Variant report

Variant	rs592712
Chromosome Location	chr11:85470941-85470942
allele	C/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	chr11:85470887-85471251	MCF-7	breast:	n/a	n/a
2	GATA3	chr11:85470753-85471433	SK-N-SH	brain:	n/a	chr11:85470981-85470991
3	EP300	chr11:85470737-85471491	SK-N-SH	brain:	n/a	chr11:85470810-85470824
4	CEBPB	chr11:85470917-85471335	IMR90	lung:	n/a	n/a
5	MAX	chr11:85470840-85471465	HCT-116	colon:	n/a	n/a
6	NR3C1	chr11:85470936-85471233	A549	lung:	n/a	n/a
7	GATA3	chr11:85470729-85471527	SK-N-SH	brain:	n/a	chr11:85470981-85470991
8	JUND	chr11:85470928-85471461	SK-N-SH	brain:	n/a	n/a
9	FOSL2	chr11:85470790-85471425	SK-N-SH	brain:	n/a	chr11:85470812-85470821
10	CEBPB	chr11:85470939-85471214	ECC-1	luminal epithelium:	n/a	n/a
11	SP1	chr11:85470862-85471378	A549	lung:	n/a	n/a
12	MAX	chr11:85470898-85471399	SK-N-SH	brain:	n/a	n/a
13	POLR2A	chr11:85470924-85470981	MCF10A-Er-Src	breast:	n/a	n/a
14	PBX3	chr11:85470827-85471498	SK-N-SH	brain:	n/a	n/a
15	TCF12	chr11:85470800-85471394	SK-N-SH	brain:	n/a	n/a
16	TCF12	chr11:85470743-85471500	SK-N-SH	brain:	n/a	n/a
17	CEBPB	chr11:85470922-85471280	Hela-S3	cervix:	n/a	n/a
18	MAX	chr11:85470850-85471316	SK-N-SH	brain:	n/a	n/a
19	POLR2A	chr11:85470868-85471354	SK-N-SH	brain:	n/a	n/a
20	CEBPB	chr11:85470816-85471428	HCT-116	colon:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:85466013..85467547-chr11:85470379..85472711,2	MCF-7	breast:
2	chr11:85470667..85472897-chr11:85479422..85481165,2	K562	blood:
3	chr11:85470232..85471819-chr11:85473605..85475832,2	K562	blood:
4	chr11:85470232..85472552-chr11:85473605..85477376,4	K562	blood:
5	chr11:85469322..85470979-chr11:85520431..85523173,2	MCF-7	breast:

Variant related genes	Relation type
SYTL2	TF binding region
ENSG00000137501	Chromatin interaction

Extended variants
information (count: 108 )
Associated
traits (count: 5 )

rSNPs within LD-proxies of this variant (count:86)

