Variant report

Variant	rs60460891
Chromosome Location	chr3:160168769-160168770
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:67)
CpG islands
(count:0)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:67 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	PBX3	chr3:160168472-160169155	SK-N-SH	brain:	n/a	n/a
2	HEY1	chr3:160166688-160168801	K562	blood:	n/a	chr3:160167195-160167210
3	MEF2A	chr3:160168483-160169326	SK-N-SH	brain:	n/a	n/a
4	EP300	chr3:160168410-160169159	SK-N-SH	brain:	n/a	n/a
5	POLR2A	chr3:160167021-160168906	K562	blood:	n/a	n/a
6	CTCF	chr3:160168660-160168810	RPTEC	kidney:	n/a	n/a
7	MAFK	chr3:160168631-160169045	IMR90	lung:	n/a	n/a
8	CTCF	chr3:160168680-160168830	HMF	breast:	n/a	n/a
9	CTCF	chr3:160168700-160168850	HCFaa	heart:	n/a	n/a
10	POLR2A	chr3:160168492-160168791	ProgFib	skin:	n/a	n/a
11	CTCF	chr3:160168660-160168810	NHDF-neo	bronchial:	n/a	n/a
12	FOSL2	chr3:160168542-160169152	SK-N-SH	brain:	n/a	n/a
13	CTCF	chr3:160168720-160168870	HBMEC	blood vessel:	n/a	n/a
14	CTCF	chr3:160168700-160168850	HPAF	blood vessel:	n/a	n/a
15	CTCF	chr3:160168680-160168830	AG09309	skin:	n/a	n/a
16	ZNF384	chr3:160167098-160168780	K562	blood:	n/a	n/a
17	CTCF	chr3:160168620-160168870	HBMEC	blood vessel:	n/a	n/a
18	CTCF	chr3:160168700-160168850	BJ	skin:	n/a	n/a
19	CTCF	chr3:160168620-160168770	HRE	kidney:	n/a	n/a
20	TBP	chr3:160166659-160168829	K562	blood:	n/a	n/a
21	CTCF	chr3:160168720-160168870	HAc	cerebellar:	n/a	n/a
22	TCF12	chr3:160168492-160169214	SK-N-SH	brain:	n/a	chr3:160168986-160168995
23	POLR2A	chr3:160168602-160169106	SK-N-SH	brain:	n/a	n/a
24	CTCF	chr3:160168700-160168850	AG04449	skin:	n/a	n/a
25	CTCF	chr3:160168720-160168870	HMF	breast:	n/a	n/a
26	CTCF	chr3:160168740-160168890	AoAF	blood vessel:	n/a	n/a
27	RCOR1	chr3:160166746-160169584	IMR90	lung:	n/a	n/a
28	CTCF	chr3:160168660-160168810	AG10803	skin:	n/a	n/a
29	POLR2A	chr3:160166686-160169075	K562	blood:	n/a	n/a
30	CTCF	chr3:160168720-160168870	AG04450	lung:	n/a	n/a
31	CTCF	chr3:160168760-160168910	AG09319	gingival:	n/a	n/a
32	POLR2A	chr3:160166664-160168917	K562	blood:	n/a	n/a
33	RXRA	chr3:160168562-160169145	SK-N-SH	brain:	n/a	n/a
34	POLR2A	chr3:160166665-160169068	GM12878	blood:	n/a	n/a
35	TEAD4	chr3:160166764-160169040	K562	blood:	n/a	n/a
36	POLR2A	chr3:160166686-160169077	K562	blood:	n/a	n/a
37	POLR2A	chr3:160166107-160169020	K562	blood:	n/a	n/a
38	TCF12	chr3:160168436-160169223	SK-N-SH	brain:	n/a	chr3:160168986-160168995
39	TEAD4	chr3:160168441-160169216	SK-N-SH	brain:	n/a	n/a
40	CTCF	chr3:160168760-160168910	AG09309	skin:	n/a	n/a
41	POLR2A	chr3:160166811-160169025	K562	blood:	n/a	n/a
42	CTCF	chr3:160168720-160168870	HFF	foreskin:	n/a	n/a
43	CTCF	chr3:160168700-160168850	HA-sp	spinal cord:	n/a	n/a
44	CTCF	chr3:160168640-160168790	NHLF	lung:	n/a	n/a
45	CTCF	chr3:160168660-160168810	HRPEpiC	eye:	n/a	n/a
46	CTCF	chr3:160168700-160168850	AG10803	skin:	n/a	n/a
47	TEAD4	chr3:160166449-160169101	K562	blood:	n/a	n/a
48	CTCF	chr3:160168640-160168790	HRE	kidney:	n/a	n/a
49	CTCF	chr3:160168720-160168870	AG09319	gingival:	n/a	n/a
50	POLR2A	chr3:160166912-160168784	K562	blood:	n/a	n/a

