Variant report

Variant	nsv1042414
Chromosome Location	chr14:42884353-43154606
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	chr14:42890942-42891236	GM12878	blood:	n/a	n/a
2	ATF2	chr14:42898123-42898538	GM12878	blood:	n/a	n/a
3	ATF2	chr14:42898121-42898501	GM12878	blood:	n/a	n/a
4	BACH1	chr14:43088748-43088782	K562	blood:	n/a	n/a
5	BATF	chr14:42890928-42891203	GM12878	blood:	n/a	chr14:42891116-42891127 chr14:42891154-42891165
6	BATF	chr14:42992903-42993204	GM12878	blood:	n/a	n/a
7	BATF	chr14:42898158-42898555	GM12878	blood:	n/a	n/a
8	BATF	chr14:42890963-42891282	GM12878	blood:	n/a	chr14:42891116-42891127 chr14:42891154-42891165
9	BCL11A	chr14:42898127-42898592	GM12878	blood:	n/a	n/a
10	BCL11A	chr14:42944608-42944827	H1-hESC	embryonic stem cell:	n/a	n/a
11	BCL11A	chr14:42992865-42993250	GM12878	blood:	n/a	n/a
12	BCL11A	chr14:42890931-42891249	GM12878	blood:	n/a	n/a
13	BCL11A	chr14:42898070-42898555	GM12878	blood:	n/a	n/a
14	BHLHE40	chr14:42898065-42898516	GM12878	blood:	n/a	n/a
15	BRCA1	chr14:43010506-43011087	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr14:43152884-43153470	Hela-S3	cervix:	n/a	n/a
17	CCNT2	chr14:42932649-42932849	K562	blood:	n/a	n/a
18	CEBPB	chr14:42968790-42969062	A549	lung:	n/a	chr14:42968894-42968905 chr14:42968918-42968929
19	CEBPB	chr14:43057650-43057809	HepG2	liver:	n/a	chr14:43057739-43057750
20	CEBPB	chr14:43152873-43153174	H1-hESC	embryonic stem cell:	n/a	chr14:43153045-43153058 chr14:43153045-43153056 chr14:43153047-43153056 chr14:43153045-43153058 chr14:43153058-43153071 chr14:43153046-43153057
21	CEBPB	chr14:43088915-43089065	HepG2	liver:	n/a	n/a
22	CEBPB	chr14:43006799-43007063	IMR90	lung:	n/a	chr14:43006914-43006925 chr14:43006916-43006925
23	CEBPB	chr14:43045458-43045742	HepG2	liver:	n/a	chr14:43045602-43045613
24	CEBPB	chr14:42947180-42947425	A549	lung:	n/a	chr14:42947307-42947320 chr14:42947309-42947320 chr14:42947307-42947318
25	CEBPB	chr14:43112092-43112319	MCF-7	breast:	n/a	chr14:43112172-43112183
26	CEBPB	chr14:42995827-42996065	HepG2	liver:	n/a	chr14:42995926-42995937 chr14:42995924-42995935
27	CEBPB	chr14:43152850-43153177	A549	lung:	n/a	chr14:43153045-43153058 chr14:43153045-43153056 chr14:43153047-43153056 chr14:43153045-43153058 chr14:43153058-43153071 chr14:43153046-43153057
28	CEBPB	chr14:43112099-43112243	K562	blood:	n/a	chr14:43112172-43112183
29	CEBPB	chr14:42973693-42973995	A549	lung:	n/a	chr14:42973833-42973846 chr14:42973851-42973862 chr14:42973834-42973845 chr14:42973849-42973860 chr14:42973851-42973860
30	CEBPB	chr14:43006767-43007104	HepG2	liver:	n/a	chr14:43006914-43006925 chr14:43006916-43006925
31	CEBPB	chr14:43058980-43059253	A549	lung:	n/a	chr14:43059110-43059121
32	CEBPB	chr14:43112050-43112355	A549	lung:	n/a	chr14:43112172-43112183
33	CEBPB	chr14:43152867-43153237	HepG2	liver:	n/a	chr14:43153045-43153058 chr14:43153045-43153056 chr14:43153047-43153056 chr14:43153045-43153058 chr14:43153058-43153071 chr14:43153046-43153057
34	CEBPB	chr14:42898784-42898952	HepG2	liver:	n/a	chr14:42898837-42898848
35	CEBPB	chr14:43020465-43020677	HepG2	liver:	n/a	chr14:43020529-43020540
36	CEBPB	chr14:43098476-43098668	HepG2	liver:	n/a	n/a
37	CEBPB	chr14:43152905-43153236	A549	lung:	n/a	chr14:43153045-43153058 chr14:43153045-43153056 chr14:43153047-43153056 chr14:43153045-43153058 chr14:43153058-43153071 chr14:43153046-43153057
38	CEBPB	chr14:43112026-43112359	IMR90	lung:	n/a	chr14:43112172-43112183
39	CEBPB	chr14:43009532-43009798	HepG2	liver:	n/a	n/a
40	CEBPB	chr14:43104496-43104820	HepG2	liver:	n/a	chr14:43104691-43104702 chr14:43104647-43104658
41	CEBPB	chr14:43152636-43153526	Hela-S3	cervix:	n/a	chr14:43153045-43153058 chr14:43153045-43153056 chr14:43153047-43153056 chr14:43153045-43153058 chr14:43153058-43153071 chr14:43153046-43153057
42	CEBPB	chr14:42968773-42969081	HepG2	liver:	n/a	chr14:42968894-42968905 chr14:42968918-42968929
43	CEBPB	chr14:43006817-43007048	A549	lung:	n/a	chr14:43006914-43006925 chr14:43006916-43006925
44	CEBPB	chr14:43094448-43094984	HepG2	liver:	n/a	chr14:43094870-43094883 chr14:43094573-43094586 chr14:43094870-43094881
45	CEBPB	chr14:43112055-43112323	Hela-S3	cervix:	n/a	chr14:43112172-43112183
46	CEBPB	chr14:42973793-42973878	K562	blood:	n/a	chr14:42973833-42973846 chr14:42973851-42973862 chr14:42973834-42973845 chr14:42973849-42973860 chr14:42973851-42973860
47	CEBPB	chr14:43112063-43112289	H1-hESC	embryonic stem cell:	n/a	chr14:43112172-43112183
48	CEBPB	chr14:43152858-43153242	IMR90	lung:	n/a	chr14:43153045-43153058 chr14:43153045-43153056 chr14:43153047-43153056 chr14:43153045-43153058 chr14:43153058-43153071 chr14:43153046-43153057
