Variant report

Variant	rs575082
Chromosome Location	chr15:44110142-44110143
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr15:44082965..44094882-chr15:44108427..44121402,26	K562	blood:
2	chr15:44109520..44111190-chr15:44111853..44114212,2	K562	blood:
3	chr15:44109134..44111631-chr15:44115239..44117473,3	MCF-7	breast:
4	chr15:44103639..44105537-chr15:44108444..44110720,3	K562	blood:

Variant related genes	Relation type
ENSG00000140264	Chromatin interaction
ENSG00000184716	Chromatin interaction
ENSG00000221792	Chromatin interaction
ENSG00000140259	Chromatin interaction
ENSG00000242028	Chromatin interaction

Extended variants
information (count: 137 )
Associated
traits (count: 16 )

rSNPs within LD-proxies of this variant (count:126)

rs_ID	r²[population]
rs10163054	0.95[CHB][hapmap];0.92[CHD][hapmap];0.90[JPT][hapmap];0.83[ASN][1000 genomes]
rs10438303	1.00[CHB][hapmap];0.94[CHD][hapmap];0.95[JPT][hapmap]
rs1053492	1.00[CEU][hapmap];0.90[EUR][1000 genomes]
rs11070408	1.00[CHB][hapmap];0.94[CHD][hapmap];0.90[JPT][hapmap]
rs11070410	0.80[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];0.93[GIH][hapmap];0.95[JPT][hapmap];1.00[MEX][hapmap];0.97[TSI][hapmap];0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11070412	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11638972	1.00[CEU][hapmap];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11852840	0.92[ASN][1000 genomes]
rs11856495	0.91[ASN][1000 genomes]
rs11856795	1.00[CHB][hapmap];0.97[CHD][hapmap];0.84[JPT][hapmap];0.83[ASN][1000 genomes]
rs12101756	0.84[ASN][1000 genomes]
rs12440573	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs12441127	1.00[CHB][hapmap];0.90[JPT][hapmap]
rs12441861	1.00[CHB][hapmap];0.94[CHD][hapmap];0.95[JPT][hapmap];0.87[ASN][1000 genomes]
rs12441984	1.00[CHB][hapmap];0.95[JPT][hapmap];0.95[ASN][1000 genomes]
rs12442129	0.87[ASN][1000 genomes]
rs12443102	0.89[CHB][hapmap];0.88[JPT][hapmap]
rs12702	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs12899922	0.81[ASN][1000 genomes]
rs12908467	0.88[EUR][1000 genomes]
rs13380397	0.88[ASN][1000 genomes]
rs16950562	1.00[CHB][hapmap];0.95[JPT][hapmap]
rs16963953	0.95[ASN][1000 genomes]
rs16965120	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs16977724	1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[JPT][hapmap];0.94[ASN][1000 genomes]
rs16977798	1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[JPT][hapmap];0.94[ASN][1000 genomes]
rs1965794	0.87[ASN][1000 genomes]
rs1965795	0.94[ASN][1000 genomes]
rs1975364	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2228368	1.00[ASN][1000 genomes]
rs2277531	1.00[CHB][hapmap];0.95[JPT][hapmap];0.87[ASN][1000 genomes]
rs2411284	0.84[EUR][1000 genomes]
rs2412823	0.82[CEU][hapmap]
rs2447193	1.00[CHB][hapmap];0.90[JPT][hapmap]
rs2447208	1.00[CHB][hapmap];0.91[CHD][hapmap];0.90[JPT][hapmap]
rs2467402	0.95[CHB][hapmap];0.94[CHD][hapmap];0.95[JPT][hapmap]
rs2470121	1.00[CHB][hapmap];0.89[JPT][hapmap]
rs2614811	1.00[CHB][hapmap];0.90[JPT][hapmap]
rs2788	1.00[CHB][hapmap];0.94[CHD][hapmap];0.95[JPT][hapmap];0.87[ASN][1000 genomes]
rs28377539	0.87[ASN][1000 genomes]
rs28413704	0.94[ASN][1000 genomes]
rs28476182	0.94[ASN][1000 genomes]
rs28509275	1.00[CHB][hapmap];0.97[CHD][hapmap];0.95[JPT][hapmap];0.98[ASN][1000 genomes]
