Variant report

Variant	esv3354861
Chromosome Location	chr14:38359630-38392369
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:299)
CpG islands
(count:183)
Chromatin interactive
region (count:10)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:299 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:38359344-38359690	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:38372828-38373175	HepG2	liver:	n/a	n/a
3	CEBPB	chr14:38365572-38365735	HepG2	liver:	n/a	n/a
4	CEBPB	chr14:38369706-38370191	Hela-S3	cervix:	n/a	chr14:38369997-38370008
5	CEBPB	chr14:38369817-38370145	IMR90	lung:	n/a	chr14:38369997-38370008
6	CEBPB	chr14:38385568-38385866	IMR90	lung:	n/a	chr14:38385721-38385732
7	CEBPB	chr14:38385527-38385864	MCF-7	breast:	n/a	chr14:38385721-38385732
8	CEBPB	chr14:38369819-38370154	HepG2	liver:	n/a	chr14:38369997-38370008
9	CEBPB	chr14:38365037-38365329	HepG2	liver:	n/a	chr14:38365146-38365163 chr14:38365149-38365160
10	CEBPB	chr14:38369868-38370087	A549	lung:	n/a	chr14:38369997-38370008
11	CEBPB	chr14:38376350-38376516	HepG2	liver:	n/a	chr14:38376407-38376418
12	CEBPB	chr14:38385588-38385892	HepG2	liver:	n/a	chr14:38385721-38385732
13	CTCF	chr14:38372900-38373050	HEEpiC	esophagus:	n/a	chr14:38372978-38372994
14	CTCF	chr14:38372940-38373090	HMF	breast:	n/a	chr14:38372978-38372994
15	CTCF	chr14:38372799-38373099	HepG2	liver:	n/a	chr14:38372978-38372994
16	CTCF	chr14:38372640-38372790	AG04450	lung:	n/a	chr14:38372649-38372657
17	CTCF	chr14:38371300-38371450	AG09309	skin:	n/a	chr14:38371301-38371314 chr14:38371301-38371310
18	CTCF	chr14:38372940-38373090	GM12878	blood:	n/a	chr14:38372978-38372994
19	CTCF	chr14:38372920-38373070	BJ	skin:	n/a	chr14:38372978-38372994
20	CTCF	chr14:38372748-38373185	IMR90	lung:	n/a	chr14:38372978-38372994
21	CTCF	chr14:38381663-38381773	MCF-7	breast:	n/a	n/a
22	CTCF	chr14:38372878-38373068	K562	blood:	n/a	chr14:38372978-38372994
23	CTCF	chr14:38372500-38372650	RPTEC	kidney:	n/a	n/a
24	CTCF	chr14:38372870-38373019	NHEK	skin:	n/a	chr14:38372978-38372994
25	CTCF	chr14:38372860-38373010	AG04449	skin:	n/a	chr14:38372978-38372994
26	CTCF	chr14:38372863-38373060	GM12878	blood:	n/a	chr14:38372978-38372994
27	CTCF	chr14:38372880-38373030	AG04450	lung:	n/a	chr14:38372978-38372994
28	CTCF	chr14:38372854-38373124	HUVEC	blood vessel:	n/a	chr14:38372978-38372994
29	CTCF	chr14:38372880-38373030	Caco-2	colon:	n/a	chr14:38372978-38372994
30	CTCF	chr14:38371180-38371330	BJ	skin:	n/a	chr14:38371301-38371314 chr14:38371301-38371310
31	CTCF	chr14:38372600-38372750	AG09309	skin:	n/a	chr14:38372649-38372657
32	CTCF	chr14:38372940-38373090	HCT-116	colon:	n/a	chr14:38372978-38372994
33	CTCF	chr14:38372860-38373010	Hela-S3	cervix:	n/a	chr14:38372978-38372994
34	CTCF	chr14:38372920-38373070	HUVEC	blood vessel:	n/a	chr14:38372978-38372994
35	CTCF	chr14:38373238-38373320	HUVEC	blood vessel:	n/a	n/a
36	CTCF	chr14:38372895-38372902	GM19238	blood:	n/a	n/a
37	CTCF	chr14:38372840-38372990	GM12870	blood:	n/a	n/a
38	CTCF	chr14:38372860-38373010	HBMEC	blood vessel:	n/a	chr14:38372978-38372994
39	CTCF	chr14:38372840-38372990	SAEC	small airway:	n/a	n/a
40	CTCF	chr14:38372480-38372630	BE2_C	brain:	n/a	n/a
41	CTCF	chr14:38372840-38372990	HCT-116	colon:	n/a	n/a
42	CTCF	chr14:38372894-38373032	HepG2	liver:	n/a	chr14:38372978-38372994
43	CTCF	chr14:38372877-38373076	LNCaP	prostate:	n/a	chr14:38372978-38372994
44	CTCF	chr14:38372878-38373099	GM10248	blood:	n/a	chr14:38372978-38372994
45	CTCF	chr14:38372780-38372930	BE2_C	brain:	n/a	n/a
46	CTCF	chr14:38372900-38373050	HRE	kidney:	n/a	chr14:38372978-38372994
47	CTCF	chr14:38372860-38373010	GM12866	blood:	n/a	chr14:38372978-38372994
48	CTCF	chr14:38372920-38373070	GM12864	blood:	n/a	chr14:38372978-38372994
49	CTCF	chr14:38372780-38372930	HAc	cerebellar:	n/a	n/a
50	CTCF	chr14:38372880-38373030	AG09319	gingival:	n/a	chr14:38372978-38372994

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:38363538-38363588	HL-60	blood:	n/a
