Variant report

Variant	rs17370180
Chromosome Location	chr1:179742819-179742820
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:179741509..179743490-chr1:179922299..179924287,2	K562	blood:

Variant related genes	Relation type
ENSG00000135837	Chromatin interaction
ENSG00000260360	Chromatin interaction

Extended variants
information (count: 27 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs11812078	0.86[CEU][hapmap];0.86[JPT][hapmap];0.80[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs16854685	0.86[CEU][hapmap];0.85[CHD][hapmap];0.83[GIH][hapmap];0.86[JPT][hapmap];0.91[TSI][hapmap]
rs16854692	0.85[CEU][hapmap];0.86[JPT][hapmap];0.80[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs17279065	0.86[JPT][hapmap]
rs2318392	0.86[CEU][hapmap];0.85[JPT][hapmap]
rs2318393	0.86[CEU][hapmap];0.85[CHD][hapmap];0.83[GIH][hapmap];0.86[JPT][hapmap];0.91[TSI][hapmap]
rs3845384	0.86[CEU][hapmap];0.86[JPT][hapmap]
rs3893369	0.81[CEU][hapmap];0.85[CHD][hapmap];0.83[GIH][hapmap];0.86[JPT][hapmap];0.91[TSI][hapmap]
rs4428843	0.86[EUR][1000 genomes]
rs4652453	0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.88[JPT][hapmap];0.88[MEX][hapmap];0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs56166650	0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs56965719	0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs58204878	0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs61828391	0.81[ASN][1000 genomes]
rs6425592	0.86[CEU][hapmap];0.85[CHD][hapmap];0.83[GIH][hapmap];0.86[JPT][hapmap];0.91[TSI][hapmap];0.80[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6425593	0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.88[JPT][hapmap];0.88[MEX][hapmap];0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6683249	0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6696060	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs68141282	0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7514717	0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7517022	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7544460	0.86[CEU][hapmap];0.86[JPT][hapmap]
rs7544925	0.86[CEU][hapmap];0.86[JPT][hapmap]
rs7549144	0.86[CEU][hapmap];0.85[JPT][hapmap];0.80[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7549263	0.86[CEU][hapmap];0.86[JPT][hapmap];0.80[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[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	nsv1009961	chr1:179714247-179790110	Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv1011407	chr1:179733193-179799430	Bivalent Enhancer Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs17370180	FAM163A	cis	parietal	SCAN
rs17370180	SOAT1	cis	multi-tissue	Pritchard

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:179737000-179756000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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