Variant report

Variant	rs1213958
Chromosome Location	chr2:124809685-124809686
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:124804089..124806526-chr2:124808703..124810618,2	K562	blood:
2	chr2:124808179..124810494-chr2:124811698..124813821,2	K562	blood:

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs1036609	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1213938	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1213942	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1213945	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1213946	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1213948	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap]
rs1213950	1.00[CEU][hapmap];0.93[CHB][hapmap];0.91[JPT][hapmap];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1213956	0.96[CEU][hapmap];0.93[CHB][hapmap];0.91[JPT][hapmap];0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1213962	0.96[CEU][hapmap];0.84[CHB][hapmap];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1228168	1.00[CEU][hapmap];0.93[CHB][hapmap];0.91[JPT][hapmap];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1347876	0.84[CEU][hapmap];0.87[CHB][hapmap];0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs17010766	0.93[CHB][hapmap];0.91[JPT][hapmap];0.89[ASN][1000 genomes]
rs17010827	0.93[CHB][hapmap];0.91[JPT][hapmap];0.89[ASN][1000 genomes]
rs17010876	0.81[CHB][hapmap]
rs17278676	0.83[CEU][hapmap];0.81[CHB][hapmap];0.82[EUR][1000 genomes]
rs1816698	1.00[CEU][hapmap];0.93[CHB][hapmap];0.91[JPT][hapmap]
rs1898788	1.00[CEU][hapmap];0.93[CHB][hapmap];0.91[JPT][hapmap];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2439003	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7567584	0.93[CHB][hapmap];0.91[JPT][hapmap];0.85[ASN][1000 genomes]
rs868995	0.81[CHB][hapmap]
rs959320	0.81[CEU][hapmap]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531408	chr2:124727329-125011247	Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr2:124805600-124810000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
2	chr2:124809600-124809800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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