Variant report

Variant	nsv563742
Chromosome Location	chr14:20085860-20438149
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	ARID3A	chr14:20387153-20387455	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:20346241-20346527	K562	blood:	n/a	n/a
3	ARID3A	chr14:20346227-20346537	HepG2	liver:	n/a	n/a
4	ATF1	chr14:20319622-20319703	K562	blood:	n/a	n/a
5	ATF1	chr14:20388271-20388560	K562	blood:	n/a	n/a
6	ATF1	chr14:20374096-20374405	K562	blood:	n/a	n/a
7	ATF1	chr14:20325048-20325100	K562	blood:	n/a	n/a
8	BACH1	chr14:20348120-20348235	K562	blood:	n/a	n/a
9	BATF	chr14:20131255-20131487	GM12878	blood:	n/a	n/a
10	BATF	chr14:20085953-20086237	GM12878	blood:	n/a	n/a
11	BHLHE40	chr14:20136685-20136689	K562	blood:	n/a	n/a
12	CEBPB	chr14:20386088-20387344	MCF-7	breast:	n/a	n/a
13	CEBPB	chr14:20144553-20144585	A549	lung:	n/a	chr14:20144569-20144580
14	CEBPB	chr14:20246382-20246627	A549	lung:	n/a	chr14:20246533-20246544
15	CEBPB	chr14:20413462-20413846	A549	lung:	n/a	n/a
16	CEBPB	chr14:20370608-20370903	IMR90	lung:	n/a	chr14:20370744-20370755 chr14:20370732-20370743
17	CEBPB	chr14:20144535-20144743	IMR90	lung:	n/a	chr14:20144569-20144580
18	CEBPB	chr14:20370568-20370914	HepG2	liver:	n/a	chr14:20370744-20370755 chr14:20370732-20370743
19	CEBPB	chr14:20245850-20246106	IMR90	lung:	n/a	chr14:20245944-20245955
20	CEBPB	chr14:20144546-20144735	HepG2	liver:	n/a	chr14:20144569-20144580
21	CEBPB	chr14:20246393-20246694	IMR90	lung:	n/a	chr14:20246533-20246544
22	CEBPB	chr14:20434694-20434707	K562	blood:	n/a	n/a
23	CEBPB	chr14:20374900-20375169	HepG2	liver:	n/a	chr14:20375036-20375045 chr14:20375036-20375047 chr14:20375036-20375045 chr14:20375034-20375045 chr14:20375036-20375045 chr14:20375034-20375047 chr14:20375036-20375047 chr14:20375036-20375045 chr14:20375034-20375047
24	CEBPB	chr14:20337012-20337281	K562	blood:	n/a	n/a
25	CEBPB	chr14:20353081-20353403	A549	lung:	n/a	n/a
26	CEBPB	chr14:20387030-20387353	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr14:20347421-20347704	K562	blood:	n/a	n/a
28	CEBPB	chr14:20346421-20346658	HepG2	liver:	n/a	chr14:20346574-20346585
29	CEBPB	chr14:20390412-20390477	HepG2	liver:	n/a	n/a
30	CEBPB	chr14:20353091-20353443	IMR90	lung:	n/a	n/a
31	CEBPB	chr14:20353121-20353345	HepG2	liver:	n/a	n/a
32	CEBPB	chr14:20388043-20388243	HepG2	liver:	n/a	chr14:20388129-20388140
33	CEBPB	chr14:20374865-20375205	K562	blood:	n/a	chr14:20375036-20375045 chr14:20375036-20375047 chr14:20375036-20375045 chr14:20375034-20375045 chr14:20375036-20375045 chr14:20375034-20375047 chr14:20375036-20375047 chr14:20375036-20375045 chr14:20375034-20375047
34	CEBPB	chr14:20386146-20386742	MCF-7	breast:	n/a	n/a
35	CEBPB	chr14:20420582-20420802	HepG2	liver:	n/a	chr14:20420660-20420671
36	CEBPB	chr14:20434386-20434443	K562	blood:	n/a	n/a
37	CEBPB	chr14:20374862-20375189	A549	lung:	n/a	chr14:20375036-20375045 chr14:20375036-20375047 chr14:20375036-20375045 chr14:20375034-20375045 chr14:20375036-20375045 chr14:20375034-20375047 chr14:20375036-20375047 chr14:20375036-20375045 chr14:20375034-20375047
38	CEBPB	chr14:20245877-20246103	HepG2	liver:	n/a	chr14:20245944-20245955
39	CEBPB	chr14:20388060-20388537	A549	lung:	n/a	chr14:20388129-20388140
40	CEBPB	chr14:20394073-20394339	HepG2	liver:	n/a	chr14:20394191-20394202
41	CEBPB	chr14:20374855-20375196	IMR90	lung:	n/a	chr14:20375036-20375045 chr14:20375036-20375047 chr14:20375036-20375045 chr14:20375034-20375045 chr14:20375036-20375045 chr14:20375034-20375047 chr14:20375036-20375047 chr14:20375036-20375045 chr14:20375034-20375047
42	CEBPB	chr14:20321015-20321026	K562	blood:	n/a	n/a
43	CEBPB	chr14:20387999-20388479	K562	blood:	n/a	chr14:20388129-20388140
44	CEBPB	chr14:20370645-20370888	K562	blood:	n/a	chr14:20370744-20370755 chr14:20370732-20370743
45	CEBPB	chr14:20387024-20387360	HepG2	liver:	n/a	n/a
46	CEBPB	chr14:20386291-20386625	HepG2	liver:	n/a	n/a
47	CEBPB	chr14:20370643-20370895	Hela-S3	cervix:	n/a	chr14:20370744-20370755 chr14:20370732-20370743
48	CEBPB	chr14:20386989-20387500	A549	lung:	n/a	n/a
49	CEBPB	chr14:20246480-20246681	HepG2	liver:	n/a	chr14:20246533-20246544
50	CEBPB	chr14:20386850-20387355	A549	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:20136822-20136872	RPTEC	kidney:	n/a
2	chr14:20136822-20136872	RPTEC	kidney:	n/a
3	chr14:20403239-20403289	GM12891	blood:	n/a
4	chr14:20134518-20134568	HepG2	liver:	n/a
5	chr14:20147652-20147702	HCM	heart:	n/a
6	chr14:20136693-20136743	ProgFib	skin:	n/a
7	chr14:20148103-20148153	HRPEpiC	eye:	n/a
8	chr14:20139478-20139528	HEEpiC	esophagus:	n/a
