Variant report

Variant	nsv427940
Chromosome Location	chr14:47386766-47562967
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	ATF2	chr14:47513971-47514339	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr14:47555354-47555385	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL11A	chr14:47514116-47514346	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL11A	chr14:47514066-47514301	H1-hESC	embryonic stem cell:	n/a	n/a
5	BRCA1	chr14:47509696-47510005	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr14:47485732-47485940	HepG2	liver:	n/a	chr14:47485846-47485857 chr14:47485886-47485898
7	CEBPB	chr14:47393770-47394030	H1-hESC	embryonic stem cell:	n/a	chr14:47393873-47393882 chr14:47393873-47393884 chr14:47393871-47393882 chr14:47393873-47393882 chr14:47393871-47393884 chr14:47393873-47393882 chr14:47393871-47393884 chr14:47393873-47393882
8	CEBPB	chr14:47550933-47551123	A549	lung:	n/a	chr14:47550992-47551005 chr14:47550994-47551005
9	CEBPB	chr14:47393713-47394028	HepG2	liver:	n/a	chr14:47393873-47393882 chr14:47393873-47393884 chr14:47393871-47393882 chr14:47393873-47393882 chr14:47393871-47393884 chr14:47393873-47393882 chr14:47393871-47393884 chr14:47393873-47393882
10	CEBPB	chr14:47404882-47405242	HepG2	liver:	n/a	n/a
11	CEBPB	chr14:47393718-47394047	IMR90	lung:	n/a	chr14:47393873-47393882 chr14:47393873-47393884 chr14:47393871-47393882 chr14:47393873-47393882 chr14:47393871-47393884 chr14:47393873-47393882 chr14:47393871-47393884 chr14:47393873-47393882
12	CEBPB	chr14:47510116-47510168	K562	blood:	n/a	n/a
13	CEBPB	chr14:47520035-47520324	A549	lung:	n/a	n/a
14	CEBPB	chr14:47404877-47405212	IMR90	lung:	n/a	n/a
15	CEBPB	chr14:47404933-47405117	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr14:47434809-47435009	HepG2	liver:	n/a	chr14:47434916-47434933
17	CEBPB	chr14:47509711-47510131	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr14:47485719-47485919	A549	lung:	n/a	chr14:47485846-47485857 chr14:47485886-47485898
19	CEBPB	chr14:47423059-47423295	HepG2	liver:	n/a	chr14:47423216-47423225 chr14:47423214-47423225 chr14:47423214-47423227
20	CEBPB	chr14:47514120-47514377	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr14:47454833-47454920	A549	lung:	n/a	n/a
22	CEBPB	chr14:47393758-47394044	A549	lung:	n/a	chr14:47393873-47393882 chr14:47393873-47393884 chr14:47393871-47393882 chr14:47393873-47393882 chr14:47393871-47393884 chr14:47393873-47393882 chr14:47393871-47393884 chr14:47393873-47393882
23	CEBPB	chr14:47545880-47546163	HepG2	liver:	n/a	chr14:47546020-47546031 chr14:47546049-47546060 chr14:47546019-47546032
24	CHD2	chr14:47514070-47514415	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr14:47393021-47393101	LNCaP	prostate:	n/a	chr14:47393063-47393084
26	CTCF	chr14:47514140-47514290	BE2_C	brain:	n/a	chr14:47514240-47514261 chr14:47514241-47514249 chr14:47514238-47514256
27	CTCF	chr14:47420260-47420410	RPTEC	kidney:	n/a	n/a
28	CTCF	chr14:47514135-47514345	HUVEC	blood vessel:	n/a	chr14:47514240-47514261 chr14:47514241-47514249 chr14:47514238-47514256
29	CTCF	chr14:47389820-47389970	GM12874	blood:	n/a	n/a
30	CTCF	chr14:47514054-47514349	H1-hESC	embryonic stem cell:	n/a	chr14:47514240-47514261 chr14:47514241-47514249 chr14:47514238-47514256
31	CTCF	chr14:47514200-47514350	HRPEpiC	eye:	n/a	chr14:47514240-47514261 chr14:47514241-47514249 chr14:47514238-47514256
32	CTCF	chr14:47420340-47420490	GM12873	blood:	n/a	n/a
33	CTCF	chr14:47509780-47509930	HAc	cerebellar:	n/a	n/a
34	CTCF	chr14:47509720-47509870	HCT-116	colon:	n/a	n/a
35	CTCF	chr14:47509750-47509998	MCF-7	breast:	n/a	n/a
36	CTCF	chr14:47420526-47420542	HUVEC	blood vessel:	n/a	n/a
37	CTCF	chr14:47514180-47514330	WERI-Rb-1	eye:	n/a	chr14:47514240-47514261 chr14:47514241-47514249 chr14:47514238-47514256
38	CTCF	chr14:47514220-47514370	RPTEC	kidney:	n/a	chr14:47514240-47514261 chr14:47514241-47514249 chr14:47514238-47514256
39	CTCF	chr14:47509787-47509943	HepG2	liver:	n/a	n/a
40	CTCF	chr14:47420512-47420520	HUVEC	blood vessel:	n/a	n/a
41	CTCF	chr14:47509840-47509990	HepG2	liver:	n/a	n/a
