Variant report

Variant	rs228504
Chromosome Location	chr1:79682046-79682047
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs170612	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs170614	0.84[AMR][1000 genomes]
rs172926	0.84[AMR][1000 genomes]
rs183458	0.90[AMR][1000 genomes]
rs228469	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs228470	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs228472	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs228473	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs228476	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs228494	0.83[AMR][1000 genomes]
rs228495	0.83[AMR][1000 genomes]
rs228496	0.85[AMR][1000 genomes]
rs228497	0.88[AMR][1000 genomes]
rs228499	0.84[AMR][1000 genomes]
rs228500	0.92[AMR][1000 genomes]
rs228502	0.92[AMR][1000 genomes]
rs228503	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs228506	0.92[AMR][1000 genomes]
rs228508	0.92[AMR][1000 genomes]
rs228510	0.85[AMR][1000 genomes]
rs228511	0.92[AMR][1000 genomes]
rs228512	0.84[AMR][1000 genomes]
rs228514	0.92[AMR][1000 genomes]
rs228515	0.92[AMR][1000 genomes]
rs228516	0.85[AMR][1000 genomes]
rs228517	0.92[AMR][1000 genomes]
rs228518	0.85[AMR][1000 genomes]
rs228519	0.83[AMR][1000 genomes]
rs228520	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs228521	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs228522	0.84[AMR][1000 genomes]
rs228523	0.85[AMR][1000 genomes]
rs228532	0.90[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs228533	0.90[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs228534	0.80[AMR][1000 genomes]
rs228535	0.84[AMR][1000 genomes]
rs228536	0.90[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs228537	0.84[AMR][1000 genomes]
rs228538	0.90[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs228540	0.90[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs228541	0.84[AMR][1000 genomes]
rs228542	0.85[AMR][1000 genomes]
rs228544	0.90[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs35764284	0.90[AMR][1000 genomes]
rs368460	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs393486	0.85[AMR][1000 genomes]
rs418641	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4650402	0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4650403	0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6424644	0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6674681	0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6697527	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 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

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:79665200-79682400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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