Variant report

Variant	esv2758355
Chromosome Location	chr14:44399205-44644481
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	chr14:44479441-44480344	HepG2	liver:	n/a	n/a
2	BACH1	chr14:44632100-44632238	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr14:44435424-44435438	GM12878	blood:	n/a	n/a
4	BRCA1	chr14:44618833-44619126	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr14:44560981-44561240	A549	lung:	n/a	chr14:44561060-44561071
6	CEBPB	chr14:44599593-44600126	A549	lung:	n/a	chr14:44599949-44599960
7	CEBPB	chr14:44595881-44596093	HepG2	liver:	n/a	n/a
8	CEBPB	chr14:44479333-44479685	ECC-1	luminal epithelium:	n/a	chr14:44479481-44479494 chr14:44479483-44479494 chr14:44479481-44479492 chr14:44479481-44479494
9	CEBPB	chr14:44605796-44606154	Hela-S3	cervix:	n/a	chr14:44605990-44606001 chr14:44605988-44606001 chr14:44605988-44605999 chr14:44605990-44606001
10	CEBPB	chr14:44606767-44606976	H1-hESC	embryonic stem cell:	n/a	chr14:44606862-44606873
11	CEBPB	chr14:44478922-44479645	HepG2	liver:	n/a	chr14:44479481-44479494 chr14:44479483-44479494 chr14:44479481-44479492 chr14:44479481-44479494
12	CEBPB	chr14:44499216-44499416	H1-hESC	embryonic stem cell:	n/a	chr14:44499342-44499351 chr14:44499340-44499353 chr14:44499340-44499353 chr14:44499243-44499254 chr14:44499245-44499254 chr14:44499340-44499351
13	CEBPB	chr14:44452992-44453227	ECC-1	luminal epithelium:	n/a	n/a
14	CEBPB	chr14:44487307-44487471	HepG2	liver:	n/a	n/a
15	CEBPB	chr14:44605865-44606139	A549	lung:	n/a	chr14:44605990-44606001 chr14:44605988-44606001 chr14:44605988-44605999 chr14:44605990-44606001
16	CEBPB	chr14:44572581-44572713	HepG2	liver:	n/a	chr14:44572646-44572657 chr14:44572645-44572658
17	CEBPB	chr14:44560929-44561184	K562	blood:	n/a	chr14:44561060-44561071
18	CEBPB	chr14:44633192-44633496	Hela-S3	cervix:	n/a	chr14:44633351-44633362
19	CEBPB	chr14:44541354-44541571	HepG2	liver:	n/a	chr14:44541425-44541436
20	CEBPB	chr14:44606738-44606986	HepG2	liver:	n/a	chr14:44606862-44606873
21	CEBPB	chr14:44478922-44479578	IMR90	lung:	n/a	chr14:44479481-44479494 chr14:44479483-44479494 chr14:44479481-44479492 chr14:44479481-44479494
22	CEBPB	chr14:44484998-44485226	HepG2	liver:	n/a	chr14:44485063-44485074
23	CEBPB	chr14:44498807-44499464	HepG2	liver:	n/a	chr14:44499342-44499351 chr14:44499340-44499353 chr14:44499340-44499353 chr14:44499243-44499254 chr14:44499245-44499254 chr14:44498983-44498994 chr14:44499340-44499351
24	CEBPB	chr14:44450644-44451128	HepG2	liver:	n/a	n/a
25	CEBPB	chr14:44444697-44444949	HepG2	liver:	n/a	chr14:44444844-44444855
26	CEBPB	chr14:44498824-44499447	IMR90	lung:	n/a	chr14:44499342-44499351 chr14:44499340-44499353 chr14:44499340-44499353 chr14:44499243-44499254 chr14:44499245-44499254 chr14:44498983-44498994 chr14:44499340-44499351
27	CEBPB	chr14:44499069-44499521	Hela-S3	cervix:	n/a	chr14:44499342-44499351 chr14:44499340-44499353 chr14:44499340-44499353 chr14:44499243-44499254 chr14:44499245-44499254 chr14:44499340-44499351
28	CEBPB	chr14:44498838-44499445	A549	lung:	n/a	chr14:44499342-44499351 chr14:44499340-44499353 chr14:44499340-44499353 chr14:44499243-44499254 chr14:44499245-44499254 chr14:44498983-44498994 chr14:44499340-44499351
29	CEBPB	chr14:44618834-44619117	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr14:44479371-44479562	MCF-7	breast:	n/a	chr14:44479481-44479494 chr14:44479483-44479494 chr14:44479481-44479492 chr14:44479481-44479494
31	CEBPB	chr14:44633186-44633505	HepG2	liver:	n/a	chr14:44633351-44633362
32	CEBPB	chr14:44560911-44561219	IMR90	lung:	n/a	chr14:44561060-44561071
33	CEBPB	chr14:44478929-44479169	A549	lung:	n/a	n/a
34	CEBPB	chr14:44582232-44582510	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr14:44479378-44479560	HepG2	liver:	n/a	chr14:44479481-44479494 chr14:44479483-44479494 chr14:44479481-44479492 chr14:44479481-44479494
36	CEBPB	chr14:44595859-44595978	A549	lung:	n/a	n/a
37	CEBPB	chr14:44560924-44561243	H1-hESC	embryonic stem cell:	n/a	chr14:44561060-44561071
38	CEBPB	chr14:44479304-44479659	ECC-1	luminal epithelium:	n/a	chr14:44479481-44479494 chr14:44479483-44479494 chr14:44479481-44479492 chr14:44479481-44479494
39	CEBPB	chr14:44560911-44561241	HepG2	liver:	n/a	chr14:44561060-44561071
40	CEBPB	chr14:44487331-44487496	A549	lung:	n/a	n/a
41	CEBPB	chr14:44448312-44448448	HepG2	liver:	n/a	chr14:44448367-44448378
42	CEBPB	chr14:44599875-44600120	HepG2	liver:	n/a	chr14:44599949-44599960
43	CEBPB	chr14:44605817-44606143	HepG2	liver:	n/a	chr14:44605990-44606001 chr14:44605988-44606001 chr14:44605988-44605999 chr14:44605990-44606001