2	chr14:38363538-38363588	HRCEpiC	kidney:	n/a
3	chr14:38371657-38371707	K562	blood:	n/a
4	chr14:38371657-38371707	HEEpiC	esophagus:	n/a
5	chr14:38363538-38363588	HepG2	liver:	n/a
6	chr14:38371657-38371707	SK-N-SH_RA	brain:	n/a
7	chr14:38371922-38371972	HCM	heart:	n/a
8	chr14:38363538-38363588	IMR90	lung:	fetal
9	chr14:38371922-38371972	HL-60	blood:	n/a
10	chr14:38371922-38371972	PrEC	prostate:	n/a
11	chr14:38371922-38371972	H1-hESC	embryonic stem cell:	embryo
12	chr14:38371922-38371972	HCPEpiC	choroid plexus:	n/a
13	chr14:38371922-38371972	GM12892	blood:	n/a
14	chr14:38371657-38371707	GM19239	blood:	n/a
15	chr14:38371922-38371972	AoSMC	blood vessel:	n/a
16	chr14:38371657-38371707	SK-N-SH	brain:	n/a
17	chr14:38371657-38371707	SK-N-MC	brain:	n/a
18	chr14:38363538-38363588	NHDF-neo	bronchial:	n/a
19	chr14:38371657-38371707	BE2_C	brain:	n/a
20	chr14:38371657-38371707	Hepatocyte	liver:	n/a
21	chr14:38363538-38363588	K562	blood:	n/a
22	chr14:38363538-38363588	BE2_C	brain:	n/a
23	chr14:38371922-38371972	RPTEC	kidney:	n/a
24	chr14:38371922-38371972	A549	lung:	n/a
25	chr14:38371657-38371707	MCF10A-Er-Src	breast:	n/a
26	chr14:38371657-38371707	HRPEpiC	eye:	n/a
27	chr14:38371657-38371707	HCM	heart:	n/a
28	chr14:38371922-38371972	U87	brain:	n/a
29	chr14:38371657-38371707	NT2-D1	testis:	n/a
30	chr14:38363538-38363588	LNCaP	prostate:	n/a
31	chr14:38371922-38371972	ovcar-3	ovarian:	n/a
32	chr14:38371922-38371972	Hela-S3	cervix:	n/a
33	chr14:38371657-38371707	ECC-1	luminal epithelium:	n/a
34	chr14:38371657-38371707	NHDF-neo	bronchial:	n/a
35	chr14:38371657-38371707	HAEpiC	amniotic membrane:	n/a
36	chr14:38371657-38371707	HUVEC	blood vessel:	n/a
37	chr14:38371657-38371707	BJ	skin:	n/a
38	chr14:38371657-38371707	HRCEpiC	kidney:	n/a
39	chr14:38371922-38371972	HCF	heart:	n/a
40	chr14:38371657-38371707	HCF	heart:	n/a
41	chr14:38363538-38363588	SK-N-MC	brain:	n/a
42	chr14:38371922-38371972	HRE	kidney:	n/a
43	chr14:38371922-38371972	MCF10A-Er-Src	breast:	n/a
44	chr14:38371922-38371972	SK-N-SH	brain:	n/a
45	chr14:38371657-38371707	H1-hESC	embryonic stem cell:	embryo
46	chr14:38363538-38363588	NT2-D1	testis:	n/a
47	chr14:38363538-38363588	SKMC	muscle:	n/a
48	chr14:38363538-38363588	AG04450	lung:	fetal
49	chr14:38371922-38371972	SAEC	small airway:	n/a
50	chr14:38363538-38363588	HNPCEpiC	eye:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:38372602..38374691-chr14:38377284..38379028,2	MCF-7	breast:
2	chr14:38363021..38365119-chr14:38365586..38368317,2	MCF-7	breast:
3	chr14:38056746..38059083-chr14:38363861..38366801,2	MCF-7	breast:
4	chr14:38372603..38373391-chr14:38619012..38619723,2	MCF-7	breast:
5	chr14:38372874..38373419-chr14:39069490..39070036,2	MCF-7	breast:
6	chr14:38372704..38373564-chr14:39336508..39337178,3	K562	blood:
7	chr14:38372517..38373229-chr14:38666364..38667063,2	MCF-7	breast:
8	chr14:38372602..38374691-chr14:38377284..38379028,2	MCF-7	breast:
9	chr14:38365851..38368436-chr14:38371004..38373198,2	MCF-7	breast:
10	chr14:38363021..38365119-chr14:38365586..38368317,2	MCF-7	breast:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FOXA1-2	chr14:38371221-38371577	ENSG00000259091.1
2	lnc-CLEC14A-4	chr14:38376599-38376755	l_970_chr14:38376598-38429748_brain
3	lnc-FOXA1-2	chr14:38371221-38371329	XLOC_010999
4	lnc-FOXA1-2	chr14:38370081-38370497	ENSG00000259091.1
5	lnc-SSTR1-3	chr14:38385712-38385759	NONHSAT036476
6	lnc-FOXA1-2	chr14:38365265-38368615	XLOC_010999
7	lnc-SSTR1-3	chr14:38385713-38385759	XLOC_010808
8	lnc-CLEC14A-4	chr14:38376771-38378159	l_970_chr14:38376598-38429748_brain

No data

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

Extended variants
