Variant report

Variant	nsv901863
Chromosome Location	chr14:46797353-47247399
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1300)
CpG islands
(count:1100)
Chromatin interactive
region (count:22)
LncRNA
region (count:19)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1300 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:47060393-47060753	HepG2	liver:	n/a	n/a
2	ATF1	chr14:47227696-47227775	K562	blood:	n/a	n/a
3	ATF1	chr14:47124636-47124919	K562	blood:	n/a	n/a
4	ATF2	chr14:47238352-47238954	GM12878	blood:	n/a	n/a
5	ATF2	chr14:47238421-47238949	GM12878	blood:	n/a	n/a
6	BACH1	chr14:47144126-47144310	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr14:47238467-47238929	GM12878	blood:	n/a	chr14:47238736-47238744
8	BATF	chr14:47238445-47238909	GM12878	blood:	n/a	chr14:47238736-47238744
9	BCL11A	chr14:47238500-47238903	GM12878	blood:	n/a	chr14:47238829-47238838 chr14:47238615-47238624
10	BCLAF1	chr14:46959550-46960028	GM12878	blood:	n/a	n/a
11	BCLAF1	chr14:47238310-47239094	GM12878	blood:	n/a	chr14:47238829-47238838 chr14:47238615-47238624
12	BHLHE40	chr14:46847543-46847870	HepG2	liver:	n/a	n/a
13	BHLHE40	chr14:47050460-47050552	GM12878	blood:	n/a	n/a
14	BHLHE40	chr14:47238505-47238975	GM12878	blood:	n/a	n/a
15	BHLHE40	chr14:47243207-47243216	GM12878	blood:	n/a	n/a
16	CBX3	chr14:47128948-47129132	K562	blood:	n/a	n/a
17	CEBPB	chr14:47099535-47099985	ECC-1	luminal epithelium:	n/a	chr14:47099772-47099783
18	CEBPB	chr14:46959424-46959778	HepG2	liver:	n/a	chr14:46959575-46959586 chr14:46959590-46959603
19	CEBPB	chr14:47007729-47007887	K562	blood:	n/a	chr14:47007809-47007820
20	CEBPB	chr14:47150417-47150717	IMR90	lung:	n/a	n/a
21	CEBPB	chr14:46887921-46888002	K562	blood:	n/a	chr14:46887964-46887975
22	CEBPB	chr14:47099640-47099928	HepG2	liver:	n/a	chr14:47099772-47099783
23	CEBPB	chr14:46889950-46890217	HepG2	liver:	n/a	chr14:46890121-46890134 chr14:46890122-46890133
24	CEBPB	chr14:46874550-46874834	MCF-7	breast:	n/a	n/a
25	CEBPB	chr14:47007646-47007959	IMR90	lung:	n/a	chr14:47007809-47007820
26	CEBPB	chr14:47068392-47068645	A549	lung:	n/a	chr14:47068490-47068503
27	CEBPB	chr14:46874491-46874834	ECC-1	luminal epithelium:	n/a	n/a
28	CEBPB	chr14:47150439-47150659	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr14:46959392-46959846	MCF-7	breast:	n/a	chr14:46959575-46959586 chr14:46959590-46959603
30	CEBPB	chr14:46901890-46901905	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr14:47184230-47184309	H1-hESC	embryonic stem cell:	n/a	chr14:47184272-47184283
32	CEBPB	chr14:46874424-46874880	ECC-1	luminal epithelium:	n/a	n/a
33	CEBPB	chr14:47184168-47184434	HepG2	liver:	n/a	chr14:47184272-47184283
34	CEBPB	chr14:47099633-47099882	H1-hESC	embryonic stem cell:	n/a	chr14:47099772-47099783
35	CEBPB	chr14:47150425-47150718	A549	lung:	n/a	n/a
36	CEBPB	chr14:46887890-46888142	HepG2	liver:	n/a	chr14:46887964-46887975
37	CEBPB	chr14:47204885-47205091	A549	lung:	n/a	n/a
38	CEBPB	chr14:47007629-47007980	A549	lung:	n/a	chr14:47007809-47007820
39	CEBPB	chr14:47191649-47191654	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr14:47163162-47163272	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr14:46817335-46817572	A549	lung:	n/a	n/a
42	CEBPB	chr14:47237873-47237945	H1-hESC	embryonic stem cell:	n/a	chr14:47237881-47237890 chr14:47237881-47237890 chr14:47237879-47237892 chr14:47237881-47237890
43	CEBPB	chr14:47217051-47217222	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr14:46874231-46874599	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr14:46959438-46959906	H1-hESC	embryonic stem cell:	n/a	chr14:46959575-46959586 chr14:46959590-46959603
46	CEBPB	chr14:47163064-47163185	HepG2	liver:	n/a	n/a
47	CEBPB	chr14:47099568-47099959	MCF-7	breast:	n/a	chr14:47099772-47099783
48	CEBPB	chr14:47191227-47191420	HepG2	liver:	n/a	chr14:47191326-47191337
49	CEBPB	chr14:47007631-47007991	HepG2	liver:	n/a	chr14:47007809-47007820
50	CEBPB	chr14:46959463-46959768	A549	lung:	n/a	chr14:46959575-46959586 chr14:46959590-46959603

