Variant report

Variant	rs11204956
Chromosome Location	chr1:152236058-152236059
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 91 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:83)

rs_ID	r²[population]
rs10749670	0.85[ASN][1000 genomes]
rs10788831	0.86[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs10888473	0.82[ASN][1000 genomes]
rs10888475	0.84[ASN][1000 genomes]
rs10888476	0.85[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs10888477	0.92[AFR][1000 genomes];0.91[AMR][1000 genomes];0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10888478	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11204944	0.82[ASN][1000 genomes]
rs11204947	0.82[ASN][1000 genomes]
rs11204948	0.82[ASN][1000 genomes]
rs11204951	0.85[ASN][1000 genomes]
rs11204952	0.81[ASN][1000 genomes]
rs11204976	0.86[ASN][1000 genomes]
rs11204980	0.82[ASN][1000 genomes]
rs11204981	0.82[ASN][1000 genomes]
rs11485508	0.91[ASN][1000 genomes]
rs11584340	0.83[ASN][1000 genomes]
rs12027807	0.90[ASN][1000 genomes]
rs12027899	0.88[ASN][1000 genomes]
rs12045492	0.88[ASN][1000 genomes]
rs12045496	0.88[ASN][1000 genomes]
rs12065368	0.88[ASN][1000 genomes]
rs12407553	0.81[ASN][1000 genomes]
rs12409802	0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12730241	0.86[ASN][1000 genomes]
rs1466757	0.82[ASN][1000 genomes]
rs1845791	0.83[ASN][1000 genomes]
rs1858479	0.82[ASN][1000 genomes]
rs1858480	0.84[ASN][1000 genomes]
rs1969019	0.83[ASN][1000 genomes]
rs2132418	0.84[ASN][1000 genomes]
rs2184950	0.86[ASN][1000 genomes]
rs2184951	0.86[ASN][1000 genomes]
rs2184953	0.83[ASN][1000 genomes]
rs2338430	0.83[ASN][1000 genomes]
rs2879174	0.81[ASN][1000 genomes]
rs3120659	0.84[ASN][1000 genomes]
rs3120661	0.84[ASN][1000 genomes]
rs3126055	0.90[ASN][1000 genomes]
rs3126056	0.88[ASN][1000 genomes]
rs3126058	0.85[ASN][1000 genomes]
rs3126060	0.85[ASN][1000 genomes]
rs3126062	0.86[ASN][1000 genomes]
rs3126066	0.83[ASN][1000 genomes]
rs3126067	0.83[ASN][1000 genomes]
rs3126072	0.84[ASN][1000 genomes]
rs3126074	0.85[ASN][1000 genomes]
rs3126079	0.85[ASN][1000 genomes]
rs3126091	0.84[ASN][1000 genomes]
rs3126094	0.84[ASN][1000 genomes]
rs3126097	0.84[ASN][1000 genomes]
rs34188926	0.82[ASN][1000 genomes]
rs36033453	0.82[ASN][1000 genomes]
rs41267154	0.83[ASN][1000 genomes]
rs4256811	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4341364	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4361987	0.89[ASN][1000 genomes]
rs4456097	0.86[ASN][1000 genomes]
rs4466659	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4511113	0.82[ASN][1000 genomes]
rs4845428	0.82[ASN][1000 genomes]
rs4845430	0.85[ASN][1000 genomes]
rs4845431	0.85[ASN][1000 genomes]
rs4845751	0.81[ASN][1000 genomes]
rs4845752	0.81[ASN][1000 genomes]
rs4845753	0.91[AFR][1000 genomes];0.90[AMR][1000 genomes];0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs55650366	0.81[ASN][1000 genomes]
rs6587666	0.82[ASN][1000 genomes]
rs6666382	0.82[ASN][1000 genomes]
rs6670891	0.83[ASN][1000 genomes]
rs6675889	0.83[ASN][1000 genomes]
rs6678951	0.82[ASN][1000 genomes]
rs6681433	0.83[ASN][1000 genomes]
rs6681457	0.82[ASN][1000 genomes]
rs6692010	0.87[ASN][1000 genomes]
rs72697000	0.82[ASN][1000 genomes]
rs7535078	0.84[ASN][1000 genomes]
rs7536879	0.85[ASN][1000 genomes]
rs7537637	0.82[ASN][1000 genomes]
rs7540844	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7543541	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9436062	0.87[ASN][1000 genomes]
rs991231	0.83[ASN][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	nsv547853	chr1:152008671-152236760	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	83 gene(s)	inside rSNPs	diseases
2	nsv1014095	chr1:152104486-152454591	Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
3	nsv946325	chr1:152221751-152240196	Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS Active TSS	lncRNA	1 gene(s)	inside rSNPs	diseases
4	esv3372510	chr1:152232828-152237226	ZNF genes & repeats Weak transcription	n/a	n/a	inside rSNPs	diseases
5	esv3422049	chr1:152234328-152238726	Weak transcription ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
6	nsv547855	chr1:152235044-152240504	Weak transcription ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
7	nsv547856	chr1:152235044-152251714	Weak transcription ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
8	nsv547857	chr1:152235564-152240504	Weak transcription ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:152231200-152236400	Weak transcription	Fetal Kidney	kidney
2	chr1:152236000-152236200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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