information (count: 569 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:569 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs78903870	chr14:38359641-38359642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs537318834	chr14:38359654-38359655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs200848448	chr14:38359683-38359684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs4901412	chr14:38359760-38359761	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs150225730	chr14:38359777-38359778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs372053571	chr14:38359806-38359807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs539025719	chr14:38359817-38359818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs552697877	chr14:38359855-38359856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs56034185	chr14:38359861-38359862	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs552319740	chr14:38359866-38359867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs542016986	chr14:38359901-38359902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs141584506	chr14:38359942-38359943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs147034661	chr14:38359954-38359955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs564126805	chr14:38359958-38359959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs4901413	chr14:38360009-38360010	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs564355874	chr14:38360024-38360025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs546366974	chr14:38360035-38360036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs532576446	chr14:38360088-38360089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs552599750	chr14:38360106-38360107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs370855452	chr14:38360131-38360132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs373968719	chr14:38360173-38360174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs564356906	chr14:38360187-38360188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs374076647	chr14:38360188-38360189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs528533671	chr14:38360191-38360192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs75465727	chr14:38360205-38360206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs568528407	chr14:38360235-38360236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs144076104	chr14:38360245-38360246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs535419508	chr14:38360264-38360265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs188370363	chr14:38360285-38360286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs570807438	chr14:38360295-38360296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs539086753	chr14:38360323-38360324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs552511457	chr14:38360401-38360402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs370068090	chr14:38360423-38360424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs566564246	chr14:38360460-38360461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs535173206	chr14:38360493-38360494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs550611782	chr14:38360635-38360636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs111926872	chr14:38360645-38360646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs374399743	chr14:38360689-38360690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs558129240	chr14:38360740-38360741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs77792388	chr14:38360794-38360795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs577971132	chr14:38360875-38360876	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs546225338	chr14:38360876-38360877	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs559462094	chr14:38360927-38360928	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs190432711	chr14:38360966-38360967	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs541993662	chr14:38361033-38361034	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs537349442	chr14:38361041-38361042	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs112521321	chr14:38361059-38361060	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs74352448	chr14:38361066-38361067	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs562190616	chr14:38361119-38361120	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs531059163	chr14:38361185-38361186	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:132 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:38359400-38360800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr14:38360800-38361400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
