Variant report

Variant	rs35501117
Chromosome Location	chr9:85046303-85046304
allele	A/G/T
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	ZNF263	chr9:85046187-85046729	HEK293-T-REx	kidney:	n/a	n/a

Variant related genes	Relation type
ENSG00000228046	TF binding region

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs10113923	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10114756	0.92[EUR][1000 genomes]
rs10123160	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10124221	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10125999	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1041392	0.94[ASN][1000 genomes]
rs10512125	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11139566	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11139569	0.91[ASN][1000 genomes]
rs11139570	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12002791	0.82[EUR][1000 genomes]
rs12350753	0.91[ASN][1000 genomes]
rs12551735	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12683121	0.83[ASN][1000 genomes]
rs12683715	0.83[ASN][1000 genomes]
rs12684844	0.94[ASN][1000 genomes]
rs12684886	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12685162	0.83[ASN][1000 genomes]
rs13290374	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs13298628	0.86[ASN][1000 genomes]
rs13299917	0.82[ASN][1000 genomes]
rs1330817	0.80[ASN][1000 genomes]
rs1411660	0.83[ASN][1000 genomes]
rs1411662	0.88[ASN][1000 genomes]
rs17085530	0.83[ASN][1000 genomes]
rs17085531	0.83[ASN][1000 genomes]
rs2026194	0.83[ASN][1000 genomes]
rs28520227	0.93[EUR][1000 genomes]
rs2889949	0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs34637520	0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs34845422	0.86[ASN][1000 genomes]
rs35089927	0.88[ASN][1000 genomes]
rs35576282	0.83[ASN][1000 genomes]
rs35677430	0.83[ASN][1000 genomes]
rs4478643	0.83[ASN][1000 genomes]
rs4877232	0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4877233	0.88[ASN][1000 genomes]
rs4877692	0.81[AFR][1000 genomes];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4877693	0.95[ASN][1000 genomes]
rs56291243	0.82[ASN][1000 genomes]
rs67968529	0.83[ASN][1000 genomes]
rs7018522	0.89[ASN][1000 genomes]
rs7021813	0.83[ASN][1000 genomes]
rs7036901	0.83[ASN][1000 genomes]
rs7037151	0.83[ASN][1000 genomes]
rs7042354	0.88[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs7046852	0.83[ASN][1000 genomes]
rs7048894	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7850751	0.89[ASN][1000 genomes]
rs7865649	0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs7869176	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7874021	0.93[EUR][1000 genomes]
rs7874946	0.91[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv893507	chr9:84799537-85097651	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv893508	chr9:84954592-85080395	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv893509	chr9:84954592-85097651	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv893510	chr9:84954592-85117420	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv982311	chr9:85041031-85052919	Enhancers Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:85046000-85046800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr9:85046000-85047200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell

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