Variant report

Variant	nsv542075
Chromosome Location	chr14:44737522-44856450
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:417)
CpG islands
(count:61)
Chromatin interactive
region (count:20)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:417 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:44786011-44786505	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:44786027-44786367	K562	blood:	n/a	n/a
3	ATF1	chr14:44786110-44786462	K562	blood:	n/a	n/a
4	ATF3	chr14:44786091-44786377	K562	blood:	n/a	n/a
5	ATF3	chr14:44786185-44786384	HepG2	liver:	n/a	n/a
6	ATF3	chr14:44786082-44786534	A549	lung:	n/a	n/a
7	ATF3	chr14:44786000-44786531	HCT-116	colon:	n/a	n/a
8	ATF3	chr14:44786106-44786596	HCT-116	colon:	n/a	n/a
9	ATF3	chr14:44786197-44786335	K562	blood:	n/a	n/a
10	BATF	chr14:44786178-44786410	GM12878	blood:	n/a	n/a
11	BATF	chr14:44786155-44786410	GM12878	blood:	n/a	n/a
12	BCL3	chr14:44786061-44786449	GM12878	blood:	n/a	n/a
13	BHLHE40	chr14:44786155-44786484	K562	blood:	n/a	n/a
14	BHLHE40	chr14:44786136-44786463	HepG2	liver:	n/a	n/a
15	CBX3	chr14:44785944-44786626	HCT-116	colon:	n/a	n/a
16	CEBPB	chr14:44801511-44801755	H1-hESC	embryonic stem cell:	n/a	chr14:44801651-44801662 chr14:44801651-44801664
17	CEBPB	chr14:44801504-44801823	HepG2	liver:	n/a	chr14:44801651-44801662 chr14:44801651-44801664
18	CEBPB	chr14:44801528-44801807	A549	lung:	n/a	chr14:44801651-44801662 chr14:44801651-44801664
19	CEBPB	chr14:44825168-44825407	HepG2	liver:	n/a	n/a
20	CEBPB	chr14:44804468-44804813	HepG2	liver:	n/a	chr14:44804642-44804653
21	CEBPB	chr14:44786074-44786501	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr14:44845840-44846035	A549	lung:	n/a	n/a
23	CEBPB	chr14:44822866-44823194	H1-hESC	embryonic stem cell:	n/a	chr14:44823024-44823035
24	CEBPB	chr14:44822884-44823206	A549	lung:	n/a	chr14:44823024-44823035
25	CEBPB	chr14:44804504-44804827	A549	lung:	n/a	chr14:44804642-44804653
26	CEBPB	chr14:44804471-44804773	IMR90	lung:	n/a	chr14:44804642-44804653
27	CEBPB	chr14:44822632-44823413	MCF-7	breast:	n/a	chr14:44823024-44823035
28	CEBPB	chr14:44801504-44801816	IMR90	lung:	n/a	chr14:44801651-44801662 chr14:44801651-44801664
29	CEBPB	chr14:44785988-44786493	A549	lung:	n/a	n/a
30	CEBPB	chr14:44822861-44823165	K562	blood:	n/a	chr14:44823024-44823035
31	CEBPB	chr14:44822915-44823413	MCF-7	breast:	n/a	chr14:44823024-44823035
32	CEBPB	chr14:44822869-44823209	HepG2	liver:	n/a	chr14:44823024-44823035
33	CEBPB	chr14:44822857-44823212	IMR90	lung:	n/a	chr14:44823024-44823035
34	CEBPB	chr14:44785605-44785900	MCF-7	breast:	n/a	n/a
35	CHD1	chr14:44785940-44786615	IMR90	lung:	n/a	n/a
36	CHD2	chr14:44785974-44786422	Hela-S3	cervix:	n/a	n/a
37	CTCF	chr14:44838714-44838896	MCF-7	breast:	n/a	n/a
38	CTCF	chr14:44838633-44838917	MCF-7	breast:	n/a	n/a
39	CTCF	chr14:44838760-44838910	Caco-2	colon:	n/a	n/a
40	CTCF	chr14:44817626-44817803	MCF-7	breast:	n/a	n/a
41	CTCF	chr14:44838700-44838850	HEK293	kidney:	n/a	n/a
42	CTCF	chr14:44838689-44838906	MCF-7	breast:	n/a	n/a
43	CTCF	chr14:44838725-44838861	LNCaP	prostate:	n/a	n/a
44	CTCF	chr14:44838680-44838830	HEK293	kidney:	n/a	n/a
45	CTCF	chr14:44838662-44838909	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr14:44817649-44817734	MCF-7	breast:	n/a	n/a
47	CTCF	chr14:44817102-44817146	Pancreas_OC	pancreas:	n/a	n/a
48	CTCF	chr14:44817631-44817772	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTCF	chr14:44817617-44817739	MCF-7	breast:	n/a	n/a
50	CTCF	chr14:44817620-44817770	HEK293	kidney:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:44853952-44854002	AG04449	skin:	fetal
2	chr14:44853952-44854002	AG09309	skin:	n/a
3	chr14:44853952-44854002	Jurkat	blood:	n/a
4	chr14:44853952-44854002	HCPEpiC	choroid plexus:	n/a
