Variant report

Variant	rs10049074
Chromosome Location	chr3:121702325-121702326
allele	C/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 2 )

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

rs_ID	r²[population]
rs10934568	0.87[YRI][hapmap];0.83[AFR][1000 genomes];0.95[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10934570	0.87[CEU][hapmap]
rs11718322	0.82[AMR][1000 genomes]
rs12637573	0.87[EUR][1000 genomes]
rs13074085	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1920289	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs3762821	0.80[AMR][1000 genomes]
rs3792597	0.80[AMR][1000 genomes]
rs4325959	0.80[AMR][1000 genomes]
rs59823080	0.80[AMR][1000 genomes]
rs6793566	0.83[AFR][1000 genomes];0.95[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6793858	0.95[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9811389	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9812869	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9824120	0.87[CEU][hapmap]
rs9825193	0.83[AFR][1000 genomes];0.95[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9844039	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9867460	0.80[AMR][1000 genomes]
rs9871743	0.90[AMR][1000 genomes];0.91[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	esv33139	chr3:121500400-122091831	Strong transcription Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs10049074	SLC15A2	cis	Artery Tibial	GTEx
rs10049074	SLC15A2	Cis_1M	lymphoblastoid	RTeQTL

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:121698400-121704800	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr3:121699000-121704800	Weak transcription	Rectal Mucosa Donor 29	rectum
3	chr3:121699000-121711200	Weak transcription	Rectal Mucosa Donor 31	rectum
4	chr3:121699400-121714200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr3:121699600-121703400	Weak transcription	Primary monocytes fromperipheralblood	blood
6	chr3:121701800-121703400	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr3:121702000-121703200	ZNF genes & repeats	Primary B cells from peripheral blood	blood
8	chr3:121702200-121703600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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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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