Variant report

Variant	rs61825254
Chromosome Location	chr1:222935479-222935480
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:222933683..222936065-chr1:222964950..222967024,2	K562	blood:

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs11490203	0.86[ASN][1000 genomes]
rs12043288	0.84[EUR][1000 genomes]
rs12073392	0.81[ASN][1000 genomes]
rs12749296	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17532708	0.87[EUR][1000 genomes]
rs2068814	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2378603	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2378607	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs28521319	0.86[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs28654270	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28765200	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28787398	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs34311160	0.86[ASN][1000 genomes]
rs34885880	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs35300015	0.85[AFR][1000 genomes];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs35725247	0.87[EUR][1000 genomes]
rs35806535	0.81[ASN][1000 genomes]
rs35968825	0.83[ASN][1000 genomes]
rs4240935	0.88[ASN][1000 genomes]
rs4282830	0.87[EUR][1000 genomes]
rs61824331	0.88[EUR][1000 genomes]
rs61825253	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs61825255	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs61825258	0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs61825259	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6700083	0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 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

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:222934400-222935600	Enhancers	HSMMtube	muscle
2	chr1:222934800-222939600	Weak transcription	Primary B cells from cord blood	blood
3	chr1:222934800-222940000	Weak transcription	Colon Smooth Muscle	Colon
4	chr1:222935200-222935600	Enhancers	Fetal Muscle Leg	muscle

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