Variant report

Variant	esv994902
Chromosome Location	chr14:38368430-38374964
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	chr14:38372828-38373175	HepG2	liver:	n/a	n/a
2	CEBPB	chr14:38369868-38370087	A549	lung:	n/a	chr14:38369997-38370008
3	CEBPB	chr14:38369706-38370191	Hela-S3	cervix:	n/a	chr14:38369997-38370008
4	CEBPB	chr14:38369819-38370154	HepG2	liver:	n/a	chr14:38369997-38370008
5	CEBPB	chr14:38369817-38370145	IMR90	lung:	n/a	chr14:38369997-38370008
6	CTCF	chr14:38372880-38373030	Hela-S3	cervix:	n/a	chr14:38372978-38372994
7	CTCF	chr14:38372802-38373169	K562	blood:	n/a	chr14:38372978-38372994
8	CTCF	chr14:38372863-38373060	GM12878	blood:	n/a	chr14:38372978-38372994
9	CTCF	chr14:38372920-38373070	HCPEpiC	choroid plexus:	n/a	chr14:38372978-38372994
10	CTCF	chr14:38372920-38373070	Caco-2	colon:	n/a	chr14:38372978-38372994
11	CTCF	chr14:38372782-38373111	ECC-1	luminal epithelium:	n/a	chr14:38372978-38372994
12	CTCF	chr14:38372940-38373090	HCM	heart:	n/a	chr14:38372978-38372994
13	CTCF	chr14:38372823-38373137	HCT-116	colon:	n/a	chr14:38372978-38372994
14	CTCF	chr14:38372840-38372990	SAEC	small airway:	n/a	n/a
15	CTCF	chr14:38372880-38373030	AoAF	blood vessel:	n/a	chr14:38372978-38372994
16	CTCF	chr14:38372620-38372770	GM12874	blood:	n/a	chr14:38372649-38372657
17	CTCF	chr14:38372880-38373030	K562	blood:	n/a	chr14:38372978-38372994
18	CTCF	chr14:38372873-38373069	Hela-S3	cervix:	n/a	chr14:38372978-38372994
19	CTCF	chr14:38372880-38373030	HBMEC	blood vessel:	n/a	chr14:38372978-38372994
20	CTCF	chr14:38371940-38372090	AG10803	skin:	n/a	n/a
21	CTCF	chr14:38372880-38373030	HPF	lung:	n/a	chr14:38372978-38372994
22	CTCF	chr14:38372655-38373290	SK-N-SH	brain:	n/a	chr14:38372978-38372994
23	CTCF	chr14:38371300-38371450	NHDF-neo	bronchial:	n/a	chr14:38371301-38371314 chr14:38371301-38371310
24	CTCF	chr14:38372880-38373030	HRPEpiC	eye:	n/a	chr14:38372978-38372994
25	CTCF	chr14:38372500-38372650	RPTEC	kidney:	n/a	n/a
26	CTCF	chr14:38372620-38372770	GM12870	blood:	n/a	chr14:38372649-38372657
27	CTCF	chr14:38372783-38373154	A549	lung:	n/a	chr14:38372978-38372994
28	CTCF	chr14:38372660-38372810	GM12873	blood:	n/a	n/a
29	CTCF	chr14:38372900-38373050	AG04449	skin:	n/a	chr14:38372978-38372994
30	CTCF	chr14:38372860-38373010	GM12875	blood:	n/a	chr14:38372978-38372994
31	CTCF	chr14:38372929-38373035	GM20000	blood:	n/a	chr14:38372978-38372994
32	CTCF	chr14:38372886-38373105	A549	lung:	n/a	chr14:38372978-38372994
33	CTCF	chr14:38372940-38373090	HRPEpiC	eye:	n/a	chr14:38372978-38372994
34	CTCF	chr14:38371220-38371370	AG04449	skin:	n/a	chr14:38371301-38371314 chr14:38371301-38371310
35	CTCF	chr14:38372980-38373130	A549	lung:	n/a	n/a
36	CTCF	chr14:38373238-38373320	HUVEC	blood vessel:	n/a	n/a
37	CTCF	chr14:38372940-38373090	HCT-116	colon:	n/a	chr14:38372978-38372994
38	CTCF	chr14:38372909-38372949	GM19240	blood:	n/a	n/a
39	CTCF	chr14:38373000-38373150	GM12871	blood:	n/a	n/a
40	CTCF	chr14:38372620-38372770	GM12864	blood:	n/a	chr14:38372649-38372657
41	CTCF	chr14:38372860-38373010	AG04449	skin:	n/a	chr14:38372978-38372994
42	CTCF	chr14:38372880-38373030	GM12873	blood:	n/a	chr14:38372978-38372994
43	CTCF	chr14:38372900-38373050	HepG2	liver:	n/a	chr14:38372978-38372994
44	CTCF	chr14:38372920-38373070	GM06990	blood:	n/a	chr14:38372978-38372994
45	CTCF	chr14:38372854-38373124	HUVEC	blood vessel:	n/a	chr14:38372978-38372994
46	CTCF	chr14:38372880-38373030	AG04450	lung:	n/a	chr14:38372978-38372994
47	CTCF	chr14:38372900-38373050	MCF-7	breast:	n/a	chr14:38372978-38372994
48	CTCF	chr14:38372877-38373076	LNCaP	prostate:	n/a	chr14:38372978-38372994
49	CTCF	chr14:38372880-38373030	HUVEC	blood vessel:	n/a	chr14:38372978-38372994
50	CTCF	chr14:38372887-38373058	GM10266	blood:	n/a	chr14:38372978-38372994

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:38371922-38371972	HEEpiC	esophagus:	n/a
2	chr14:38371657-38371707	BJ	skin:	n/a
3	chr14:38371922-38371972	HRPEpiC	eye:	n/a
4	chr14:38371922-38371972	AG09319	gingival:	n/a