44	CEBPB	chr14:44499135-44499425	MCF-7	breast:	n/a	chr14:44499342-44499351 chr14:44499340-44499353 chr14:44499340-44499353 chr14:44499243-44499254 chr14:44499245-44499254 chr14:44499340-44499351
45	CHD2	chr14:44618838-44619102	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr14:44618799-44619104	T-47D	breast:	n/a	chr14:44618936-44618957 chr14:44618941-44618959 chr14:44618942-44618958
47	CTCF	chr14:44618880-44619030	HMEC	breast:	n/a	chr14:44618936-44618957 chr14:44618941-44618959 chr14:44618942-44618958
48	CTCF	chr14:44619020-44619170	A549	lung:	n/a	n/a
49	CTCF	chr14:44618920-44619070	HCM	heart:	n/a	chr14:44618936-44618957 chr14:44618941-44618959 chr14:44618942-44618958
50	CTCF	chr14:44618860-44619010	HPAF	blood vessel:	n/a	chr14:44618936-44618957 chr14:44618941-44618959 chr14:44618942-44618958

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:44408473-44408523	HCPEpiC	choroid plexus:	n/a
2	chr14:44408473-44408523	HCPEpiC	choroid plexus:	n/a
3	chr14:44418808-44418858	NHBE	bronchial:	n/a
4	chr14:44408339-44408389	HCM	heart:	n/a
5	chr14:44408339-44408389	ProgFib	skin:	n/a
6	chr14:44408339-44408389	HPAEpiC	pulmonary alveolar:	n/a
7	chr14:44408473-44408523	HRCEpiC	kidney:	n/a
8	chr14:44418808-44418858	ECC-1	luminal epithelium:	n/a
9	chr14:44418808-44418858	HUVEC	blood vessel:	n/a
10	chr14:44408417-44408467	U87	brain:	n/a
11	chr14:44408339-44408389	GM12878	blood:	n/a
12	chr14:44408417-44408467	GM19239	blood:	n/a
13	chr14:44408339-44408389	NH-A	brain:	n/a
14	chr14:44418808-44418858	AG10803	skin:	n/a
15	chr14:44408473-44408523	AG10803	skin:	n/a
16	chr14:44418808-44418858	SAEC	small airway:	n/a
17	chr14:44418808-44418858	HRE	kidney:	n/a
18	chr14:44408417-44408467	SKMC	muscle:	n/a
19	chr14:44418808-44418858	SK-N-SH	brain:	n/a
20	chr14:44408339-44408389	K562	blood:	n/a
21	chr14:44418808-44418858	HMEC	breast:	n/a
22	chr14:44408339-44408389	PrEC	prostate:	n/a
23	chr14:44418808-44418858	U87	brain:	n/a
24	chr14:44418808-44418858	H1-hESC	embryonic stem cell:	embryo
25	chr14:44418808-44418858	SK-N-MC	brain:	n/a
26	chr14:44408473-44408523	SAEC	small airway:	n/a
27	chr14:44408473-44408523	NHDF-neo	bronchial:	n/a
28	chr14:44408339-44408389	Caco-2	colon:	n/a
29	chr14:44408473-44408523	NH-A	brain:	n/a
30	chr14:44408473-44408523	HAEpiC	amniotic membrane:	n/a
31	chr14:44408417-44408467	HCF	heart:	n/a
32	chr14:44408339-44408389	BJ	skin:	n/a
33	chr14:44408473-44408523	NT2-D1	testis:	n/a
34	chr14:44408417-44408467	NHDF-neo	bronchial:	n/a
35	chr14:44408417-44408467	ProgFib	skin:	n/a
36	chr14:44408473-44408523	PrEC	prostate:	n/a
37	chr14:44408473-44408523	A549	lung:	n/a
38	chr14:44408417-44408467	PFSK-1	brain:	n/a
39	chr14:44408339-44408389	HUVEC	blood vessel:	n/a
40	chr14:44408473-44408523	HRE	kidney:	n/a
41	chr14:44408417-44408467	HIPEpiC	eye:	n/a
42	chr14:44408339-44408389	BE2_C	brain:	n/a
43	chr14:44408473-44408523	GM12892	blood:	n/a
44	chr14:44408339-44408389	U87	brain:	n/a
45	chr14:44408473-44408523	AG04450	lung:	fetal
46	chr14:44408339-44408389	A549	lung:	n/a
47	chr14:44408339-44408389	IMR90	lung:	fetal
48	chr14:44408417-44408467	GM12878	blood:	n/a
49	chr14:44408417-44408467	HepG2	liver:	n/a
50	chr14:44418808-44418858	GM06990	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:44480170..44481920-chr14:44484152..44486382,2	MCF-7	breast:
2	chr14:44600217..44602036-chr14:44604194..44606588,2	K562	blood:
3	chr14:44370246..44372256-chr14:44617257..44619025,2	MCF-7	breast:
4	chr14:44562970..44563903-chr14:44618440..44619350,3	MCF-7	breast:
5	chr14:44606810..44610792-chr14:44612494..44615788,3	K562	blood:
6	chr14:44606810..44610792-chr14:44612494..44615788,3	K562	blood:
7	chr14:44370633..44373508-chr14:44616084..44618482,2	MCF-7	breast:
8	chr14:44569949..44570449-chr8:101630587..101631141,2	MCF-7	breast:
9	chr14:44430928..44433388-chr14:44437033..44439809,2	MCF-7	breast:
10	chr14:44480170..44481920-chr14:44484152..44486382,2	MCF-7	breast:
11	chr14:44430928..44433388-chr14:44437033..44439809,2	MCF-7	breast:
12	chr14:44562970..44563903-chr14:44618440..44619350,3	MCF-7	breast:
13	chr14:44429802..44430574-chr20:39327036..39327797,2	MCF-7	breast:
14	chr14:44600217..44602036-chr14:44604194..44606588,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FSCB-6	chr14:44621313-44621629	l_977_chr14:44621312-44622966_testes
2	lnc-FSCB-2	chr14:44518586-44518710	ENSG00000258969
3	lnc-FSCB-2	chr14:44464984-44465046	ENSG00000258969
