Variant report

Variant	rs2225960
Chromosome Location	chr6:118315426-118315427
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs1338972	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs1338973	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs1416414	1.00[AFR][1000 genomes]
rs2355795	0.90[AFR][1000 genomes]
rs2760228	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs2760230	1.00[YRI][hapmap];0.83[AFR][1000 genomes]
rs2763008	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs2789011	1.00[AFR][1000 genomes]
rs2789012	1.00[YRI][hapmap]
rs4113074	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs4245489	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs4245491	1.00[YRI][hapmap]
rs4946310	1.00[AFR][1000 genomes]
rs6908566	1.00[YRI][hapmap];0.90[AFR][1000 genomes]
rs6934820	1.00[YRI][hapmap];0.90[AFR][1000 genomes]
rs6942098	1.00[AFR][1000 genomes]
rs7753286	1.00[YRI][hapmap]
rs7768494	0.90[AFR][1000 genomes]
rs9372490	0.90[AFR][1000 genomes]
rs9372491	0.90[AFR][1000 genomes]
rs9387523	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs9387534	1.00[YRI][hapmap];0.90[AFR][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	nsv530526	chr6:118027339-118718476	Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
2	esv3351599	chr6:118315359-118315730	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:118313600-118315600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr6:118313600-118315600	Enhancers	Brain Anterior Caudate	brain
3	chr6:118315400-118324400	Weak transcription	Cortex derived primary cultured neurospheres	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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