rs28513374	1.00[CHB][hapmap];0.95[ASN][1000 genomes]
rs28519630	0.94[ASN][1000 genomes]
rs28524541	0.95[ASN][1000 genomes]
rs28531819	0.95[ASN][1000 genomes]
rs28546844	0.90[ASN][1000 genomes]
rs28564774	0.95[ASN][1000 genomes]
rs28578398	0.93[ASN][1000 genomes]
rs28583806	1.00[ASN][1000 genomes]
rs28590651	0.98[ASN][1000 genomes]
rs28595038	0.85[ASN][1000 genomes]
rs28636829	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs28674750	0.98[ASN][1000 genomes]
rs28678901	0.94[ASN][1000 genomes]
rs28679673	0.95[ASN][1000 genomes]
rs28684672	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs28687459	0.95[ASN][1000 genomes]
rs28696802	0.95[ASN][1000 genomes]
rs28707214	0.95[ASN][1000 genomes]
rs28718261	0.85[ASN][1000 genomes]
rs28780699	0.95[ASN][1000 genomes]
rs28781888	0.95[ASN][1000 genomes]
rs28823973	0.86[ASN][1000 genomes]
rs28858500	0.85[ASN][1000 genomes]
rs28866846	0.93[ASN][1000 genomes]
rs28891769	0.93[ASN][1000 genomes]
rs2920781	0.90[CHB][hapmap];0.91[CHD][hapmap];0.90[JPT][hapmap]
rs2927071	0.95[CEU][hapmap];1.00[CHB][hapmap];0.91[CHD][hapmap];0.90[JPT][hapmap];1.00[MEX][hapmap];0.97[TSI][hapmap]
rs2927072	1.00[CHB][hapmap];0.90[JPT][hapmap]
rs2927085	0.86[CEU][hapmap]
rs2955969	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3087657	1.00[CEU][hapmap];0.86[GIH][hapmap];1.00[MEX][hapmap];0.97[TSI][hapmap];0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs3101443	1.00[CHB][hapmap];0.90[JPT][hapmap]
rs35654783	0.81[EUR][1000 genomes]
rs35866764	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs3736180	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs3742982	1.00[CHB][hapmap];0.81[ASN][1000 genomes]
rs3759790	1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[JPT][hapmap];0.95[ASN][1000 genomes]
rs3759791	0.95[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs3816792	0.95[CHB][hapmap];0.97[CHD][hapmap];0.95[JPT][hapmap];0.98[ASN][1000 genomes]
rs3825783	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs3862142	1.00[CHB][hapmap];0.91[CHD][hapmap];0.94[JPT][hapmap]
rs4332723	0.87[EUR][1000 genomes]
rs4617832	0.84[EUR][1000 genomes]
rs4924720	0.81[EUR][1000 genomes]
rs4924722	0.90[EUR][1000 genomes]
rs4997480	1.00[CHB][hapmap];0.95[JPT][hapmap]
rs524908	0.80[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.84[JPT][hapmap];0.81[MKK][hapmap];0.93[TSI][hapmap];0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs533143	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.84[JPT][hapmap];0.81[EUR][1000 genomes]
rs56008017	0.94[ASN][1000 genomes]
rs56909447	0.95[ASN][1000 genomes]
rs60883262	0.94[ASN][1000 genomes]
rs61390361	0.83[ASN][1000 genomes]
rs62018947	0.84[EUR][1000 genomes]
rs62018952	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs663214	1.00[CEU][hapmap];0.93[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs667476	0.91[CEU][hapmap];0.95[CHB][hapmap]
rs68079546	0.95[ASN][1000 genomes]
rs686666	0.95[CEU][hapmap];0.84[YRI][hapmap];0.89[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs688009	0.95[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.83[YRI][hapmap];0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs693919	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.93[LWK][hapmap];1.00[MEX][hapmap];0.90[MKK][hapmap];0.95[TSI][hapmap];0.88[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs694461	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7168158	0.85[ASN][1000 genomes]
