Variant report

Variant	esv2756847
Chromosome Location	chr1:77238418-77302885
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	CEBPB	chr1:77248403-77248809	HepG2	liver:	n/a	chr1:77248584-77248593 chr1:77248582-77248595 chr1:77248582-77248595 chr1:77248582-77248593 chr1:77248584-77248593 chr1:77248582-77248593 chr1:77248583-77248594 chr1:77248584-77248593 chr1:77248584-77248593 chr1:77248582-77248595
2	CEBPB	chr1:77256460-77256657	A549	lung:	n/a	n/a
3	CEBPB	chr1:77248438-77248766	A549	lung:	n/a	chr1:77248584-77248593 chr1:77248582-77248595 chr1:77248582-77248595 chr1:77248582-77248593 chr1:77248584-77248593 chr1:77248582-77248593 chr1:77248583-77248594 chr1:77248584-77248593 chr1:77248584-77248593 chr1:77248582-77248595
4	CEBPB	chr1:77248431-77248783	IMR90	lung:	n/a	chr1:77248584-77248593 chr1:77248582-77248595 chr1:77248582-77248595 chr1:77248582-77248593 chr1:77248584-77248593 chr1:77248582-77248593 chr1:77248583-77248594 chr1:77248584-77248593 chr1:77248584-77248593 chr1:77248582-77248595
5	CEBPB	chr1:77249976-77250146	A549	lung:	n/a	chr1:77250003-77250014 chr1:77250003-77250016
6	CEBPB	chr1:77248449-77248821	Hela-S3	cervix:	n/a	chr1:77248584-77248593 chr1:77248582-77248595 chr1:77248582-77248595 chr1:77248582-77248593 chr1:77248584-77248593 chr1:77248582-77248593 chr1:77248583-77248594 chr1:77248584-77248593 chr1:77248584-77248593 chr1:77248582-77248595
7	CHD1	chr1:77287433-77287446	H1-hESC	embryonic stem cell:	n/a	n/a
8	CTCF	chr1:77263300-77263450	WERI-Rb-1	eye:	n/a	n/a
9	CTCF	chr1:77251256-77251289	GM13976	blood:	n/a	n/a
10	CTCF	chr1:77288453-77288539	GM20000	blood:	n/a	n/a
11	CTCF	chr1:77263258-77263437	Medullo	brain:	n/a	n/a
12	CTCF	chr1:77249200-77249350	GM12869	blood:	n/a	n/a
13	CTCF	chr1:77257140-77257290	GM12869	blood:	n/a	n/a
14	CTCF	chr1:77299775-77299849	ProgFib	skin:	n/a	n/a
15	E2F4	chr1:77301559-77301645	MCF10A-Er-Src	breast:	n/a	n/a
16	E2F4	chr1:77293467-77293654	MCF10A-Er-Src	breast:	n/a	n/a
17	E2F4	chr1:77291860-77292116	MCF10A-Er-Src	breast:	n/a	n/a
18	E2F4	chr1:77239360-77239543	MCF10A-Er-Src	breast:	n/a	n/a
19	E2F4	chr1:77248453-77248759	MCF10A-Er-Src	breast:	n/a	n/a
20	EBF1	chr1:77296296-77296313	GM12878	blood:	n/a	n/a
21	EP300	chr1:77267261-77268598	SK-N-SH	brain:	n/a	n/a
22	EP300	chr1:77298289-77298459	SK-N-SH_RA	brain:	n/a	n/a
23	EP300	chr1:77265015-77267069	SK-N-SH	brain:	n/a	n/a
24	EP300	chr1:77296086-77296411	SK-N-SH_RA	brain:	n/a	n/a
25	EP300	chr1:77291698-77292084	SK-N-SH_RA	brain:	n/a	n/a
26	EP300	chr1:77251899-77252545	SK-N-SH_RA	brain:	n/a	chr1:77252175-77252184 chr1:77252044-77252052
27	EP300	chr1:77300784-77301276	SK-N-SH_RA	brain:	n/a	n/a
28	EP300	chr1:77291683-77292101	SK-N-SH_RA	brain:	n/a	n/a
29	EP300	chr1:77259256-77259531	SK-N-SH_RA	brain:	n/a	n/a
30	EP300	chr1:77267724-77268202	SK-N-SH_RA	brain:	n/a	n/a
31	EP300	chr1:77259152-77259753	SK-N-SH	brain:	n/a	chr1:77259700-77259710
32	EP300	chr1:77251856-77252535	SK-N-SH_RA	brain:	n/a	chr1:77252175-77252184 chr1:77252044-77252052
33	EP300	chr1:77300824-77301276	SK-N-SH_RA	brain:	n/a	n/a
34	EP300	chr1:77291569-77292273	SK-N-SH	brain:	n/a	n/a
35	EP300	chr1:77265472-77265699	SK-N-SH_RA	brain:	n/a	n/a
36	EP300	chr1:77267779-77268107	SK-N-SH_RA	brain:	n/a	n/a
37	FOS	chr1:77264831-77265045	MCF10A-Er-Src	breast:	n/a	chr1:77264978-77264985 chr1:77264978-77264987 chr1:77264978-77264986 chr1:77264976-77264987 chr1:77264977-77264986
38	FOS	chr1:77289808-77290194	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr1:77289886-77290139	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr1:77264868-77265076	HUVEC	blood vessel:	n/a	chr1:77264978-77264985 chr1:77264978-77264987 chr1:77264978-77264986 chr1:77264976-77264987 chr1:77264977-77264986
41	FOS	chr1:77291710-77292437	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr1:77248499-77248807	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr1:77291700-77292595	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr1:77301051-77301265	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr1:77298821-77299159	MCF10A-Er-Src	breast:	n/a	chr1:77298991-77299000 chr1:77298990-77299000 chr1:77298991-77298999 chr1:77298992-77298999
46	FOS	chr1:77264936-77265025	MCF10A-Er-Src	breast:	n/a	chr1:77264978-77264985 chr1:77264978-77264987 chr1:77264978-77264986 chr1:77264976-77264987 chr1:77264977-77264986
47	FOS	chr1:77300977-77301279	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr1:77248426-77248902	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr1:77248426-77248810	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr1:77252120-77252320	MCF10A-Er-Src	breast:	n/a	chr1:77252175-77252185 chr1:77252175-77252185 chr1:77252175-77252185 chr1:77252175-77252185 chr1:77252176-77252185