9	chr14:20295616-20295666	MCF-7	breast:	n/a
10	chr14:20403845-20403895	HCF	heart:	n/a
11	chr14:20387292-20387342	NT2-D1	testis:	n/a
12	chr14:20215980-20216030	A549	lung:	n/a
13	chr14:20247919-20247969	SK-N-SH	brain:	n/a
14	chr14:20148103-20148153	AG10803	skin:	n/a
15	chr14:20295616-20295666	Hepatocyte	liver:	n/a
16	chr14:20134518-20134568	HCM	heart:	n/a
17	chr14:20136822-20136872	GM19239	blood:	n/a
18	chr14:20147187-20147237	AG10803	skin:	n/a
19	chr14:20344083-20344133	PANC-1	pancreas:	n/a
20	chr14:20215980-20216030	HepG2	liver:	n/a
21	chr14:20147187-20147237	NT2-D1	testis:	n/a
22	chr14:20389177-20389227	HRE	kidney:	n/a
23	chr14:20106919-20106969	K562	blood:	n/a
24	chr14:20387292-20387342	RPTEC	kidney:	n/a
25	chr14:20137365-20137415	HEK293	kidney:	embryo
26	chr14:20404281-20404331	GM12891	blood:	n/a
27	chr14:20136822-20136872	PANC-1	pancreas:	n/a
28	chr14:20137365-20137415	SKMC	muscle:	n/a
29	chr14:20344394-20344444	CMK	blood:	n/a
30	chr14:20387292-20387342	ovcar-3	ovarian:	n/a
31	chr14:20247697-20247747	AG04450	lung:	fetal
32	chr14:20404281-20404331	Jurkat	blood:	n/a
33	chr14:20344083-20344133	NT2-D1	testis:	n/a
34	chr14:20387292-20387342	HEEpiC	esophagus:	n/a
35	chr14:20344083-20344133	HL-60	blood:	n/a
36	chr14:20106919-20106969	SK-N-SH	brain:	n/a
37	chr14:20389177-20389227	IMR90	lung:	fetal
38	chr14:20387292-20387342	NB4	blood:	n/a
39	chr14:20404281-20404331	NT2-D1	testis:	n/a
40	chr14:20147652-20147702	PANC-1	pancreas:	n/a
41	chr14:20344394-20344444	HNPCEpiC	eye:	n/a
42	chr14:20137365-20137415	HIPEpiC	eye:	n/a
43	chr14:20139478-20139528	PFSK-1	brain:	n/a
44	chr14:20403239-20403289	NHDF-neo	bronchial:	n/a
45	chr14:20247697-20247747	HRPEpiC	eye:	n/a
46	chr14:20387292-20387342	HMEC	breast:	n/a
47	chr14:20146493-20146543	AG04450	lung:	fetal
48	chr14:20135228-20135278	GM12892	blood:	n/a
49	chr14:20148103-20148153	HL-60	blood:	n/a
50	chr14:20136824-20136874	HCM	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:20330082..20332945-chr14:20336237..20338891,2	K562	blood:
2	chr14:20382435..20385861-chr14:20389212..20390807,3	K562	blood:
3	chr14:20421291..20423829-chr14:20424473..20427279,2	MCF-7	breast:
4	chr14:20378405..20379102-chr22:33621834..33622612,2	MCF-7	breast:
5	chr14:20382435..20385861-chr14:20389212..20390807,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-POTEM-4	chr14:20145803-20146140	ENSG00000259069.1
2	lnc-POTEM-4	chr14:20146951-20147175	ENSG00000259069.1
3	lnc-OR4N2-1	chr14:20149579-20149748	ENSG00000257395
4	lnc-OR4N2-1	chr14:20151685-20152898	ENSG00000257395
5	lnc-OR4N2-1	chr14:20150010-20150118	ENSG00000257395
6	lnc-OR4K14-1	chr14:20376255-20376808	NONHSAT035546

Variant related genes	Relation type
ENSG00000259016	TF binding region
OR4K5	TF binding region
ENSG00000257142	TF binding region
ENSG00000259069	TF binding region
OR4K4P	TF binding region
ENSG00000257884	TF binding region
ENSG00000258324	TF binding region
OR4K3	TF binding region
ARHGAP42P4	TF binding region
ENSG00000238492	TF binding region
OR4K16P	TF binding region
ENSG00000257846	TF binding region
OR11H2	TF binding region
ENSG00000257357	TF binding region
OR4N2	TF binding region
OR4K1	TF binding region
OR4M1	TF binding region
OR11K2P	TF binding region
ENSG00000257395	TF binding region
OR4N1P	TF binding region
ENSG00000257493	TF binding region
OR4Q3	TF binding region
OR4H12P	TF binding region
OR4K6P	TF binding region
ENSG00000257751	TF binding region
ENSG00000257432	TF binding region
OR4K2	TF binding region
ENSG00000259016	CpG island
OR4K5	CpG island
ENSG00000257142	CpG island
ENSG00000259069	CpG island
OR4K4P	CpG island
ENSG00000257884	CpG island
ENSG00000258324	CpG island
OR4K3	CpG island
ARHGAP42P4	CpG island
ENSG00000238492	CpG island
OR4K16P	CpG island
ENSG00000257846	CpG island
OR11H2	CpG island
ENSG00000257357	CpG island
OR4N2	CpG island
OR4K1	CpG island
OR4M1	CpG island
OR11K2P	CpG island
ENSG00000257395	CpG island
OR4N1P	CpG island
ENSG00000257493	CpG island
OR4Q3	CpG island
OR4H12P	CpG island
OR4K6P	CpG island
ENSG00000257751	CpG island
ENSG00000257432	CpG island
OR4K2	CpG island
ENSG00000258822	chromatin interactions
ENSG00000176290	chromatin interactions

Extended variants
information (count: 5595 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:5595 , 50 per page) page: 1 2 3 4 5 6 7 ... 112

