Variant report

Variant	rs10468955
Chromosome Location	chr18:39119258-39119259
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10048345	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10083938	0.94[AFR][1000 genomes]
rs10084019	1.00[AMR][1000 genomes]
rs10163863	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10163951	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10164168	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10502768	1.00[AMR][1000 genomes]
rs12327187	1.00[AMR][1000 genomes]
rs13381786	0.81[AFR][1000 genomes]
rs1545056	1.00[AMR][1000 genomes]
rs16974747	1.00[AMR][1000 genomes]
rs16974835	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16974997	1.00[AMR][1000 genomes]
rs16975126	1.00[AMR][1000 genomes]
rs55946383	0.81[AFR][1000 genomes]
rs57557970	0.81[AFR][1000 genomes]
rs58356161	1.00[AMR][1000 genomes]
rs73950952	1.00[AMR][1000 genomes]
rs73953311	1.00[AMR][1000 genomes]
rs73953336	0.81[AFR][1000 genomes]
rs9807141	1.00[AMR][1000 genomes]
rs9807239	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9807489	1.00[AMR][1000 genomes]
rs9963615	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv909564	chr18:38739067-39179256	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv1066869	chr18:38742896-39680723	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	nsv543685	chr18:38742896-39680723	Flanking Active TSS Enhancers Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:39118600-39125800	Weak transcription	Fetal Heart	heart
2	chr18:39119200-39119400	Enhancers	Fetal Brain Male	brain

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Input of quick search could be:

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

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