4	lnc-FSCB-7	chr14:44546737-44547087	NONHSAT036603
5	lnc-FSCB-6	chr14:44622029-44622354	l_977_chr14:44621312-44622966_testes
6	lnc-FSCB-8	chr14:44477505-44479523	ucscGeneNc_uc001wvs_1
7	lnc-FSCB-6	chr14:44622425-44622966	l_977_chr14:44621312-44622966_testes
8	lnc-FSCB-6	chr14:44621821-44621918	l_977_chr14:44621312-44622966_testes

Variant related genes	Relation type
ENSG00000259137	TF binding region
ENSG00000259019	TF binding region
ENSG00000259137	CpG island
ENSG00000259019	CpG island
ENSG00000253740	chromatin interactions
ENSG00000174226	chromatin interactions
ENSG00000229771	chromatin interactions

Extended variants
information (count: 2536 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:2536 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs79900818	chr14:44403840-44403841	Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs564138226	chr14:44403843-44403844	Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs531417164	chr14:44403901-44403902	Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs138461598	chr14:44403945-44403946	Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs370992079	chr14:44404033-44404034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs76031519	chr14:44404061-44404062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs535648986	chr14:44404085-44404086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs146109535	chr14:44404091-44404092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs565848583	chr14:44404135-44404136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs534166812	chr14:44404143-44404144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs569448423	chr14:44404154-44404155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs558656191	chr14:44404158-44404159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs144541030	chr14:44404190-44404191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs549173199	chr14:44404327-44404328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs368649246	chr14:44404328-44404329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs537948822	chr14:44404336-44404337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs188520212	chr14:44404341-44404342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs191388754	chr14:44404384-44404385	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs558176796	chr14:44404415-44404416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs542034848	chr14:44404421-44404422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs8013639	chr14:44404471-44404472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs141546950	chr14:44404576-44404577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs567033702	chr14:44404580-44404581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs183217650	chr14:44404703-44404704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs150844937	chr14:44404750-44404751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs79070940	chr14:44404764-44404765	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs188276250	chr14:44404789-44404790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs375893240	chr14:44404914-44404915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs555555584	chr14:44404962-44404963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs139325227	chr14:44405007-44405008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs534622050	chr14:44405080-44405081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs145332535	chr14:44405100-44405101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs191123571	chr14:44405101-44405102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs183667834	chr14:44405104-44405105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs78633736	chr14:44405112-44405113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs543628336	chr14:44405122-44405123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs556536120	chr14:44405144-44405145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs371690250	chr14:44405145-44405146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs187635123	chr14:44405206-44405207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs543596020	chr14:44405207-44405208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs201958032	chr14:44405208-44405209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs576801151	chr14:44405211-44405212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs563754285	chr14:44405249-44405250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs535581753	chr14:44405293-44405294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs147673225	chr14:44405326-44405327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs572638008	chr14:44405338-44405339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs375980707	chr14:44405474-44405475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs115184623	chr14:44405475-44405476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs139717817	chr14:44405495-44405496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs145303162	chr14:44405497-44405498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

