Variant report

Variant	esv34106
Chromosome Location	chr14:56346245-56550642
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:668)
CpG islands
(count:489)
Chromatin interactive
region (count:23)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:668 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:56392908-56392994	HepG2	liver:	n/a	n/a
2	ATF1	chr14:56435287-56435393	K562	blood:	n/a	n/a
3	ATF1	chr14:56430046-56430347	K562	blood:	n/a	n/a
4	ATF2	chr14:56424561-56424968	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr14:56471967-56472411	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr14:56348351-56348997	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr14:56471561-56471773	GM12878	blood:	n/a	n/a
8	BATF	chr14:56430910-56431177	GM12878	blood:	n/a	n/a
9	BCL11A	chr14:56471546-56471754	GM12878	blood:	n/a	n/a
10	BCL11A	chr14:56469651-56469858	GM12878	blood:	n/a	n/a
11	BCL11A	chr14:56424730-56425076	H1-hESC	embryonic stem cell:	n/a	n/a
12	BCL11A	chr14:56424621-56425049	H1-hESC	embryonic stem cell:	n/a	n/a
13	BCL11A	chr14:56471476-56471791	GM12878	blood:	n/a	n/a
14	BCL3	chr14:56355867-56356423	A549	lung:	n/a	n/a
15	BHLHE40	chr14:56416936-56417199	K562	blood:	n/a	chr14:56417046-56417059 chr14:56417048-56417057 chr14:56417047-56417056 chr14:56417049-56417058 chr14:56417048-56417057 chr14:56417042-56417063
16	BHLHE40	chr14:56471537-56471775	GM12878	blood:	n/a	n/a
17	BHLHE40	chr14:56469594-56470188	GM12878	blood:	n/a	n/a
18	BHLHE40	chr14:56541113-56541282	K562	blood:	n/a	n/a
19	BHLHE40	chr14:56348635-56348852	K562	blood:	n/a	n/a
20	CEBPB	chr14:56397190-56397403	A549	lung:	n/a	chr14:56397285-56397296
21	CEBPB	chr14:56531530-56531562	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr14:56525729-56526025	IMR90	lung:	n/a	n/a
23	CEBPB	chr14:56408785-56409257	MCF-7	breast:	n/a	chr14:56409034-56409043 chr14:56409032-56409045 chr14:56409034-56409043 chr14:56409034-56409045 chr14:56409032-56409043 chr14:56409034-56409043 chr14:56409034-56409045 chr14:56409032-56409045 chr14:56409034-56409043 chr14:56409032-56409045
24	CEBPB	chr14:56548039-56548181	K562	blood:	n/a	chr14:56548092-56548103
25	CEBPB	chr14:56355785-56356338	Hela-S3	cervix:	n/a	chr14:56356310-56356321 chr14:56356310-56356321 chr14:56356308-56356321
26	CEBPB	chr14:56359715-56359925	K562	blood:	n/a	chr14:56359827-56359844
27	CEBPB	chr14:56471986-56472269	A549	lung:	n/a	chr14:56472080-56472091 chr14:56472103-56472120
28	CEBPB	chr14:56403626-56403789	Hela-S3	cervix:	n/a	chr14:56403688-56403699
29	CEBPB	chr14:56488684-56489013	HepG2	liver:	n/a	chr14:56488860-56488871
30	CEBPB	chr14:56493968-56494253	IMR90	lung:	n/a	chr14:56494104-56494115
31	CEBPB	chr14:56397205-56397477	HepG2	liver:	n/a	chr14:56397285-56397296
32	CEBPB	chr14:56397183-56397440	MCF-7	breast:	n/a	chr14:56397285-56397296
33	CEBPB	chr14:56443422-56443698	ECC-1	luminal epithelium:	n/a	n/a
34	CEBPB	chr14:56359667-56359988	A549	lung:	n/a	chr14:56359827-56359844
35	CEBPB	chr14:56430032-56430317	K562	blood:	n/a	n/a
36	CEBPB	chr14:56400385-56400688	HepG2	liver:	n/a	chr14:56400560-56400571
37	CEBPB	chr14:56429982-56430311	K562	blood:	n/a	n/a
38	CEBPB	chr14:56547966-56548259	HepG2	liver:	n/a	chr14:56548092-56548103
39	CEBPB	chr14:56534129-56534312	HepG2	liver:	n/a	chr14:56534223-56534234
40	CEBPB	chr14:56547993-56548200	H1-hESC	embryonic stem cell:	n/a	chr14:56548092-56548103
41	CEBPB	chr14:56355865-56356281	ECC-1	luminal epithelium:	n/a	n/a
42	CEBPB	chr14:56443013-56443642	ECC-1	luminal epithelium:	n/a	n/a
43	CEBPB	chr14:56403526-56403836	HepG2	liver:	n/a	chr14:56403688-56403699
44	CEBPB	chr14:56355814-56356400	A549	lung:	n/a	chr14:56356310-56356321 chr14:56356310-56356321 chr14:56356308-56356321
45	CEBPB	chr14:56547930-56548231	IMR90	lung:	n/a	chr14:56548092-56548103
46	CEBPB	chr14:56355850-56356350	MCF-7	breast:	n/a	chr14:56356310-56356321 chr14:56356310-56356321 chr14:56356308-56356321
47	CEBPB	chr14:56403493-56403911	H1-hESC	embryonic stem cell:	n/a	chr14:56403688-56403699
48	CEBPB	chr14:56355882-56356319	A549	lung:	n/a	n/a
49	CEBPB	chr14:56397126-56397397	ECC-1	luminal epithelium:	n/a	chr14:56397285-56397296
50	CEBPB	chr14:56355806-56356532	MCF-7	breast:	n/a	chr14:56356310-56356321 chr14:56356310-56356321 chr14:56356308-56356321