49	CEBPB	chr14:43081131-43081221	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr14:42973667-42974028	HepG2	liver:	n/a	chr14:42973833-42973846 chr14:42973851-42973862 chr14:42973834-42973845 chr14:42973849-42973860 chr14:42973851-42973860

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:43123081-43123131	RPTEC	kidney:	n/a
2	chr14:43123081-43123131	RPTEC	kidney:	n/a
3	chr14:43123081-43123131	HCM	heart:	n/a
4	chr14:43123081-43123131	Hela-S3	cervix:	n/a
5	chr14:43123081-43123131	HL-60	blood:	n/a
6	chr14:43123081-43123131	SK-N-SH_RA	brain:	n/a
7	chr14:43123081-43123131	HCPEpiC	choroid plexus:	n/a
8	chr14:43123081-43123131	AG09319	gingival:	n/a
9	chr14:43123081-43123131	PANC-1	pancreas:	n/a
10	chr14:43123081-43123131	GM12892	blood:	n/a
11	chr14:43123081-43123131	HepG2	liver:	n/a
12	chr14:43123081-43123131	MCF-7	breast:	n/a
13	chr14:43123081-43123131	HAEpiC	amniotic membrane:	n/a
14	chr14:43123081-43123131	AG10803	skin:	n/a
15	chr14:43123081-43123131	HIPEpiC	eye:	n/a
16	chr14:43123081-43123131	HCT-116	colon:	n/a
17	chr14:43123081-43123131	HUVEC	blood vessel:	n/a
18	chr14:43123081-43123131	U87	brain:	n/a
19	chr14:43123081-43123131	NHDF-neo	bronchial:	n/a
20	chr14:43123081-43123131	SKMC	muscle:	n/a
21	chr14:43123081-43123131	PFSK-1	brain:	n/a
22	chr14:43123081-43123131	BJ	skin:	n/a
23	chr14:43123081-43123131	NB4	blood:	n/a
24	chr14:43123081-43123131	AG04449	skin:	fetal
25	chr14:43123081-43123131	T-47D	breast:	n/a
26	chr14:43123081-43123131	A549	lung:	n/a
27	chr14:43123081-43123131	Jurkat	blood:	n/a
28	chr14:43123081-43123131	AoSMC	blood vessel:	n/a
29	chr14:43123081-43123131	NT2-D1	testis:	n/a
30	chr14:43123081-43123131	Caco-2	colon:	n/a
31	chr14:43123081-43123131	Hepatocyte	liver:	n/a
32	chr14:43123081-43123131	LNCaP	prostate:	n/a
33	chr14:43123081-43123131	HRE	kidney:	n/a
34	chr14:43123081-43123131	HRPEpiC	eye:	n/a
35	chr14:43123081-43123131	GM12891	blood:	n/a
36	chr14:43123081-43123131	HPAEpiC	pulmonary alveolar:	n/a
37	chr14:43123081-43123131	SK-N-MC	brain:	n/a
38	chr14:43123081-43123131	CMK	blood:	n/a
39	chr14:43123081-43123131	SAEC	small airway:	n/a
40	chr14:43123081-43123131	ECC-1	luminal epithelium:	n/a
41	chr14:43123081-43123131	HRCEpiC	kidney:	n/a
42	chr14:43123081-43123131	BE2_C	brain:	n/a
43	chr14:43123081-43123131	GM06990	blood:	n/a
44	chr14:43123081-43123131	ovcar-3	ovarian:	n/a
45	chr14:43123081-43123131	HMEC	breast:	n/a
46	chr14:43123081-43123131	AG04450	lung:	fetal
47	chr14:43123081-43123131	HCF	heart:	n/a
48	chr14:43123081-43123131	ProgFib	skin:	n/a
49	chr14:43123081-43123131	HEK293	kidney:	embryo
50	chr14:43123081-43123131	K562	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:42995581..42997108-chr14:42999086..43001857,2	K562	blood:
2	chr14:42579463..42579970-chr14:43055430..43056355,2	MCF-7	breast:
3	chr14:42933700..42935505-chr14:42937514..42939043,2	MCF-7	breast:
4	chr14:43134052..43134776-chr3:181029654..181030646,2	MCF-7	breast:
5	chr14:43090850..43092635-chr14:43095537..43098102,2	K562	blood:
6	chr14:43140328..43142020-chr14:43153445..43155405,2	MCF-7	breast:
7	chr14:43055616..43058571-chr14:43062767..43065185,2	MCF-7	breast:
8	chr14:42995581..42997108-chr14:42999086..43001857,2	K562	blood:
9	chr14:42955061..42956041-chr18:32446617..32447280,2	MCF-7	breast:
10	chr14:43090850..43092635-chr14:43095537..43098102,2	K562	blood:
11	chr14:42933286..42933984-chr3:29810719..29811455,2	MCF-7	breast:
12	chr14:42933700..42935505-chr14:42937514..42939043,2	MCF-7	breast:
13	chr14:43055616..43058571-chr14:43062767..43065185,2	MCF-7	breast:
14	chr14:43078769..43080628-chr14:43081211..43084199,2	MCF-7	breast:
15	chr14:43078769..43080628-chr14:43081211..43084199,2	MCF-7	breast:
16	chr14:43140328..43142020-chr14:43153445..43155405,2	MCF-7	breast:
17	chr14:43030553..43031053-chr17:8338863..8339416,2	Hela-S3	cervix:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-214N1.1.1-2	chr14:42998014-42998060	NONHSAT036588
2	lnc-RP11-214N1.1.1-2	chr14:42997872-42998091	ENSG00000258850.1
3	lnc-RP11-214N1.1.1-2	chr14:42972301-42972709	NONHSAT036588
4	lnc-RP11-214N1.1.1-3	chr14:43078071-43078780	NONHSAT036591
5	lnc-RP11-214N1.1.1-2	chr14:42997872-42998001	NONHSAT036588

Variant related genes	Relation type
ENSG00000258622	TF binding region
ENSG00000258505	TF binding region
ENSG00000258622	CpG island
ENSG00000258505	CpG island
ENSG00000166579	chromatin interactions

Extended variants
information (count: 4164 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:4164 , 50 per page) page: 1 2 3 4 5 6 7 ... 84