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs376753688	chr14:20092810-20092811	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs575611947	chr14:20093399-20093400	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs201335100	chr14:20093453-20093454	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs199493219	chr14:20093473-20093474	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs375624685	chr14:20093477-20093478	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs201635539	chr14:20093548-20093549	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs113296003	chr14:20093568-20093569	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs542730278	chr14:20093592-20093593	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs531692102	chr14:20093673-20093674	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs561440537	chr14:20093753-20093754	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs528230349	chr14:20093757-20093758	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs200891289	chr14:20093807-20093808	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs373870210	chr14:20093854-20093855	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs61977247	chr14:20094227-20094228	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs200977027	chr14:20094243-20094244	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs540470555	chr14:20094321-20094322	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs377387964	chr14:20094353-20094354	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs565173112	chr14:20094394-20094395	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs532474444	chr14:20094403-20094404	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs550578429	chr14:20094427-20094428	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs56163945	chr14:20094467-20094468	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs200246748	chr14:20094500-20094501	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs202198765	chr14:20094510-20094511	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs568723788	chr14:20094554-20094555	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs61977250	chr14:20094578-20094579	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs549011991	chr14:20094626-20094627	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs529714755	chr14:20094627-20094628	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs547938000	chr14:20094635-20094636	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs566602872	chr14:20094716-20094717	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs377520217	chr14:20094738-20094739	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs201742618	chr14:20094829-20094830	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs375120019	chr14:20094832-20094833	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs534886277	chr14:20094917-20094918	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs553180401	chr14:20094938-20094939	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs7492427	chr14:20094956-20094957	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs571594848	chr14:20094971-20094972	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs371232553	chr14:20094995-20094996	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs574563650	chr14:20097080-20097081	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs542080658	chr14:20097081-20097082	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs553787553	chr14:20097102-20097103	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs7149714	chr14:20097110-20097111	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs571669441	chr14:20097142-20097143	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs546774034	chr14:20097144-20097145	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs545431228	chr14:20097154-20097155	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs202046186	chr14:20097163-20097164	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs563837925	chr14:20097179-20097180	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs531336049	chr14:20097211-20097212	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs58853141	chr14:20097227-20097228	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs369006852	chr14:20097277-20097278	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs369491802	chr14:20097278-20097279	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:72)

Disease	PMID	Source
Cancer	20164920	CNVD
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cone-rod dystrophy	18421352	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myelofibrosis	22110671	CNVD
Alzheimer''s disease	21482944	CNVD
Mental retardation	19951919	CNVD
Neuroblastoma	21899760	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Heart disease	21282601	CNVD