No.	Distal block	Cell Line	Cell type
1	chr1:77268124..77270530-chr1:77274080..77275666,2	MCF-7	breast:
2	chr1:77297526..77298368-chr2:54890998..54891931,2	MCF-7	breast:
3	chr1:77263566..77264086-chr12:6643239..6643753,2	HCT-116	colon:
4	chr1:77169289..77170251-chr1:77243231..77243897,2	MCF-7	breast:
5	chr1:77268124..77270530-chr1:77274080..77275666,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PIGK-2	chr1:77244675-77244952	XLOC_000873

Variant related genes	Relation type
ENSG00000237552	TF binding region
ENSG00000111640	chromatin interactions

Extended variants
information (count: 1856 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:1856 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6687408	chr1:77238418-77238419	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs532403260	chr1:77238427-77238428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs34624638	chr1:77238429-77238430	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs189794731	chr1:77238458-77238459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs181467449	chr1:77238461-77238462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs543756862	chr1:77238479-77238480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs184623373	chr1:77238499-77238500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs574388538	chr1:77238545-77238546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs144654984	chr1:77238621-77238622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs148592140	chr1:77238624-77238625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs527455964	chr1:77238631-77238632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs546038387	chr1:77238634-77238635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs7530899	chr1:77238731-77238732	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs531641560	chr1:77238734-77238735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs540070513	chr1:77238777-77238778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs530130738	chr1:77238822-77238823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs532974485	chr1:77238827-77238828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs550146838	chr1:77238958-77238959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs569227654	chr1:77238959-77238960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs61783193	chr1:77238963-77238964	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs548633762	chr1:77238975-77238976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs566867421	chr1:77239000-77239001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs534361818	chr1:77239002-77239003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs563677181	chr1:77239005-77239006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs112471413	chr1:77239098-77239099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs188300446	chr1:77239134-77239135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs115032803	chr1:77239140-77239141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs376641719	chr1:77239161-77239162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs538138116	chr1:77239206-77239207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs556470959	chr1:77239236-77239237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs143027612	chr1:77239268-77239269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs535128001	chr1:77239291-77239292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs553798834	chr1:77239330-77239331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs572058722	chr1:77239333-77239334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs545974783	chr1:77239335-77239336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs564270284	chr1:77239448-77239449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs552630144	chr1:77239453-77239454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs566188456	chr1:77239493-77239494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs576346713	chr1:77239517-77239518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs146134344	chr1:77239557-77239558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs561856018	chr1:77239560-77239561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs530069858	chr1:77239586-77239587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs560586080	chr1:77239588-77239589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs180769421	chr1:77239641-77239642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs553760755	chr1:77239652-77239653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs569936279	chr1:77239678-77239679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs528615976	chr1:77239728-77239729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs78723925	chr1:77239773-77239774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs113265504	chr1:77239802-77239803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs186450647	chr1:77239829-77239830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:103)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Ewing''s sarcoma	17952124	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:107 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:77238200-77243600	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr1:77243400-77243600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr1:77243600-77243800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr1:77243600-77244000	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr1:77243600-77244600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr1:77243600-77244800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr1:77243600-77246600	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr1:77243800-77245000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr1:77244600-77244800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr1:77244800-77245000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr1:77244800-77245400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr1:77245000-77245800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr1:77245000-77245800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr1:77245000-77245800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr1:77245400-77251200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr1:77245800-77246800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr1:77245800-77246800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr1:77246400-77247400	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr1:77246600-77247200	Weak transcription	Cortex derived primary cultured neurospheres	brain
20	chr1:77246800-77247000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr1:77246800-77247000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr1:77246800-77247200	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr1:77247000-77250000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr1:77247200-77247400	Enhancers	Cortex derived primary cultured neurospheres	brain
25	chr1:77247400-77247600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr1:77247400-77247800	Enhancers	Fetal Brain Male	brain
27	chr1:77247800-77249000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr1:77249000-77249400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr1:77249000-77255800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr1:77249800-77250000	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
31	chr1:77250000-77250200	Bivalent/Poised TSS	ES-UCSF4 Cell Line	embryonic stem cell
32	chr1:77251200-77252600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr1:77251600-77252400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr1:77252000-77252400	Enhancers	Fetal Lung	lung
35	chr1:77252400-77254600	Weak transcription	Fetal Lung	lung
36	chr1:77254600-77255000	Enhancers	Fetal Lung	lung
37	chr1:77263200-77264400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr1:77263600-77264000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr1:77264000-77266800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr1:77265400-77265800	Enhancers	Fetal Lung	lung
41	chr1:77265600-77266000	Enhancers	Brain Germinal Matrix	brain
42	chr1:77266800-77268000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr1:77268000-77273000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr1:77273000-77273400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr1:77273000-77273600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr1:77273000-77274200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr1:77273200-77274200	Enhancers	NHDF-Ad	bronchial
48	chr1:77273400-77278400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr1:77278200-77278400	Enhancers	Spleen	Spleen
50	chr1:77278400-77279200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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