Variant report

Variant	rs1551233
Chromosome Location	chr18:44095365-44095366
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs4133965	0.81[JPT][hapmap]
rs426303	0.84[AFR][1000 genomes]
rs9807265	0.89[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs986117	0.81[JPT][hapmap]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3407279	chr18:44094554-44098852	Enhancers Bivalent Enhancer Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:44086000-44114400	Weak transcription	Spleen	Spleen
2	chr18:44086800-44099200	Weak transcription	Right Ventricle	heart
3	chr18:44088000-44096400	Strong transcription	Monocytes-CD14+_RO01746	blood
4	chr18:44093200-44118600	Strong transcription	Primary monocytes fromperipheralblood	blood
5	chr18:44093200-44120400	Strong transcription	Primary neutrophils fromperipheralblood	blood
6	chr18:44094000-44126000	Weak transcription	Adipose Nuclei	Adipose

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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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