Variant report

Variant	rs61605094
Chromosome Location	chr7:117686024-117686025
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs17140971	1.00[AMR][1000 genomes]
rs73477483	1.00[AMR][1000 genomes]
rs73477495	1.00[AMR][1000 genomes]
rs73479305	1.00[AMR][1000 genomes]
rs7780015	1.00[AMR][1000 genomes]
rs7792745	1.00[AMR][1000 genomes]
rs7792854	1.00[AMR][1000 genomes]
rs7802235	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	nsv869971	chr7:117420583-118274149	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	40 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	chr7:117683200-117691600	Weak transcription	Fetal Brain Male	brain
2	chr7:117683200-117692000	Weak transcription	Fetal Brain Female	brain
3	chr7:117685800-117686400	Enhancers	Fetal Heart	heart
4	chr7:117686000-117687800	Enhancers	Brain Germinal Matrix	brain

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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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