Variant report

Variant	nsv886466
Chromosome Location	chr6:102327303-102432398
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	chr6:102327575-102327933	GM12878	blood:	n/a	n/a
2	BATF	chr6:102331364-102331593	GM12878	blood:	n/a	n/a
3	BATF	chr6:102327588-102327954	GM12878	blood:	n/a	n/a
4	CEBPB	chr6:102359527-102359859	HepG2	liver:	n/a	chr6:102359688-102359699
5	CEBPB	chr6:102430470-102430482	K562	blood:	n/a	n/a
6	CEBPB	chr6:102340481-102340681	HepG2	liver:	n/a	chr6:102340605-102340618 chr6:102340605-102340618 chr6:102340519-102340530 chr6:102340606-102340617
7	CEBPB	chr6:102379676-102379923	IMR90	lung:	n/a	chr6:102379822-102379835
8	CEBPB	chr6:102331363-102331953	IMR90	lung:	n/a	n/a
9	CEBPB	chr6:102331435-102331696	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr6:102335573-102335864	HepG2	liver:	n/a	chr6:102335715-102335726
11	CEBPB	chr6:102335594-102335841	A549	lung:	n/a	chr6:102335715-102335726
12	CEBPB	chr6:102359560-102359811	A549	lung:	n/a	chr6:102359688-102359699
13	CEBPB	chr6:102355347-102355775	HepG2	liver:	n/a	n/a
14	CEBPB	chr6:102359504-102359870	IMR90	lung:	n/a	chr6:102359688-102359699
15	CEBPB	chr6:102379717-102379919	ECC-1	luminal epithelium:	n/a	chr6:102379822-102379835
16	CEBPB	chr6:102340485-102340685	K562	blood:	n/a	chr6:102340605-102340618 chr6:102340605-102340618 chr6:102340519-102340530 chr6:102340606-102340617
17	CREB1	chr6:102327645-102328015	GM12878	blood:	n/a	n/a
18	CTCF	chr6:102409385-102409477	GM12891	blood:	n/a	n/a
19	CTCF	chr6:102409360-102409510	GM12865	blood:	n/a	n/a
20	CTCF	chr6:102409340-102409490	HepG2	liver:	n/a	n/a
21	CTCF	chr6:102409395-102409522	MCF-7	breast:	n/a	n/a
22	CTCF	chr6:102409300-102409450	WERI-Rb-1	eye:	n/a	n/a
23	CTCF	chr6:102409465-102409468	A549	lung:	n/a	n/a
24	CTCF	chr6:102409440-102409590	GM12865	blood:	n/a	n/a
25	CTCF	chr6:102409300-102409450	Caco-2	colon:	n/a	n/a
26	CTCF	chr6:102409380-102409530	HEK293	kidney:	n/a	n/a
27	CTCF	chr6:102409369-102409493	GM12878	blood:	n/a	n/a
28	CTCF	chr6:102409347-102409493	HepG2	liver:	n/a	n/a
29	CTCF	chr6:102409415-102409503	HepG2	liver:	n/a	n/a
30	CTCF	chr6:102346499-102346520	GM13976	blood:	n/a	n/a
31	CTCF	chr6:102409417-102409472	Hela-S3	cervix:	n/a	n/a
32	CTCF	chr6:102409361-102409524	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr6:102409277-102409614	GM12878	blood:	n/a	n/a
34	CTCF	chr6:102409361-102409478	MCF-7	breast:	n/a	n/a
35	CTCF	chr6:102409364-102409560	MCF-7	breast:	n/a	n/a
36	CTCF	chr6:102409434-102409464	A549	lung:	n/a	n/a
37	CTCF	chr6:102409365-102409527	MCF-7	breast:	n/a	n/a
38	CTCF	chr6:102409398-102409542	MCF-7	breast:	n/a	n/a
39	CTCF	chr6:102409470-102409478	A549	lung:	n/a	n/a
40	CTCF	chr6:102409386-102409480	Fibrobl	skin:	n/a	n/a
41	E2F4	chr6:102332181-102332519	MCF10A-Er-Src	breast:	n/a	chr6:102332365-102332374
42	E2F4	chr6:102333344-102333467	MCF10A-Er-Src	breast:	n/a	n/a
43	E2F4	chr6:102412723-102412793	MCF10A-Er-Src	breast:	n/a	n/a
44	EBF1	chr6:102400186-102400280	GM12878	blood:	n/a	n/a
45	EBF1	chr6:102388029-102388293	GM12878	blood:	n/a	chr6:102388184-102388195 chr6:102388185-102388194
46	EP300	chr6:102428835-102429115	SK-N-SH_RA	brain:	n/a	chr6:102429041-102429054
47	EP300	chr6:102331383-102331590	GM12878	blood:	n/a	n/a
48	EP300	chr6:102428558-102429349	SK-N-SH	brain:	n/a	chr6:102429041-102429054 chr6:102428823-102428837
49	FOS	chr6:102379544-102380170	MCF10A-Er-Src	breast:	n/a	chr6:102380033-102380044 chr6:102379978-102379987 chr6:102380032-102380039 chr6:102380032-102380040
50	FOS	chr6:102379668-102380203	MCF10A-Er-Src	breast:	n/a	chr6:102380033-102380044 chr6:102379978-102379987 chr6:102380032-102380039 chr6:102380032-102380040

No.	Distal block	Cell Line	Cell type
1	chr6:102353130..102355186-chr6:102359232..102361862,2	K562	blood:
2	chr6:102423740..102426359-chr6:102431274..102433245,2	K562	blood:
3	chr6:102352732..102355186-chr6:102357901..102361862,3	K562	blood:
4	chr6:102423740..102426359-chr6:102431274..102433245,2	K562	blood:
5	chr6:102368803..102370851-chr6:102488591..102491392,2	K562	blood:
6	chr6:102427557..102429881-chr6:102433659..102436642,2	MCF-7	breast:
7	chr6:102352732..102355186-chr6:102357901..102361862,3	K562	blood:
8	chr6:102388911..102391649-chr6:102394397..102396742,2	MCF-7	breast:
9	chr6:102408799..102411775-chr6:102415336..102416958,2	MCF-7	breast:
10	chr6:102377981..102380751-chr6:102384114..102385937,2	K562	blood:
11	chr6:102353130..102355186-chr6:102359232..102361862,2	K562	blood:
12	chr6:102332291..102334019-chr6:102343556..102346119,2	MCF-7	breast:
13	chr6:102377981..102380751-chr6:102384114..102385937,2	K562	blood:
14	chr6:102332291..102334019-chr6:102343556..102346119,2	MCF-7	breast:
15	chr6:102388911..102391649-chr6:102394397..102396742,2	MCF-7	breast:
16	chr6:102312465..102314279-chr6:102350590..102352223,2	K562	blood:
