Variant report

Variant	rs10051090
Chromosome Location	chr5:114527392-114527393
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 1 )

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

rs_ID	r²[population]
rs11241317	0.81[ASN][1000 genomes]
rs12054867	0.91[CHB][hapmap]
rs1422074	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1422075	0.91[CHB][hapmap];0.98[CHD][hapmap];0.80[ASN][1000 genomes]
rs1559080	0.91[CHB][hapmap];0.98[CHD][hapmap]
rs1990897	0.97[ASN][1000 genomes]
rs2112363	0.91[CHB][hapmap]
rs267291	0.81[CHB][hapmap]
rs7713151	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][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	nsv830453	chr5:114277261-114546536	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Weak transcription Bivalent/Poised TSS Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
2	nsv830454	chr5:114453864-114607159	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs10051090	PGGT1B	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:114522800-114543400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr5:114523400-114576200	Weak transcription	Psoas Muscle	Psoas
3	chr5:114525400-114527400	Enhancers	iPS-15b Cell Line	embryonic stem cell
4	chr5:114525400-114531400	Enhancers	Rectal Mucosa Donor 31	rectum
5	chr5:114525600-114528200	Enhancers	Stomach Mucosa	stomach
6	chr5:114525800-114544800	Weak transcription	Primary T cells from cord blood	blood
7	chr5:114526000-114528600	Enhancers	Duodenum Mucosa	Duodenum
8	chr5:114526400-114527800	Weak transcription	Gastric	stomach
9	chr5:114526600-114527600	Enhancers	Sigmoid Colon	Sigmoid Colon
10	chr5:114526800-114527400	Weak transcription	Colonic Mucosa	Colon
11	chr5:114527000-114527400	Enhancers	Rectal Mucosa Donor 29	rectum
12	chr5:114527200-114527800	Enhancers	Breast Myoepithelial Primary Cells	Breast

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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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