Variant report

Variant	rs635375
Chromosome Location	chr11:65621995-65621996
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:80)
CpG islands
(count:0)
Chromatin interactive
region (count:16)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:80 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr11:65617944-65626197	K562	blood:	n/a	n/a
2	POLR2A	chr11:65621776-65622014	GM12878	blood:	n/a	n/a
3	POLR2A	chr11:65617092-65633870	K562	blood:	n/a	n/a
4	POLR2A	chr11:65617861-65622588	Hela-S3	cervix:	n/a	n/a
5	POLR2A	chr11:65617610-65622326	U87	brain:	n/a	n/a
6	FOXA2	chr11:65621751-65622030	HepG2	liver:	n/a	n/a
7	POLR2A	chr11:65620617-65622149	HCT-116	colon:	n/a	n/a
8	RXRA	chr11:65621618-65622088	HepG2	liver:	n/a	n/a
9	POLR2A	chr11:65621589-65622005	GM12878	blood:	n/a	n/a
10	NFIC	chr11:65621585-65622100	HepG2	liver:	n/a	n/a
11	MXI1	chr11:65621747-65622004	HepG2	liver:	n/a	n/a
12	POLR2A	chr11:65621969-65622082	K562	blood:	n/a	n/a
13	POLR2A	chr11:65616755-65639999	U87	brain:	n/a	n/a
14	ARID3A	chr11:65621814-65622014	HepG2	liver:	n/a	n/a
15	POLR2A	chr11:65617198-65628973	PANC-1	pancreas:	n/a	n/a
16	MTA3	chr11:65617490-65622077	GM12878	blood:	n/a	n/a
17	POLR2A	chr11:65621606-65622326	U87	brain:	n/a	n/a
18	HNF4A	chr11:65621608-65622108	HepG2	liver:	n/a	chr11:65621809-65621824
19	POLR2A	chr11:65617082-65622141	SK-N-SH	brain:	n/a	n/a
20	POLR2A	chr11:65618517-65622566	PFSK-1	brain:	n/a	n/a
21	POLR2A	chr11:65618005-65623075	PFSK-1	brain:	n/a	n/a
22	POLR2A	chr11:65621993-65622242	ProgFib	skin:	n/a	n/a
23	POLR2A	chr11:65621905-65622244	SK-N-SH	brain:	n/a	n/a
24	RXRA	chr11:65621655-65622018	HepG2	liver:	n/a	n/a
25	POLR2A	chr11:65617784-65622663	PANC-1	pancreas:	n/a	n/a
26	POLR2A	chr11:65617323-65622533	H1-hESC	embryonic stem cell:	n/a	n/a
27	POLR2A	chr11:65617465-65622308	HUVEC	blood vessel:	n/a	n/a
28	POLR2A	chr11:65617215-65622257	MCF-7	breast:	n/a	n/a
29	POLR2A	chr11:65617118-65622730	Hela-S3	cervix:	n/a	n/a
30	HNF4A	chr11:65621576-65622048	HepG2	liver:	n/a	chr11:65621809-65621824
31	POLR2A	chr11:65617531-65622640	HUVEC	blood vessel:	n/a	n/a
32	POLR2A	chr11:65618467-65622327	HL-60	blood:	n/a	n/a
33	ATF2	chr11:65621270-65622162	H1-hESC	embryonic stem cell:	n/a	n/a
34	POLR2A	chr11:65616422-65629961	H1-hESC	embryonic stem cell:	n/a	n/a
35	POLR2A	chr11:65616827-65622249	GM12878	blood:	n/a	n/a
36	POLR2A	chr11:65617007-65628594	GM12891	blood:	n/a	n/a
37	POLR2A	chr11:65617073-65630131	GM12892	blood:	n/a	n/a
38	FOSL2	chr11:65621655-65622061	HepG2	liver:	n/a	chr11:65621865-65621876 chr11:65621831-65621839 chr11:65621867-65621879 chr11:65621830-65621841
39	POLR2A	chr11:65617574-65622131	ECC-1	luminal epithelium:	n/a	n/a
40	POLR2A	chr11:65616778-65626416	Hela-S3	cervix:	n/a	n/a
41	POLR2A	chr11:65617276-65622614	HUVEC	blood vessel:	n/a	n/a
42	POLR2A	chr11:65621772-65622122	HUVEC	blood vessel:	n/a	n/a
43	POLR2A	chr11:65621351-65622250	H1-neurons	neurons:	n/a	n/a
44	POLR2A	chr11:65617393-65622537	GM12892	blood:	n/a	n/a
45	POLR2A	chr11:65619408-65622282	HepG2	liver:	n/a	n/a
46	POLR2A	chr11:65616706-65640269	U87	brain:	n/a	n/a
47	POLR2A	chr11:65619434-65622500	K562	blood:	n/a	n/a
48	POLR2A	chr11:65619602-65622114	K562	blood:	n/a	n/a
49	PML	chr11:65617492-65622005	GM12878	blood:	n/a	n/a
50	POLR2A	chr11:65621387-65622264	H1-hESC	embryonic stem cell:	n/a	n/a