5	chr14:38371922-38371972	T-47D	breast:	n/a
6	chr14:38371922-38371972	HMEC	breast:	n/a
7	chr14:38371657-38371707	AG04449	skin:	fetal
8	chr14:38371922-38371972	SK-N-SH_RA	brain:	n/a
9	chr14:38371922-38371972	AG10803	skin:	n/a
10	chr14:38371657-38371707	HMEC	breast:	n/a
11	chr14:38371657-38371707	AG10803	skin:	n/a
12	chr14:38371657-38371707	A549	lung:	n/a
13	chr14:38371657-38371707	HepG2	liver:	n/a
14	chr14:38371922-38371972	HL-60	blood:	n/a
15	chr14:38371922-38371972	AG04449	skin:	fetal
16	chr14:38371922-38371972	HRCEpiC	kidney:	n/a
17	chr14:38371657-38371707	HIPEpiC	eye:	n/a
18	chr14:38371922-38371972	NB4	blood:	n/a
19	chr14:38371657-38371707	NH-A	brain:	n/a
20	chr14:38371922-38371972	HepG2	liver:	n/a
21	chr14:38371922-38371972	Hela-S3	cervix:	n/a
22	chr14:38371922-38371972	HCF	heart:	n/a
23	chr14:38371657-38371707	Caco-2	colon:	n/a
24	chr14:38371922-38371972	GM06990	blood:	n/a
25	chr14:38371922-38371972	ECC-1	luminal epithelium:	n/a
26	chr14:38371657-38371707	MCF-7	breast:	n/a
27	chr14:38371922-38371972	PANC-1	pancreas:	n/a
28	chr14:38371657-38371707	NT2-D1	testis:	n/a
29	chr14:38371922-38371972	AoSMC	blood vessel:	n/a
30	chr14:38371922-38371972	CMK	blood:	n/a
31	chr14:38371657-38371707	HEK293	kidney:	embryo
32	chr14:38371922-38371972	GM12891	blood:	n/a
33	chr14:38371657-38371707	Hepatocyte	liver:	n/a
34	chr14:38371657-38371707	SK-N-MC	brain:	n/a
35	chr14:38371657-38371707	MCF10A-Er-Src	breast:	n/a
36	chr14:38371922-38371972	PrEC	prostate:	n/a
37	chr14:38371657-38371707	HRE	kidney:	n/a
38	chr14:38371922-38371972	IMR90	lung:	fetal
39	chr14:38371922-38371972	NH-A	brain:	n/a
40	chr14:38371922-38371972	HCPEpiC	choroid plexus:	n/a
41	chr14:38371657-38371707	K562	blood:	n/a
42	chr14:38371922-38371972	ovcar-3	ovarian:	n/a
43	chr14:38371922-38371972	SK-N-SH	brain:	n/a
44	chr14:38371922-38371972	AG04450	lung:	fetal
45	chr14:38371657-38371707	HCM	heart:	n/a
46	chr14:38371922-38371972	HEK293	kidney:	embryo
47	chr14:38371922-38371972	HCT-116	colon:	n/a
48	chr14:38371922-38371972	NHDF-neo	bronchial:	n/a
49	chr14:38371922-38371972	SKMC	muscle:	n/a
50	chr14:38371922-38371972	HUVEC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:38372517..38373229-chr14:38666364..38667063,2	MCF-7	breast:
2	chr14:38372602..38374691-chr14:38377284..38379028,2	MCF-7	breast:
3	chr14:38372603..38373391-chr14:38619012..38619723,2	MCF-7	breast:
4	chr14:38372874..38373419-chr14:39069490..39070036,2	MCF-7	breast:
5	chr14:38365851..38368436-chr14:38371004..38373198,2	MCF-7	breast:
6	chr14:38372704..38373564-chr14:39336508..39337178,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FOXA1-2	chr14:38370081-38370497	ENSG00000259091.1
2	lnc-FOXA1-2	chr14:38365265-38368615	XLOC_010999
3	lnc-FOXA1-2	chr14:38371221-38371329	XLOC_010999
4	lnc-FOXA1-2	chr14:38371221-38371577	ENSG00000259091.1

Variant related genes	Relation type
LINC00517	TF binding region
LINC00517	CpG island
ENSG00000259091	chromatin interactions

Extended variants
information (count: 189 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:189 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs116551781	chr14:38368505-38368506	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
2	rs79211361	chr14:38368601-38368602	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
3	rs529451001	chr14:38368673-38368674	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs186084923	chr14:38368686-38368687	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs116345984	chr14:38368713-38368714	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs577830467	chr14:38368720-38368721	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs571025498	chr14:38368731-38368732	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs539455881	chr14:38368735-38368736	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs553306620	chr14:38368752-38368753	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs573271984	chr14:38368800-38368801	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs541955176	