(count:1100 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:46916080-46916130	HRE	kidney:	n/a
2	chr14:47121132-47121182	GM06990	blood:	n/a
3	chr14:46916080-46916130	HRE	kidney:	n/a
4	chr14:47121132-47121182	GM06990	blood:	n/a
5	chr14:46916080-46916130	NT2-D1	testis:	n/a
6	chr14:47120507-47120557	NHBE	bronchial:	n/a
7	chr14:47121156-47121206	SK-N-SH	brain:	n/a
8	chr14:46916528-46916578	NHDF-neo	bronchial:	n/a
9	chr14:47104140-47104190	HUVEC	blood vessel:	n/a
10	chr14:46874779-46874829	HEEpiC	esophagus:	n/a
11	chr14:46916528-46916578	AG09319	gingival:	n/a
12	chr14:46874779-46874829	HAEpiC	amniotic membrane:	n/a
13	chr14:47121156-47121206	HRE	kidney:	n/a
14	chr14:47123088-47123138	HEEpiC	esophagus:	n/a
15	chr14:47120795-47120845	HIPEpiC	eye:	n/a
16	chr14:47121158-47121208	HIPEpiC	eye:	n/a
17	chr14:46874779-46874829	AG04449	skin:	fetal
18	chr14:47120507-47120557	MCF10A-Er-Src	breast:	n/a
19	chr14:47123088-47123138	HPAEpiC	pulmonary alveolar:	n/a
20	chr14:47096230-47096280	ProgFib	skin:	n/a
21	chr14:47096230-47096280	HRCEpiC	kidney:	n/a
22	chr14:47123088-47123138	SK-N-MC	brain:	n/a
23	chr14:46874779-46874829	SK-N-MC	brain:	n/a
24	chr14:46874779-46874829	A549	lung:	n/a
25	chr14:47121117-47121167	RPTEC	kidney:	n/a
26	chr14:47096230-47096280	ovcar-3	ovarian:	n/a
27	chr14:47120507-47120557	HAEpiC	amniotic membrane:	n/a
28	chr14:47123088-47123138	AG04449	skin:	fetal
29	chr14:47104140-47104190	ECC-1	luminal epithelium:	n/a
30	chr14:47120920-47120970	NHDF-neo	bronchial:	n/a
31	chr14:47121158-47121208	MCF-7	breast:	n/a
32	chr14:47096230-47096280	MCF10A-Er-Src	breast:	n/a
33	chr14:47123298-47123348	HRE	kidney:	n/a
34	chr14:46916080-46916130	GM12892	blood:	n/a
35	chr14:47123088-47123138	SKMC	muscle:	n/a
36	chr14:46916528-46916578	HRE	kidney:	n/a
37	chr14:47120920-47120970	HCF	heart:	n/a
38	chr14:47121158-47121208	GM06990	blood:	n/a
39	chr14:47123088-47123138	H1-hESC	embryonic stem cell:	embryo
40	chr14:47123088-47123138	BE2_C	brain:	n/a
41	chr14:47123088-47123138	AG04450	lung:	fetal
42	chr14:46916528-46916578	CMK	blood:	n/a
43	chr14:47121002-47121052	SK-N-SH_RA	brain:	n/a
44	chr14:47121156-47121206	HIPEpiC	eye:	n/a
45	chr14:47120507-47120557	U87	brain:	n/a
46	chr14:47118100-47118150	IMR90	lung:	fetal
47	chr14:47121158-47121208	PrEC	prostate:	n/a
48	chr14:47120845-47120895	HPAEpiC	pulmonary alveolar:	n/a
49	chr14:47121158-47121208	HCPEpiC	choroid plexus:	n/a
50	chr14:47120920-47120970	HCM	heart:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:46878574..46881068-chr14:46881642..46884417,2	K562	blood:
2	chr14:47110358..47111900-chr14:47112511..47115228,2	K562	blood:
3	chr14:47110358..47111900-chr14:47112511..47115228,2	K562	blood:
4	chr14:47050051..47050804-chr14:48867648..48868551,2	MCF-7	breast:
5	chr14:47229054..47230571-chr14:47239361..47241042,2	K562	blood:
6	chr14:47190435..47193179-chr14:47198084..47200809,2	MCF-7	breast:
7	chr14:47049935..47050932-chr14:48008149..48008898,3	MCF-7	breast:
8	chr14:47049606..47051836-chr14:47067092..47069403,2	K562	blood:
9	chr14:46719211..46719811-chr14:46813566..46814094,2	MCF-7	breast:
10	chr14:46984156..46986673-chr14:46987478..46989928,2	K562	blood:
11	chr14:47196544..47199011-chr14:47199972..47202196,2	K562	blood:
12	chr14:47050439..47051198-chr14:48008059..48008561,2	MCF-7	breast:
13	chr14:47196544..47199011-chr14:47199972..47202196,2	K562	blood:
14	chr14:47190435..47193179-chr14:47198084..47200809,2	MCF-7	breast:
15	chr14:47229054..47230571-chr14:47239361..47241042,2	K562	blood:
16	chr14:46517075..46517958-chr14:46813262..46814074,4	MCF-7	breast:
17	chr14:46984156..46986673-chr14:46987478..46989928,2	K562	blood:
18	chr14:47049606..47051836-chr14:47067092..47069403,2	K562	blood:
19	chr14:46517458..46517985-chr14:47049934..47050581,2	MCF-7	breast:
20	chr14:46718996..46719973-chr14:46813315..46814211,4	MCF-7	breast:
21	chr14:46878574..46881068-chr14:46881642..46884417,2	K562	blood:
22	chr14:47050056..47050875-chr14:47509400..47510237,2	MCF-7	breast:

(count:19 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FANCM-6	chr14:46959395-46959490	NONHSAT036681
2	lnc-FANCM-6	chr14:46907384-46907453	ENSG00000258700
3	lnc-FANCM-6	chr14:46940564-46940714	ENSG00000258700
4	lnc-FANCM-6	chr14:46915388-46915429	ENSG00000258700
5	lnc-FANCM-6	chr14:46919111-46919157	ENSG00000258700
6	lnc-FANCM-6	chr14:46907384-46907453	NONHSAT036678
7	lnc-FANCM-6	chr14:46970510-46971104	NONHSAT036679
8	lnc-FANCM-6	chr14:46940562-46940714	NONHSAT036680
9	lnc-FANCM-6	chr14:46970510-46971026	ENSG00000258700
10	lnc-FANCM-6	chr14:46940562-46940714	ENSG00000258700
11	lnc-FANCM-6	chr14:46919111-46919157	NONHSAT036678
12	lnc-FANCM-6	chr14:46970510-46970814	ENSG00000258700
13	lnc-FANCM-6	chr14:46970510-46970814	ENSG00000258700
14	lnc-FANCM-6	chr14:46916512-46916578	ENSG00000258700
15	lnc-FANCM-6	chr14:46959395-46959490	ENSG00000258700
16	lnc-FANCM-6	chr14:46940562-46940714	NONHSAT036681
17	lnc-FANCM-6	chr14:46970510-46971104	NONHSAT036678
18	lnc-FANCM-6	chr14:46970510-46971104	NONHSAT036680
19	lnc-FANCM-6	chr14:46970510-46971104	NONHSAT036681

No data

Variant related genes	Relation type
LINC00871	TF binding region
RPL10L	TF binding region
LINC00871	CpG island
RPL10L	CpG island

Extended variants
information (count: 8626 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:8626 , 50 per page) page: 1 2 3 4 5 6 7 ... 173