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:56348939-56348989	ProgFib	skin:	n/a
2	chr14:56348939-56348989	ProgFib	skin:	n/a
3	chr14:56359470-56359520	HIPEpiC	eye:	n/a
4	chr14:56348939-56348989	BJ	skin:	n/a
5	chr14:56403510-56403560	GM06990	blood:	n/a
6	chr14:56374714-56374764	T-47D	breast:	n/a
7	chr14:56471704-56471754	HUVEC	blood vessel:	n/a
8	chr14:56524388-56524438	H1-hESC	embryonic stem cell:	embryo
9	chr14:56403510-56403560	IMR90	lung:	fetal
10	chr14:56348939-56348989	SKMC	muscle:	n/a
11	chr14:56348939-56348989	H1-hESC	embryonic stem cell:	embryo
12	chr14:56391960-56392010	NH-A	brain:	n/a
13	chr14:56403510-56403560	HAEpiC	amniotic membrane:	n/a
14	chr14:56403510-56403560	HMEC	breast:	n/a
15	chr14:56524388-56524438	HNPCEpiC	eye:	n/a
16	chr14:56471704-56471754	SKMC	muscle:	n/a
17	chr14:56359470-56359520	GM12892	blood:	n/a
18	chr14:56403510-56403560	BJ	skin:	n/a
19	chr14:56391960-56392010	GM06990	blood:	n/a
20	chr14:56471704-56471754	LNCaP	prostate:	n/a
21	chr14:56524388-56524438	NHDF-neo	bronchial:	n/a
22	chr14:56374714-56374764	HCPEpiC	choroid plexus:	n/a
23	chr14:56471704-56471754	ovcar-3	ovarian:	n/a
24	chr14:56391960-56392010	HL-60	blood:	n/a
25	chr14:56424872-56424922	IMR90	lung:	fetal
26	chr14:56524388-56524438	AG10803	skin:	n/a
27	chr14:56359470-56359520	AG10803	skin:	n/a
28	chr14:56524388-56524438	IMR90	lung:	fetal
29	chr14:56348939-56348989	T-47D	breast:	n/a
30	chr14:56359470-56359520	H1-hESC	embryonic stem cell:	embryo
31	chr14:56471704-56471754	GM12878	blood:	n/a
32	chr14:56391960-56392010	PFSK-1	brain:	n/a
33	chr14:56374714-56374764	U87	brain:	n/a
34	chr14:56374714-56374764	HRCEpiC	kidney:	n/a
35	chr14:56524388-56524438	SK-N-MC	brain:	n/a
36	chr14:56359470-56359520	HAEpiC	amniotic membrane:	n/a
37	chr14:56524388-56524438	Hepatocyte	liver:	n/a
38	chr14:56359470-56359520	AG09309	skin:	n/a
39	chr14:56374714-56374764	ProgFib	skin:	n/a
40	chr14:56374714-56374764	HUVEC	blood vessel:	n/a
41	chr14:56403510-56403560	NB4	blood:	n/a
42	chr14:56424872-56424922	LNCaP	prostate:	n/a
43	chr14:56524388-56524438	RPTEC	kidney:	n/a
44	chr14:56424872-56424922	H1-hESC	embryonic stem cell:	embryo
45	chr14:56374714-56374764	MCF10A-Er-Src	breast:	n/a
46	chr14:56424872-56424922	GM19239	blood:	n/a
47	chr14:56524388-56524438	HCF	heart:	n/a
48	chr14:56524388-56524438	GM19239	blood:	n/a
49	chr14:56359470-56359520	IMR90	lung:	fetal
50	chr14:56359470-56359520	AG04450	lung:	fetal

