Variant report

Variant	rs7687956
Chromosome Location	chr4:110810224-110810225
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs11736783	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11937583	0.97[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs13117220	0.97[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1978231	0.90[AMR][1000 genomes]
rs6852679	0.85[EUR][1000 genomes]
rs7669266	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9918080	0.97[AMR][1000 genomes];0.91[EUR][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	nsv530156	chr4:110721397-110911297	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 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	chr4:110807600-110810800	Weak transcription	Psoas Muscle	Psoas
2	chr4:110807800-110811400	Weak transcription	Skeletal Muscle Male	skeletal muscle
3	chr4:110807800-110811400	Weak transcription	Skeletal Muscle Female	skeletal muscle
4	chr4:110808400-110810800	Weak transcription	HSMMtube	muscle

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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