rs7169322	1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[JPT][hapmap];0.94[ASN][1000 genomes]
rs7169382	1.00[ASN][1000 genomes]
rs7169988	0.90[CHB][hapmap];0.90[JPT][hapmap]
rs7170167	0.86[ASN][1000 genomes]
rs7170751	0.88[ASN][1000 genomes]
rs7171750	1.00[CHB][hapmap];0.94[JPT][hapmap]
rs7174208	1.00[CHB][hapmap];0.95[JPT][hapmap];0.85[ASN][1000 genomes]
rs7175032	1.00[CHB][hapmap];0.94[CHD][hapmap];0.95[JPT][hapmap];0.87[ASN][1000 genomes]
rs7175129	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.87[EUR][1000 genomes]
rs7178343	0.84[EUR][1000 genomes]
rs7179388	0.95[ASN][1000 genomes]
rs7180818	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7183809	0.95[ASN][1000 genomes]
rs8023458	1.00[CHB][hapmap];0.94[CHD][hapmap];0.95[JPT][hapmap]
rs8023508	1.00[CHB][hapmap];1.00[CHD][hapmap];0.85[JPT][hapmap];0.82[ASN][1000 genomes]
rs8032649	1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[JPT][hapmap];0.95[ASN][1000 genomes]
rs8034451	0.83[EUR][1000 genomes]
rs8040839	0.97[ASN][1000 genomes]
rs8042868	1.00[CHB][hapmap];0.91[CHD][hapmap];0.90[JPT][hapmap]
rs9944216	1.00[CHB][hapmap];0.91[CHD][hapmap];0.84[JPT][hapmap];0.83[ASN][1000 genomes]
rs9989313	1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[JPT][hapmap];0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1846172	chr15:43632138-44116986	Bivalent Enhancer Weak transcription Genic enhancers Strong transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	101 gene(s)	inside rSNPs	diseases
2	esv1846701	chr15:43759774-44116986	Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
3	esv2758379	chr15:43823158-44148641	Strong transcription Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	84 gene(s)	inside rSNPs	diseases
4	esv2760028	chr15:43823158-44148641	Genic enhancers Enhancers Active TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	84 gene(s)	inside rSNPs	diseases
5	nsv427960	chr15:43823158-44148641	Flanking Active TSS Active TSS Strong transcription Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Enhancers Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	84 gene(s)	inside rSNPs	diseases
6	nsv1037786	chr15:43888926-44318587	Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Enhancers Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
7	nsv542370	chr15:43888926-44318587	Weak transcription Genic enhancers Flanking Active TSS Active TSS Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
8	nsv431387	chr15:43929378-44862930	Weak transcription Strong transcription Active TSS ZNF genes & repeats Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	158 gene(s)	inside rSNPs	diseases
9	nsv931051	chr15:43988761-44833518	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	154 gene(s)	inside rSNPs	diseases
10	nsv1036318	chr15:44053617-44160773	Flanking Active TSS Strong transcription Genic enhancers Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	68 gene(s)	inside rSNPs	diseases
11	nsv1050263	chr15:44093927-44204047	Strong transcription Flanking Active TSS Weak transcription Bivalent/Poised TSS Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	n/a