No data

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:65472429..65485450-chr11:65615794..65629774,38	K562	blood:
2	chr11:65620395..65622230-chr6:26030977..26033729,2	K562	blood:
3	chr11:65575640..65578882-chr11:65620145..65623092,3	K562	blood:
4	chr11:65562689..65564854-chr11:65621006..65623868,2	K562	blood:
5	chr11:64883013..64884898-chr11:65620612..65622205,2	K562	blood:
6	chr11:65194112..65195843-chr11:65621752..65623385,2	K562	blood:
7	chr11:65397945..65399959-chr11:65620228..65622246,2	K562	blood:
8	chr11:65485004..65489716-chr11:65621545..65626984,9	K562	blood:
9	chr11:65616798..65622478-chr11:65727555..65733013,6	MCF-7	breast:
10	chr11:65486395..65489048-chr11:65619139..65622077,3	MCF-7	breast:
11	chr11:65485735..65490975-chr11:65621882..65626984,8	K562	blood:
12	chr11:65478964..65482539-chr11:65616975..65622123,6	K562	blood:
13	chr11:65484120..65486209-chr11:65619696..65622078,2	MCF-7	breast:
14	chr11:65340642..65343423-chr11:65617979..65623594,4	K562	blood:
15	chr11:65562689..65566411-chr11:65620359..65624603,6	K562	blood:
16	chr11:65492532..65494079-chr11:65621451..65623321,2	K562	blood:

No data

Variant related genes	Relation type
MUS81	TF binding region
ENSG00000172922	Chromatin interaction
ENSG00000175467	Chromatin interaction
ENSG00000124693	Chromatin interaction
ENSG00000255173	Chromatin interaction
ENSG00000172977	Chromatin interaction
ENSG00000255404	Chromatin interaction

Extended variants
information (count: 44 )
Associated
traits (count: 14 )

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10791828	0.81[CEU][hapmap];0.85[AMR][1000 genomes]
rs10896053	0.88[GIH][hapmap]
rs11227311	0.84[GIH][hapmap]
rs1204772	0.88[GIH][hapmap]
rs12575663	0.80[GIH][hapmap]
rs13817	0.93[ASW][hapmap];0.92[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.96[MEX][hapmap];0.97[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1939212	0.81[CEU][hapmap];0.92[CHB][hapmap];0.89[CHD][hapmap];0.97[GIH][hapmap];0.88[MEX][hapmap];0.87[TSI][hapmap];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4621	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs508548	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs538394	1.00[CEU][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs545500	0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs558114	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[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];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs570387	0.80[GIH][hapmap]
rs601887	0.88[GIH][hapmap]
rs621348	0.88[GIH][hapmap]
rs630303	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.81[LWK][hapmap];1.00[MEX][hapmap];0.97[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs630755	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs633800	0.80[GIH][hapmap]
rs633877	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs648732	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.97[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.97[TSI][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs652021	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.97[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs656040	1.00[ASW][hapmap];0.92[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.94[LWK][hapmap];0.96[MEX][hapmap];1.00[MKK][hapmap];0.97[TSI][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs659824	0.80[GIH][hapmap];0.86[MKK][hapmap]
rs659857	1.00[ASW][hapmap];0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.91[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap]
rs665306	1.00[ASW][hapmap];0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.91[LWK][hapmap];1.00[MEX][hapmap];0.99[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs667555	0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs668356	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.91[LWK][hapmap];1.00[MEX][hapmap];0.99[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs679147	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7107912	0.84[GIH][hapmap]
rs7114014	0.92[CHB][hapmap];0.86[CHD][hapmap];0.95[GIH][hapmap]
rs7114237	0.88[GIH][hapmap]
rs7125986	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7947741	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7947929	0.92[AMR][1000 genomes];0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv897736	chr11:65335705-65676516	Flanking Active TSS Active TSS Enhancers Weak transcription 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	227 gene(s)	inside rSNPs	diseases
2	nsv430401	chr11:65419324-65788024	Enhancers Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	224 gene(s)	inside rSNPs	diseases
3	esv2758274	chr11:65559893-65722363	Genic enhancers Active TSS Flanking Active TSS Strong transcription Weak transcription Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	178 gene(s)	inside rSNPs	diseases
4	esv2759834	chr11:65559893-65722363	Flanking Active TSS Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	178 gene(s)	inside rSNPs	diseases
5	nsv427890	chr11:65559893-65722363	Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	178 gene(s)	inside rSNPs	diseases
6	nsv897761	chr11:65580638-65738566	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	186 gene(s)	inside rSNPs	diseases
7	nsv555215	chr11:65581579-65676516	Strong transcription Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	165 gene(s)	inside rSNPs	diseases
8	nsv897762	chr11:65613218-65758854	Active TSS Flanking Active TSS Genic enhancers Enhancers Flanking Bivalent TSS/Enh Strong transcription Weak transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	185 gene(s)	inside rSNPs	diseases
9	nsv897763	chr11:65613348-65644027	Weak transcription Genic enhancers Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	121 gene(s)	inside rSNPs	diseases
10	nsv897764	chr11:65613348-65695222	Flanking Bivalent TSS/Enh Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	176 gene(s)	inside rSNPs	diseases

mRNA abundance (count:14)

