Variant report

Variant	rs4557238
Chromosome Location	chr4:153061400-153061401
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10030518	0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11099843	0.91[ASN][1000 genomes]
rs11721407	0.91[ASN][1000 genomes]
rs11721782	0.91[ASN][1000 genomes]
rs11726930	0.91[ASN][1000 genomes]
rs11727862	0.91[ASN][1000 genomes]
rs11733393	0.85[ASN][1000 genomes]
rs11733971	0.91[ASN][1000 genomes]
rs11736628	0.96[ASN][1000 genomes]
rs11737156	0.96[ASN][1000 genomes]
rs13112841	0.96[ASN][1000 genomes]
rs13131134	0.96[ASN][1000 genomes]
rs13147317	0.84[EUR][1000 genomes]
rs2406622	0.96[ASN][1000 genomes]
rs2406625	0.98[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2897478	0.96[ASN][1000 genomes]
rs34069606	0.91[ASN][1000 genomes]
rs34276148	0.96[ASN][1000 genomes]
rs34909306	0.96[ASN][1000 genomes]
rs35296212	0.91[ASN][1000 genomes]
rs56780740	0.89[ASN][1000 genomes]
rs61226564	0.90[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6535839	0.98[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6535840	0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6823091	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6833264	0.96[ASN][1000 genomes]
rs6837375	0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6843300	0.84[EUR][1000 genomes]
rs6843947	0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6848307	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7662581	0.96[ASN][1000 genomes]
rs7671283	0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7674458	0.96[ASN][1000 genomes]
rs7675252	0.96[ASN][1000 genomes]
rs7675481	0.96[ASN][1000 genomes]
rs7682931	0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv880341	chr4:152861685-153110256	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv931416	chr4:152877808-153440553	Genic enhancers Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
3	nsv880774	chr4:153035743-153121818	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:153060400-153064800	Weak transcription	Thymus	Thymus
2	chr4:153060600-153061600	Weak transcription	Dnd41	blood

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