mRNA abundance (count:16)

SNP	Gene	Cis/trans	Tissue	Source
rs575082	TGM5	cis	lymphoblastoid	seeQTL
rs575082	WDR76	cis	parietal	SCAN
rs575082	ZSCAN29	cis	Thyroid	GTEx
rs575082	AC011330.5	cis	Artery Tibial	GTEx
rs575082	ADAL	cis	parietal	SCAN
rs575082	ELL3	cis	multi-tissue	Pritchard
rs575082	STRCP1	cis	Thyroid	GTEx
rs575082	DUOX2	cis	parietal	SCAN
rs575082	TGM5	cis	Lymphoblastoid	GTEx
rs575082	C15orf43	cis	cerebellum	SCAN
rs575082	STRCP1	cis	Whole Blood	GTEx
rs575082	PATL2	cis	cerebellum	SCAN
rs575082	SERF2	cis	lymphoblastoid	seeQTL
rs575082	STRC	cis	multi-tissue	Pritchard
rs575082	AC011330.5	cis	Thyroid	GTEx
rs575082	NAP1L2	trans	lymphoblastoid	seeQTL

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:44093600-44116000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr15:44093600-44116400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr15:44093800-44112800	Strong transcription	Thymus	Thymus
4	chr15:44093800-44113800	Weak transcription	Stomach Mucosa	stomach
5	chr15:44093800-44115800	Weak transcription	Right Atrium	heart
6	chr15:44094000-44110200	Strong transcription	HUES64 Cell Line	embryonic stem cell
7	chr15:44094000-44110200	Strong transcription	Primary T cells fromperipheralblood	blood
8	chr15:44094000-44110200	Strong transcription	Fetal Intestine Large	intestine
9	chr15:44094000-44110400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr15:44094000-44110400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
11	chr15:44094000-44110800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
12	chr15:44094000-44111200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr15:44094000-44111200	Strong transcription	Fetal Muscle Trunk	muscle
14	chr15:44094000-44113200	Strong transcription	Fetal Muscle Leg	muscle
15	chr15:44094000-44113400	Strong transcription	Fetal Stomach	stomach
16	chr15:44094000-44114600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr15:44094000-44114800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr15:44094200-44110200	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
19	chr15:44094200-44110200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr15:44094200-44110200	Strong transcription	Sigmoid Colon	Sigmoid Colon
21	chr15:44094200-44110600	Strong transcription	HUES48 Cell Line	embryonic stem cell
22	chr15:44094200-44111200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr15:44094200-44111200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr15:44094200-44111400	Strong transcription	Primary T cells from cord blood	blood
25	chr15:44094200-44111600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
26	chr15:44094200-44113000	Strong transcription	Cortex derived primary cultured neurospheres	brain
27	chr15:44094200-44113200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr15:44094400-44110200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
29	chr15:44094400-44110200	Strong transcription	Liver	Liver
30	chr15:44094400-44110400	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
31	chr15:44094400-44111000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr15:44094400-44111200	Strong transcription	Rectal Mucosa Donor 29	rectum
33	chr15:44094400-44113200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr15:44094400-44113200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr15:44095000-44110400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr15:44095400-44110200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
37	chr15:44096000-44110800	Strong transcription	Primary T helper cells PMA-I stimulated	--
38	chr15:44096400-44110200	Strong transcription	HUES6 Cell Line	embryonic stem cell
39	chr15:44096400-44110200	Strong transcription	Duodenum Smooth Muscle	Duodenum
40	chr15:44096400-44110600	Strong transcription	HepG2	liver
41	chr15:44096400-44111200	Strong transcription	Osteobl	bone
42	chr15:44096400-44111600	Strong transcription	Hela-S3	cervix
43	chr15:44097000-44110200	Strong transcription	Colonic Mucosa	Colon
44	chr15:44097000-44110200	Strong transcription	HSMM	muscle
45	chr15:44098200-44110200	Strong transcription	Primary T helper naive cells from peripheral blood	blood
46	chr15:44100800-44111200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
47	chr15:44101000-44113200	Strong transcription	Fetal Intestine Small	intestine
48	chr15:44102200-44110200	Strong transcription	Primary monocytes fromperipheralblood	blood
49	chr15:44102200-44110600	Strong transcription	Monocytes-CD14+_RO01746	blood
50	chr15:44102800-44110200	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links