Variant report

Variant	rs17754667
Chromosome Location	chr14:78654373-78654374
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs11628166	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs11628271	0.92[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12878262	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12880798	0.95[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs12883548	0.95[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs12897003	0.94[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12897190	0.94[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs17107053	0.83[EUR][1000 genomes]
rs1882818	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2049818	0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs61975962	0.91[AMR][1000 genomes];0.82[EUR][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	nsv1366	chr14:78633044-78677718	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
2	nsv1038627	chr14:78635498-78657912	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:78648000-78659000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr14:78651600-78654600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr14:78652600-78660200	Weak transcription	Brain Germinal Matrix	brain

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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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