Variant report

Variant	rs7761061
Chromosome Location	chr6:77999779-77999780
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 60 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs10455106	0.92[AFR][1000 genomes]
rs10455329	0.92[AFR][1000 genomes]
rs10755354	0.90[AFR][1000 genomes]
rs10943436	0.87[AFR][1000 genomes]
rs10943437	0.91[AFR][1000 genomes]
rs10943438	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10943441	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1115314	0.92[AFR][1000 genomes]
rs12192404	0.92[AFR][1000 genomes]
rs12525774	0.85[AFR][1000 genomes]
rs1342624	0.94[AFR][1000 genomes]
rs1342627	0.94[AFR][1000 genomes]
rs1342629	0.85[AFR][1000 genomes]
rs1342638	0.92[AFR][1000 genomes]
rs1418584	0.94[AFR][1000 genomes]
rs1418585	0.94[AFR][1000 genomes]
rs1418586	0.94[AFR][1000 genomes]
rs1592219	0.91[AFR][1000 genomes]
rs16879515	0.92[AFR][1000 genomes]
rs1857201	0.89[AFR][1000 genomes]
rs1935724	0.84[AFR][1000 genomes]
rs1935729	0.93[AFR][1000 genomes]
rs1935732	0.92[AFR][1000 genomes]
rs2153886	0.94[AFR][1000 genomes]
rs2211408	0.92[AFR][1000 genomes]
rs2320293	0.89[AFR][1000 genomes]
rs2874222	0.92[AFR][1000 genomes]
rs2874223	0.94[AFR][1000 genomes]
rs4142469	0.92[AFR][1000 genomes]
rs4499894	0.92[AFR][1000 genomes]
rs6904292	0.94[AFR][1000 genomes]
rs756232	0.92[AFR][1000 genomes]
rs7744314	0.94[AFR][1000 genomes]
rs7752306	0.92[AFR][1000 genomes]
rs7756606	0.92[AFR][1000 genomes]
rs9341654	0.92[AFR][1000 genomes]
rs9341655	0.94[AFR][1000 genomes]
rs9341656	0.94[AFR][1000 genomes]
rs9341657	0.92[AFR][1000 genomes]
rs9343587	0.92[AFR][1000 genomes]
rs9343588	0.92[AFR][1000 genomes]
rs9343589	0.92[AFR][1000 genomes]
rs9343590	0.92[AFR][1000 genomes]
rs9343591	0.92[AFR][1000 genomes]
rs9352462	0.84[AFR][1000 genomes]
rs9352464	0.89[AMR][1000 genomes]
rs9352473	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9359257	0.94[AFR][1000 genomes]
rs9359258	0.94[AFR][1000 genomes]
rs9359259	0.94[AFR][1000 genomes]
rs9359264	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9361214	0.89[AFR][1000 genomes]
rs9361215	0.91[AFR][1000 genomes]
rs9361216	0.92[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1017082	chr6:77585310-78258237	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv534282	chr6:77764575-78351994	Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv1034979	chr6:77781244-78426249	Active TSS Weak transcription ZNF genes & repeats Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv538324	chr6:77781244-78426249	Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	esv2753543	chr6:77791848-78059351	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Genic enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv1015307	chr6:77902559-78352291	Weak transcription Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:77990800-78000400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr6:77998000-77999800	Weak transcription	NHEK	skin
3	chr6:77998200-78000000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr6:77999000-78005400	Enhancers	HUVEC	blood vessel
5	chr6:77999400-78000400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links