SNP	Gene	Cis/trans	Tissue	Source
rs635375	MTA2	cis	parietal	SCAN
rs635375	SNX32	cis	Whole Blood	GTEx
rs635375	SNX32	cis	cerebellum	SCAN
rs635375	SNX32	cis	Esophagus Muscularis	GTEx
rs635375	PACS1	cis	parietal	SCAN
rs635375	RAB3IL1	cis	cerebellum	SCAN
rs635375	FIBP	cis	cerebellum	SCAN
rs635375	SNX32	cis	parietal	SCAN
rs635375	DPP3	cis	lymphoblastoid	seeQTL
rs635375	SNX32	cis	Artery Tibial	GTEx
rs635375	CARNS1	cis	cerebellum	SCAN
rs635375	SNX32	cis	Thyroid	GTEx
rs635375	FIBP	Cis_1M	lymphoblastoid	RTeQTL
rs635375	PLCB3	cis	parietal	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:65602200-65623800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr11:65616800-65625000	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr11:65617000-65622000	Genic enhancers	Fetal Intestine Small	intestine
4	chr11:65618000-65624000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr11:65618000-65624600	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr11:65618200-65622000	Strong transcription	NHLF	lung
7	chr11:65618200-65622400	Strong transcription	Primary B cells from cord blood	blood
8	chr11:65618200-65623200	Strong transcription	Right Ventricle	heart
9	chr11:65618200-65623800	Strong transcription	Placenta Amnion	Placenta Amnion
10	chr11:65618400-65622400	Weak transcription	Fetal Brain Male	brain
11	chr11:65618400-65622600	Strong transcription	Primary T cells from cord blood	blood
12	chr11:65618400-65623000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr11:65618600-65622800	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
14	chr11:65618600-65623000	Strong transcription	Brain Hippocampus Middle	brain
15	chr11:65618600-65623000	Strong transcription	Pancreas	Pancrea
16	chr11:65618600-65623200	Strong transcription	Osteobl	bone
17	chr11:65618600-65623400	Strong transcription	Brain Angular Gyrus	brain
18	chr11:65618800-65622400	Strong transcription	Primary hematopoietic stem cells	blood
19	chr11:65618800-65622800	Genic enhancers	Fetal Intestine Large	intestine
20	chr11:65618800-65623000	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
21	chr11:65618800-65623000	Strong transcription	Left Ventricle	heart
22	chr11:65619000-65622000	Strong transcription	Muscle Satellite Cultured Cells	--
23	chr11:65619000-65622600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr11:65619000-65622800	Strong transcription	Dnd41	blood
25	chr11:65619000-65623000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr11:65619000-65623000	Strong transcription	HMEC	breast
27	chr11:65619000-65623600	Strong transcription	Fetal Lung	lung
28	chr11:65619000-65623800	Strong transcription	Aorta	Aorta
29	chr11:65619200-65622000	Strong transcription	Monocytes-CD14+_RO01746	blood
30	chr11:65619200-65623000	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
31	chr11:65619200-65623000	Strong transcription	Adipose Nuclei	Adipose
32	chr11:65619200-65623000	Strong transcription	Duodenum Smooth Muscle	Duodenum
33	chr11:65619200-65623000	Strong transcription	NHEK	skin
34	chr11:65619200-65623400	Strong transcription	Brain Cingulate Gyrus	brain
35	chr11:65619200-65623400	Strong transcription	Brain Inferior Temporal Lobe	brain
36	chr11:65619200-65623600	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr11:65619200-65623600	Strong transcription	iPS-15b Cell Line	embryonic stem cell
38	chr11:65619400-65622600	Strong transcription	Placenta	Placenta
39	chr11:65619400-65623000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr11:65619400-65623200	Strong transcription	Cortex derived primary cultured neurospheres	brain
41	chr11:65619400-65623400	Strong transcription	K562	blood
42	chr11:65619400-65623600	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr11:65619400-65623800	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr11:65619600-65622400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr11:65619600-65622600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr11:65619600-65623000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
47	chr11:65619600-65623400	Strong transcription	H1 Cell Line	embryonic stem cell
48	chr11:65619600-65623400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr11:65619600-65623400	Strong transcription	Fetal Stomach	stomach
50	chr11:65619800-65622600	Strong transcription	Primary monocytes fromperipheralblood	blood

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