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4405459	chr14:46797353-46797354	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs191620459	chr14:46797355-46797356	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs145789438	chr14:46797404-46797405	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs73232343	chr14:46797418-46797419	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs549964362	chr14:46797435-46797436	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs200758593	chr14:46797471-46797472	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs139989451	chr14:46797478-46797479	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs369948974	chr14:46797497-46797498	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs537296304	chr14:46797572-46797573	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs555786075	chr14:46797584-46797585	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs565981839	chr14:46797633-46797634	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs73232346	chr14:46797665-46797666	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs541384460	chr14:46797671-46797672	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs553117414	chr14:46797728-46797729	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs183728062	chr14:46797738-46797739	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs570606106	chr14:46797749-46797750	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs145493460	chr14:46797768-46797769	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs147693031	chr14:46797785-46797786	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs530720012	chr14:46797812-46797813	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs145308215	chr14:46797815-46797816	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs542458349	chr14:46797819-46797820	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs189449191	chr14:46797820-46797821	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs34469417	chr14:46797833-46797834	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs397724855	chr14:46797834-46797835	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs73232348	chr14:46797850-46797851	Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs377342910	chr14:46797855-46797856	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs568435544	chr14:46797923-46797924	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs10498396	chr14:46797956-46797957	Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs570894427	chr14:46798000-46798001	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs532019134	chr14:46798093-46798094	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs566916122	chr14:46798108-46798109	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs114969995	chr14:46798167-46798168	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs570016314	chr14:46798216-46798217	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs187392121	chr14:46798226-46798227	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs2415953	chr14:46798259-46798260	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs190271566	chr14:46798288-46798289	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs534783384	chr14:46798289-46798290	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs2415954	chr14:46798358-46798359	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs199828978	chr14:46798395-46798396	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs554889581	chr14:46799205-46799206	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs550838217	chr14:46799257-46799258	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs543016596	chr14:46799276-46799277	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs540424007	chr14:46799314-46799315	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs564165240	chr14:46799352-46799353	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs564595797	chr14:46799356-46799357	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs113808945	chr14:46799398-46799399	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs543775531	chr14:46799399-46799400	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs572223912	chr14:46813075-46813076	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs190736589	chr14:46813088-46813089	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs146046821	chr14:46813089-46813090	Enhancers	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
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
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
Acute lymphoblastic leukemia	21098271	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	19907438	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD

Chromatin state (count:403 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:46793400-46797400	Weak transcription	Ovary	ovary
2	chr14:46797200-46797400	Enhancers	Primary hematopoietic stem cells	blood
3	chr14:46797200-46798200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr14:46797200-46798400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr14:46797400-46797600	Enhancers	Pancreatic Islets	Pancreatic Islet
6	chr14:46797400-46797800	Enhancers	Ovary	ovary
7	chr14:46797600-46798000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr14:46797600-46798200	Active TSS	Pancreatic Islets	Pancreatic Islet
9	chr14:46799200-46799400	Enhancers	Fetal Kidney	kidney
10	chr14:46813000-46814000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr14:46813600-46814000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr14:46814800-46815800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr14:46818800-46821200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
14	chr14:46836800-46838000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr14:46837400-46839000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr14:46837600-46838200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr14:46838000-46838800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr14:46838200-46838800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr14:46838800-46839000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr14:46838800-46839800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr14:46844800-46845000	Enhancers	H9 Cell Line	embryonic stem cell
22	chr14:46845600-46847600	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr14:46846200-46846400	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
24	chr14:46846200-46846800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr14:46846200-46846800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr14:46846200-46847200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
27	chr14:46846200-46847200	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr14:46846400-46846800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr14:46846400-46847200	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr14:46846400-46847200	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr14:46846400-46847200	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr14:46846600-46850800	Weak transcription	H9 Cell Line	embryonic stem cell
33	chr14:46846800-46848000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr14:46847200-46847600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
35	chr14:46847200-46850400	Weak transcription	HUES6 Cell Line	embryonic stem cell
36	chr14:46847200-46850400	Weak transcription	HUES64 Cell Line	embryonic stem cell
37	chr14:46847600-46847800	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr14:46847600-46850400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
39	chr14:46847800-46850800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
40	chr14:46850400-46851000	Enhancers	HUES64 Cell Line	embryonic stem cell
41	chr14:46850400-46851400	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr14:46850400-46851600	Enhancers	HUES6 Cell Line	embryonic stem cell
43	chr14:46850400-46852000	Enhancers	HUES48 Cell Line	embryonic stem cell
44	chr14:46850600-46851400	Enhancers	iPS-18 Cell Line	embryonic stem cell
45	chr14:46850600-46851400	Enhancers	iPS-20b Cell Line	embryonic stem cell
46	chr14:46850800-46851200	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr14:46850800-46851200	Enhancers	H9 Cell Line	embryonic stem cell
48	chr14:46850800-46851200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
49	chr14:46851600-46854800	Weak transcription	HUES6 Cell Line	embryonic stem cell
50	chr14:46852000-46855000	Weak transcription	HUES48 Cell Line	embryonic stem cell

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