Variant report

Variant	rs2101854
Chromosome Location	chr8:90675745-90675746
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:90674028..90676742-chr8:90677317..90680172,3	K562	blood:

Extended variants
information (count: 66 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:57)

rs_ID	r²[population]
rs10108588	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1032516	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1040327	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10956209	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12216864	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12545569	0.83[ASN][1000 genomes]
rs12675281	0.86[ASN][1000 genomes]
rs13266524	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs13278061	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1603289	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs160423	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs160424	0.88[EUR][1000 genomes]
rs160427	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs160429	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs160437	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs160441	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs160447	0.82[EUR][1000 genomes]
rs160448	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs160449	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs160450	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs160451	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs160453	0.83[AMR][1000 genomes]
rs1605996	0.89[ASN][1000 genomes]
rs1605997	0.89[ASN][1000 genomes]
rs183363	0.83[EUR][1000 genomes]
rs216989	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs218882	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs218884	0.83[EUR][1000 genomes]
rs218885	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs218886	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs218887	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs218888	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs218889	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs218890	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs218899	0.95[CHB][hapmap]
rs218900	0.90[CHB][hapmap]
rs218901	0.86[CHB][hapmap]
rs218902	0.86[CHB][hapmap]
rs218903	0.90[CHB][hapmap]
rs218916	0.81[ASN][1000 genomes]
rs218917	0.96[CEU][hapmap];0.88[EUR][1000 genomes]
rs218918	0.89[CEU][hapmap];0.82[EUR][1000 genomes]
rs2202990	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs28374917	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2840206	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28819479	0.81[EUR][1000 genomes]
rs28875294	0.84[EUR][1000 genomes]
rs34036322	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4961154	0.91[ASN][1000 genomes]
rs4961155	0.91[ASN][1000 genomes]
rs4961157	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4961158	0.85[ASN][1000 genomes]
rs56237088	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs56291556	0.91[ASN][1000 genomes]
rs56403153	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7003919	0.88[EUR][1000 genomes]
rs7004089	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv465735	chr8:89760311-90729507	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
2	nsv611714	chr8:89760311-90729507	Enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Weak transcription Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
3	nsv870380	chr8:90546585-90720182	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
4	nsv1028026	chr8:90553930-90678631	Genic enhancers Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
5	nsv982109	chr8:90556188-90703631	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
6	nsv1026523	chr8:90558935-90722580	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
7	nsv831389	chr8:90575517-90753120	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
8	nsv1017263	chr8:90605445-90722580	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
9	nsv1031578	chr8:90670102-90757821	Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs2101854	RP11-37B2.1	cis	Skin Sun Exposed Lower leg	GTEx

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:90674400-90676000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
2	chr8:90675200-90675800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr8:90675200-90675800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr8:90675200-90675800	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr8:90675200-90676000	ZNF genes & repeats	Brain Hippocampus Middle	brain
6	chr8:90675200-90676000	ZNF genes & repeats	Pancreas	Pancrea
7	chr8:90675200-90676200	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links