Variant report

Variant	esv2759982
Chromosome Location	chr14:41766561-41880727
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	ATF1	chr14:41852997-41853203	K562	blood:	n/a	n/a
2	ATF3	chr14:41831395-41831637	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr14:41853134-41853209	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr14:41843406-41843570	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr14:41772715-41773048	A549	lung:	n/a	chr14:41772874-41772883 chr14:41772872-41772885 chr14:41772874-41772883 chr14:41772873-41772884 chr14:41772872-41772885 chr14:41772874-41772883 chr14:41772872-41772883 chr14:41772874-41772883 chr14:41772872-41772885
6	CEBPB	chr14:41843343-41843675	MCF-7	breast:	n/a	n/a
7	CEBPB	chr14:41825972-41826222	HepG2	liver:	n/a	chr14:41826057-41826068
8	CEBPB	chr14:41843283-41843667	HepG2	liver:	n/a	n/a
9	CEBPB	chr14:41772732-41773141	IMR90	lung:	n/a	chr14:41772874-41772883 chr14:41772872-41772885 chr14:41772874-41772883 chr14:41772873-41772884 chr14:41772872-41772885 chr14:41772874-41772883 chr14:41772872-41772883 chr14:41772874-41772883 chr14:41772872-41772885
10	CEBPB	chr14:41860008-41860342	HepG2	liver:	n/a	chr14:41860189-41860200
11	CEBPB	chr14:41772746-41773072	H1-hESC	embryonic stem cell:	n/a	chr14:41772874-41772883 chr14:41772872-41772885 chr14:41772874-41772883 chr14:41772873-41772884 chr14:41772872-41772885 chr14:41772874-41772883 chr14:41772872-41772883 chr14:41772874-41772883 chr14:41772872-41772885
12	CEBPB	chr14:41843330-41843647	A549	lung:	n/a	n/a
13	CEBPB	chr14:41801056-41801376	HepG2	liver:	n/a	chr14:41801209-41801220
14	CEBPB	chr14:41843358-41843671	IMR90	lung:	n/a	n/a
15	CEBPB	chr14:41771959-41772333	ECC-1	luminal epithelium:	n/a	n/a
16	CEBPB	chr14:41772728-41772983	K562	blood:	n/a	chr14:41772874-41772883 chr14:41772872-41772885 chr14:41772874-41772883 chr14:41772873-41772884 chr14:41772872-41772885 chr14:41772874-41772883 chr14:41772872-41772883 chr14:41772874-41772883 chr14:41772872-41772885
17	CEBPB	chr14:41772696-41773134	HepG2	liver:	n/a	chr14:41772874-41772883 chr14:41772872-41772885 chr14:41772874-41772883 chr14:41772873-41772884 chr14:41772872-41772885 chr14:41772874-41772883 chr14:41772872-41772883 chr14:41772874-41772883 chr14:41772872-41772885
18	CEBPB	chr14:41772723-41773057	ECC-1	luminal epithelium:	n/a	chr14:41772874-41772883 chr14:41772872-41772885 chr14:41772874-41772883 chr14:41772873-41772884 chr14:41772872-41772885 chr14:41772874-41772883 chr14:41772872-41772883 chr14:41772874-41772883 chr14:41772872-41772885
19	CEBPB	chr14:41855036-41855437	ECC-1	luminal epithelium:	n/a	n/a
20	CEBPB	chr14:41772781-41773093	ECC-1	luminal epithelium:	n/a	chr14:41772874-41772883 chr14:41772872-41772885 chr14:41772874-41772883 chr14:41772873-41772884 chr14:41772872-41772885 chr14:41772874-41772883 chr14:41772872-41772883 chr14:41772874-41772883 chr14:41772872-41772885
21	CEBPZ	chr14:41793109-41793167	HepG2	liver:	n/a	n/a
22	CTCF	chr14:41769180-41769330	RPTEC	kidney:	n/a	n/a
23	CTCF	chr14:41769289-41769319	LNCaP	prostate:	n/a	n/a
24	CTCF	chr14:41862861-41862985	HepG2	liver:	n/a	n/a
25	CTCF	chr14:41769227-41769406	MCF-7	breast:	n/a	n/a
26	CTCF	chr14:41879455-41879792	MCF-7	breast:	n/a	chr14:41879612-41879633 chr14:41879617-41879635 chr14:41879622-41879630
27	CTCF	chr14:41769180-41769330	BE2_C	brain:	n/a	n/a
28	CTCF	chr14:41787540-41787690	HPAF	blood vessel:	n/a	n/a
29	CTCF	chr14:41862920-41863070	A549	lung:	n/a	n/a
30	CTCF	chr14:41769219-41769408	HepG2	liver:	n/a	n/a
31	CTCF	chr14:41862860-41863010	HepG2	liver:	n/a	n/a
32	CTCF	chr14:41769300-41769450	HPAF	blood vessel:	n/a	n/a
33	CTCF	chr14:41802438-41802476	Lung_OC	lung:	n/a	n/a
34	CTCF	chr14:41879572-41879685	MCF-7	breast:	n/a	chr14:41879612-41879633 chr14:41879617-41879635 chr14:41879622-41879630
35	CTCF	chr14:41769160-41769310	MCF-7	breast:	n/a	n/a
36	CTCF	chr14:41769243-41769377	MCF-7	breast:	n/a	n/a
37	CTCF	chr14:41769284-41769353	K562	blood:	n/a	n/a
38	CTCF	chr14:41777820-41777970	HCM	heart:	n/a	n/a
39	CTCF	chr14:41769231-41769490	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr14:41862847-41862988	HepG2	liver:	n/a	n/a
41	CTCF	chr14:41812722-41812833	GM13976	blood:	n/a	n/a
