Variant report

Variant	rs368460
Chromosome Location	chr1:79709724-79709725
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs170612	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs17102981	0.85[AMR][1000 genomes]
rs228467	0.82[AMR][1000 genomes]
rs228469	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs228470	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs228472	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs228473	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs228474	0.82[AMR][1000 genomes]
rs228475	0.82[AMR][1000 genomes]
rs228476	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs228477	0.82[AMR][1000 genomes]
rs228478	0.82[AMR][1000 genomes]
rs228479	0.82[AMR][1000 genomes]
rs228480	0.82[AMR][1000 genomes]
rs228482	0.88[AMR][1000 genomes]
rs228484	0.81[AMR][1000 genomes]
rs228486	0.81[AMR][1000 genomes]
rs228489	0.81[AMR][1000 genomes]
rs228503	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs228504	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs228520	0.84[EUR][1000 genomes]
rs418641	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs427551	0.83[AMR][1000 genomes]
rs4650402	0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4650403	0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs61766097	0.85[AMR][1000 genomes]
rs6424643	0.86[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs6424644	0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6424645	0.82[AMR][1000 genomes]
rs6674681	0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6681555	0.83[AMR][1000 genomes]
rs6697527	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7553133	0.82[AMR][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	nsv491784	chr1:79146141-79853482	Enhancers Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv830326	chr1:79573379-79735667	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv871182	chr1:79614989-79822735	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv999471	chr1:79650363-79774433	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv870657	chr1:79701220-79890774	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 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	chr1:79705800-79710000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr1:79709200-79710200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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