42	CTCF	chr14:47509785-47509967	LNCaP	prostate:	n/a	n/a
43	CTCF	chr14:47509620-47509770	A549	lung:	n/a	n/a
44	CTCF	chr14:47514160-47514310	GM06990	blood:	n/a	chr14:47514240-47514261 chr14:47514241-47514249 chr14:47514238-47514256
45	CTCF	chr14:47451843-47451976	Kidney_OC	kidney:	n/a	n/a
46	CTCF	chr14:47420620-47420770	HCPEpiC	choroid plexus:	n/a	n/a
47	CTCF	chr14:47514126-47514303	MCF-7	breast:	n/a	chr14:47514240-47514261 chr14:47514241-47514249 chr14:47514238-47514256
48	CTCF	chr14:47509720-47509870	HCPEpiC	choroid plexus:	n/a	n/a
49	CTCF	chr14:47393000-47393150	HCPEpiC	choroid plexus:	n/a	chr14:47393063-47393084
50	CTCF	chr14:47509716-47509974	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:47544244-47544294	BJ	skin:	n/a
2	chr14:47411755-47411805	HRE	kidney:	n/a
3	chr14:47411755-47411805	SKMC	muscle:	n/a
4	chr14:47411755-47411805	AG09309	skin:	n/a
5	chr14:47544244-47544294	HCF	heart:	n/a
6	chr14:47513774-47513824	HRE	kidney:	n/a
7	chr14:47513774-47513824	HEK293	kidney:	embryo
8	chr14:47411755-47411805	Caco-2	colon:	n/a
9	chr14:47411755-47411805	AG10803	skin:	n/a
10	chr14:47544244-47544294	SK-N-MC	brain:	n/a
11	chr14:47411755-47411805	NB4	blood:	n/a
12	chr14:47513774-47513824	HCT-116	colon:	n/a
13	chr14:47544244-47544294	AoSMC	blood vessel:	n/a
14	chr14:47513774-47513824	AG10803	skin:	n/a
15	chr14:47544244-47544294	MCF10A-Er-Src	breast:	n/a
16	chr14:47411755-47411805	HAEpiC	amniotic membrane:	n/a
17	chr14:47544244-47544294	A549	lung:	n/a
18	chr14:47411755-47411805	AG04449	skin:	fetal
19	chr14:47411755-47411805	HMEC	breast:	n/a
20	chr14:47411755-47411805	HCF	heart:	n/a
21	chr14:47513774-47513824	PrEC	prostate:	n/a
22	chr14:47411755-47411805	Hepatocyte	liver:	n/a
23	chr14:47544244-47544294	NT2-D1	testis:	n/a
24	chr14:47411755-47411805	LNCaP	prostate:	n/a
25	chr14:47411755-47411805	AG04450	lung:	fetal
26	chr14:47411755-47411805	IMR90	lung:	fetal
27	chr14:47513774-47513824	Caco-2	colon:	n/a
28	chr14:47411755-47411805	ProgFib	skin:	n/a
29	chr14:47513774-47513824	HRCEpiC	kidney:	n/a
30	chr14:47544244-47544294	ECC-1	luminal epithelium:	n/a
31	chr14:47513774-47513824	GM19239	blood:	n/a
32	chr14:47411755-47411805	GM06990	blood:	n/a
33	chr14:47411755-47411805	GM12892	blood:	n/a
34	chr14:47411755-47411805	A549	lung:	n/a
35	chr14:47411755-47411805	SAEC	small airway:	n/a
36	chr14:47544244-47544294	HCM	heart:	n/a
37	chr14:47544244-47544294	GM06990	blood:	n/a
38	chr14:47513774-47513824	HCPEpiC	choroid plexus:	n/a
39	chr14:47513774-47513824	NHBE	bronchial:	n/a
40	chr14:47544244-47544294	GM12878	blood:	n/a
41	chr14:47544244-47544294	Caco-2	colon:	n/a
42	chr14:47513774-47513824	MCF-7	breast:	n/a
43	chr14:47513774-47513824	SK-N-MC	brain:	n/a
44	chr14:47544244-47544294	SK-N-SH_RA	brain:	n/a
45	chr14:47513774-47513824	NT2-D1	testis:	n/a
46	chr14:47544244-47544294	PANC-1	pancreas:	n/a
47	chr14:47411755-47411805	HRPEpiC	eye:	n/a
48	chr14:47513774-47513824	ovcar-3	ovarian:	n/a
49	chr14:47513774-47513824	U87	brain:	n/a
50	chr14:47544244-47544294	PFSK-1	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:47417689..47420302-chr14:47420799..47423183,3	MCF-7	breast:
2	chr14:47417689..47420302-chr14:47420799..47423183,3	MCF-7	breast:
3	chr14:47409007..47410877-chr14:47415123..47417216,2	K562	blood:
4	chr14:47409007..47410877-chr14:47415123..47417216,2	K562	blood:
5	chr14:47050056..47050875-chr14:47509400..47510237,2	MCF-7	breast:
6	chr14:47401862..47402382-chr2:190007804..190008571,2	MCF-7	breast:
7	chr14:47525262..47526210-chr14:47747163..47747902,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FANCM-11	chr14:47465657-47466377	NONHSAT036685

Variant related genes	Relation type
RPA2P1	TF binding region
ENSG00000251735	TF binding region
MDGA2	TF binding region
RPA2P1	CpG island
ENSG00000251735	CpG island
MDGA2	CpG island

Extended variants