No data

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:160099375..160102379-chr3:160166288..160168879,3	MCF-7	breast:
2	chr3:160116116..160127665-chr3:160158037..160169627,42	K562	blood:
3	chr3:160167035..160169821-chr3:160232708..160234646,2	K562	blood:
4	chr3:160113853..160115916-chr3:160167790..160169810,2	K562	blood:
5	chr3:160166147..160168803-chr3:160282163..160283900,2	MCF-7	breast:
6	chr3:160166836..160169216-chr3:161090028..161092220,2	MCF-7	breast:
7	chr3:160167702..160169385-chr3:160272825..160274892,2	K562	blood:
8	chr3:160164471..160170330-chr3:160281681..160284179,8	K562	blood:
9	chr3:160165891..160168986-chr3:160283501..160286413,4	K562	blood:

No data

Variant related genes	Relation type
TRIM59	TF binding region
ENSG00000244009	TF binding region
ENSG00000248710	TF binding region
ENSG00000229320	Chromatin interaction
ENSG00000196542	Chromatin interaction
ENSG00000238741	Chromatin interaction
ENSG00000186432	Chromatin interaction
ENSG00000068885	Chromatin interaction
ENSG00000113810	Chromatin interaction
ENSG00000198987	Chromatin interaction
ENSG00000207779	Chromatin interaction

Extended variants
information (count: 93 )
Associated
traits (count: 1 )

