Variant report

Variant	rs58243356
Chromosome Location	chr5:74313801-74313802
allele	C/T
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:30)

rs_ID	r²[population]
rs10462510	0.86[ASN][1000 genomes]
rs11957690	0.88[EUR][1000 genomes]
rs12515891	0.85[ASN][1000 genomes]
rs12516438	0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs34018438	0.89[EUR][1000 genomes]
rs3811986	0.87[EUR][1000 genomes]
rs3811987	0.88[EUR][1000 genomes]
rs4285200	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4290996	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4492095	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4704166	0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs56682994	0.88[EUR][1000 genomes]
rs58323964	0.86[ASN][1000 genomes]
rs59923116	0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs59992473	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs60661930	0.95[ASN][1000 genomes]
rs61342638	0.86[ASN][1000 genomes]
rs61616736	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62369160	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs62369161	0.80[ASN][1000 genomes]
rs62369164	0.90[EUR][1000 genomes]
rs62369166	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs62369167	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6874469	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs72768311	0.99[ASN][1000 genomes]
rs7706858	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7725085	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7726378	0.84[EUR][1000 genomes]
rs7734427	0.88[EUR][1000 genomes]
rs7736471	0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830352	chr5:74189495-74337944	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv1018865	chr5:74246293-74494552	Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:74303600-74316000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr5:74313400-74314600	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr5:74313600-74318200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr5:74313600-74341800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr5:74313800-74314200	Weak transcription	NHDF-Ad	bronchial

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