Variant report

Variant	rs61362928
Chromosome Location	chr1:215500510-215500511
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 101 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:93)

rs_ID	r²[population]
rs10127809	0.86[ASN][1000 genomes]
rs10494998	0.93[ASN][1000 genomes]
rs10494999	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11120554	1.00[ASN][1000 genomes]
rs11120588	1.00[AMR][1000 genomes]
rs12041872	1.00[AFR][1000 genomes]
rs12062740	0.93[ASN][1000 genomes]
rs12064396	0.93[ASN][1000 genomes]
rs12066481	0.93[ASN][1000 genomes]
rs12070874	0.93[ASN][1000 genomes]
rs12080428	0.93[ASN][1000 genomes]
rs12084684	0.93[ASN][1000 genomes]
rs12093830	0.93[ASN][1000 genomes]
rs13376274	0.93[ASN][1000 genomes]
rs13376355	0.93[ASN][1000 genomes]
rs1395722	0.93[ASN][1000 genomes]
rs17024732	0.93[ASN][1000 genomes]
rs17024744	0.86[ASN][1000 genomes]
rs17024755	0.86[ASN][1000 genomes]
rs17024758	0.86[ASN][1000 genomes]
rs1876407	0.93[ASN][1000 genomes]
rs1876408	0.93[ASN][1000 genomes]
rs2885989	0.86[ASN][1000 genomes]
rs35134381	0.86[ASN][1000 genomes]
rs3845523	0.93[ASN][1000 genomes]
rs4607849	0.86[ASN][1000 genomes]
rs56802573	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs56956076	1.00[AMR][1000 genomes]
rs56988669	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57110734	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs57179404	1.00[AMR][1000 genomes]
rs57309511	0.86[ASN][1000 genomes]
rs57379455	1.00[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs57628126	1.00[AMR][1000 genomes]
rs57758604	1.00[AMR][1000 genomes]
rs57792259	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58163611	1.00[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs58330534	1.00[AMR][1000 genomes]
rs58342290	0.93[ASN][1000 genomes]
rs58425452	1.00[AMR][1000 genomes]
rs58557470	1.00[AMR][1000 genomes]
rs58629829	1.00[AMR][1000 genomes]
rs58682085	1.00[AMR][1000 genomes]
rs58836680	1.00[AMR][1000 genomes]
rs58919310	1.00[AMR][1000 genomes]
rs59040705	1.00[AMR][1000 genomes]
rs59233975	1.00[AMR][1000 genomes]
rs59577074	1.00[AMR][1000 genomes]
rs59628625	1.00[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs60026262	1.00[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs60365921	1.00[AMR][1000 genomes]
rs60404320	1.00[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs60620576	0.86[ASN][1000 genomes]
rs61057668	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs61059263	0.93[ASN][1000 genomes]
rs61167296	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs61343540	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61368758	1.00[AMR][1000 genomes]
rs61400453	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs61600848	1.00[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs61618553	1.00[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs61633090	1.00[AMR][1000 genomes]
rs61685588	1.00[AMR][1000 genomes]
rs6674016	0.93[ASN][1000 genomes]
rs6678049	0.93[ASN][1000 genomes]
rs6679048	0.93[ASN][1000 genomes]
rs6686570	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs73081443	1.00[AMR][1000 genomes]
rs73081447	1.00[AMR][1000 genomes]
rs73081459	1.00[AMR][1000 genomes]
rs73081470	1.00[AMR][1000 genomes]
rs73081479	1.00[AMR][1000 genomes]
rs73081487	1.00[AMR][1000 genomes]
rs73081497	1.00[AMR][1000 genomes]
rs73083403	1.00[AMR][1000 genomes]
rs73083410	1.00[AMR][1000 genomes]
rs73083415	1.00[AMR][1000 genomes]
rs73083420	1.00[AMR][1000 genomes]
rs73090166	0.93[ASN][1000 genomes]
rs73090172	0.93[ASN][1000 genomes]
rs73090177	0.93[ASN][1000 genomes]
rs73090179	0.93[ASN][1000 genomes]
rs73091959	0.93[ASN][1000 genomes]
rs73091984	0.86[ASN][1000 genomes]
rs73091986	0.86[ASN][1000 genomes]
rs73091998	0.86[ASN][1000 genomes]
rs73094106	1.00[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs73094120	1.00[AMR][1000 genomes]
rs73094142	1.00[AMR][1000 genomes]
rs73100105	1.00[AMR][1000 genomes]
rs73100108	1.00[AMR][1000 genomes]
rs73100129	1.00[AMR][1000 genomes]
rs73100141	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1014878	chr1:215453286-215527616	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv1003660	chr1:215453286-215529747	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
3	esv4176	chr1:215492233-215501083	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
4	esv3321142	chr1:215492265-215501079	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
5	esv3321141	chr1:215492277-215501111	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
6	esv3321139	chr1:215492331-215501079	Enhancers ZNF genes & repeats Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
7	esv3321143	chr1:215492422-215500995	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv1009296	chr1:215498152-215520123	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:215499400-215504000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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