Variant report

Variant	rs499188
Chromosome Location	chr11:57434122-57434123
allele	G/T
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	chr11:57433949-57435625	Hela-S3	cervix:	n/a	chr11:57435144-57435161 chr11:57434007-57434018 chr11:57435270-57435278
2	CEBPB	chr11:57433873-57434405	HepG2	liver:	n/a	chr11:57434007-57434018
3	POLR2A	chr11:57434105-57435969	U87	brain:	n/a	n/a
4	SP1	chr11:57434077-57436206	HCT-116	colon:	n/a	chr11:57434555-57434567 chr11:57434556-57434565 chr11:57435446-57435467 chr11:57435268-57435289
5	STAT3	chr11:57434062-57434403	MCF10A-Er-Src	breast:	n/a	chr11:57434217-57434238 chr11:57434222-57434233 chr11:57434218-57434238
6	ZNF384	chr11:57434051-57435838	K562	blood:	n/a	n/a
7	POLR2A	chr11:57434030-57436393	PFSK-1	brain:	n/a	n/a
8	REST	chr11:57434068-57436003	HL-60	blood:	n/a	chr11:57435543-57435556 chr11:57435908-57435921 chr11:57435908-57435921
9	MAX	chr11:57434068-57436263	HepG2	liver:	n/a	n/a
10	JUN	chr11:57433825-57437028	K562	blood:	n/a	chr11:57435449-57435458 chr11:57435783-57435797 chr11:57435546-57435555 chr11:57435271-57435280
11	TBP	chr11:57434092-57435876	Hela-S3	cervix:	n/a	n/a
12	MAZ	chr11:57434060-57436738	IMR90	lung:	n/a	n/a
13	MYBL2	chr11:57434087-57435882	HepG2	liver:	n/a	n/a
14	MYC	chr11:57434118-57435919	A549	lung:	n/a	n/a
15	RELA	chr11:57434102-57436334	GM12891	blood:	n/a	n/a
16	MYC	chr11:57434097-57435653	MCF10A-Er-Src	breast:	n/a	n/a
17	POLR2A	chr11:57434024-57436095	HUVEC	blood vessel:	n/a	n/a
18	CEBPB	chr11:57433869-57434354	IMR90	lung:	n/a	chr11:57434007-57434018
19	ELF1	chr11:57434102-57436009	GM12878	blood:	n/a	chr11:57435689-57435698 chr11:57435377-57435386 chr11:57435948-57435960 chr11:57435688-57435699 chr11:57435566-57435578 chr11:57435539-57435548 chr11:57434554-57434566 chr11:57435149-57435160
20	STAT3	chr11:57433934-57434458	MCF10A-Er-Src	breast:	n/a	chr11:57434217-57434238 chr11:57434222-57434233 chr11:57434218-57434238
21	CEBPB	chr11:57433853-57434417	A549	lung:	n/a	chr11:57434007-57434018
22	SREBP1	chr11:57433965-57437117	GM12878	blood:	n/a	n/a
23	MAX	chr11:57434122-57435961	ECC-1	luminal epithelium:	n/a	n/a
24	POLR2A	chr11:57434072-57436738	PFSK-1	brain:	n/a	n/a
25	EP300	chr11:57434116-57434199	HepG2	liver:	n/a	n/a
26	REST	chr11:57434099-57436333	H1-neurons	neurons:	n/a	chr11:57435543-57435556 chr11:57435908-57435921 chr11:57436142-57436160 chr11:57435908-57435921
27	POLR2A	chr11:57434055-57436358	HL-60	blood:	n/a	n/a
28	POLR2A	chr11:57434037-57436441	GM12878	blood:	n/a	n/a
29	POLR2A	chr11:57434054-57436216	SK-N-MC	brain:	n/a	n/a
30	MTA3	chr11:57433963-57436684	GM12878	blood:	n/a	n/a
31	POLR2A	chr11:57434095-57436818	MCF10A-Er-Src	breast:	n/a	n/a
32	CEBPB	chr11:57433841-57434202	K562	blood:	n/a	chr11:57434007-57434018
33	MAX	chr11:57434096-57436350	Hela-S3	cervix:	n/a	n/a
34	MAX	chr11:57434057-57436498	A549	lung:	n/a	n/a
35	HCFC1	chr11:57433860-57436999	Hela-S3	cervix:	n/a	n/a
36	POLR2A	chr11:57434122-57436773	Hela-S3	cervix:	n/a	n/a
37	POLR2A	chr11:57434031-57436579	GM12891	blood:	n/a	n/a
38	POLR2A	chr11:57434120-57436357	Hela-S3	cervix:	n/a	n/a
39	POLR2A	chr11:57433643-57436169	HepG2	liver:	n/a	n/a
40	CHD1	chr11:57433867-57436848	IMR90	lung:	n/a	n/a
41	JUND	chr11:57434029-57436175	SK-N-SH	brain:	n/a	chr11:57435449-57435458 chr11:57435783-57435797 chr11:57435546-57435555 chr11:57435271-57435280
42	CEBPB	chr11:57433840-57434408	K562	blood:	n/a	chr11:57434007-57434018
43	MYC	chr11:57434051-57435949	NB4	blood:	n/a	n/a
44	NR2F2	chr11:57434019-57436152	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:57423375..57427275-chr11:57433374..57437610,8	MCF-7	breast:
2	chr11:57431371..57436913-chr11:57505728..57511660,10	K562	blood:
3	chr11:57433532..57435196-chr11:57508492..57510425,2	MCF-7	breast:
4	chr11:57433936..57437289-chr11:57477964..57482818,9	K562	blood:
5	chr11:57433251..57435131-chr11:58346916..58348765,2	K562	blood:
6	chr11:57281807..57284360-chr11:57431208..57434169,2	K562	blood:
7	chr11:57433884..57439071-chr11:57477629..57483930,15	K562	blood:
8	chr11:57243239..57245827-chr11:57433789..57436480,2	K562	blood:
9	chr11:57433251..57437103-chr11:58344962..58348416,5	K562	blood:
10	chr11:57423095..57430151-chr11:57432283..57438412,24	K562	blood:
11	chr11:57424563..57426708-chr11:57434107..57436084,3	MCF-7	breast:
12	chr11:57433015..57436358-chr11:57440099..57444661,8	MCF-7	breast:
13	chr11:57434008..57435608-chr11:57507270..57509557,2	MCF-7	breast:
14	chr11:57433212..57437810-chr11:57477098..57481918,8	MCF-7	breast:

Variant related genes	Relation type
ZDHHC5	TF binding region
ENSG00000213593	Chromatin interaction
ENSG00000172409	Chromatin interaction
ENSG00000255073	Chromatin interaction
ENSG00000254732	Chromatin interaction
ENSG00000254462	Chromatin interaction
ENSG00000186660	Chromatin interaction
ENSG00000255301	Chromatin interaction
ENSG00000156599	Chromatin interaction
ENSG00000211450	Chromatin interaction
ENSG00000110031	Chromatin interaction
ENSG00000156603	Chromatin interaction
ENSG00000149150	Chromatin interaction

Extended variants
information (count: 67 )
Associated
traits (count: 9 )

rSNPs within LD-proxies of this variant (count:60)

rs_ID	r²[population]
rs10792112	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10896633	0.95[CEU][hapmap];0.89[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.93[MEX][hapmap];0.94[TSI][hapmap];0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10896636	0.95[CEU][hapmap];0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10896647	0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11229066	1.00[JPT][hapmap]
rs11229067	1.00[JPT][hapmap]
rs11229113	0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11229116	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11229130	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11229131	0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11229148	0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11570190	1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[CHD][hapmap];0.82[GIH][hapmap];1.00[JPT][hapmap];0.93[MEX][hapmap];0.94[TSI][hapmap];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11601320	0.83[ASN][1000 genomes]
rs11601449	0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11602109	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11603020	0.82[CHD][hapmap];1.00[JPT][hapmap]
rs11604325	0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11604333	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11605731	1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11606396	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11606677	1.00[JPT][hapmap]
rs11607056	1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[CHD][hapmap];0.82[GIH][hapmap];1.00[JPT][hapmap];0.93[MEX][hapmap];1.00[TSI][hapmap];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12146541	0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12362166	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12785533	0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12790196	0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12804972	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12805841	1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12807250	1.00[CEU][hapmap];0.84[CHB][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1647405	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17455520	0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2081361	0.85[CHB][hapmap];1.00[JPT][hapmap]
rs2847308	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2926656	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs35808061	0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs3781885	0.83[EUR][1000 genomes]
rs3824988	0.82[CHD][hapmap];1.00[JPT][hapmap]
rs4827	0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs488769	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4926	1.00[JPT][hapmap]
rs527528	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs543725	0.93[AFR][1000 genomes];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs547891	0.83[AFR][1000 genomes];0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs576859	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.97[TSI][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6591434	0.85[ASN][1000 genomes]
rs682503	0.83[ASN][1000 genomes]
rs708228	1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[CHD][hapmap];0.82[GIH][hapmap];1.00[JPT][hapmap];0.93[MEX][hapmap];0.94[TSI][hapmap];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7116341	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7117205	0.83[ASN][1000 genomes]
rs7117878	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7121169	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7129727	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs71484461	0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs71484468	0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs731384	0.86[CHD][hapmap];1.00[JPT][hapmap];0.87[MEX][hapmap]
rs7932091	0.80[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7936998	0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7938083	0.93[EUR][1000 genomes]
rs7949841	0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9420	1.00[ASW][hapmap];0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.91[LWK][hapmap];0.93[MEX][hapmap];0.97[MKK][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap];0.81[AFR][1000 genomes];0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1044030	chr11:57073395-58035564	Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	136 gene(s)	inside rSNPs	diseases
2	nsv541047	chr11:57073395-58035564	Active TSS Enhancers Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	136 gene(s)	inside rSNPs	diseases
3	nsv530621	chr11:57139699-57703639	Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Weak transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	109 gene(s)	inside rSNPs	diseases
4	nsv832163	chr11:57299354-57481050	Strong transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
5	nsv1040913	chr11:57315006-57696122	Active TSS Flanking Active TSS Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	93 gene(s)	inside rSNPs	diseases
6	nsv832164	chr11:57407617-57578825	Enhancers Strong transcription Genic enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
7	nsv508633	chr11:57419585-57560045	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases

mRNA abundance (count:9)

SNP	Gene	Cis/trans	Tissue	Source
rs499188	LRRC55	cis	parietal	SCAN
rs499188	OR5T1	cis	cerebellum	SCAN
rs499188	MED19	Cis_1M	lymphoblastoid	RTeQTL
rs499188	OR4D10	cis	parietal	SCAN
rs499188	TIMM10	cis	parietal	SCAN
rs499188	DDB1	cis	cerebellum	SCAN
rs499188	MED19	cis	cerebellum	SCAN
rs499188	MS4A7	cis	parietal	SCAN
rs499188	PRG3	cis	parietal	SCAN

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:57426000-57434200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr11:57426000-57434200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr11:57428400-57434200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr11:57428800-57434200	Weak transcription	Fetal Brain Male	brain
5	chr11:57429000-57434200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr11:57429000-57434200	Weak transcription	Aorta	Aorta
7	chr11:57429000-57434200	Weak transcription	Esophagus	oesophagus
8	chr11:57429000-57434200	Weak transcription	Left Ventricle	heart
9	chr11:57429000-57434400	Weak transcription	Gastric	stomach
10	chr11:57429000-57434400	Weak transcription	Small Intestine	intestine
11	chr11:57429200-57434200	Weak transcription	Brain Substantia Nigra	brain
12	chr11:57429200-57434200	Weak transcription	Colonic Mucosa	Colon
13	chr11:57429600-57434200	Weak transcription	Ovary	ovary
14	chr11:57429800-57434200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr11:57430400-57434200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
16	chr11:57430600-57434200	Weak transcription	Thymus	Thymus
17	chr11:57430600-57434200	Weak transcription	Spleen	Spleen
18	chr11:57431400-57434200	Weak transcription	Fetal Stomach	stomach
19	chr11:57431400-57434400	Weak transcription	Lung	lung
20	chr11:57433600-57434200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
21	chr11:57433600-57434400	Enhancers	Stomach Mucosa	stomach
22	chr11:57433600-57434800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
23	chr11:57433800-57434200	Enhancers	Breast Myoepithelial Primary Cells	Breast
24	chr11:57433800-57434200	Enhancers	Primary T cells from cord blood	blood
25	chr11:57433800-57434200	Enhancers	Primary T cells fromperipheralblood	blood
26	chr11:57433800-57434200	Enhancers	Primary T helper cells PMA-I stimulated	--
27	chr11:57433800-57434200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
28	chr11:57433800-57434200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
29	chr11:57433800-57434200	Enhancers	Fetal Muscle Leg	muscle
30	chr11:57433800-57434200	Enhancers	Fetal Thymus	thymus
31	chr11:57433800-57434200	Enhancers	Pancreas	Pancrea
32	chr11:57433800-57434400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr11:57433800-57434400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr11:57433800-57434400	Enhancers	Placenta Amnion	Placenta Amnion
35	chr11:57433800-57434400	Flanking Active TSS	Hela-S3	cervix
36	chr11:57433800-57434400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
37	chr11:57433800-57434600	Flanking Active TSS	Dnd41	blood
38	chr11:57433800-57436600	Active TSS	iPS-18 Cell Line	embryonic stem cell
39	chr11:57434000-57434200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr11:57434000-57434200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr11:57434000-57434200	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
42	chr11:57434000-57434200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
43	chr11:57434000-57434200	Enhancers	Primary B cells from peripheral blood	blood
44	chr11:57434000-57434200	Enhancers	Primary T helper naive cells from peripheral blood	blood
45	chr11:57434000-57434200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
46	chr11:57434000-57434200	Enhancers	Primary T helper cells fromperipheralblood	blood
47	chr11:57434000-57434200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
48	chr11:57434000-57434200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
49	chr11:57434000-57434200	Enhancers	Primary T killer memory cells from peripheral blood	blood
50	chr11:57434000-57434200	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin

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