42	CTCF	chr14:41769257-41769397	GM13977	blood:	n/a	n/a
43	CTCF	chr14:41879560-41879710	MCF-7	breast:	n/a	chr14:41879612-41879633 chr14:41879617-41879635 chr14:41879622-41879630
44	CTCF	chr14:41862900-41863050	HCM	heart:	n/a	n/a
45	CTCF	chr14:41805585-41805622	GM10248	blood:	n/a	n/a
46	CTCF	chr14:41769220-41769370	HEK293	kidney:	n/a	n/a
47	CTCF	chr14:41769260-41769410	HepG2	liver:	n/a	n/a
48	CTCF	chr14:41769258-41769351	Gliobla	brain:	n/a	n/a
49	CTCF	chr14:41769220-41769370	AoAF	blood vessel:	n/a	n/a
50	CTCF	chr14:41769211-41769365	LNCaP	prostate:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:41771257-41771307	MCF-7	breast:	n/a
2	chr14:41771257-41771307	BE2_C	brain:	n/a
3	chr14:41771257-41771307	NH-A	brain:	n/a
4	chr14:41771257-41771307	Jurkat	blood:	n/a
5	chr14:41771257-41771307	NB4	blood:	n/a
6	chr14:41771257-41771307	U87	brain:	n/a
7	chr14:41771257-41771307	HAEpiC	amniotic membrane:	n/a
8	chr14:41771257-41771307	Caco-2	colon:	n/a
9	chr14:41771257-41771307	SK-N-SH_RA	brain:	n/a
10	chr14:41771257-41771307	PFSK-1	brain:	n/a
11	chr14:41771257-41771307	NHBE	bronchial:	n/a
12	chr14:41771257-41771307	HIPEpiC	eye:	n/a
13	chr14:41771257-41771307	AG04450	lung:	fetal
14	chr14:41771257-41771307	AG09319	gingival:	n/a
15	chr14:41771257-41771307	LNCaP	prostate:	n/a
16	chr14:41771257-41771307	NT2-D1	testis:	n/a
17	chr14:41771257-41771307	HUVEC	blood vessel:	n/a
18	chr14:41771257-41771307	AG10803	skin:	n/a
19	chr14:41771257-41771307	K562	blood:	n/a
20	chr14:41771257-41771307	SK-N-SH	brain:	n/a
21	chr14:41771257-41771307	BJ	skin:	n/a
22	chr14:41771257-41771307	GM19239	blood:	n/a
23	chr14:41771257-41771307	ovcar-3	ovarian:	n/a
24	chr14:41771257-41771307	IMR90	lung:	fetal
25	chr14:41771257-41771307	HepG2	liver:	n/a
26	chr14:41771257-41771307	GM12892	blood:	n/a
27	chr14:41771257-41771307	HEK293	kidney:	embryo
28	chr14:41771257-41771307	HL-60	blood:	n/a
29	chr14:41771257-41771307	A549	lung:	n/a
30	chr14:41771257-41771307	HPAEpiC	pulmonary alveolar:	n/a
31	chr14:41771257-41771307	GM12891	blood:	n/a
32	chr14:41771257-41771307	HRPEpiC	eye:	n/a
33	chr14:41771257-41771307	SK-N-MC	brain:	n/a
34	chr14:41771257-41771307	AG04449	skin:	fetal
35	chr14:41771257-41771307	HCM	heart:	n/a
36	chr14:41771257-41771307	CMK	blood:	n/a
37	chr14:41771257-41771307	PrEC	prostate:	n/a
38	chr14:41771257-41771307	RPTEC	kidney:	n/a
39	chr14:41771257-41771307	HCT-116	colon:	n/a
40	chr14:41771257-41771307	MCF10A-Er-Src	breast:	n/a
41	chr14:41771257-41771307	ProgFib	skin:	n/a
42	chr14:41771257-41771307	GM12878	blood:	n/a
43	chr14:41771257-41771307	GM06990	blood:	n/a
44	chr14:41771257-41771307	HRE	kidney:	n/a
45	chr14:41771257-41771307	SAEC	small airway:	n/a
46	chr14:41771257-41771307	HCPEpiC	choroid plexus:	n/a
47	chr14:41771257-41771307	HEEpiC	esophagus:	n/a
48	chr14:41771257-41771307	HNPCEpiC	eye:	n/a
49	chr14:41771257-41771307	Hepatocyte	liver:	n/a
50	chr14:41771257-41771307	AoSMC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:41856073..41858584-chr14:41859093..41860987,2	MCF-7	breast:
2	chr14:41792593..41793113-chr2:63668078..63668598,2	MCF-7	breast:
3	chr14:41856073..41858584-chr14:41859093..41860987,2	MCF-7	breast:
4	chr14:41873770..41876020-chr14:41877862..41880665,2	MCF-7	breast:
5	chr14:41873770..41876020-chr14:41877862..41880665,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LRFN5-5	chr14:41765489-41767937	NONHSAT036568

Variant related genes	Relation type
ENSG00000221695	TF binding region
ENSG00000221695	CpG island
ENSG00000143951	chromatin interactions

Extended variants
information (count: 980 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:980 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1778365	chr14:41766561-41766562	Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs539051906	chr14:41766572-41766573	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
3	rs1778366	chr14:41766603-41766604	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
4	rs200518315	chr14:41766640-41766641	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
5	rs36203452	chr14:41766641-41766642	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
