Variant report

Variant	rs417738
Chromosome Location	chr1:76643830-76643831
allele	C/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:47)

rs_ID	r²[population]
rs10873868	0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11162094	0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11162100	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11584719	0.89[EUR][1000 genomes]
rs12031035	0.88[AFR][1000 genomes];0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12080978	0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12083141	0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12085592	0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12086586	0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12089339	0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12089419	0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12089425	0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12136476	0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12136538	0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12138879	0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12138975	0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12139114	0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1318243	0.83[EUR][1000 genomes]
rs1684945	0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2631794	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2631795	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2706179	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2706180	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs28485639	0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs376878	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs409936	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs411756	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs417932	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs432956	0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs592872	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs60164283	0.86[ASN][1000 genomes]
rs638947	0.90[EUR][1000 genomes]
rs66489023	0.86[ASN][1000 genomes]
rs7512081	0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7514776	0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7521939	0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7528649	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7528680	0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7528766	0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7532337	0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7534087	0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7536455	0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7540069	0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7551529	0.83[AFR][1000 genomes]
rs7552671	0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs923244	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs923245	0.88[AMR][1000 genomes];0.90[EUR][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	nsv870621	chr1:76620313-76997071	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:76619800-76646400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr1:76636000-76646600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr1:76636600-76652800	Weak transcription	Primary B cells from cord blood	blood
4	chr1:76643400-76644600	Enhancers	HepG2	liver
5	chr1:76643800-76651800	Weak transcription	Fetal Kidney	kidney

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