17	chr6:102408799..102411775-chr6:102415336..102416958,2	MCF-7	breast:

Variant related genes	Relation type
GRIK2	TF binding region

Extended variants
information (count: 1012 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:1012 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4840200	chr6:102327303-102327304	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs564422094	chr6:102327374-102327375	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs531527987	chr6:102327376-102327377	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs561195637	chr6:102327383-102327384	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs141232041	chr6:102327410-102327411	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs562951256	chr6:102327470-102327471	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs539833440	chr6:102327496-102327497	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs548680003	chr6:102327530-102327531	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs113205517	chr6:102327553-102327554	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs67965320	chr6:102327554-102327555	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs34632401	chr6:102327566-102327567	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs200138669	chr6:102327567-102327568	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs566712328	chr6:102327677-102327678	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs527690012	chr6:102327678-102327679	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs528399436	chr6:102327734-102327735	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs182806979	chr6:102327751-102327752	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs117588217	chr6:102327783-102327784	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs538033163	chr6:102327784-102327785	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs556366853	chr6:102327786-102327787	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs531981562	chr6:102327794-102327795	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs547734519	chr6:102327796-102327797	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs150380870	chr6:102327848-102327849	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs138072532	chr6:102327855-102327856	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs368477725	chr6:102327857-102327858	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs553837675	chr6:102327894-102327895	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs2791843	chr6:102327950-102327951	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs373662667	chr6:102327995-102327996	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs545826737	chr6:102328000-102328001	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs558072044	chr6:102328019-102328020	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs576435069	chr6:102328063-102328064	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs533417185	chr6:102328122-102328123	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs543764554	chr6:102328193-102328194	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs561831410	chr6:102328221-102328222	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs373530094	chr6:102328228-102328229	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs186766964	chr6:102328258-102328259	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs142645108	chr6:102328259-102328260	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs560681982	chr6:102328303-102328304	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs145950021	chr6:102328345-102328346	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs372292862	chr6:102328387-102328388	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs370454889	chr6:102328403-102328404	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs191611945	chr6:102328433-102328434	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs564416780	chr6:102328676-102328677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs531854372	chr6:102328681-102328682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs368537578	chr6:102328766-102328767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs550076037	chr6:102328819-102328820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs73761461	chr6:102328858-102328859	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs536048421	chr6:102328862-102328863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs547169864	chr6:102328864-102328865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs73761462	chr6:102328878-102328879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs116610671	chr6:102328936-102328937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:109)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Autism	22495311	CNVD