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
Melanoma	17363583	CNVD
Breast cancer	21364760	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:133 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:44403800-44404000	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
2	chr14:44404000-44406000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr14:44405400-44408000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr14:44406000-44406400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
5	chr14:44406200-44406400	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
6	chr14:44406200-44406400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr14:44406400-44409200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr14:44408000-44408400	Active TSS	HepG2	liver
9	chr14:44408000-44408800	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr14:44408800-44409000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr14:44409000-44409200	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr14:44409000-44409400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr14:44409000-44409400	Enhancers	Spleen	Spleen
14	chr14:44409200-44409400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr14:44409200-44409400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr14:44409400-44409600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr14:44411800-44415000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr14:44415000-44418000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr14:44417800-44418800	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr14:44417800-44419400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr14:44418000-44419600	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr14:44418000-44419600	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr14:44418000-44419600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr14:44418200-44419400	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr14:44418400-44419200	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr14:44418400-44419400	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr14:44418400-44419600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr14:44418600-44419000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr14:44418600-44419200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr14:44418600-44419400	Enhancers	H1 Cell Line	embryonic stem cell
31	chr14:44418600-44419400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr14:44418600-44419600	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr14:44418800-44419200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
34	chr14:44419000-44419200	Enhancers	H9 Cell Line	embryonic stem cell
35	chr14:44419200-44419600	Enhancers	iPS-20b Cell Line	embryonic stem cell
36	chr14:44419200-44422200	Weak transcription	H9 Cell Line	embryonic stem cell
37	chr14:44422200-44422400	Enhancers	H9 Cell Line	embryonic stem cell
38	chr14:44425600-44427200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr14:44443800-44444200	Enhancers	Fetal Brain Male	brain
40	chr14:44447800-44448000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr14:44448000-44449800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr14:44450400-44450800	Enhancers	Fetal Intestine Small	intestine
43	chr14:44450400-44451200	Enhancers	Liver	Liver
44	chr14:44450400-44451200	Enhancers	Fetal Intestine Large	intestine
45	chr14:44450600-44451200	Enhancers	Pancreatic Islets	Pancreatic Islet
46	chr14:44450600-44451200	Enhancers	HepG2	liver
47	chr14:44450800-44451400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr14:44464800-44465000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr14:44472800-44473000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr14:44473600-44473800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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