Variant report

Variant	rs74129118
Chromosome Location	chr10:26514043-26514044
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10466097	1.00[AMR][1000 genomes]
rs11015041	1.00[AMR][1000 genomes]
rs11015042	1.00[AMR][1000 genomes]
rs11015044	1.00[AMR][1000 genomes]
rs11015045	1.00[AMR][1000 genomes]
rs11015062	1.00[AMR][1000 genomes]
rs12245905	1.00[AMR][1000 genomes]
rs12256340	1.00[AMR][1000 genomes]
rs12263068	1.00[AMR][1000 genomes]
rs12269473	1.00[AMR][1000 genomes]
rs55923319	1.00[AMR][1000 genomes]
rs56194212	1.00[AMR][1000 genomes]
rs56201961	1.00[AMR][1000 genomes]
rs57729809	1.00[AMR][1000 genomes]
rs61012151	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74126404	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74126408	1.00[AMR][1000 genomes]
rs74126411	1.00[AMR][1000 genomes]
rs74126455	1.00[AMR][1000 genomes]
rs74129117	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74129120	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74129123	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74129124	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8190619	1.00[ASN][1000 genomes]
rs8190673	1.00[AMR][1000 genomes]
rs8190778	1.00[AMR][1000 genomes]
rs8190797	1.00[AMR][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	nsv894975	chr10:26343356-27014467	Strong transcription Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 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	chr10:26512000-26515200	Weak transcription	Brain Germinal Matrix	brain
2	chr10:26512600-26514200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr10:26513600-26514600	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
4	chr10:26513800-26514200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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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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