rs_ID	r²[population]
rs10501595	0.88[JPT][hapmap]
rs10898410	0.81[CEU][hapmap]
rs11234410	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1151152	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11604141	0.95[CHB][hapmap];0.97[CHD][hapmap];0.88[JPT][hapmap];0.88[ASN][1000 genomes]
rs11604178	0.88[ASN][1000 genomes]
rs1192	0.82[JPT][hapmap]
rs1214001	0.82[JPT][hapmap]
rs12419172	0.88[JPT][hapmap]
rs12792050	0.80[AFR][1000 genomes];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1445513	0.95[CHB][hapmap];0.88[JPT][hapmap];0.88[ASN][1000 genomes]
rs17208492	0.88[JPT][hapmap]
rs17208519	0.88[JPT][hapmap]
rs17810659	0.88[JPT][hapmap]
rs17817179	0.90[CHB][hapmap];0.94[CHD][hapmap];0.82[JPT][hapmap]
rs188311	0.96[CEU][hapmap];0.84[CHB][hapmap];0.88[CHD][hapmap];0.86[GIH][hapmap];0.94[JPT][hapmap];0.84[TSI][hapmap]
rs1892872	0.88[JPT][hapmap]
rs1991923	0.88[JPT][hapmap]
rs2290823	0.88[JPT][hapmap]
rs2374683	0.81[CEU][hapmap]
rs2467059	0.94[JPT][hapmap]
rs290173	0.84[CEU][hapmap]
rs290175	0.96[CEU][hapmap];0.84[CHB][hapmap];0.94[JPT][hapmap]
rs290177	0.94[JPT][hapmap]
rs290182	0.88[JPT][hapmap]
rs290186	0.94[JPT][hapmap]
rs290190	0.91[CEU][hapmap]
rs290194	0.96[CEU][hapmap];0.84[CHB][hapmap];0.94[JPT][hapmap]
rs290195	0.87[CEU][hapmap]
rs290196	0.95[CEU][hapmap];0.84[CHB][hapmap];0.94[JPT][hapmap]
rs290199	0.91[CEU][hapmap];0.80[CHB][hapmap];0.94[JPT][hapmap]
rs290200	0.83[CEU][hapmap]
rs290202	0.92[CEU][hapmap]
rs3862785	0.84[CHB][hapmap]
rs491867	0.83[CEU][hapmap]
rs493673	0.82[ASN][1000 genomes]
rs4943925	0.80[CHB][hapmap];0.93[JPT][hapmap]
rs4944529	0.88[JPT][hapmap]
rs4944531	0.88[JPT][hapmap]
rs4944539	0.91[CHD][hapmap]
rs496187	0.83[CEU][hapmap]
rs497158	0.83[ASN][1000 genomes]
rs510948	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap];0.89[TSI][hapmap];0.96[ASN][1000 genomes]
rs520629	0.91[CEU][hapmap];0.89[CHB][hapmap];0.97[CHD][hapmap];0.82[GIH][hapmap];0.88[JPT][hapmap];0.84[TSI][hapmap];0.89[ASN][1000 genomes]
rs521764	0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs537266	0.96[CEU][hapmap];0.90[CHB][hapmap];0.85[CHD][hapmap];0.86[GIH][hapmap];0.94[JPT][hapmap];0.89[TSI][hapmap]
rs537604	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.82[GIH][hapmap];1.00[JPT][hapmap];0.89[TSI][hapmap];0.96[ASN][1000 genomes]
rs540063	0.87[CEU][hapmap]
rs543995	0.87[ASN][1000 genomes]
rs550404	0.87[CEU][hapmap];0.86[YRI][hapmap]
rs556669	0.87[CEU][hapmap]
rs558377	0.88[ASN][1000 genomes]
rs565494	0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs56579	0.94[JPT][hapmap]
rs573766	0.91[CEU][hapmap];0.83[CHB][hapmap];1.00[JPT][hapmap]
rs578324	0.96[CEU][hapmap];0.90[CHB][hapmap];0.91[CHD][hapmap];0.95[GIH][hapmap];0.94[JPT][hapmap];0.88[MEX][hapmap];0.92[TSI][hapmap];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs580459	0.87[CEU][hapmap]
rs583122	0.90[CEU][hapmap];0.90[CHB][hapmap];0.94[JPT][hapmap];0.88[ASN][1000 genomes]
rs589327	0.95[CEU][hapmap]
rs592380	0.88[ASN][1000 genomes]
rs597480	0.92[CEU][hapmap]
rs609012	1.00[ASW][hapmap];0.96[CEU][hapmap];0.90[CHB][hapmap];0.94[CHD][hapmap];0.95[GIH][hapmap];0.88[JPT][hapmap];0.98[LWK][hapmap];0.88[MEX][hapmap];1.00[MKK][hapmap];0.92[TSI][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs613973	0.96[CEU][hapmap];0.87[CHB][hapmap];0.92[JPT][hapmap];0.87[YRI][hapmap];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs61907272	0.80[ASN][1000 genomes]
rs631104	0.96[ASN][1000 genomes]
rs631410	0.91[CEU][hapmap]
rs639688	0.91[CEU][hapmap];0.95[CHB][hapmap];0.97[CHD][hapmap];0.84[GIH][hapmap];0.94[JPT][hapmap];0.81[TSI][hapmap];0.90[ASN][1000 genomes]
rs641393	0.92[CEU][hapmap]
rs644558	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs644972	0.91[CEU][hapmap]
rs647912	0.91[CEU][hapmap]
rs650036	1.00[ASW][hapmap];0.96[CEU][hapmap];0.95[CHB][hapmap];0.94[CHD][hapmap];0.93[GIH][hapmap];0.94[JPT][hapmap];1.00[LWK][hapmap];0.96[MEX][hapmap];0.92[MKK][hapmap];0.89[TSI][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs650970	0.92[ASN][1000 genomes]
rs653559	0.91[CEU][hapmap];0.95[CHB][hapmap];0.85[CHD][hapmap];0.89[GIH][hapmap];0.94[JPT][hapmap];0.84[TSI][hapmap];0.87[ASN][1000 genomes]
rs666176	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs667080	0.83[ASN][1000 genomes]
rs679204	0.96[CEU][hapmap]
rs680498	0.91[CEU][hapmap]
rs681044	0.96[CEU][hapmap];0.95[CHB][hapmap];0.88[JPT][hapmap];0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs683903	0.87[ASN][1000 genomes]
rs688741	0.96[CEU][hapmap];0.84[CHB][hapmap];0.91[CHD][hapmap];0.95[GIH][hapmap];0.94[JPT][hapmap];0.88[MEX][hapmap];0.92[TSI][hapmap];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7119617	0.82[JPT][hapmap]
rs7943586	0.88[JPT][hapmap]
rs881121	0.88[JPT][hapmap]
rs947861	0.88[JPT][hapmap]
rs947863	0.88[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:22 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1051155	chr11:85006564-85721261	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
2	nsv541110	chr11:85006564-85721261	Enhancers Strong transcription Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
3	esv2758279	chr11:85180480-85603988	Flanking Active TSS Active TSS Weak transcription Enhancers Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
4	esv2759845	chr11:85180480-85603988	Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
5	nsv832222	chr11:85405712-85603981	Enhancers Active TSS Bivalent Enhancer Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
6	nsv898050	chr11:85406915-85499290	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv1052123	chr11:85425856-85471132	Enhancers Genic enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	nsv555633	chr11:85426330-85473883	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
9	nsv1036110	chr11:85429074-85471132	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
10	nsv1054027	chr11:85429074-85477283	Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
11	esv3471508	chr11:85429687-85472395	Active TSS Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
12	esv3471519	chr11:85429687-85472395	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
13	nsv1047001	chr11:85433687-85470941	Enhancers Weak transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
14	nsv1042942	chr11:85433687-85471132	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
15	nsv1048844	chr11:85434057-85470941	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
16	nsv1051644	chr11:85434057-85471132	Genic enhancers Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
17	nsv555639	chr11:85436352-85495269	Enhancers Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
18	nsv1048750	chr11:85436840-85471132	Enhancers Genic enhancers Active TSS Strong transcription Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
19	esv2757459	chr11:85436868-85473347	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
20	nsv1047147	chr11:85459235-85594800	Flanking Active TSS Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
21	nsv541114	chr11:85459235-85594800	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
22	esv2762927	chr11:85468051-85559618	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases

mRNA abundance (count:5)

SNP	Gene	Cis/trans	Tissue	Source
rs592712	SYTL2	cis	lymphoblastoid	seeQTL
rs592712	SYTL2	cis	cerebellum	SCAN
rs592712	CCT4	trans	parietal	SCAN
rs592712	SYTL2	cis	Muscle Skeletal	GTEx
rs592712	ME3	cis	cerebellum	SCAN

Chromatin state (count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:85430400-85480400	Weak transcription	Aorta	Aorta
2	chr11:85448000-85480600	Weak transcription	Fetal Stomach	stomach
3	chr11:85449200-85478400	Weak transcription	Right Ventricle	heart
4	chr11:85453000-85471000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr11:85460600-85483800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr11:85461600-85471000	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr11:85462000-85471000	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr11:85463200-85478800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr11:85463400-85472400	Weak transcription	Fetal Muscle Leg	muscle
10	chr11:85464400-85471000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr11:85464600-85471800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
12	chr11:85464600-85472600	Enhancers	Primary T helper cells fromperipheralblood	blood
13	chr11:85467600-85471800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
14	chr11:85467600-85472200	Enhancers	Primary T helper cells PMA-I stimulated	--
15	chr11:85467600-85477600	Weak transcription	Sigmoid Colon	Sigmoid Colon
16	chr11:85467800-85472000	Enhancers	Primary T cells from cord blood	blood
17	chr11:85467800-85472200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
18	chr11:85468000-85472600	Enhancers	Primary T helper naive cells from peripheral blood	blood
19	chr11:85468800-85471000	Weak transcription	Small Intestine	intestine
20	chr11:85468800-85472000	Weak transcription	Psoas Muscle	Psoas
21	chr11:85469200-85471000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
22	chr11:85469200-85471600	Weak transcription	Brain Inferior Temporal Lobe	brain
23	chr11:85469400-85471000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
24	chr11:85469400-85471000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr11:85469400-85471200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr11:85469400-85471400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr11:85469400-85471800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
28	chr11:85469400-85472400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr11:85469400-85472400	Weak transcription	Gastric	stomach
30	chr11:85469400-85485400	Weak transcription	Rectal Mucosa Donor 29	rectum
31	chr11:85469800-85471000	Weak transcription	Stomach Mucosa	stomach
32	chr11:85469800-85477000	Weak transcription	Duodenum Mucosa	Duodenum
33	chr11:85469800-85477800	Weak transcription	Rectal Mucosa Donor 31	rectum
34	chr11:85470000-85471000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
35	chr11:85470200-85471000	Weak transcription	Primary T cells fromperipheralblood	blood
36	chr11:85470200-85472200	Enhancers	Fetal Kidney	kidney
37	chr11:85470400-85471800	Enhancers	A549	lung
38	chr11:85470400-85473600	Enhancers	NHDF-Ad	bronchial
39	chr11:85470400-85473800	Enhancers	HMEC	breast
40	chr11:85470600-85471000	Weak transcription	Skeletal Muscle Female	skeletal muscle
41	chr11:85470600-85471800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr11:85470600-85471800	Enhancers	Primary T killer memory cells from peripheral blood	blood
43	chr11:85470600-85471800	Enhancers	Hela-S3	cervix
44	chr11:85470600-85471800	Enhancers	NHEK	skin
45	chr11:85470600-85472000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr11:85470600-85472000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr11:85470600-85472000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
48	chr11:85470600-85472600	Enhancers	HSMM	muscle
49	chr11:85470800-85471200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr11:85470800-85471400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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