Variant report

Variant	rs4498222
Chromosome Location	chr5:54084234-54084235
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10064404	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10066485	0.90[EUR][1000 genomes]
rs10072474	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10074079	0.90[EUR][1000 genomes]
rs10075754	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4425466	0.90[CEU][hapmap]
rs4572962	0.81[CEU][hapmap]
rs57059470	0.86[AMR][1000 genomes]
rs7703792	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv880717	chr5:54025701-54106378	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv830300	chr5:54056300-54257344	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	esv3358092	chr5:54077828-54189150	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	esv2754136	chr5:54083387-54107727	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:54073000-54097600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr5:54082000-54088600	Weak transcription	Fetal Stomach	stomach
3	chr5:54082400-54087600	Weak transcription	Fetal Muscle Trunk	muscle
4	chr5:54083200-54084400	Weak transcription	Left Ventricle	heart
5	chr5:54083200-54088000	Weak transcription	Fetal Heart	heart
6	chr5:54083200-54088800	Weak transcription	Aorta	Aorta
7	chr5:54083400-54087400	Weak transcription	Fetal Muscle Leg	muscle

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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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