Variant report

Variant	rs10829226
Chromosome Location	chr10:27573952-27573953
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:27531276..27533998-chr10:27572512..27575307,2	K562	blood:

Variant related genes	Relation type
ENSG00000262412	Chromatin interaction

Extended variants
information (count: 38 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10764692	0.97[AFR][1000 genomes];0.94[EUR][1000 genomes]
rs10829222	0.83[ASN][1000 genomes]
rs10829223	0.84[ASN][1000 genomes]
rs10829224	0.83[ASN][1000 genomes]
rs10829225	0.84[ASN][1000 genomes]
rs10829227	0.84[ASN][1000 genomes]
rs10829228	0.82[ASN][1000 genomes]
rs10829229	0.82[ASN][1000 genomes]
rs10829231	0.94[EUR][1000 genomes]
rs10829233	0.83[ASN][1000 genomes]
rs11015635	0.82[ASN][1000 genomes]
rs11015637	0.83[ASN][1000 genomes]
rs11015640	0.82[ASN][1000 genomes]
rs11015642	0.84[ASN][1000 genomes]
rs11015643	0.84[ASN][1000 genomes]
rs11015644	0.82[ASN][1000 genomes]
rs11015646	0.84[ASN][1000 genomes]
rs11015647	0.84[ASN][1000 genomes]
rs11015650	0.80[ASN][1000 genomes]
rs1832019	0.84[ASN][1000 genomes]
rs1832020	0.83[ASN][1000 genomes]
rs1832021	0.84[ASN][1000 genomes]
rs2184165	0.84[ASN][1000 genomes]
rs35724729	0.83[ASN][1000 genomes]
rs35891243	0.84[ASN][1000 genomes]
rs3818746	0.82[ASN][1000 genomes]
rs4396190	0.84[ASN][1000 genomes]
rs4607976	0.84[ASN][1000 genomes]
rs4617487	0.84[ASN][1000 genomes]
rs61849692	0.82[ASN][1000 genomes]
rs7076087	0.84[ASN][1000 genomes]
rs7090358	0.80[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2422253	chr10:27431366-27575370	Strong transcription Genic enhancers Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
2	esv3337781	chr10:27472216-27666703	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
3	nsv8614	chr10:27504487-27828406	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
4	nsv550241	chr10:27569521-28025771	Enhancers ZNF genes & repeats Strong transcription Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
5	esv3413607	chr10:27569733-27577795	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv1045257	chr10:27572440-27926946	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs10829226	ARMC4P1	cis	Esophagus Muscularis	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:27573200-27574200	Enhancers	Liver	Liver

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