Variant report

Variant	rs62567925
Chromosome Location	chr9:94766571-94766572
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2)
CpG islands
(count:0)
Chromatin interactive
region (count:2)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr9:94766562-94766667	H1-hESC	embryonic stem cell:	n/a	n/a
2	RAD21	chr9:94766280-94766668	H1-hESC	embryonic stem cell:	n/a	n/a

No data

(count:2 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:94766208..94767936-chr9:94768192..94770688,2	K562	blood:
2	chr9:94759552..94762482-chr9:94762532..94767082,4	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SPTLC1-1	chr9:94766310-94766591	XLOC_007778

No data

Variant related genes	Relation type
ENSG00000227399	TF binding region
ENSG00000227399	Chromatin interaction

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10820921	0.82[EUR][1000 genomes]
rs10820922	0.85[AFR][1000 genomes];0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs10820928	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10820933	0.93[AMR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10820934	1.00[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10820939	0.98[AMR][1000 genomes]
rs10820942	0.82[AMR][1000 genomes]
rs10992161	0.81[EUR][1000 genomes]
rs10992166	0.81[EUR][1000 genomes]
rs10992168	0.81[EUR][1000 genomes]
rs10992196	0.94[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10992208	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10992218	0.98[AMR][1000 genomes]
rs10992219	0.98[AMR][1000 genomes]
rs10992224	0.98[AMR][1000 genomes]
rs11790093	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs11790991	0.98[AMR][1000 genomes]
rs12377635	0.98[AMR][1000 genomes]
rs12380093	0.98[AMR][1000 genomes]
rs12554018	0.86[AMR][1000 genomes]
rs17749165	0.85[AMR][1000 genomes]
rs1892263	0.81[EUR][1000 genomes]
rs1919101	0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3932420	0.82[EUR][1000 genomes]
rs55939422	0.98[AMR][1000 genomes]
rs56013831	0.81[EUR][1000 genomes]
rs56272949	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs56280154	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs56309039	0.81[EUR][1000 genomes]
rs62565755	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs62567926	0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs62567930	0.98[AMR][1000 genomes]
rs62567931	0.98[AMR][1000 genomes]
rs72746299	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs72748323	0.85[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs7857759	1.00[AMR][1000 genomes];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	nsv949008	chr9:94500776-95182133	Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
2	nsv1050845	chr9:94687959-95312406	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
3	nsv1046733	chr9:94690622-95138564	Genic enhancers Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
4	nsv831653	chr9:94692454-94867542	Strong transcription Enhancers Weak transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
5	nsv530947	chr9:94697309-95093377	Weak transcription Bivalent Enhancer Strong transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
6	nsv972417	chr9:94766194-94769276	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:94764800-94767200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr9:94765600-94766600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr9:94766200-94767000	Enhancers	Placenta	Placenta

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