Esophageal cancer	20955586	CNVD
Neurodevelopmental disorder	22521361	CNVD
Lung cancer	16773561	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17440070	CNVD
Breast cancer	16272173	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
severe speech impairment	20736978	CNVD
speech impairment	20736978	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
Breast cancer	21509527	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Ependymoma	20639864	CNVD
Autism	20531469	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	17431168	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:131 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:20094600-20095000	Enhancers	Adipose Nuclei	Adipose
2	chr14:20094600-20095000	Enhancers	Placenta	Placenta
3	chr14:20136400-20136600	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
4	chr14:20136400-20137600	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
5	chr14:20136400-20137800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
6	chr14:20136400-20138000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr14:20136600-20136800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
8	chr14:20137200-20137800	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr14:20144800-20145000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
10	chr14:20195400-20198600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr14:20201600-20203400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
12	chr14:20210800-20211400	Enhancers	Pancreatic Islets	Pancreatic Islet
13	chr14:20213200-20215400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
14	chr14:20214000-20214800	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr14:20214200-20215400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr14:20216000-20217600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr14:20218800-20220200	Enhancers	Brain Angular Gyrus	brain
18	chr14:20219000-20220600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr14:20220800-20223200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr14:20228800-20229400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
21	chr14:20239000-20239800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr14:20239400-20240600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
23	chr14:20241400-20242200	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
24	chr14:20251200-20252000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr14:20255000-20255200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
26	chr14:20266600-20266800	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr14:20268000-20269200	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr14:20268000-20269400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr14:20268000-20269600	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
30	chr14:20268000-20269600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
31	chr14:20268400-20268600	Flanking Active TSS	Brain Cingulate Gyrus	brain
32	chr14:20268400-20268600	Bivalent Enhancer	Brain Inferior Temporal Lobe	brain
33	chr14:20268400-20269000	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr14:20268600-20269200	Bivalent/Poised TSS	Brain Inferior Temporal Lobe	brain
35	chr14:20269000-20269200	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr14:20269200-20269600	Active TSS	Brain Inferior Temporal Lobe	brain
37	chr14:20269400-20269600	Flanking Bivalent TSS/Enh	Brain Dorsolateral Prefrontal Cortex	brain
38	chr14:20273000-20275200	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
39	chr14:20274600-20275000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr14:20281200-20281400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr14:20281400-20281800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr14:20281400-20281800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr14:20281800-20282600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr14:20291000-20291600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr14:20291400-20292800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr14:20291600-20291800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr14:20291600-20292800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr14:20291800-20292200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr14:20291800-20292800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr14:20292200-20292400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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