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

rs_ID	r²[population]
rs10212236	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10513551	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11918749	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs13403	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1451761	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1451762	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1451764	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1551190	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1584688	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs17236544	0.85[ASN][1000 genomes]
rs1882127	0.80[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1920642	0.85[ASN][1000 genomes]
rs1920662	0.85[ASN][1000 genomes]
rs1920664	0.85[ASN][1000 genomes]
rs1953506	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2152425	0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2279457	0.85[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2305407	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs28705750	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2886825	0.81[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs3773372	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs3851366	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4091703	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs41272947	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4621370	0.85[ASN][1000 genomes]
rs4679881	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4679885	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4679888	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4679889	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4679890	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4679891	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4679899	0.85[ASN][1000 genomes]
rs4680576	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4680579	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4680580	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4680585	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4680587	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4680588	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs55687857	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs55731730	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs56197102	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs56394279	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs58322641	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs58665246	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs60009222	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs62272186	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs62272791	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs62272792	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs62272794	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs62272800	0.85[EUR][1000 genomes]
rs6441313	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6441314	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6441319	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6441320	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6441324	0.85[ASN][1000 genomes]
rs6768975	0.85[ASN][1000 genomes]
rs6791261	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6792612	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6793560	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6798668	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6801300	0.85[ASN][1000 genomes]
rs6803828	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6808083	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs721023	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs73154592	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7356111	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7611130	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7618974	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7621724	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7624902	0.84[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs7627749	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7627756	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7629	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7629202	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7631792	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7634108	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7634826	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7640072	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7643779	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7645832	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7647873	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs869468	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9798898	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9799314	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs9862595	0.86[ASN][1000 genomes]
rs9968151	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[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	nsv532666	chr3:159777847-160703202	Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	271 gene(s)	inside rSNPs	diseases
2	nsv1000453	chr3:159853305-160366357	Active TSS Flanking Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	259 gene(s)	inside rSNPs	diseases
3	nsv536779	chr3:159853305-160366357	Strong transcription Enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	259 gene(s)	inside rSNPs	diseases
4	esv1800136	chr3:159950498-160278160	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	213 gene(s)	inside rSNPs	diseases
5	esv1801767	chr3:159950498-160279411	Strong transcription Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	213 gene(s)	inside rSNPs	diseases
6	nsv1008519	chr3:160038710-160292589	Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Enhancers Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	255 gene(s)	inside rSNPs	diseases
7	esv1801686	chr3:160089896-160248363	Strong transcription Weak transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	211 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs60460891	SMC4	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:53 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:160164800-160169000	Active TSS	H1 Cell Line	embryonic stem cell
2	chr3:160165000-160169000	Active TSS	HUES6 Cell Line	embryonic stem cell
3	chr3:160165400-160169000	Active TSS	ES-I3 Cell Line	embryonic stem cell
4	chr3:160166400-160169000	Active TSS	iPS-20b Cell Line	embryonic stem cell
5	chr3:160167600-160168800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr3:160167800-160168800	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr3:160167800-160168800	Flanking Active TSS	Muscle Satellite Cultured Cells	--
8	chr3:160167800-160168800	Flanking Active TSS	Colon Smooth Muscle	Colon
9	chr3:160167800-160168800	Flanking Active TSS	HSMMtube	muscle
10	chr3:160167800-160168800	Flanking Active TSS	NH-A	brain
11	chr3:160167800-160168800	Flanking Active TSS	Osteobl	bone
12	chr3:160168000-160169800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr3:160168200-160168800	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr3:160168200-160168800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr3:160168200-160168800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr3:160168200-160169000	Enhancers	Fetal Heart	heart
17	chr3:160168400-160168800	Flanking Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr3:160168400-160168800	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
19	chr3:160168400-160168800	Enhancers	Primary monocytes fromperipheralblood	blood
20	chr3:160168400-160168800	Enhancers	A549	lung
21	chr3:160168400-160169000	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
22	chr3:160168400-160169000	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
23	chr3:160168400-160169000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr3:160168400-160169400	Weak transcription	Hela-S3	cervix
25	chr3:160168400-160169600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr3:160168400-160169600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr3:160168400-160170200	Weak transcription	Lung	lung
28	chr3:160168400-160172600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr3:160168400-160172600	Weak transcription	Brain Substantia Nigra	brain
30	chr3:160168400-160172800	Weak transcription	Brain Anterior Caudate	brain
31	chr3:160168600-160168800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr3:160168600-160168800	Flanking Active TSS	H9 Cell Line	embryonic stem cell
33	chr3:160168600-160168800	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr3:160168600-160168800	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
35	chr3:160168600-160168800	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
36	chr3:160168600-160168800	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr3:160168600-160168800	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr3:160168600-160168800	Active TSS	Brain Germinal Matrix	brain
39	chr3:160168600-160168800	Enhancers	Fetal Kidney	kidney
40	chr3:160168600-160168800	Enhancers	Fetal Muscle Leg	muscle
41	chr3:160168600-160168800	Enhancers	Fetal Stomach	stomach
42	chr3:160168600-160168800	Active TSS	GM12878-XiMat	blood
43	chr3:160168600-160169000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr3:160168600-160169000	Enhancers	Fetal Thymus	thymus
45	chr3:160168600-160169000	Bivalent Enhancer	NHEK	skin
46	chr3:160168600-160169600	Flanking Active TSS	K562	blood
47	chr3:160168600-160169600	Enhancers	NHLF	lung
48	chr3:160168600-160169800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr3:160168600-160169800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr3:160168600-160169800	Enhancers	HSMM	muscle

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links