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:56361180..56363338-chr14:56369643..56372390,2	MCF-7	breast:
2	chr14:56487196..56488964-chr14:56491977..56494936,2	MCF-7	breast:
3	chr14:56489100..56490654-chr14:56494380..56496682,2	MCF-7	breast:
4	chr14:56357306..56359037-chr14:56360348..56362523,2	K562	blood:
5	chr14:56514146..56516367-chr14:56517394..56520149,2	K562	blood:
6	chr14:56514146..56516367-chr14:56517394..56520149,2	K562	blood:
7	chr14:56361180..56363338-chr14:56369643..56372390,2	MCF-7	breast:
8	chr10:70939625..70940171-chr14:56500071..56501060,2	Hela-S3	cervix:
9	chr14:56396115..56397620-chr14:56399759..56401612,2	K562	blood:
10	chr14:56396115..56397620-chr14:56399759..56401612,2	K562	blood:
11	chr14:56467248..56469891-chr14:56470182..56472447,2	K562	blood:
12	chr14:56390153..56391038-chr18:24814712..24815423,2	MCF-7	breast:
13	chr14:56399761..56402429-chr14:56440899..56442886,2	K562	blood:
14	chr14:56467248..56469891-chr14:56470182..56472447,2	K562	blood:
15	chr14:56492963..56495703-chr14:56498948..56501320,2	K562	blood:
16	chr14:56543596..56545113-chr5:172750348..172752553,2	MCF-7	breast:
17	chr14:56399761..56402429-chr14:56440899..56442886,2	K562	blood:
18	chr14:56489100..56490654-chr14:56494380..56496682,2	MCF-7	breast:
19	chr12:9799281..9800002-chr14:56409811..56410509,2	MCF-7	breast:
20	chr14:56487196..56488964-chr14:56491977..56494936,2	MCF-7	breast:
21	chr14:56492963..56495703-chr14:56498948..56501320,2	K562	blood:
22	chr14:56258843..56261080-chr14:56411606..56413589,2	K562	blood:
23	chr14:56357306..56359037-chr14:56360348..56362523,2	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PELI2-3	chr14:56512565-56512682	NONHSAT037035
2	lnc-PELI2-3	chr14:56515171-56515402	NONHSAT037035
3	lnc-PELI2-3	chr14:56512566-56512682	XLOC_010838
4	lnc-PELI2-5	chr14:56382445-56383044	ENSG00000259868.1
5	lnc-KTN1-AS1-2	chr14:56464932-56465307	NONHSAT037034
6	lnc-PELI2-3	chr14:56515172-56515402	XLOC_010838
7	lnc-PELI2-5	chr14:56382445-56383047	NONHSAT037033

No data

Variant related genes	Relation type
ENSG00000221254	TF binding region
ENSG00000259868	TF binding region
ENSG00000213622	TF binding region
ENSG00000212522	TF binding region
ENSG00000221254	CpG island
ENSG00000259868	CpG island
ENSG00000213622	CpG island
ENSG00000212522	CpG island
ENSG00000258791	chromatin interactions
ENSG00000156502	chromatin interactions
ENSG00000113739	chromatin interactions

Extended variants
information (count: 6971 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:6971 , 50 per page) page: 1 2 3 4 5 6 7 ... 140

