Variant report

Variant	rs10253383
Chromosome Location	chr7:38138584-38138585
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs10227310	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10272947	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12113670	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs55683740	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56253086	0.85[AFR][1000 genomes]
rs73691930	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73691943	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73691974	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73691976	1.00[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	nsv8074	chr7:37865340-38210087	ZNF genes & repeats Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	nsv887962	chr7:38093233-38203341	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:38138400-38138800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell

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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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