5	chr14:44853952-44854002	Caco-2	colon:	n/a
6	chr14:44853952-44854002	AoSMC	blood vessel:	n/a
7	chr14:44853952-44854002	AG04450	lung:	fetal
8	chr14:44853952-44854002	A549	lung:	n/a
9	chr14:44853952-44854002	ovcar-3	ovarian:	n/a
10	chr14:44853952-44854002	SK-N-SH_RA	brain:	n/a
11	chr14:44853952-44854002	BJ	skin:	n/a
12	chr14:44853952-44854002	PrEC	prostate:	n/a
13	chr14:44853952-44854002	HCF	heart:	n/a
14	chr14:44853952-44854002	GM12892	blood:	n/a
15	chr14:44853952-44854002	HEK293	kidney:	embryo
16	chr14:44853952-44854002	MCF-7	breast:	n/a
17	chr14:44853952-44854002	RPTEC	kidney:	n/a
18	chr14:44853952-44854002	HepG2	liver:	n/a
19	chr14:44853952-44854002	IMR90	lung:	fetal
20	chr14:44853952-44854002	HCM	heart:	n/a
21	chr14:44853952-44854002	HL-60	blood:	n/a
22	chr14:44853952-44854002	AG10803	skin:	n/a
23	chr14:44853952-44854002	PFSK-1	brain:	n/a
24	chr14:44853952-44854002	BE2_C	brain:	n/a
25	chr14:44853952-44854002	SK-N-SH	brain:	n/a
26	chr14:44853952-44854002	NT2-D1	testis:	n/a
27	chr14:44853952-44854002	Hela-S3	cervix:	n/a
28	chr14:44853952-44854002	HEEpiC	esophagus:	n/a
29	chr14:44853952-44854002	GM19239	blood:	n/a
30	chr14:44853952-44854002	ProgFib	skin:	n/a
31	chr14:44853952-44854002	HPAEpiC	pulmonary alveolar:	n/a
32	chr14:44853952-44854002	U87	brain:	n/a
33	chr14:44853952-44854002	H1-hESC	embryonic stem cell:	embryo
34	chr14:44853952-44854002	GM12878	blood:	n/a
35	chr14:44853952-44854002	SKMC	muscle:	n/a
36	chr14:44853952-44854002	ECC-1	luminal epithelium:	n/a
37	chr14:44853952-44854002	K562	blood:	n/a
38	chr14:44853952-44854002	NH-A	brain:	n/a
39	chr14:44853952-44854002	NHBE	bronchial:	n/a
40	chr14:44853952-44854002	NB4	blood:	n/a
41	chr14:44853952-44854002	T-47D	breast:	n/a
42	chr14:44853952-44854002	HMEC	breast:	n/a
43	chr14:44853952-44854002	MCF10A-Er-Src	breast:	n/a
44	chr14:44853952-44854002	Hepatocyte	liver:	n/a
45	chr14:44853952-44854002	HCT-116	colon:	n/a
46	chr14:44853952-44854002	HUVEC	blood vessel:	n/a
47	chr14:44853952-44854002	HNPCEpiC	eye:	n/a
48	chr14:44853952-44854002	SAEC	small airway:	n/a
49	chr14:44853952-44854002	SK-N-MC	brain:	n/a
50	chr14:44853952-44854002	HIPEpiC	eye:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:44836359..44838272-chr14:44839234..44841841,2	K562	blood:
2	chr14:44803036..44805789-chr14:44807681..44809917,2	MCF-7	breast:
3	chr14:44785511..44787603-chr14:44801475..44804165,2	MCF-7	breast:
4	chr14:44838166..44839882-chr14:44873785..44875324,2	MCF-7	breast:
5	chr14:44754776..44756782-chr14:44760420..44763272,3	MCF-7	breast:
6	chr14:44755644..44758887-chr14:44761125..44763162,3	K562	blood:
7	chr14:44836359..44838272-chr14:44839234..44841841,3	K562	blood:
8	chr14:44803036..44805789-chr14:44807681..44809917,2	MCF-7	breast:
9	chr14:44836359..44838272-chr14:44839234..44841841,3	K562	blood:
10	chr14:44795723..44798432-chr14:44798850..44801579,2	MCF-7	breast:
11	chr14:44785511..44787603-chr14:44801475..44804165,2	MCF-7	breast:
12	chr14:44838296..44838875-chr14:45126583..45127520,3	MCF-7	breast:
13	chr14:44838612..44839205-chr14:44974588..44975472,2	MCF-7	breast:
14	chr14:44834762..44837688-chr14:44839758..44841386,2	MCF-7	breast:
15	chr14:44799704..44802515-chr14:44803665..44805548,2	K562	blood:
16	chr14:44755644..44758887-chr14:44761125..44763162,3	K562	blood:
17	chr14:44836359..44838272-chr14:44839234..44841841,2	K562	blood:
18	chr14:44799704..44802515-chr14:44803665..44805548,2	K562	blood:
19	chr14:44795723..44798432-chr14:44798850..44801579,2	MCF-7	breast:
20	chr14:44834762..44837688-chr14:44839758..44841386,2	MCF-7	breast:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FSCB-5	chr14:44760200-44760921	NONHSAT036604
2	lnc-FSCB-2	chr14:44853680-44853748	ENSG00000258969