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10498479	chr14:56346245-56346246	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs111822065	chr14:56346249-56346250	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs149059625	chr14:56346273-56346274	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs143056719	chr14:56346288-56346289	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs192527518	chr14:56346319-56346320	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs574948379	chr14:56346483-56346484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs151166287	chr14:56346495-56346496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs184865923	chr14:56346514-56346515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs141172588	chr14:56346633-56346634	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs8012251	chr14:56346641-56346642	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs34627712	chr14:56346718-56346719	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs146925102	chr14:56346769-56346770	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs550523476	chr14:56346792-56346793	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs571841342	chr14:56346817-56346818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs189277032	chr14:56346857-56346858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs181645105	chr14:56346858-56346859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs566046801	chr14:56346986-56346987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs75326838	chr14:56347008-56347009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs554659450	chr14:56347019-56347020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs73274384	chr14:56347042-56347043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs184253367	chr14:56347043-56347044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs138225484	chr14:56347060-56347061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs577380097	chr14:56347114-56347115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs140670182	chr14:56347126-56347127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs373047962	chr14:56347130-56347131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs538455353	chr14:56347132-56347133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs374764292	chr14:56347210-56347211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs572042610	chr14:56347216-56347217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs113437926	chr14:56347281-56347282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs542748131	chr14:56347322-56347323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs560701106	chr14:56347325-56347326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs143694526	chr14:56347333-56347334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs150146628	chr14:56347336-56347337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs138559908	chr14:56347349-56347350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs4901616	chr14:56347427-56347428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs371672934	chr14:56347448-56347449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs113602024	chr14:56347449-56347450	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs567257179	chr14:56347468-56347469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs115146802	chr14:56347474-56347475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs79490086	chr14:56347494-56347495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs548688217	chr14:56347500-56347501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs537841201	chr14:56347509-56347510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs372123763	chr14:56347513-56347514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs554579578	chr14:56347514-56347515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs149591177	chr14:56347522-56347523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs549622398	chr14:56347528-56347529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs190140048	chr14:56347529-56347530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs538593546	chr14:56347570-56347571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs181337248	chr14:56347610-56347611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs572239238	chr14:56347630-56347631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:65)

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
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
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	21633010	CNVD
Breast cancer	22032731	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
small cell lung cancer	20016488	CNVD
Ovarian cancer	21720365	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21364760	CNVD
Medulloblastoma	19270706	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Breast cancer	17603634	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Neuroblastoma	18923191	CNVD
Medulloblastoma	21163964	CNVD
Cancer	20164919	CNVD
ocular or pituitary abnormalities	19965921	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1254 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:56339600-56348600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr14:56345000-56346600	Weak transcription	Colon Smooth Muscle	Colon
3	chr14:56346200-56346400	Enhancers	Breast Myoepithelial Primary Cells	Breast
4	chr14:56346400-56348600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr14:56346600-56346800	Enhancers	Colon Smooth Muscle	Colon
6	chr14:56346800-56347000	Weak transcription	Colon Smooth Muscle	Colon
7	chr14:56348000-56348400	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr14:56348000-56348600	Enhancers	Hela-S3	cervix
9	chr14:56348000-56348800	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr14:56348000-56349000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr14:56348000-56349000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr14:56348000-56349200	Enhancers	NHDF-Ad	bronchial
13	chr14:56348200-56348400	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr14:56348200-56348400	Bivalent Enhancer	HSMMtube	muscle
15	chr14:56348200-56348600	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr14:56348200-56348800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
17	chr14:56348200-56348800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
18	chr14:56348200-56349000	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr14:56348200-56349000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr14:56348200-56349000	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr14:56348200-56349000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr14:56348200-56349000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr14:56348200-56349200	Enhancers	H1 Cell Line	embryonic stem cell
24	chr14:56348200-56350000	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr14:56348400-56348600	Enhancers	HSMMtube	muscle
26	chr14:56348400-56348800	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
27	chr14:56348400-56348800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr14:56348400-56348800	Enhancers	Osteobl	bone
29	chr14:56348400-56349000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr14:56348400-56349000	Enhancers	H9 Cell Line	embryonic stem cell
31	chr14:56348400-56349000	Enhancers	Skeletal Muscle Female	skeletal muscle
32	chr14:56348400-56349000	Enhancers	A549	lung
33	chr14:56348400-56349000	Enhancers	HMEC	breast
34	chr14:56348400-56349000	Enhancers	NHEK	skin
35	chr14:56348600-56348800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr14:56348600-56348800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr14:56348600-56348800	Enhancers	Esophagus	oesophagus
38	chr14:56348600-56349000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr14:56348600-56349000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr14:56348600-56349000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr14:56348600-56349000	Enhancers	Breast Myoepithelial Primary Cells	Breast
42	chr14:56348600-56349000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
43	chr14:56348600-56349000	Flanking Active TSS	Hela-S3	cervix
44	chr14:56348600-56349000	Enhancers	NH-A	brain
45	chr14:56348600-56349600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
46	chr14:56348800-56349000	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr14:56348800-56349000	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
48	chr14:56348800-56350800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr14:56348800-56350800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr14:56348800-56355200	Weak transcription	Esophagus	oesophagus

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