Variant report

Variant	rs7655488
Chromosome Location	chr4:21183041-21183042
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 1 )

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

rs_ID	r²[population]
rs1319225	0.91[CHB][hapmap];0.91[CHD][hapmap];0.86[JPT][hapmap]
rs1433482	0.87[CHD][hapmap];0.86[JPT][hapmap];0.85[ASN][1000 genomes]
rs1812828	0.90[CHB][hapmap];0.90[JPT][hapmap];0.95[ASN][1000 genomes]
rs1836087	0.89[CHD][hapmap];0.81[GIH][hapmap];0.86[JPT][hapmap]
rs2060326	0.87[CHD][hapmap];0.82[JPT][hapmap]
rs2322870	0.86[JPT][hapmap]
rs2322873	0.86[JPT][hapmap]
rs2322874	0.91[ASN][1000 genomes]
rs4263402	0.90[JPT][hapmap]
rs4697206	0.80[ASN][1000 genomes]
rs6448023	0.87[CHD][hapmap];0.86[JPT][hapmap];0.85[ASN][1000 genomes]
rs6448027	0.86[JPT][hapmap]
rs6821250	0.82[CHB][hapmap];0.89[CHD][hapmap];0.81[GIH][hapmap];0.86[JPT][hapmap]
rs6854413	0.89[CHD][hapmap];0.86[JPT][hapmap];0.87[ASN][1000 genomes]
rs7658047	0.83[CHB][hapmap];0.86[JPT][hapmap]
rs7687191	0.87[CHD][hapmap];0.82[JPT][hapmap]
rs892314	0.86[JPT][hapmap]

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	nsv1014941	chr4:20611726-21345226	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	nsv537053	chr4:20611726-21345226	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	nsv1013365	chr4:20834054-21609078	Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases
4	nsv4264	chr4:21138131-21199262	Weak transcription Enhancers Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs7655488	PACRGL	cis	cerebellum	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:21182600-21183800	Enhancers	Fetal Lung	lung

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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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