No data

Variant related genes	Relation type
ENSG00000259148	TF binding region
ENSG00000258969	TF binding region
ENSG00000259148	CpG island
ENSG00000258969	CpG island
ENSG00000259148	chromatin interactions

Extended variants
information (count: 2244 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:2244 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs60903115	chr14:44743025-44743026	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs570882148	chr14:44743054-44743055	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs78891717	chr14:44743079-44743080	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs556812740	chr14:44743116-44743117	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs112382161	chr14:44743146-44743147	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs181826472	chr14:44743162-44743163	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs185962822	chr14:44743170-44743171	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs554738476	chr14:44743202-44743203	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs190378206	chr14:44743244-44743245	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs76824543	chr14:44743246-44743247	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs559803646	chr14:44743285-44743286	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs182570201	chr14:44743304-44743305	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs547915021	chr14:44743321-44743322	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs545400630	chr14:44743330-44743331	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs142229126	chr14:44743368-44743369	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs34305165	chr14:44743397-44743398	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs186326073	chr14:44743400-44743401	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs76269791	chr14:44743403-44743404	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs150167588	chr14:44743411-44743412	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs115287735	chr14:44743416-44743417	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs546855639	chr14:44743431-44743432	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs571592655	chr14:44743435-44743436	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs538273693	chr14:44743436-44743437	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs113660092	chr14:44743437-44743438	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs556911793	chr14:44743516-44743517	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs372987505	chr14:44743606-44743607	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs62013168	chr14:44743623-44743624	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs536302177	chr14:44743635-44743636	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs554467799	chr14:44743643-44743644	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs573043553	chr14:44743688-44743689	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs533962460	chr14:44743798-44743799	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs540938530	chr14:44752207-44752208	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs115565902	chr14:44752265-44752266	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs201865479	chr14:44752295-44752296	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs554537422	chr14:44752312-44752313	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs11157392	chr14:44752330-44752331	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs548165819	chr14:44752414-44752415	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs566632396	chr14:44752426-44752427	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs557902420	chr14:44752464-44752465	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs181449736	chr14:44752478-44752479	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs559126863	chr14:44752479-44752480	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs377125868	chr14:44752508-44752509	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs185547141	chr14:44752604-44752605	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs62013171	chr14:44752620-44752621	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs189858414	chr14:44752647-44752648	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs556946854	chr14:44752685-44752686	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs575204400	chr14:44752686-44752687	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs541856204	chr14:44752700-44752701	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs560143535	chr14:44752704-44752705	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs17654975	chr14:44752716-44752717	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:67)

