Variant report

Variant	rs2265242
Chromosome Location	chr1:160939134-160939135
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 28 )
Associated
traits (count: 1 )

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

rs_ID	r²[population]
rs2184065	0.87[ASN][1000 genomes]
rs2245672	0.94[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs2246145	0.94[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs2246484	0.91[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs2246485	0.91[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs2249409	0.94[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs2249933	0.86[AMR][1000 genomes]
rs2250174	0.89[AMR][1000 genomes]
rs2250193	0.89[AMR][1000 genomes]
rs2250304	0.89[AMR][1000 genomes]
rs2256505	0.85[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs2256625	0.86[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs2265239	0.92[AMR][1000 genomes]
rs2265240	0.94[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs2481073	0.92[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs2483139	0.86[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs2483140	0.95[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs2483142	0.82[AMR][1000 genomes]
rs2779801	0.95[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs2988722	0.84[AMR][1000 genomes]
rs2990694	0.92[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs3007155	0.88[AMR][1000 genomes]
rs6427563	0.95[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs6427571	0.86[AMR][1000 genomes]
rs6677526	0.84[AMR][1000 genomes]
rs6677533	0.94[AMR][1000 genomes];0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530077	chr1:160836448-161284904	Enhancers Weak transcription Strong transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	119 gene(s)	inside rSNPs	diseases
2	nsv548058	chr1:160925455-160989614	Flanking Active TSS Genic enhancers Active TSS Enhancers Bivalent Enhancer Weak transcription Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs2265242	F11R	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:160931000-160942000	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr1:160938000-160941200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr1:160939000-160941200	Weak transcription	H1 Cell Line	embryonic stem cell

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Input of quick search could be:

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

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