Variant report

Variant	rs2156282
Chromosome Location	chr18:44120193-44120194
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs11082532	1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs12607120	0.89[ASN][1000 genomes]
rs1564130	0.84[ASN][1000 genomes]
rs1868711	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1893566	0.81[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs426303	0.82[ASN][1000 genomes]
rs4890668	0.90[ASN][1000 genomes]
rs7235681	0.95[ASN][1000 genomes]
rs7239183	0.91[ASN][1000 genomes]

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:44093200-44120400	Strong transcription	Primary neutrophils fromperipheralblood	blood
2	chr18:44094000-44126000	Weak transcription	Adipose Nuclei	Adipose
3	chr18:44109200-44126200	Weak transcription	Right Ventricle	heart
4	chr18:44111200-44126000	Weak transcription	Brain Angular Gyrus	brain
5	chr18:44118400-44126000	Weak transcription	Spleen	Spleen
6	chr18:44118600-44121400	Weak transcription	Primary monocytes fromperipheralblood	blood
7	chr18:44119400-44121400	Weak transcription	Monocytes-CD14+_RO01746	blood

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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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