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
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
Oral squamous cell carcinoma	17134496	CNVD
Renal cell carcinoma	18194544	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21364760	CNVD
Melanoma	17363583	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ovarian cancer	21781307	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Williams Syndrome	20824207	CNVD

Chromatin state (count:110 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:44743000-44743800	Enhancers	Fetal Heart	heart
2	chr14:44752200-44752800	Enhancers	NHDF-Ad	bronchial
3	chr14:44756800-44757200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr14:44760000-44761600	Enhancers	Fetal Heart	heart
5	chr14:44766000-44766200	Enhancers	Fetal Muscle Trunk	muscle
6	chr14:44770000-44771400	Enhancers	HUVEC	blood vessel
7	chr14:44770200-44771000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr14:44778000-44779600	Enhancers	HMEC	breast
9	chr14:44778200-44778400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr14:44778200-44779800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr14:44778400-44779400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr14:44778600-44779000	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr14:44778600-44779200	Enhancers	HUES64 Cell Line	embryonic stem cell
14	chr14:44779400-44780000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr14:44780000-44785200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr14:44784200-44787000	Enhancers	HUVEC	blood vessel
17	chr14:44785000-44786800	Enhancers	NHDF-Ad	bronchial
18	chr14:44785200-44787000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr14:44785200-44787000	Enhancers	HMEC	breast
20	chr14:44785400-44785600	Active TSS	NHEK	skin
21	chr14:44785400-44786000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr14:44785400-44786000	Enhancers	A549	lung
23	chr14:44785400-44786600	Enhancers	Hela-S3	cervix
24	chr14:44785600-44785800	Flanking Active TSS	NHEK	skin
25	chr14:44785600-44786800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr14:44785600-44786800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr14:44785600-44786800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr14:44785600-44786800	Enhancers	NH-A	brain
29	chr14:44785600-44787000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr14:44785800-44786800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr14:44785800-44786800	Enhancers	Fetal Intestine Large	intestine
32	chr14:44785800-44787000	Enhancers	NHEK	skin
33	chr14:44786000-44786400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr14:44786000-44786800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr14:44786000-44786800	Flanking Active TSS	A549	lung
36	chr14:44786000-44787000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr14:44786200-44786800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr14:44786200-44786800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr14:44786200-44786800	Enhancers	Lung	lung
40	chr14:44786400-44786600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr14:44786400-44786800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr14:44786400-44787000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr14:44786600-44787000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr14:44786800-44787000	Enhancers	A549	lung
45	chr14:44786800-44789000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr14:44787000-44787800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr14:44795000-44795200	Enhancers	NHDF-Ad	bronchial
48	chr14:44795000-44798600	Enhancers	Fetal Heart	heart
49	chr14:44795800-44796000	Enhancers	NHDF-Ad	bronchial
50	chr14:44798400-44798800	Enhancers	Brain Germinal Matrix	brain

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