Variant report

Variant	rs16884736
Chromosome Location	chr8:36075940-36075941
allele	C/G/T
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:5)

rs_ID	r²[population]
rs16884618	1.00[AMR][1000 genomes]
rs16884638	1.00[AMR][1000 genomes]
rs2105023	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs41503248	1.00[AMR][1000 genomes]
rs7015832	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533420	chr8:35358115-36227536	Enhancers Strong transcription Weak transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
2	nsv1024552	chr8:35655964-36210907	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
3	nsv539548	chr8:35655964-36210907	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
4	nsv890718	chr8:35948467-36224134	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
5	nsv819958	chr8:36073740-36080027	Weak transcription Enhancers	n/a	n/a	inside rSNPs	n/a
6	esv2422113	chr8:36075155-36078341	Enhancers Weak transcription	n/a	n/a	inside rSNPs	n/a
7	nsv442104	chr8:36075155-36078341	Enhancers Weak transcription	n/a	n/a	inside rSNPs	n/a
8	nsv824596	chr8:36075478-36078619	Enhancers Weak transcription	n/a	n/a	inside rSNPs	n/a
9	nsv824597	chr8:36075478-36079997	Weak transcription Enhancers	n/a	n/a	inside rSNPs	n/a
10	nsv515078	chr8:36075678-36078358	Enhancers Weak transcription	n/a	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:36075800-36076600	Enhancers	Adipose Nuclei	Adipose

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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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