information (count: 2618 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:2618 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs78663219	chr14:47389502-47389503	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs573181072	chr14:47389529-47389530	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs540209658	chr14:47389550-47389551	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs565189787	chr14:47389564-47389565	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs143746534	chr14:47389713-47389714	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs373556248	chr14:47389737-47389738	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs527273826	chr14:47389755-47389756	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs183901105	chr14:47389802-47389803	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs188790312	chr14:47389811-47389812	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs535638069	chr14:47389882-47389883	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs538937065	chr14:47389909-47389910	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs555612314	chr14:47389917-47389918	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs575207565	chr14:47389923-47389924	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs569096138	chr14:47389929-47389930	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs148119916	chr14:47390007-47390008	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs554641709	chr14:47390073-47390074	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs141907446	chr14:47390078-47390079	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs564152479	chr14:47391407-47391408	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs531203506	chr14:47391417-47391418	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs542968412	chr14:47391434-47391435	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs562852321	chr14:47391500-47391501	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs530296040	chr14:47391503-47391504	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs190341769	chr14:47391510-47391511	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs146033476	chr14:47391531-47391532	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs139953434	chr14:47391545-47391546	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs376455339	chr14:47391556-47391557	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs182512318	chr14:47391580-47391581	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs570868660	chr14:47391594-47391595	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs538244247	chr14:47391652-47391653	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs374260723	chr14:47391686-47391687	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs540250773	chr14:47391687-47391688	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs184983760	chr14:47391711-47391712	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs188249968	chr14:47391719-47391720	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs567497123	chr14:47391722-47391723	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs369576685	chr14:47391723-47391724	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs535727174	chr14:47391748-47391749	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs553969493	chr14:47391769-47391770	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs181086771	chr14:47391898-47391899	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs185516967	chr14:47391931-47391932	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs553582279	chr14:47391936-47391937	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs149303249	chr14:47392011-47392012	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs575691763	chr14:47392013-47392014	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs191650229	chr14:47392031-47392032	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs561318954	chr14:47392036-47392037	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs371561477	chr14:47392057-47392058	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs183425157	chr14:47392074-47392075	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs538098942	chr14:47392079-47392080	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs560777710	chr14:47392088-47392089	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs573441685	chr14:47392091-47392092	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs558382640	chr14:47392108-47392109	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:59)

