Variant report

Variant	rs59866505
Chromosome Location	chr1:224040327-224040328
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:224039824..224041644-chr1:224060638..224062824,2	K562	blood:
2	chr1:224031495..224036851-chr1:224037356..224045519,10	MCF-7	breast:

Variant related genes	Relation type
ENSG00000143514	Chromatin interaction

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs10799327	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10915882	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10915892	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10915917	0.84[EUR][1000 genomes]
rs10915946	0.81[EUR][1000 genomes]
rs10915948	0.81[EUR][1000 genomes]
rs10915950	0.80[EUR][1000 genomes]
rs10915956	0.81[EUR][1000 genomes]
rs1124943	0.87[EUR][1000 genomes]
rs11801971	0.83[EUR][1000 genomes]
rs11802505	0.82[EUR][1000 genomes]
rs11806886	0.84[EUR][1000 genomes]
rs12021759	0.86[EUR][1000 genomes]
rs12021785	0.85[EUR][1000 genomes]
rs12024535	0.86[EUR][1000 genomes]
rs12026098	0.86[EUR][1000 genomes]
rs12026835	0.84[EUR][1000 genomes]
rs12027539	0.85[EUR][1000 genomes]
rs12030094	0.81[EUR][1000 genomes]
rs12040633	0.81[EUR][1000 genomes]
rs12042503	0.81[EUR][1000 genomes]
rs12045776	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12730520	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12731254	0.88[EUR][1000 genomes]
rs17559050	0.89[EUR][1000 genomes]
rs2014441	0.90[AFR][1000 genomes];0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2126389	0.86[EUR][1000 genomes]
rs2169459	0.82[EUR][1000 genomes]
rs34124959	0.86[EUR][1000 genomes]
rs35634773	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs3856161	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4653644	0.84[EUR][1000 genomes]
rs4653645	0.84[EUR][1000 genomes]
rs56280097	0.81[EUR][1000 genomes]
rs61823593	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs61823594	0.89[EUR][1000 genomes]
rs61823595	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6658752	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6677956	0.82[EUR][1000 genomes]
rs6678103	0.81[EUR][1000 genomes]
rs6688246	0.85[EUR][1000 genomes]
rs6693324	0.82[EUR][1000 genomes]
rs6702843	0.86[EUR][1000 genomes]
rs723999	0.86[EUR][1000 genomes]
rs745697	0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7516059	0.86[EUR][1000 genomes]
rs7519753	0.85[EUR][1000 genomes]
rs7533614	0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7554109	0.84[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3361888	chr1:223725597-224114846	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
2	nsv1007380	chr1:223834380-224042190	Strong transcription Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
3	nsv535310	chr1:223834380-224042190	ZNF genes & repeats Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
4	esv34082	chr1:223851018-224144509	Enhancers Genic enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
5	nsv1008800	chr1:223904653-224061032	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
6	esv2757772	chr1:223935220-224363163	Genic enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Strong transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
7	esv2759000	chr1:223935220-224363163	Enhancers Weak transcription Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 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	chr1:224034800-224041200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr1:224035000-224041200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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