Variant report

Variant	rs10919234
Chromosome Location	chr1:169732443-169732444
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10157398	0.93[CEU][hapmap];0.92[CHB][hapmap];0.89[JPT][hapmap];0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10753794	0.92[CHB][hapmap]
rs10800474	0.89[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10800476	0.92[CEU][hapmap];0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10919238	0.84[CHB][hapmap]
rs10919242	0.84[CHB][hapmap]
rs12063022	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12129417	0.84[CHB][hapmap]
rs2076059	0.96[CEU][hapmap];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2420507	0.81[ASN][1000 genomes]
rs3917389	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs3917419	0.96[CEU][hapmap];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6427218	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6686522	0.84[CHB][hapmap]
rs722511	0.84[CHB][hapmap]
rs7526645	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7531675	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7543618	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7549412	1.00[CEU][hapmap];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes]

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	esv3451367	chr1:169630075-169976964	Strong transcription Flanking Active TSS Genic enhancers Enhancers Weak transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:169728000-169732800	Weak transcription	Adipose Nuclei	Adipose
2	chr1:169730800-169732600	Enhancers	Sigmoid Colon	Sigmoid Colon
3	chr1:169731200-169733200	Enhancers	Rectal Mucosa Donor 31	rectum
4	chr1:169731600-169732800	Enhancers	Rectal Mucosa Donor 29	rectum
5	chr1:169731800-169732600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr1:169732200-169732800	Enhancers	Breast Myoepithelial Primary Cells	Breast
7	chr1:169732200-169732800	Bivalent Enhancer	Small Intestine	intestine
8	chr1:169732200-169733000	Enhancers	Fetal Intestine Large	intestine

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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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