..21031156-chr3:21036432..21038394,3	K562	blood:
9	chr3:21132848..21134885-chr3:21136213..21138179,2	K562	blood:
10	chr3:21088992..21091588-chr3:21092168..21094857,2	K562	blood:
11	chr3:21087665..21089357-chr3:21090092..21092558,2	MCF-7	breast:
12	chr3:21058401..21059994-chr3:21063772..21066035,2	K562	blood:
13	chr3:21034419..21036332-chr3:21040045..21042156,2	MCF-7	breast:
14	chr3:21132848..21134885-chr3:21136213..21138179,2	K562	blood:
15	chr3:21034419..21036332-chr3:21040045..21042156,2	MCF-7	breast:
16	chr3:21018630..21020462-chr3:21036904..21039487,2	K562	blood:
17	chr3:21097762..21100655-chr3:21104242..21105984,2	MCF-7	breast:
18	chr3:21188799..21190342-chr3:21193601..21195363,2	K562	blood:
19	chr3:21097762..21100655-chr3:21104242..21105984,2	MCF-7	breast:
20	chr20:22586398..22587122-chr3:21089488..21090217,2	MCF-7	breast:
21	chr3:21194222..21197075-chr3:21200094..21202897,2	K562	blood:
22	chr3:21188799..21190342-chr3:21193601..21195363,2	K562	blood:
23	chr3:21049220..21051443-chr3:21113228..21114946,2	K562	blood:
24	chr3:21088992..21091588-chr3:21092168..21094857,2	K562	blood:
25	chr3:21058395..21059158-chr3:21525879..21526450,3	MCF-7	breast:
26	chr3:21058134..21059174-chr3:21592293..21593050,3	MCF-7	breast:
27	chr3:21058438..21059584-chr3:21257830..21258577,6	MCF-7	breast:
28	chr3:21100031..21101592-chr3:21111513..21113234,2	K562	blood:
29	chr3:21018630..21020462-chr3:21036904..21039487,2	K562	blood:
30	chr3:21058401..21059994-chr3:21063772..21066035,2	K562	blood:
31	chr3:21175037..21177371-chr3:21182384..21184259,2	K562	blood:
32	chr3:21027317..21031156-chr3:21036432..21038394,3	K562	blood:
33	chr3:21062603..21065448-chr3:21079335..21081512,2	K562	blood:
34	chr3:21049220..21051443-chr3:21113228..21114946,2	K562	blood:
35	chr3:21194222..21197075-chr3:21200094..21202897,2	K562	blood:
36	chr3:21100031..21101592-chr3:21111513..21113234,2	K562	blood:
37	chr3:21067350..21069805-chr3:21070647..21072179,2	K562	blood:
38	chr3:21175037..21177371-chr3:21182384..21184259,2	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KAT2B-10	chr3:21011020-21011417	NONHSAT088634
2	lnc-KAT2B-11	chr3:21084468-21084602	NONHSAT088635
3	lnc-KAT2B-10	chr3:21011809-21011871	NONHSAT088634
4	lnc-KAT2B-11	chr3:21082738-21082849	NONHSAT088635
5	lnc-KAT2B-11	chr3:21083244-21083384	NONHSAT088635

No data

Variant related genes	Relation type
ENSG00000221659	TF binding region
ENSG00000221659	CpG island

Extended variants
information (count: 4136 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:4136 , 50 per page) page: 1 2 3 4 5 6 7 ... 83

