Variant report

Variant	rs2821127
Chromosome Location	chr1:197309594-197309595
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs1337169	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1415214	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1615444	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1764622	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1764623	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1764624	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1764625	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1764786	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1764787	0.88[EUR][1000 genomes]
rs1764788	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1764791	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1764792	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2786108	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2786110	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2786111	0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2786112	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2786113	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2786115	0.89[AFR][1000 genomes];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2821131	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs482526	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs550098	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs554009	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs570845	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs572447	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs580067	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs643025	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs658409	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs664767	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs675699	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]

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	nsv528460	chr1:196542567-197446702	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	26 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	chr1:197299000-197323400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr1:197302400-197312800	Weak transcription	Brain Anterior Caudate	brain
3	chr1:197308400-197309600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr1:197309000-197309600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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