Variant report

Variant	rs55766784
Chromosome Location	chr6:75151391-75151392
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs11751066	1.00[AFR][1000 genomes]
rs11752582	1.00[AFR][1000 genomes]
rs16884854	0.87[EUR][1000 genomes]
rs1830595	1.00[AFR][1000 genomes]
rs41367946	0.83[EUR][1000 genomes]
rs56168999	0.92[EUR][1000 genomes]
rs56206543	0.83[EUR][1000 genomes]
rs71555263	1.00[AFR][1000 genomes]
rs72958951	1.00[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs72958964	0.94[EUR][1000 genomes]
rs72958991	1.00[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs72960912	1.00[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs72960934	1.00[AFR][1000 genomes]
rs72969247	0.83[EUR][1000 genomes]
rs72969251	0.81[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2759442	chr6:74961996-75162222	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	esv35015	chr6:75031337-75154143	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	esv2757178	chr6:75060947-75162222	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv886166	chr6:75082067-75155303	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv886167	chr6:75102625-75175449	Enhancers Weak transcription Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv886168	chr6:75112715-75166715	Enhancers Weak transcription Active TSS	Chromatin interactive region lncRNA	1 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	chr6:75149800-75155800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	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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