Variant report

Variant	rs1912136
Chromosome Location	chr11:24616743-24616744
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs10767215	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10834383	0.81[ASN][1000 genomes]
rs10834389	0.83[EUR][1000 genomes]
rs10834390	0.83[EUR][1000 genomes]
rs10834391	0.83[EUR][1000 genomes]
rs10834393	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11028005	0.81[ASN][1000 genomes]
rs11028028	0.83[EUR][1000 genomes]
rs11600443	0.83[EUR][1000 genomes]
rs12284708	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12293149	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1396849	0.81[ASN][1000 genomes]
rs35783821	0.81[ASN][1000 genomes]
rs7115380	0.83[EUR][1000 genomes]
rs7118822	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7131395	0.83[EUR][1000 genomes]
rs981895	0.83[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1055026	chr11:24151133-24737122	Enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv1037744	chr11:24174588-24737122	Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv553820	chr11:24583891-24633951	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv897092	chr11:24609026-24648325	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:24615800-24616800	Weak transcription	Fetal Heart	heart
2	chr11:24616000-24620000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland

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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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