Variant report

Variant	rs7181163
Chromosome Location	chr15:31699508-31699509
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:31695571..31697566-chr15:31697893..31699568,2	K562	blood:

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs11071009	0.97[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs12101667	0.90[AFR][1000 genomes];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs28405352	0.89[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs28424256	0.90[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs28623689	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs28629861	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs28767583	0.90[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs28882498	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs56258992	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs57050120	0.88[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs57499356	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs60349856	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs60455079	0.90[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs61521461	0.92[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs6493657	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7169573	0.91[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs7174859	0.94[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs7182014	0.96[AFR][1000 genomes]
rs74010627	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs8039613	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8039819	0.90[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs8041303	0.88[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs8042812	0.90[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs8042871	1.00[AMR][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	nsv903831	chr15:30986051-31723279	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	84 gene(s)	inside rSNPs	diseases
2	nsv1054147	chr15:31014507-31972706	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription 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 miRNA target site	87 gene(s)	inside rSNPs	diseases
3	nsv542306	chr15:31014507-31972706	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
4	nsv932896	chr15:31292475-31730445	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
5	esv34100	chr15:31496514-31792591	Active TSS Enhancers ZNF genes & repeats Weak transcription Genic enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
6	nsv903840	chr15:31589970-31800149	Weak transcription Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
7	nsv903843	chr15:31672947-31723279	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:31696400-31700600	Enhancers	Primary B cells from cord blood	blood
2	chr15:31696400-31704200	Weak transcription	HMEC	breast
3	chr15:31696600-31704200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr15:31697600-31699600	Enhancers	Stomach Mucosa	stomach
5	chr15:31698200-31700400	Weak transcription	Primary T cells from cord blood	blood
6	chr15:31698200-31704200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr15:31698400-31700600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
8	chr15:31699200-31700800	Enhancers	Monocytes-CD14+_RO01746	blood
9	chr15:31699400-31699800	Enhancers	Primary monocytes fromperipheralblood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links