Variant report

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs10007142	0.82[AMR][1000 genomes]
rs10488877	0.91[JPT][hapmap];0.85[ASN][1000 genomes]
rs12640239	0.93[JPT][hapmap]
rs12647173	0.92[JPT][hapmap]
rs13120461	0.85[ASN][1000 genomes]
rs13126849	0.93[JPT][hapmap]
rs13133009	0.86[ASN][1000 genomes]
rs16997032	0.82[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs17039959	0.93[JPT][hapmap]
rs2158469	0.92[JPT][hapmap];0.85[ASN][1000 genomes]
rs35164053	0.85[ASN][1000 genomes]
rs35473845	0.91[ASN][1000 genomes]
rs4956247	0.92[JPT][hapmap]
rs4956254	0.91[ASN][1000 genomes]
rs6857867	0.85[ASN][1000 genomes]
rs7675039	0.93[JPT][hapmap];0.85[ASN][1000 genomes]
rs7682615	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7692025	0.92[JPT][hapmap];0.85[ASN][1000 genomes]
rs7695378	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs987123	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9993777	0.94[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];1.00[ASN][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	nsv461613	chr4:109922064-110593460	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
2	nsv595129	chr4:109922064-110593460	Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
3	nsv461614	chr4:110165434-110220384	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv595131	chr4:110165434-110220384	Enhancers Weak transcription Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	2 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	chr4:110155200-110192200	Weak transcription	Hela-S3	cervix
2	chr4:110186000-110215200	Weak transcription	HSMM	muscle
3	chr4:110188400-110189400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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