Variant report

Variant	rs4119502
Chromosome Location	chr13:48332418-48332419
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs12429525	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12430596	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs17337616	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2224914	0.89[EUR][1000 genomes]
rs4119501	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4941603	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4941604	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4941609	0.96[ASN][1000 genomes]
rs4942691	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4942692	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4942694	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs57427955	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs59890896	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs61972192	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7324490	0.90[EUR][1000 genomes]
rs7981324	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7982387	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7986517	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7988528	0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7989376	0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7999699	0.90[EUR][1000 genomes]
rs9526394	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9526397	0.82[EUR][1000 genomes]
rs9534771	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9534812	0.96[ASN][1000 genomes]
rs9534822	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9534830	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[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	nsv832600	chr13:48183118-48341417	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	esv3510679	chr13:48236624-48498185	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	esv3510680	chr13:48236624-48498185	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv561589	chr13:48251736-48420218	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv437785	chr13:48329584-48333991	Enhancers	TF binding region	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:48332400-48332600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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