Variant report

Variant	rs304754
Chromosome Location	chr7:79982759-79982760
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:79971854..79974583-chr7:79981836..79984361,2	K562	blood:

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs10262955	0.92[ASN][1000 genomes]
rs10264032	0.95[ASN][1000 genomes]
rs10269308	0.94[ASN][1000 genomes]
rs10486931	0.99[EUR][1000 genomes]
rs12667354	0.96[ASN][1000 genomes]
rs12667590	0.83[ASN][1000 genomes]
rs13234446	0.95[ASN][1000 genomes]
rs17153795	0.83[ASN][1000 genomes]
rs17547287	0.83[ASN][1000 genomes]
rs2906199	0.84[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs304738	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs304739	0.90[EUR][1000 genomes]
rs304741	0.97[EUR][1000 genomes]
rs304742	0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs304743	0.97[EUR][1000 genomes]
rs304744	0.97[EUR][1000 genomes]
rs304745	0.97[EUR][1000 genomes]
rs304746	0.97[EUR][1000 genomes]
rs304747	0.97[EUR][1000 genomes]
rs304748	0.99[EUR][1000 genomes]
rs304749	0.99[EUR][1000 genomes]
rs304750	0.85[AFR][1000 genomes];0.99[EUR][1000 genomes]
rs304751	0.99[EUR][1000 genomes]
rs304753	0.99[EUR][1000 genomes]
rs304755	0.98[EUR][1000 genomes]
rs304766	0.84[CHB][hapmap];1.00[JPT][hapmap]
rs304784	0.83[ASN][1000 genomes]
rs304785	0.83[ASN][1000 genomes]
rs4636124	0.91[ASN][1000 genomes]
rs485217	0.90[EUR][1000 genomes]
rs534589	0.90[EUR][1000 genomes]
rs57803210	0.94[ASN][1000 genomes]
rs58665903	0.81[ASN][1000 genomes]
rs6467133	0.84[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs6467134	0.84[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs6967989	0.90[EUR][1000 genomes]
rs6978235	1.00[CEU][hapmap];0.99[EUR][1000 genomes]
rs726458	0.94[ASN][1000 genomes]
rs764907	0.83[ASN][1000 genomes]
rs7790699	0.87[EUR][1000 genomes]
rs7792158	0.83[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv429785	chr7:79589749-80177049	Bivalent/Poised TSS Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv1024312	chr7:79832637-80004812	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
3	nsv1029180	chr7:79832637-80017560	Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:79978400-79984600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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