chr14:38368905-38368906	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs561825612	chr14:38368937-38368938	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs188385608	chr14:38368951-38368952	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs544390730	chr14:38368966-38368967	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs181246935	chr14:38369022-38369023	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs533627881	chr14:38369048-38369049	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs185750859	chr14:38369061-38369062	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs560057816	chr14:38369156-38369157	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs528865350	chr14:38369220-38369221	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs528801532	chr14:38369250-38369251	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs568969112	chr14:38369283-38369284	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs145469274	chr14:38369302-38369303	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs147681060	chr14:38369404-38369405	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs571476635	chr14:38369415-38369416	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs534060671	chr14:38369432-38369433	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs541539727	chr14:38369476-38369477	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs190406015	chr14:38369589-38369590	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs546740213	chr14:38369633-38369634	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs117132233	chr14:38369649-38369650	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs149140776	chr14:38369802-38369803	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs555479605	chr14:38369803-38369804	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs8005895	chr14:38369816-38369817	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs544404872	chr14:38369819-38369820	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs183804954	chr14:38369825-38369826	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs375339902	chr14:38369844-38369845	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs551313898	chr14:38369857-38369858	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs560599160	chr14:38369962-38369963	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs187155043	chr14:38370009-38370010	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs528941261	chr14:38370064-38370065	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs566644173	chr14:38370078-38370079	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs58800582	chr14:38370084-38370085	Weak transcription Flanking Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
42	rs542606224	chr14:38370174-38370175	Weak transcription Flanking Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
43	rs562575368	chr14:38370182-38370183	Weak transcription Flanking Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
44	rs531408930	chr14:38370303-38370304	Weak transcription Enhancers Flanking Active TSS Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
45	rs543086001	chr14:38370322-38370323	Weak transcription Enhancers Flanking Active TSS Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
46	rs369900188	chr14:38370323-38370324	Weak transcription Enhancers Flanking Active TSS Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
47	rs571453953	chr14:38370397-38370398	Weak transcription Enhancers Flanking Active TSS Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
48	rs569361105	chr14:38370416-38370417	Weak transcription Enhancers Flanking Active TSS Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
49	rs12590816	chr14:38370422-38370423	Weak transcription Enhancers Flanking Active TSS Active TSS	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs558147455	chr14:38370423-38370424	Weak transcription Enhancers Flanking Active TSS Active TSS	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