6	rs201858676	chr14:41766645-41766646	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
7	rs575813664	chr14:41766655-41766656	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
8	rs3985197	chr14:41766668-41766669	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
9	rs562276020	chr14:41766699-41766700	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
10	rs554908584	chr14:41766792-41766793	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
11	rs142908386	chr14:41766819-41766820	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
12	rs374475900	chr14:41766839-41766840	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
13	rs575916433	chr14:41766846-41766847	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
14	rs61991580	chr14:41766973-41766974	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
15	rs540596040	chr14:41766996-41766997	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
16	rs112888672	chr14:41767002-41767003	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
17	rs1431041	chr14:41767006-41767007	Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs151190249	chr14:41767036-41767037	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
19	rs544624926	chr14:41767067-41767068	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
20	rs190462174	chr14:41767109-41767110	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
21	rs180859530	chr14:41767124-41767125	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
22	rs549059714	chr14:41767129-41767130	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
23	rs185961011	chr14:41767156-41767157	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
24	rs528275592	chr14:41767175-41767176	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
25	rs546784648	chr14:41767184-41767185	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
26	rs571589225	chr14:41767198-41767199	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
27	rs140405449	chr14:41767289-41767290	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
28	rs145525487	chr14:41767293-41767294	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
29	rs569229200	chr14:41767295-41767296	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
30	rs536389591	chr14:41767391-41767392	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
31	rs555023078	chr14:41767420-41767421	Enhancers Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
32	rs573389906	chr14:41767435-41767436	Enhancers Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
33	rs137889481	chr14:41767472-41767473	Enhancers Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
34	rs113331049	chr14:41767476-41767477	Enhancers Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
35	rs140755356	chr14:41767518-41767519	Enhancers Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
36	rs577122405	chr14:41767536-41767537	Enhancers Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
37	rs544463338	chr14:41767575-41767576	Enhancers Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
38	rs562984699	chr14:41767588-41767589	Enhancers Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
39	rs370721424	chr14:41767638-41767639	Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
40	rs144604733	chr14:41767703-41767704	Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
41	rs542390905	chr14:41767792-41767793	Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
42	rs561053755	chr14:41767794-41767795	Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
43	rs191244985	chr14:41767804-41767805	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
44	rs546817679	chr14:41767815-41767816	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
45	rs571424161	chr14:41767816-41767817	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
46	rs559487934	chr14:41767879-41767880	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
47	rs532486556	chr14:41767890-41767891	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
48	rs370665032	chr14:41767902-41767903	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
49	rs1782164	chr14:41767924-41767925	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs1778367	chr14:41767938-41767939	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:62)