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
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	19907438	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	20967226	CNVD
Osteosarcoma	21215367	CNVD
Gastric cancer	18160780	CNVD

Chromatin state (count:91 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:47391400-47392000	Enhancers	HUES48 Cell Line	embryonic stem cell
2	chr14:47391600-47393000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr14:47404400-47405000	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr14:47406400-47407000	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
5	chr14:47410400-47410800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr14:47410400-47410800	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr14:47410400-47410800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
8	chr14:47410600-47411000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr14:47430000-47437000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr14:47431400-47431800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr14:47433200-47434000	Enhancers	Liver	Liver
12	chr14:47433400-47433800	Enhancers	Fetal Kidney	kidney
13	chr14:47436400-47437200	Weak transcription	Liver	Liver
14	chr14:47437600-47438000	Weak transcription	Liver	Liver
15	chr14:47442200-47443000	Enhancers	Liver	Liver
16	chr14:47447600-47448600	Enhancers	HUVEC	blood vessel
17	chr14:47454800-47455000	Enhancers	Brain Germinal Matrix	brain
18	chr14:47454800-47455400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr14:47454800-47456000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr14:47455000-47455400	Enhancers	NH-A	brain
21	chr14:47455000-47455800	Enhancers	Brain Hippocampus Middle	brain
22	chr14:47455000-47463400	Weak transcription	Brain Germinal Matrix	brain
23	chr14:47455200-47455600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr14:47455200-47455600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr14:47455200-47455600	Enhancers	Brain Substantia Nigra	brain
26	chr14:47455200-47455600	Enhancers	Fetal Brain Female	brain
27	chr14:47455200-47455800	Enhancers	Cortex derived primary cultured neurospheres	brain
28	chr14:47455200-47455800	Enhancers	Brain Cingulate Gyrus	brain
29	chr14:47455400-47457800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr14:47455600-47458400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr14:47455600-47458600	Weak transcription	Fetal Brain Female	brain
32	chr14:47455600-47460600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr14:47457600-47458000	Enhancers	Fetal Brain Male	brain
34	chr14:47457800-47459400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr14:47458000-47460000	Weak transcription	Fetal Brain Male	brain
36	chr14:47458400-47459000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr14:47458600-47458800	Enhancers	Fetal Brain Female	brain
38	chr14:47460000-47460400	Enhancers	Fetal Brain Male	brain
39	chr14:47460600-47461400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr14:47461400-47477400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr14:47463400-47463600	Enhancers	Brain Germinal Matrix	brain
42	chr14:47471000-47473800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr14:47478800-47479200	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr14:47478800-47479200	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr14:47478800-47479200	Enhancers	Fetal Kidney	kidney
46	chr14:47478800-47479400	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr14:47478800-47479400	Enhancers	iPS-15b Cell Line	embryonic stem cell
48	chr14:47479000-47479400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr14:47479000-47479400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr14:47486200-47486600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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