Variant report

Variant	rs74111690
Chromosome Location	chr10:4786946-4786947
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs11816368	1.00[AMR][1000 genomes]
rs55943502	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56884859	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57042805	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58392847	1.00[AMR][1000 genomes]
rs7074452	0.87[AFR][1000 genomes]
rs74111688	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74111694	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74111695	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74111698	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74111699	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74111701	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74113604	0.90[AFR][1000 genomes];1.00[AMR][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	nsv894787	chr10:4385379-4857717	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
2	nsv549880	chr10:4781029-4810561	Enhancers Genic enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:4779200-4791200	Weak transcription	HMEC	breast
2	chr10:4783400-4793400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr10:4784800-4787000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr10:4786000-4787200	Strong transcription	NHDF-Ad	bronchial
5	chr10:4786600-4791400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr10:4786800-4787600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	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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