Variant report

Variant	rs988213
Chromosome Location	chr18:44124967-44124968
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs12327030	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12456713	0.87[EUR][1000 genomes]
rs12458442	0.82[ASN][1000 genomes]
rs1450425	0.88[ASN][1000 genomes]
rs1868712	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4263029	0.86[ASN][1000 genomes]
rs4890330	0.87[EUR][1000 genomes]
rs4890667	0.81[CHD][hapmap];0.95[JPT][hapmap];0.88[ASN][1000 genomes]
rs4890669	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs59252058	0.81[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7237393	0.81[ASN][1000 genomes]
rs9951898	0.89[ASN][1000 genomes]

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:44094000-44126000	Weak transcription	Adipose Nuclei	Adipose
2	chr18:44109200-44126200	Weak transcription	Right Ventricle	heart
3	chr18:44111200-44126000	Weak transcription	Brain Angular Gyrus	brain
4	chr18:44118400-44126000	Weak transcription	Spleen	Spleen
5	chr18:44121000-44125600	Strong transcription	Primary neutrophils fromperipheralblood	blood
6	chr18:44121400-44125200	Strong transcription	Primary monocytes fromperipheralblood	blood
7	chr18:44121400-44125200	Strong transcription	Monocytes-CD14+_RO01746	blood
8	chr18:44122600-44126000	Weak transcription	Brain Anterior Caudate	brain

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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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