Variant report

Variant	rs9609516
Chromosome Location	chr22:32755074-32755075
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	22:32529813-32538538..22:32750950-32761732	K562	blood:
2	22:32360288-32405313..22:32750950-32761732	K562	blood:
3	22:32665993-32670527..22:32750950-32761732	K562	blood:
4	22:31936958-31958600..22:32750950-32761732	Hela-S3	cervix:
5	22:32513817-32522138..22:32750950-32761732	H1-hESC	embryonic stem cell:	embryo
6	22:32750950-32761732..22:33253287-33262063	Hela-S3	cervix:
7	22:32284948-32287956..22:32750950-32761732	K562	blood:

Variant related genes	Relation type
ENSG00000240647	Chromatin interaction
ENSG00000214093	Chromatin interaction
ENSG00000227813	Chromatin interaction
ENSG00000232707	Chromatin interaction
ENSG00000224050	Chromatin interaction
ENSG00000239674	Chromatin interaction
ENSG00000230866	Chromatin interaction
ENSG00000183531	Chromatin interaction
ENSG00000234479	Chromatin interaction

Extended variants
information (count: 32 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs12530	0.82[ASW][hapmap];0.85[CEU][hapmap];1.00[GIH][hapmap];1.00[MKK][hapmap];0.86[TSI][hapmap];0.81[EUR][1000 genomes]
rs5754074	0.80[EUR][1000 genomes]
rs73166349	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs73166359	0.85[EUR][1000 genomes]
rs73166393	0.80[EUR][1000 genomes]
rs73168721	0.80[EUR][1000 genomes]
rs73168729	0.80[EUR][1000 genomes]
rs734809	0.92[CEU][hapmap];1.00[GIH][hapmap];0.86[TSI][hapmap]
rs9606939	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs9606940	0.92[CEU][hapmap];0.85[EUR][1000 genomes]
rs9606942	0.91[CEU][hapmap];0.88[EUR][1000 genomes]
rs9606944	0.82[EUR][1000 genomes]
rs9606945	0.91[CEU][hapmap];0.82[EUR][1000 genomes]
rs9606947	0.80[EUR][1000 genomes]
rs9606950	0.80[EUR][1000 genomes]
rs9609513	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs9609514	0.84[EUR][1000 genomes]
rs9609515	0.92[CEU][hapmap];0.81[GIH][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.81[TSI][hapmap];0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs9609523	0.91[CEU][hapmap];0.82[EUR][1000 genomes]
rs9609527	0.82[ASW][hapmap];0.92[CEU][hapmap];1.00[GIH][hapmap];1.00[MKK][hapmap];0.86[TSI][hapmap];0.80[EUR][1000 genomes]
rs9609529	0.80[EUR][1000 genomes]
rs9609530	0.80[EUR][1000 genomes]
rs9609531	0.80[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948789	chr22:32462505-32764760	Enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
2	nsv1065175	chr22:32467617-32761093	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
3	nsv544680	chr22:32467617-32761093	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
4	esv2830423	chr22:32477718-32767825	Enhancers Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
5	esv2422247	chr22:32486448-32788258	Strong transcription Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	44 gene(s)	inside rSNPs	diseases
6	nsv459874	chr22:32574274-32866934	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
7	nsv588895	chr22:32574274-32866934	Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
8	nsv1064737	chr22:32603912-32829725	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
9	nsv979671	chr22:32753870-32755199	Weak transcription	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs9609516	C22orf28	cis	cerebellum	SCAN
rs9609516	LIN7A	trans	lymphoblastoid	seeQTL
rs9609516	SASH1	trans	lymphoblastoid	seeQTL

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:32750800-32755600	Weak transcription	Ovary	ovary

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