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
Invasive pancreatic ductal carcinoma	16982739	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
abnormal development	18461090	CNVD
Prostate cancer	21298110	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21858162	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Prostate cancer	21147910	CNVD
Thyroid cancer	19470727	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:92 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:38363800-38371000	Weak transcription	Psoas Muscle	Psoas
2	chr14:38364400-38369200	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr14:38365000-38372600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr14:38368000-38368600	Enhancers	NHDF-Ad	bronchial
5	chr14:38368000-38370200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr14:38368200-38369400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr14:38368400-38369000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr14:38368600-38369600	Weak transcription	NHDF-Ad	bronchial
9	chr14:38369000-38369400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
10	chr14:38369000-38370000	Enhancers	Hela-S3	cervix
11	chr14:38369000-38370200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr14:38369200-38369400	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr14:38369400-38370000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr14:38369600-38370000	Flanking Active TSS	NHDF-Ad	bronchial
15	chr14:38369600-38371600	Enhancers	Fetal Lung	lung
16	chr14:38370000-38370200	Enhancers	NHDF-Ad	bronchial
17	chr14:38370000-38371200	Weak transcription	Hela-S3	cervix
18	chr14:38370000-38371400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr14:38370200-38371000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr14:38370200-38371200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr14:38370200-38371600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr14:38370200-38371800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr14:38370200-38372200	Flanking Active TSS	NHDF-Ad	bronchial
24	chr14:38370400-38370600	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
25	chr14:38370400-38371600	Enhancers	Muscle Satellite Cultured Cells	--
26	chr14:38370800-38371000	Enhancers	Osteobl	bone
27	chr14:38370800-38371200	Active TSS	NHLF	lung
28	chr14:38370800-38372200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
29	chr14:38371000-38371200	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr14:38371000-38371400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr14:38371000-38371400	Flanking Active TSS	Osteobl	bone
32	chr14:38371000-38371600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr14:38371200-38371400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr14:38371200-38371400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr14:38371200-38371400	Flanking Bivalent TSS/Enh	Esophagus	oesophagus
36	chr14:38371200-38371400	Enhancers	NHLF	lung
37	chr14:38371200-38371600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr14:38371200-38371600	Enhancers	Hela-S3	cervix
39	chr14:38371200-38371800	Enhancers	NH-A	brain
40	chr14:38371400-38371600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr14:38371400-38371600	Enhancers	Osteobl	bone
42	chr14:38371400-38372200	Weak transcription	NHLF	lung
43	chr14:38371400-38372600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr14:38371400-38373000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr14:38371400-38373000	Enhancers	Adipose Nuclei	Adipose
46	chr14:38371600-38372600	Weak transcription	Muscle Satellite Cultured Cells	--
47	chr14:38371600-38372600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr14:38371600-38372600	Weak transcription	Hela-S3	cervix
49	chr14:38371600-38372800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr14:38371600-38372800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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