Variant report

Variant	rs1898319
Chromosome Location	chr10:44825783-44825784
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs1144483	0.99[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1144484	0.99[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1370158	0.98[AFR][1000 genomes];0.80[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1436931	0.98[AFR][1000 genomes];0.80[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs17156117	0.82[ASN][1000 genomes]
rs1836982	0.98[AFR][1000 genomes];0.80[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1898317	0.96[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs1898318	0.93[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs2028102	0.98[AFR][1000 genomes];0.80[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2457481	0.96[AFR][1000 genomes];0.91[EUR][1000 genomes]
rs2476351	0.86[EUR][1000 genomes]
rs2505737	0.84[EUR][1000 genomes]
rs2505739	0.84[EUR][1000 genomes]
rs2505740	0.89[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs2505743	0.94[AFR][1000 genomes];0.91[EUR][1000 genomes]
rs2505744	0.85[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs977754	0.84[EUR][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	nsv1038511	chr10:44596885-44870030	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	nsv1052337	chr10:44821390-44865015	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:44822400-44826000	Weak transcription	Small Intestine	intestine
2	chr10:44823000-44827200	Weak transcription	Skeletal Muscle Female	skeletal muscle
3	chr10:44823200-44830200	Weak transcription	Pancreas	Pancrea

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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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