Variant report

Variant	rs328131
Chromosome Location	chr18:44264578-44264579
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs1710431	0.88[ASN][1000 genomes]
rs328114	1.00[CEU][hapmap];1.00[CHB][hapmap];0.88[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.88[MEX][hapmap];0.96[MKK][hapmap];0.95[TSI][hapmap];0.85[YRI][hapmap];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs328115	1.00[CHB][hapmap];0.83[ASN][1000 genomes]
rs328116	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs328119	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs328120	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[YRI][hapmap];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs328134	0.88[ASN][1000 genomes]
rs371346	0.94[ASN][1000 genomes]
rs430361	0.94[ASN][1000 genomes]
rs433296	0.94[ASN][1000 genomes]
rs447137	0.94[ASN][1000 genomes]
rs645631	0.94[ASN][1000 genomes]
rs9950834	1.00[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv428355	chr18:44160181-44406285	Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
2	nsv1058904	chr18:44224972-44264578	Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:44253000-44291400	Weak transcription	Brain Cingulate Gyrus	brain
2	chr18:44253600-44269600	Weak transcription	Brain Angular Gyrus	brain
3	chr18:44254000-44269200	Weak transcription	Right Atrium	heart
4	chr18:44256600-44274000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr18:44258200-44280000	Weak transcription	HSMMtube	muscle
6	chr18:44260800-44286600	Weak transcription	Brain Germinal Matrix	brain
7	chr18:44261000-44271800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr18:44261000-44271800	Weak transcription	Fetal Muscle Trunk	muscle
9	chr18:44261200-44269200	Weak transcription	Skeletal Muscle Male	skeletal muscle
10	chr18:44261400-44269200	Weak transcription	Skeletal Muscle Female	skeletal muscle
11	chr18:44261600-44270400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland

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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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