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs35323580	chr14:42890210-42890211	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs528847374	chr14:42890222-42890223	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs185326130	chr14:42890323-42890324	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs527463281	chr14:42890325-42890326	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs371107444	chr14:42890334-42890335	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs565736089	chr14:42890342-42890343	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs2813721	chr14:42890397-42890398	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs372269149	chr14:42890405-42890406	Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs77051257	chr14:42890456-42890457	Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs567479494	chr14:42890509-42890510	Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs557715943	chr14:42890517-42890518	Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs569901907	chr14:42890518-42890519	Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs533246280	chr14:42890519-42890520	Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs536140314	chr14:42890542-42890543	Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs188531172	chr14:42890552-42890553	Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs151338668	chr14:42890570-42890571	Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs114867624	chr14:42890582-42890583	Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs577991067	chr14:42890587-42890588	Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs544326414	chr14:42890612-42890613	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs34069645	chr14:42890619-42890620	Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs141849316	chr14:42890641-42890642	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs79744165	chr14:42890648-42890649	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs138273705	chr14:42890650-42890651	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs561924612	chr14:42890685-42890686	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs529220678	chr14:42890703-42890704	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs540994776	chr14:42890717-42890718	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs559066520	chr14:42890722-42890723	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs117010096	chr14:42890735-42890736	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs551182278	chr14:42890743-42890744	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs181283188	chr14:42890749-42890750	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs530967275	chr14:42890759-42890760	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs142327904	chr14:42890770-42890771	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs373336598	chr14:42890782-42890783	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs567588859	chr14:42890863-42890864	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs112247213	chr14:42890891-42890892	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs75834239	chr14:42890904-42890905	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs146566933	chr14:42890929-42890930	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs571511532	chr14:42890937-42890938	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs376754818	chr14:42890949-42890950	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs7151394	chr14:42890951-42890952	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs142695607	chr14:42890956-42890957	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs371624691	chr14:42890965-42890966	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs539026418	chr14:42890969-42890970	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs10149763	chr14:42891004-42891005	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs575848354	chr14:42891015-42891016	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs183578254	chr14:42891024-42891025	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs575258027	chr14:42891060-42891061	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs188218309	chr14:42891065-42891066	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs138756737	chr14:42891072-42891073	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs181989247	chr14:42891130-42891131	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
