Variant report

Variant	rs57105192
Chromosome Location	chr5:97773566-97773567
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs10074098	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1079976	0.86[ASN][1000 genomes]
rs11241508	0.80[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11953740	0.80[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2368554	0.80[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs28373396	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs28842778	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs28852712	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs28871124	0.86[ASN][1000 genomes]
rs2887281	0.82[ASN][1000 genomes]
rs35251688	0.80[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4577723	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs62369958	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs62369959	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6595256	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6862099	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6862827	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6873673	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6890113	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6891474	0.81[ASN][1000 genomes]
rs73145738	0.81[EUR][1000 genomes];0.86[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	nsv882407	chr5:97553255-97783046	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv882408	chr5:97616089-97836794	Enhancers Strong transcription ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv830419	chr5:97653713-97829079	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
4	nsv1018555	chr5:97719032-97873906	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
5	nsv882409	chr5:97761687-97817930	Enhancers Flanking Active TSS Strong transcription Weak transcription ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	n/a	n/a	inside rSNPs	diseases
6	nsv882410	chr5:97764522-97810693	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	inside rSNPs	diseases
7	nsv882411	chr5:97764867-97817930	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:97765000-97780200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr5:97768800-97774600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr5:97773200-97781000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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