3	chr14:38361200-38361400	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
4	chr14:38361200-38361600	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
5	chr14:38361200-38362200	Enhancers	HepG2	liver
6	chr14:38361400-38362200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr14:38361400-38363400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr14:38361600-38362800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr14:38362200-38362400	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr14:38362400-38362800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr14:38362400-38364400	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr14:38362800-38364800	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr14:38362800-38365000	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr14:38362800-38365200	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr14:38363200-38364200	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr14:38363200-38364400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
17	chr14:38363400-38363600	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr14:38363400-38363600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr14:38363400-38363800	Enhancers	H1 Cell Line	embryonic stem cell
20	chr14:38363400-38363800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr14:38363400-38364200	Enhancers	H9 Cell Line	embryonic stem cell
22	chr14:38363600-38363800	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
23	chr14:38363600-38363800	Enhancers	Psoas Muscle	Psoas
24	chr14:38363600-38364400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr14:38363800-38364000	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr14:38363800-38371000	Weak transcription	Psoas Muscle	Psoas
27	chr14:38364000-38364200	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
28	chr14:38364200-38364400	Enhancers	Adipose Nuclei	Adipose
29	chr14:38364200-38364600	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr14:38364400-38364600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr14:38364400-38365400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
32	chr14:38364400-38369200	Weak transcription	HUES64 Cell Line	embryonic stem cell
33	chr14:38364600-38366000	Weak transcription	HUES6 Cell Line	embryonic stem cell
34	chr14:38365000-38372600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
35	chr14:38365400-38365600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
36	chr14:38365400-38365600	Enhancers	Fetal Lung	lung
37	chr14:38366200-38366400	Enhancers	HUES6 Cell Line	embryonic stem cell
38	chr14:38367800-38368200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr14:38368000-38368600	Enhancers	NHDF-Ad	bronchial
40	chr14:38368000-38370200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr14:38368200-38369400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr14:38368400-38369000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr14:38368600-38369600	Weak transcription	NHDF-Ad	bronchial
44	chr14:38369000-38369400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
45	chr14:38369000-38370000	Enhancers	Hela-S3	cervix
46	chr14:38369000-38370200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr14:38369200-38369400	Enhancers	HUES64 Cell Line	embryonic stem cell
48	chr14:38369400-38370000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr14:38369600-38370000	Flanking Active TSS	NHDF-Ad	bronchial
50	chr14:38369600-38371600	Enhancers	Fetal Lung	lung

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