Variant report

Variant	rs10874701
Chromosome Location	chr1:103737633-103737634
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10782929	0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10874693	0.86[EUR][1000 genomes]
rs10874699	0.81[ASN][1000 genomes]
rs11164723	0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11164727	0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12024454	0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12030718	0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12034204	0.80[EUR][1000 genomes]
rs12047707	0.88[EUR][1000 genomes]
rs12125734	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12128315	0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12129353	0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12129963	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12136508	0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12143297	0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1358460	0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1406130	0.81[ASN][1000 genomes]
rs1528208	0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1528209	0.81[ASN][1000 genomes]
rs1528210	0.81[ASN][1000 genomes]
rs1830300	0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2056752	0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs35091045	0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs35483270	0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4908294	0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs71655813	0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv522922	chr1:103305021-103764640	Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv931600	chr1:103548397-104161031	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
3	nsv498007	chr1:103573857-104107589	Genic enhancers Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
4	nsv432554	chr1:103673437-104128773	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
5	nsv870954	chr1:103730700-103940483	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:103732400-103741200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr1:103736800-103737800	Enhancers	Muscle Satellite Cultured Cells	--
3	chr1:103737600-103741400	Weak transcription	HSMM	muscle

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