Gastric cancer	17908304	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Ependymoma	16718352	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Leukemia	18688285	CNVD
Prostate cancer	19242612	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Lung adenocarcinoma	21935476	CNVD
Prostate cancer	17245344	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Cancer	20164920	CNVD
Burkitt''s lymphoma	20823134	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	17640729	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
small cell lung cancer	20016488	CNVD
Burkitt''s lymphoma	18698080	CNVD
Ovarian cancer	21720365	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	17170743	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21785460	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Myelofibrosis	22110671	CNVD
Obesity	21045960	CNVD
Liver carcinoma	19366792	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	16461572	CNVD
Neurocytoma	17123091	CNVD
Urothelial carcinoma	21177765	CNVD
Autism	22543975	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:52 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:102327000-102327400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr6:102327000-102331600	Weak transcription	Fetal Heart	heart
3	chr6:102327200-102327600	Enhancers	GM12878-XiMat	blood
4	chr6:102327200-102331400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr6:102327400-102327800	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr6:102327400-102327800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr6:102327400-102328200	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr6:102327800-102328000	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr6:102327800-102328600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr6:102331400-102332000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr6:102331400-102332000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr6:102331400-102332000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr6:102331400-102333200	Enhancers	Muscle Satellite Cultured Cells	--
14	chr6:102331600-102332000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr6:102331600-102332400	Enhancers	Fetal Heart	heart
16	chr6:102332000-102333000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr6:102333000-102333200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr6:102335400-102335800	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr6:102340000-102340400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr6:102345600-102346800	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr6:102354600-102355600	Enhancers	Liver	Liver
22	chr6:102355200-102356000	Enhancers	HepG2	liver
23	chr6:102355600-102356000	Flanking Active TSS	Liver	Liver
24	chr6:102358600-102359000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr6:102358800-102360800	Enhancers	Cortex derived primary cultured neurospheres	brain
26	chr6:102359000-102360000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr6:102360000-102360600	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr6:102360200-102360600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr6:102360200-102360600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr6:102360200-102360600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr6:102360200-102360600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr6:102360600-102360800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr6:102370600-102370800	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr6:102371000-102372400	Weak transcription	HUES48 Cell Line	embryonic stem cell
35	chr6:102372400-102372800	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr6:102374600-102374800	Enhancers	Liver	Liver
37	chr6:102376600-102377200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr6:102377200-102379200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr6:102379200-102380200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr6:102379400-102380000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr6:102379600-102381200	Enhancers	Liver	Liver
42	chr6:102380200-102385000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr6:102381000-102382400	Active TSS	Skeletal Muscle Female	skeletal muscle
44	chr6:102381200-102383600	Weak transcription	Liver	Liver
45	chr6:102383200-102385800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr6:102383600-102384000	Enhancers	Liver	Liver
47	chr6:102384400-102385200	Enhancers	Cortex derived primary cultured neurospheres	brain
48	chr6:102385000-102385400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr6:102385000-102385400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr6:102387800-102388200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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