Variant report

Variant	rs6030100
Chromosome Location	chr20:40893759-40893760
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 89 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:87)

rs_ID	r²[population]
rs1014757	0.90[CHB][hapmap];0.80[JPT][hapmap];0.86[ASN][1000 genomes]
rs11907691	0.89[ASN][1000 genomes]
rs12625238	0.86[CHB][hapmap];0.82[JPT][hapmap]
rs13040788	0.90[CHB][hapmap];0.91[JPT][hapmap]
rs16986670	0.86[JPT][hapmap]
rs1883376	0.86[CHB][hapmap]
rs1883377	0.90[CHB][hapmap];0.81[JPT][hapmap]
rs1883378	0.86[CHB][hapmap];0.85[AMR][1000 genomes]
rs1984399	0.86[CHB][hapmap];0.86[JPT][hapmap];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2143008	0.90[CHB][hapmap];0.81[JPT][hapmap];0.86[AMR][1000 genomes]
rs2143632	0.85[CHB][hapmap];0.90[JPT][hapmap];0.88[ASN][1000 genomes]
rs2179336	0.90[CHB][hapmap];0.81[JPT][hapmap];0.83[AMR][1000 genomes]
rs2206168	0.91[CHB][hapmap];0.83[AMR][1000 genomes]
rs2206169	0.90[CHB][hapmap];0.85[JPT][hapmap];0.88[AMR][1000 genomes]
rs2223425	0.95[CHB][hapmap];0.91[JPT][hapmap];0.88[AMR][1000 genomes]
rs2223718	0.90[CHB][hapmap];0.85[JPT][hapmap]
rs2867061	0.81[CHB][hapmap]
rs2867062	0.81[CHB][hapmap]
rs2867063	0.95[CHB][hapmap];0.90[JPT][hapmap]
rs2903465	0.90[CHB][hapmap];0.91[JPT][hapmap]
rs4140521	0.95[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4331574	0.95[CHB][hapmap];0.86[JPT][hapmap];0.80[AMR][1000 genomes]
rs4425144	0.95[CHB][hapmap];0.90[JPT][hapmap];0.85[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs4507153	1.00[YRI][hapmap]
rs6016705	0.95[CHB][hapmap];0.85[JPT][hapmap]
rs6016707	0.90[CHB][hapmap];0.91[JPT][hapmap]
rs6016710	0.95[CHB][hapmap];0.95[JPT][hapmap]
rs6016711	0.86[CHB][hapmap];0.82[JPT][hapmap]
rs6016712	0.86[CHB][hapmap];0.82[JPT][hapmap]
rs6016716	0.85[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs6016726	0.95[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6030011	0.80[CHB][hapmap]
rs6030023	0.90[CHB][hapmap]
rs6030026	0.86[CHB][hapmap];0.82[JPT][hapmap]
rs6030027	0.90[CHB][hapmap];0.86[JPT][hapmap]
rs6030033	0.91[CHB][hapmap];0.82[JPT][hapmap];0.88[AMR][1000 genomes]
rs6030035	0.86[CHB][hapmap];0.82[JPT][hapmap]
rs6030036	0.90[CHB][hapmap];0.85[JPT][hapmap]
rs6030037	0.86[CHB][hapmap];0.82[JPT][hapmap]
rs6030056	0.86[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs6030058	0.81[CHB][hapmap]
rs6030061	0.90[CHB][hapmap];0.95[JPT][hapmap];0.92[ASN][1000 genomes]
rs6030069	0.87[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs6030070	0.81[CHB][hapmap];0.90[JPT][hapmap];0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6030071	0.80[CHB][hapmap];0.81[JPT][hapmap];0.82[EUR][1000 genomes]
rs6030073	0.81[CHB][hapmap];0.85[JPT][hapmap];0.84[ASN][1000 genomes]
rs6030076	0.95[CHB][hapmap];0.95[JPT][hapmap];0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6030078	0.90[ASN][1000 genomes]
rs6030081	0.84[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs6030082	0.90[CHB][hapmap];0.87[JPT][hapmap];0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6030083	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6030084	0.82[CHB][hapmap];0.87[JPT][hapmap]
rs6030085	0.90[CHB][hapmap];0.95[JPT][hapmap];0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6030087	0.95[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6030088	0.95[CHB][hapmap];0.95[JPT][hapmap];0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6030089	0.87[CHB][hapmap];0.82[EUR][1000 genomes]
rs6030096	0.90[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.91[AMR][1000 genomes];0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6030101	0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6065450	0.95[CHB][hapmap];0.95[JPT][hapmap];0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6065451	0.88[AFR][1000 genomes];0.92[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs6072651	0.90[CHB][hapmap];0.86[JPT][hapmap];0.88[AMR][1000 genomes]
rs6072672	0.82[CHB][hapmap];0.82[JPT][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs6093584	0.90[CHB][hapmap];0.81[JPT][hapmap]
rs6093588	0.86[CHB][hapmap];0.82[JPT][hapmap]
rs6093589	0.86[CHB][hapmap];0.82[JPT][hapmap]
rs6093598	0.81[JPT][hapmap]
rs6102713	0.95[CHB][hapmap];0.90[JPT][hapmap]
rs6124427	0.90[CHB][hapmap];0.91[JPT][hapmap]
rs6124435	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6130062	0.81[CHB][hapmap]
rs6130068	0.80[CHB][hapmap];0.82[JPT][hapmap]
rs6130071	0.90[CHB][hapmap];0.85[JPT][hapmap]
rs6130073	0.85[CHB][hapmap];0.81[JPT][hapmap]
rs6130074	0.90[CHB][hapmap];0.85[JPT][hapmap]
rs6130076	0.90[CHB][hapmap];0.91[JPT][hapmap]
rs6130081	0.85[CHB][hapmap];0.85[JPT][hapmap];0.86[ASN][1000 genomes]
rs6130091	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7270492	0.85[CHB][hapmap];0.85[JPT][hapmap];0.85[ASN][1000 genomes]
rs727336	0.82[CHB][hapmap];0.82[JPT][hapmap];0.83[EUR][1000 genomes]
rs727337	0.91[CHB][hapmap];0.87[JPT][hapmap];1.00[YRI][hapmap]
rs728373	0.82[CHB][hapmap];0.86[JPT][hapmap];0.84[AMR][1000 genomes]
rs728374	0.87[CHB][hapmap];0.86[JPT][hapmap];0.86[AMR][1000 genomes]
rs742290	0.90[CHB][hapmap];0.85[JPT][hapmap]
rs742291	0.90[CHB][hapmap];0.85[JPT][hapmap]
rs926647	0.90[CHB][hapmap];0.91[JPT][hapmap];0.88[AMR][1000 genomes];0.80[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs932358	0.91[CHB][hapmap];0.82[JPT][hapmap];0.88[AMR][1000 genomes]
rs979634	0.86[CHB][hapmap];0.85[JPT][hapmap]

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	esv2751913	chr20:40422982-41269321	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
2	nsv532516	chr20:40451059-41097155	Weak transcription Strong transcription Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:40885400-40902800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr20:40885800-40896800	Weak transcription	Cortex derived primary cultured neurospheres	brain
3	chr20:40893200-40901200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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