Variant report

Variant	rs7969702
Chromosome Location	chr12:51429130-51429131
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 45 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs10876126	0.87[EUR][1000 genomes]
rs11169679	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12423207	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs150909	0.85[EUR][1000 genomes]
rs161044	0.85[EUR][1000 genomes]
rs161045	0.88[EUR][1000 genomes]
rs161046	0.88[EUR][1000 genomes]
rs161047	0.88[EUR][1000 genomes]
rs224564	0.85[EUR][1000 genomes]
rs224566	0.85[EUR][1000 genomes]
rs224569	0.85[EUR][1000 genomes]
rs224570	0.85[EUR][1000 genomes]
rs224573	0.92[EUR][1000 genomes]
rs224574	0.92[EUR][1000 genomes]
rs224578	0.88[EUR][1000 genomes]
rs224585	0.86[EUR][1000 genomes]
rs224586	0.85[EUR][1000 genomes]
rs224590	0.88[EUR][1000 genomes]
rs224592	0.88[EUR][1000 genomes]
rs224593	0.88[EUR][1000 genomes]
rs2630362	0.85[EUR][1000 genomes]
rs364627	0.92[EUR][1000 genomes]
rs390424	0.88[EUR][1000 genomes]
rs394384	0.85[EUR][1000 genomes]
rs416062	0.92[EUR][1000 genomes]
rs4238110	0.92[EUR][1000 genomes]
rs435965	0.92[EUR][1000 genomes]
rs445520	0.88[EUR][1000 genomes]
rs452587	0.92[EUR][1000 genomes]
rs4768875	0.92[EUR][1000 genomes]
rs613977	0.90[EUR][1000 genomes]
rs618510	0.89[EUR][1000 genomes]
rs6580779	0.86[EUR][1000 genomes]
rs6580780	0.92[EUR][1000 genomes]
rs6580781	0.83[EUR][1000 genomes]
rs686528	0.92[EUR][1000 genomes]
rs706803	0.83[EUR][1000 genomes]
rs706804	0.83[EUR][1000 genomes]
rs7299484	0.92[EUR][1000 genomes]
rs7969536	0.83[EUR][1000 genomes]
rs7971712	0.85[EUR][1000 genomes]
rs829021	0.83[EUR][1000 genomes]
rs9739943	0.85[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	esv3414501	chr12:51174503-51534707	Strong transcription Weak transcription Genic enhancers Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
2	esv34039	chr12:51326702-51671911	Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	93 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs7969702	SLC11A2	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:51422800-51432000	Weak transcription	Stomach Mucosa	stomach
2	chr12:51423800-51431800	Weak transcription	Hela-S3	cervix
3	chr12:51427600-51429200	Weak transcription	HepG2	liver
4	chr12:51428600-51429600	Weak transcription	Fetal Intestine Small	intestine

Quick Search:

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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