Variant report

Variant	rs7019474
Chromosome Location	chr9:103159112-103159113
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs13284374	0.87[AFR][1000 genomes]
rs13286077	0.87[AFR][1000 genomes]
rs13286964	0.80[AFR][1000 genomes]
rs13290800	0.87[AFR][1000 genomes]
rs13298673	0.87[AFR][1000 genomes]
rs34069247	0.91[AFR][1000 genomes]
rs34407044	0.87[AFR][1000 genomes]
rs34772962	0.89[AFR][1000 genomes]
rs34821647	0.87[AFR][1000 genomes]
rs34872449	0.87[AFR][1000 genomes]
rs35563956	0.87[AFR][1000 genomes]
rs35997802	0.87[AFR][1000 genomes]
rs36068962	0.87[AFR][1000 genomes]
rs71507680	0.87[AFR][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	nsv893623	chr9:102648036-103405197	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
2	nsv825012	chr9:103152205-103256281	Flanking Active TSS Active TSS Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:103151800-103160000	Weak transcription	iPS-15b Cell Line	embryonic stem cell

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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