Variant report

Variant	rs35598853
Chromosome Location	chr5:177588954-177588955
allele	A/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	ELF1	chr5:177588865-177589323	K562	blood:	n/a	chr5:177589134-177589145 chr5:177589134-177589145
2	ZNF263	chr5:177588746-177589471	HEK293-T-REx	kidney:	n/a	chr5:177589043-177589064 chr5:177589045-177589054

No.	Distal block	Cell Line	Cell type
1	chr5:177583003..177586938-chr5:177587427..177591419,5	K562	blood:
2	chr5:177583402..177586432-chr5:177587427..177590932,3	K562	blood:
3	chr5:177588875..177592834-chr5:177630545..177633533,4	K562	blood:

Variant related genes	Relation type
ENSG00000251211	TF binding region
ENSG00000197451	Chromatin interaction

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10060446	0.89[ASN][1000 genomes]
rs10074810	0.91[ASN][1000 genomes]
rs11948118	0.81[ASN][1000 genomes]
rs12655707	0.85[ASN][1000 genomes]
rs13155699	0.97[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13163671	0.83[ASN][1000 genomes]
rs13165989	0.99[ASN][1000 genomes]
rs13175750	0.86[ASN][1000 genomes]
rs13180226	0.82[ASN][1000 genomes]
rs13185017	0.81[ASN][1000 genomes]
rs13185763	0.97[ASN][1000 genomes]
rs34093388	0.89[ASN][1000 genomes]
rs34343747	0.97[ASN][1000 genomes]
rs34353050	0.91[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs35027513	0.80[ASN][1000 genomes]
rs35433113	0.87[ASN][1000 genomes]
rs35865171	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs3812073	0.84[ASN][1000 genomes]
rs3812077	0.83[ASN][1000 genomes]
rs3812080	0.83[ASN][1000 genomes]
rs3924305	0.84[ASN][1000 genomes]
rs6601217	0.93[ASN][1000 genomes]
rs6870545	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6873523	0.80[ASN][1000 genomes]
rs6886057	0.92[ASN][1000 genomes]
rs7443359	0.93[ASN][1000 genomes]
rs7448252	0.93[ASN][1000 genomes]
rs7710363	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7716860	0.93[ASN][1000 genomes]
rs7722349	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948342	chr5:177384542-178168737	Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Strong transcription Weak transcription Bivalent/Poised 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	141 gene(s)	inside rSNPs	diseases
2	nsv1021198	chr5:177386267-177611648	Enhancers Bivalent/Poised TSS Flanking Active TSS Genic enhancers Weak transcription Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
3	nsv1029398	chr5:177502106-178070654	Flanking Active TSS Enhancers Weak transcription Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	136 gene(s)	inside rSNPs	diseases
4	nsv1019404	chr5:177507080-177859089	Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	126 gene(s)	inside rSNPs	diseases
5	nsv883190	chr5:177532201-177620189	Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Enhancers Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
6	nsv600394	chr5:177549491-177608195	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
7	nsv1017664	chr5:177578194-177633116	Active TSS Enhancers Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	93 gene(s)	inside rSNPs	diseases
8	nsv482872	chr5:177580298-177744381	Active TSS Strong transcription Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	106 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	chr5:177581400-177591000	Weak transcription	Right Atrium	heart
2	chr5:177587600-177591000	Weak transcription	GM12878-XiMat	blood

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