Variant report

Variant	rs12143824
Chromosome Location	chr1:165547306-165547307
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 50 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs1011469	0.83[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs1025159	1.00[CHB][hapmap];0.90[JPT][hapmap]
rs1157861	0.93[ASN][1000 genomes]
rs12126717	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs12137629	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs1326374	0.92[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs1409413	0.98[ASN][1000 genomes]
rs1425753	0.81[ASN][1000 genomes]
rs16846547	0.88[ASN][1000 genomes]
rs16846623	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs16846756	0.93[ASN][1000 genomes]
rs16847073	0.98[ASN][1000 genomes]
rs16847083	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs16847085	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs16847110	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs16847312	0.83[AFR][1000 genomes]
rs16847331	0.92[CHB][hapmap]
rs16847570	0.84[CHB][hapmap]
rs1913836	0.91[CHB][hapmap]
rs2152818	0.83[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs2252342	0.98[ASN][1000 genomes]
rs285421	0.81[ASN][1000 genomes]
rs285422	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs285435	0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs285438	0.83[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs34201742	0.98[ASN][1000 genomes]
rs41267552	1.00[ASN][1000 genomes]
rs41267554	1.00[ASN][1000 genomes]
rs4147146	0.91[CHB][hapmap]
rs55890197	0.95[ASN][1000 genomes]
rs55957417	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56201005	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56277222	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs57799548	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs58058936	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6657863	0.91[CEU][hapmap];0.85[CHB][hapmap];0.94[EUR][1000 genomes]
rs6669449	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs6696050	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs722260	0.97[ASN][1000 genomes]
rs72693816	0.90[ASN][1000 genomes]
rs72693826	0.90[ASN][1000 genomes]
rs74120755	0.93[ASN][1000 genomes]
rs7521982	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs7533908	0.93[ASN][1000 genomes]
rs7535829	0.93[ASN][1000 genomes]
rs7535979	0.93[ASN][1000 genomes]
rs7539622	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs7554080	0.84[CHB][hapmap]
rs927844	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv429902	chr1:165531342-165574342	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:165547000-165547400	Enhancers	Psoas Muscle	Psoas
2	chr1:165547200-165547400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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