Variant report

Variant	rs1413395
Chromosome Location	chr10:25642125-25642126
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs1334057	0.84[ASN][1000 genomes]
rs1341967	0.81[ASN][1000 genomes]
rs1361633	0.89[ASN][1000 genomes]
rs1410935	0.82[ASN][1000 genomes]
rs1413398	0.86[ASN][1000 genomes]
rs1418126	0.89[ASN][1000 genomes]
rs1576319	0.84[ASN][1000 genomes]
rs1612726	0.89[ASN][1000 genomes]
rs1754248	0.89[ASN][1000 genomes]
rs1754252	0.84[ASN][1000 genomes]
rs1754259	0.84[ASN][1000 genomes]
rs1754263	0.81[ASN][1000 genomes]
rs1754270	0.89[ASN][1000 genomes]
rs1754276	0.82[ASN][1000 genomes]
rs1754277	0.87[ASN][1000 genomes]
rs1773604	0.82[ASN][1000 genomes]
rs1773615	0.83[ASN][1000 genomes]
rs1773652	0.91[ASN][1000 genomes]
rs1773655	0.87[ASN][1000 genomes]
rs1773656	0.89[ASN][1000 genomes]
rs1773657	0.89[ASN][1000 genomes]
rs1773658	0.89[ASN][1000 genomes]
rs1773659	0.81[ASN][1000 genomes]
rs1773688	0.87[ASN][1000 genomes]
rs7081326	0.89[ASN][1000 genomes]
rs7097708	0.89[ASN][1000 genomes]
rs7924230	0.82[ASN][1000 genomes]
rs824591	0.82[ASN][1000 genomes]
rs824594	0.90[ASN][1000 genomes]
rs824596	0.81[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	esv2761583	chr10:25525657-25722444	Weak transcription Enhancers ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	esv3349863	chr10:25614571-25946379	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:25632400-25642600	Weak transcription	Cortex derived primary cultured neurospheres	brain

Quick Search:

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

what's new

Quick links