Variant report

Variant	rs1418840
Chromosome Location	chr1:158411545-158411546
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs16840136	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16840139	1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16840141	1.00[ASW][hapmap];1.00[LWK][hapmap];0.95[MKK][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16840143	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16840182	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16840184	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2023633	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2213945	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2220631	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2860016	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28866916	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs55702828	1.00[AMR][1000 genomes]
rs56773217	1.00[AMR][1000 genomes]
rs58592764	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59604063	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6684251	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6691971	1.00[AMR][1000 genomes]
rs73012005	1.00[AMR][1000 genomes]
rs73013915	1.00[AMR][1000 genomes]
rs73013919	1.00[AMR][1000 genomes]
rs73013923	1.00[AMR][1000 genomes]
rs73013934	1.00[AMR][1000 genomes]
rs73013940	1.00[AMR][1000 genomes]
rs73015825	1.00[AMR][1000 genomes]
rs73017709	1.00[AMR][1000 genomes]
rs73017717	1.00[AMR][1000 genomes]
rs73017739	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73019705	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73019756	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73021774	1.00[AFR][1000 genomes]
rs73021929	1.00[AMR][1000 genomes]
rs73023804	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73023822	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73023829	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73023942	1.00[AMR][1000 genomes]
rs73023945	1.00[AMR][1000 genomes]
rs73023947	1.00[AMR][1000 genomes]
rs73025843	1.00[AMR][1000 genomes]
rs73027731	1.00[AMR][1000 genomes]
rs73027744	1.00[AMR][1000 genomes]
rs74121843	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74121844	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74121858	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7532088	1.00[AMR][1000 genomes]
rs9651044	1.00[ASW][hapmap]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv872479	chr1:158118787-158484285	Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv872480	chr1:158153526-158450238	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
3	nsv998569	chr1:158317392-158443389	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:158406600-158415000	Weak transcription	Thymus	Thymus
2	chr1:158410000-158411600	Enhancers	Primary neutrophils fromperipheralblood	blood
3	chr1:158410200-158411600	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr1:158411400-158412200	Enhancers	Monocytes-CD14+_RO01746	blood

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