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
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
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	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
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Burkitt''s lymphoma	19759907	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21858162	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Thyroid cancer	19470727	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	23813976	CNVD
Immune disease	21076436	CNVD
Immune disease	21042300	CNVD
Neurodevelopmental disorder	22521361	CNVD
Renal cell carcinoma	18194544	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Glioblastoma multiforme	21569311	CNVD
Schizophrenia	21346763	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:247 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:42890200-42891200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr14:42890400-42890600	Bivalent/Poised TSS	Gastric	stomach
3	chr14:42890400-42890800	Enhancers	NHEK	skin
4	chr14:42890400-42891000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr14:42890600-42890800	Active TSS	Gastric	stomach
6	chr14:42891000-42891400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr14:42891400-42891600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr14:42891600-42898000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr14:42893800-42894600	Enhancers	Primary B cells from peripheral blood	blood
10	chr14:42894600-42897800	Weak transcription	Primary B cells from peripheral blood	blood
11	chr14:42897800-42899200	Enhancers	Primary B cells from peripheral blood	blood
12	chr14:42898000-42899000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr14:42898000-42899000	Enhancers	NHEK	skin
14	chr14:42898400-42899200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr14:42919800-42920200	Enhancers	Pancreatic Islets	Pancreatic Islet
16	chr14:42929200-42929400	Enhancers	Esophagus	oesophagus
17	chr14:42929400-42933400	Weak transcription	Esophagus	oesophagus
18	chr14:42933400-42933600	ZNF genes & repeats	Esophagus	oesophagus
19	chr14:42938400-42938800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr14:42938600-42939400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr14:42938800-42939200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr14:42938800-42939600	Active TSS	A549	lung
23	chr14:42939000-42939400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr14:42939200-42939600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr14:42942000-42942200	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr14:42942000-42942200	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr14:42942200-42943200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
28	chr14:42942200-42943600	Weak transcription	HUES48 Cell Line	embryonic stem cell
29	chr14:42943000-42951600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr14:42943200-42944600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr14:42943200-42946400	Enhancers	iPS-15b Cell Line	embryonic stem cell
32	chr14:42943400-42943800	Enhancers	H1 Cell Line	embryonic stem cell
33	chr14:42943600-42944400	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr14:42943600-42944600	Enhancers	H9 Cell Line	embryonic stem cell
35	chr14:42943600-42946400	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr14:42943800-42944400	Enhancers	ES-I3 Cell Line	embryonic stem cell
37	chr14:42943800-42944400	Enhancers	iPS-20b Cell Line	embryonic stem cell
38	chr14:42943800-42944600	Weak transcription	H1 Cell Line	embryonic stem cell
39	chr14:42943800-42944600	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr14:42943800-42946000	Enhancers	iPS-18 Cell Line	embryonic stem cell
41	chr14:42944200-42948400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
42	chr14:42944400-42944600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
43	chr14:42944400-42944800	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
44	chr14:42944600-42944800	Enhancers	H1 Cell Line	embryonic stem cell
45	chr14:42944600-42944800	Active TSS	iPS-20b Cell Line	embryonic stem cell
46	chr14:42944600-42945800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr14:42944800-42946200	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr14:42944800-42948400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
49	chr14:42945800-42946000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr14:42946000-42946200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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