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
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	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
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:41766200-41767200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr14:41766800-41767200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr14:41766800-41767600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr14:41767000-41767400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr14:41767400-41767800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr14:41767400-41767800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr14:41767600-41770400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr14:41769000-41769600	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr14:41769200-41769400	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr14:41769400-41770000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr14:41769400-41770800	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr14:41769600-41770000	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr14:41770000-41770600	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr14:41770000-41770800	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr14:41770000-41772000	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr14:41770000-41772400	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr14:41770200-41770400	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr14:41770200-41770800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr14:41770200-41772200	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr14:41770400-41771800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr14:41770400-41773000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr14:41770600-41771600	Weak transcription	HUES6 Cell Line	embryonic stem cell
23	chr14:41770600-41771800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
24	chr14:41770800-41771200	Weak transcription	HUES48 Cell Line	embryonic stem cell
25	chr14:41770800-41771200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
26	chr14:41770800-41771200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr14:41771200-41772400	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr14:41771200-41772400	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr14:41771200-41772400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
30	chr14:41771600-41772400	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr14:41771600-41773200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr14:41771800-41772400	Enhancers	iPS-20b Cell Line	embryonic stem cell
33	chr14:41772400-41773600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr14:41773600-41774000	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
35	chr14:41799200-41799600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr14:41817200-41818600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr14:41817200-41818800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr14:41818400-41819000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr14:41819400-41820000	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr14:41819800-41820000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr14:41824400-41825800	Enhancers	Fetal Lung	lung
42	chr14:41837200-41837400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
43	chr14:41837400-41837600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
44	chr14:41837400-41837600	Flanking Bivalent TSS/Enh	Breast Myoepithelial Primary Cells	Breast
45	chr14:41855000-41855400	Enhancers	Cortex derived primary cultured neurospheres	brain
46	chr14:41866400-41867400	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr14:41866400-41868000	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr14:41866600-41867600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
49	chr14:41866600-41868600	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr14:41866800-41868000	Enhancers	HUES64 Cell Line	embryonic stem cell

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