Variant report

Variant	rs61825255
Chromosome Location	chr1:222935785-222935786
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs12749296	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2068814	0.83[EUR][1000 genomes]
rs2378603	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2378607	0.82[EUR][1000 genomes]
rs28521319	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs28654270	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs28765200	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs28787398	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs34885880	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs35300015	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs61825253	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs61825254	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs61825258	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs61825259	0.85[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs6700083	0.87[AMR][1000 genomes];0.87[EUR][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	nsv999185	chr1:222500725-223278032	Strong transcription Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
2	nsv535304	chr1:222500725-223278032	Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
3	nsv1012537	chr1:222755091-223512243	Weak transcription Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
4	esv3369664	chr1:222935606-222958164	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	Chromatin interactive region	1 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	chr1:222934800-222939600	Weak transcription	Primary B cells from cord blood	blood
2	chr1:222934800-222940000	Weak transcription	Colon Smooth Muscle	Colon

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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