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4462987	chr3:21008710-21008711	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs372726055	chr3:21008771-21008772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs536133321	chr3:21008779-21008780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs557732595	chr3:21008816-21008817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs190940944	chr3:21008824-21008825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs539410994	chr3:21008870-21008871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs558136908	chr3:21008918-21008919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs573229615	chr3:21008924-21008925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs182075591	chr3:21008949-21008950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs73187054	chr3:21008982-21008983	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs78235919	chr3:21009001-21009002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs111617679	chr3:21009008-21009009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs185272189	chr3:21009025-21009026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs190617457	chr3:21009041-21009042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs112826654	chr3:21009062-21009063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs563478491	chr3:21009092-21009093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs530835236	chr3:21009112-21009113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs182861261	chr3:21009143-21009144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs564122174	chr3:21009242-21009243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs549481802	chr3:21009250-21009251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs569961049	chr3:21009291-21009292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs148732847	chr3:21009295-21009296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs187872250	chr3:21009309-21009310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs142334773	chr3:21009326-21009327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs151281745	chr3:21009366-21009367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs375620722	chr3:21009413-21009414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs569403665	chr3:21009435-21009436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs540149034	chr3:21009437-21009438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs538540344	chr3:21009529-21009530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs557833985	chr3:21009538-21009539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs369403866	chr3:21009542-21009543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs566563608	chr3:21009566-21009567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs4257567	chr3:21009567-21009568	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs555491456	chr3:21009578-21009579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs191486033	chr3:21009616-21009617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs60022634	chr3:21009663-21009664	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs557139448	chr3:21009674-21009675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs575413430	chr3:21009691-21009692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs546110356	chr3:21009699-21009700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs563903757	chr3:21009705-21009706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs528137922	chr3:21009722-21009723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs540321557	chr3:21009745-21009746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs561725407	chr3:21009754-21009755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs6769179	chr3:21009780-21009781	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs550867173	chr3:21009846-21009847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs569451241	chr3:21009875-21009876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs533444420	chr3:21009898-21009899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs182836611	chr3:21009915-21009916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs571463283	chr3:21009921-21009922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs376971712	chr3:21009925-21009926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	17327916	CNVD
Glioblastoma multiforme	21080181	CNVD
Neuroblastoma	18923191	CNVD
Colorectal cancer	21297112	CNVD
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
lymphocytic leukemia	21291569	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Esophageal cancer	20955586	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Squamous cell cancer	20885788	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Breast cancer	17133270	CNVD
Developmental delay	21147756	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Melanoma	20688739	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:253 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:21000800-21015600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr3:21007400-21011000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr3:21010800-21011000	Active TSS	HUES6 Cell Line	embryonic stem cell
4	chr3:21011000-21011400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr3:21011000-21013600	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr3:21011000-21016800	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr3:21011400-21012400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr3:21012400-21014000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr3:21013600-21014000	Active TSS	HUES6 Cell Line	embryonic stem cell
10	chr3:21014000-21014800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr3:21014000-21016000	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr3:21014800-21015600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr3:21015600-21016000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr3:21015600-21016400	Enhancers	K562	blood
15	chr3:21015600-21017600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr3:21015800-21016000	Enhancers	Fetal Muscle Trunk	muscle
17	chr3:21016000-21016200	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr3:21016000-21016400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr3:21016000-21016600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr3:21016000-21017200	Enhancers	Fetal Muscle Leg	muscle
21	chr3:21016000-21018400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr3:21016200-21016600	Weak transcription	HUES6 Cell Line	embryonic stem cell
23	chr3:21016200-21016600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr3:21016200-21017000	Enhancers	Aorta	Aorta
25	chr3:21016200-21017600	Enhancers	Adipose Nuclei	Adipose
26	chr3:21016400-21016800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr3:21016400-21017000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr3:21016400-21017000	Enhancers	Left Ventricle	heart
29	chr3:21016400-21017200	Enhancers	Right Ventricle	heart
30	chr3:21016400-21017200	Enhancers	NHDF-Ad	bronchial
31	chr3:21016400-21017400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr3:21016600-21017200	Enhancers	Psoas Muscle	Psoas
33	chr3:21016600-21017600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr3:21016600-21017600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr3:21016600-21018600	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr3:21016800-21017200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr3:21016800-21017600	Enhancers	H9 Cell Line	embryonic stem cell
38	chr3:21016800-21017600	Enhancers	iPS-20b Cell Line	embryonic stem cell
39	chr3:21016800-21017600	Enhancers	Skeletal Muscle Male	skeletal muscle
40	chr3:21016800-21017800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr3:21017000-21019200	Enhancers	ES-I3 Cell Line	embryonic stem cell
42	chr3:21017000-21019800	Enhancers	HUES64 Cell Line	embryonic stem cell
43	chr3:21017200-21017600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr3:21017400-21017600	Enhancers	iPS-15b Cell Line	embryonic stem cell
45	chr3:21017400-21018000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
46	chr3:21017600-21018000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
47	chr3:21017600-21018200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr3:21017600-21019000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr3:21017600-21020200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
50	chr3:21017600-21020400	Weak transcription	H9 Cell Line	embryonic stem cell

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