Variant report

Variant	rs10477427
Chromosome Location	chr5:108019422-108019423
allele	G/T
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]
rs10477928	1.00[CEU][hapmap];0.86[CHB][hapmap];0.91[JPT][hapmap];0.84[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11952230	1.00[CEU][hapmap];0.86[CHB][hapmap];0.91[JPT][hapmap];0.84[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11952282	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs35842524	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4623197	1.00[CEU][hapmap];0.87[CHB][hapmap];0.91[JPT][hapmap];0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4957781	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs56915053	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7703883	1.00[CEU][hapmap];0.86[CHB][hapmap];0.91[JPT][hapmap];0.80[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7704020	0.80[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7704155	0.80[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7704581	0.94[EUR][1000 genomes]
rs7735104	0.86[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7737443	1.00[CEU][hapmap];0.80[AMR][1000 genomes];0.93[EUR][1000 genomes]

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	nsv882689	chr5:107595383-108299744	Enhancers ZNF genes & repeats Active TSS Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
2	nsv1024076	chr5:107991426-108028223	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:108007000-108034800	Weak transcription	Right Atrium	heart
2	chr5:108014200-108020800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr5:108017400-108021000	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr5:108017400-108021000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr5:108017400-108021200	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr5:108017400-108022000	Weak transcription	Brain Angular Gyrus	brain
7	chr5:108017600-108020800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr5:108017600-108021000	Weak transcription	Primary B cells from peripheral blood	blood
9	chr5:108017600-108021200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr5:108017600-108021200	Weak transcription	HepG2	liver
11	chr5:108017600-108021600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
12	chr5:108017600-108023600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr5:108017600-108023600	Weak transcription	Primary monocytes fromperipheralblood	blood
14	chr5:108017800-108020800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
15	chr5:108018200-108023000	Weak transcription	GM12878-XiMat	blood

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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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