Variant report

Variant	rs73586366
Chromosome Location	chr8:36139235-36139236
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr8:36139222-36139571	K562	blood:	n/a	n/a
2	MAFF	chr8:36139223-36139582	K562	blood:	n/a	chr8:36139401-36139419
3	MAFK	chr8:36139226-36139588	HepG2	liver:	n/a	chr8:36139402-36139417
4	MAFK	chr8:36139218-36139591	HepG2	liver:	n/a	chr8:36139402-36139417
5	MAFK	chr8:36139087-36139657	GM12878	blood:	n/a	chr8:36139402-36139417
6	MAFF	chr8:36139220-36139593	HepG2	liver:	n/a	chr8:36139401-36139419
7	MAFK	chr8:36139223-36139591	K562	blood:	n/a	chr8:36139402-36139417
8	BACH1	chr8:36139227-36139586	H1-hESC	embryonic stem cell:	n/a	n/a
9	MAFK	chr8:36138934-36139629	H1-hESC	embryonic stem cell:	n/a	chr8:36139402-36139417
10	MAFK	chr8:36139220-36139595	IMR90	lung:	n/a	chr8:36139402-36139417

Variant related genes	Relation type
ENSG00000253504	TF binding region
ENSG00000253685	TF binding region

Extended variants
information (count: 40 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1107566	0.80[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs1107567	0.82[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs1107568	0.82[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs16884807	0.83[AMR][1000 genomes]
rs16884876	0.80[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs16884883	0.80[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs16884894	0.80[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs16884902	0.83[AMR][1000 genomes]
rs41408344	0.80[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs6468359	0.83[AMR][1000 genomes]
rs6983120	0.98[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs6984135	0.80[AFR][1000 genomes]
rs6987238	0.80[AFR][1000 genomes]
rs7015213	0.83[AMR][1000 genomes]
rs73578572	0.80[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs73586355	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs73586362	0.80[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs73586363	0.80[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs73586369	0.80[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs73592006	0.83[AMR][1000 genomes]
rs73592008	0.83[AMR][1000 genomes]
rs73592010	0.83[AMR][1000 genomes]
rs73592012	0.83[AMR][1000 genomes]
rs73592013	0.87[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs73592014	0.83[AMR][1000 genomes]
rs73592019	0.83[AMR][1000 genomes]
rs73592021	0.83[AMR][1000 genomes]
rs73592024	0.83[AMR][1000 genomes]
rs73592026	0.83[AMR][1000 genomes]
rs7819939	0.82[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs7831591	0.80[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs7834732	0.80[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs7835665	0.80[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs7837634	0.83[AMR][1000 genomes]
rs879317	0.81[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs879318	0.82[AFR][1000 genomes];0.83[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533420	chr8:35358115-36227536	Enhancers Strong transcription Weak transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
2	nsv1024552	chr8:35655964-36210907	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
3	nsv539548	chr8:35655964-36210907	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
4	nsv890718	chr8:35948467-36224134	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
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