Variant report

Variant	rs6459035
Chromosome Location	chr6:54757520-54757521
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs10485136	0.98[EUR][1000 genomes]
rs12525787	0.93[EUR][1000 genomes]
rs12662124	0.93[EUR][1000 genomes]
rs1393776	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs148109	0.83[ASN][1000 genomes]
rs1503140	0.86[EUR][1000 genomes]
rs1503146	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1503147	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2064432	0.93[EUR][1000 genomes]
rs239850	0.83[ASN][1000 genomes]
rs239854	0.83[ASN][1000 genomes]
rs4141552	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4712081	0.95[EUR][1000 genomes]
rs6902245	0.86[EUR][1000 genomes]
rs6902422	0.86[EUR][1000 genomes]
rs6908170	0.91[EUR][1000 genomes]
rs6922186	0.86[EUR][1000 genomes]
rs6926997	0.86[EUR][1000 genomes]
rs6929930	0.86[EUR][1000 genomes]
rs6939778	0.93[EUR][1000 genomes]
rs72645372	0.93[EUR][1000 genomes]
rs7744592	0.85[EUR][1000 genomes]
rs7746374	0.88[EUR][1000 genomes]
rs9296771	0.93[EUR][1000 genomes]
rs932452	0.93[EUR][1000 genomes]
rs9349740	0.86[EUR][1000 genomes]
rs9357822	0.81[EUR][1000 genomes]
rs9367597	0.93[EUR][1000 genomes]
rs9370344	0.85[EUR][1000 genomes]
rs9370345	0.86[EUR][1000 genomes]
rs9382396	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9382397	0.93[EUR][1000 genomes]
rs9382398	0.93[EUR][1000 genomes]
rs9382402	0.87[EUR][1000 genomes]
rs9382403	0.86[EUR][1000 genomes]
rs9396006	0.93[EUR][1000 genomes]
rs9396007	0.92[EUR][1000 genomes]
rs9475068	0.93[EUR][1000 genomes]
rs9475069	0.89[EUR][1000 genomes]
rs9475078	0.87[EUR][1000 genomes]
rs9475081	0.90[EUR][1000 genomes]
rs960834	0.83[EUR][1000 genomes]
rs960835	0.91[EUR][1000 genomes]
rs988913	0.90[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv885900	chr6:54517968-54852462	Active TSS Bivalent Enhancer Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	esv2763553	chr6:54687979-54820487	Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:54739800-54763000	Weak transcription	Small Intestine	intestine
2	chr6:54744200-54757600	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr6:54744400-54761000	Weak transcription	Duodenum Mucosa	Duodenum
4	chr6:54746400-54757800	Weak transcription	Hela-S3	cervix
5	chr6:54752200-54759000	Weak transcription	Rectal Mucosa Donor 29	rectum
6	chr6:54752400-54758600	Weak transcription	Rectal Mucosa Donor 31	rectum
7	chr6:54755800-54758000	Enhancers	Breast Myoepithelial Primary Cells	Breast
8	chr6:54755800-54758000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr6:54756200-54758400	Enhancers	HMEC	breast
10	chr6:54757000-54757800	Enhancers	NHEK	skin
11	chr6:54757200-54757600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr6:54757200-54763000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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