Variant report

Variant	rs10873735
Chromosome Location	chr1:76300317-76300318
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 65 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:58)

rs_ID	r²[population]
rs10873724	0.81[ASN][1000 genomes]
rs10873727	0.83[ASN][1000 genomes]
rs10873728	0.83[ASN][1000 genomes]
rs10873738	0.83[ASN][1000 genomes]
rs10873739	0.83[ASN][1000 genomes]
rs11161700	0.83[ASN][1000 genomes]
rs11161704	0.87[ASN][1000 genomes]
rs1144328	0.86[ASN][1000 genomes]
rs1144331	0.87[ASN][1000 genomes]
rs1144333	0.87[ASN][1000 genomes]
rs1144337	0.87[ASN][1000 genomes]
rs1144338	0.83[ASN][1000 genomes]
rs1144339	0.87[ASN][1000 genomes]
rs1144341	0.87[ASN][1000 genomes]
rs1144342	0.87[ASN][1000 genomes]
rs1146602	0.80[ASN][1000 genomes]
rs1146616	0.82[ASN][1000 genomes]
rs1146645	0.86[ASN][1000 genomes]
rs1146647	0.86[ASN][1000 genomes]
rs1146648	0.82[ASN][1000 genomes]
rs1146649	0.85[ASN][1000 genomes]
rs1146651	0.87[ASN][1000 genomes]
rs1146652	0.87[ASN][1000 genomes]
rs1146656	0.83[ASN][1000 genomes]
rs11579355	0.83[ASN][1000 genomes]
rs12076093	0.83[ASN][1000 genomes]
rs12078151	0.83[ASN][1000 genomes]
rs12081710	0.83[ASN][1000 genomes]
rs12090712	0.83[ASN][1000 genomes]
rs12385715	0.83[ASN][1000 genomes]
rs12401729	0.83[ASN][1000 genomes]
rs12403889	0.83[ASN][1000 genomes]
rs12405178	0.83[ASN][1000 genomes]
rs1250881	0.84[ASN][1000 genomes]
rs1250882	0.87[ASN][1000 genomes]
rs1251270	0.87[ASN][1000 genomes]
rs1251272	0.83[ASN][1000 genomes]
rs1251273	0.87[ASN][1000 genomes]
rs1251274	0.87[ASN][1000 genomes]
rs1251275	0.83[ASN][1000 genomes]
rs12703	0.86[ASN][1000 genomes]
rs1812589	0.81[ASN][1000 genomes]
rs2012536	0.86[ASN][1000 genomes]
rs34045364	0.82[ASN][1000 genomes]
rs34177389	0.82[ASN][1000 genomes]
rs35591768	0.82[ASN][1000 genomes]
rs3765682	0.81[ASN][1000 genomes]
rs4347163	0.82[ASN][1000 genomes]
rs4949884	0.83[ASN][1000 genomes]
rs5019550	0.83[ASN][1000 genomes]
rs56350137	0.83[ASN][1000 genomes]
rs5745327	0.86[ASN][1000 genomes]
rs5745343	0.87[ASN][1000 genomes]
rs5745354	0.87[ASN][1000 genomes]
rs5745392	0.87[ASN][1000 genomes]
rs61676733	0.83[ASN][1000 genomes]
rs7514912	0.82[ASN][1000 genomes]
rs7548391	0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv519329	chr1:75830438-76358591	Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
2	nsv1014072	chr1:76200531-76460726	Genic enhancers Enhancers Strong transcription Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
3	nsv535005	chr1:76200531-76460726	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
4	esv1795237	chr1:76268573-76383565	Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	esv1800125	chr1:76269439-76379497	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	esv1799260	chr1:76269439-76383297	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
7	esv1847721	chr1:76269439-76383565	Weak transcription ZNF genes & repeats Enhancers Strong transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:76295800-76307800	Weak transcription	Skeletal Muscle Female	skeletal muscle

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