Variant report

Variant	rs13104799
Chromosome Location	chr4:110255140-110255141
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:110255115..110257197-chr4:110258103..110260350,2	K562	blood:
2	chr4:109755793..109756631-chr4:110255007..110255987,2	K562	blood:

Extended variants
information (count: 66 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:64)

rs_ID	r²[population]
rs10005198	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10007410	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10014623	1.00[ASN][1000 genomes]
rs10031251	0.89[ASN][1000 genomes]
rs10031399	0.89[ASN][1000 genomes]
rs10155246	1.00[CEU][hapmap];0.82[CHB][hapmap];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10516557	0.84[CHD][hapmap]
rs11933172	1.00[CEU][hapmap];1.00[MEX][hapmap];0.87[TSI][hapmap];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11937053	0.84[CHD][hapmap]
rs11939924	0.88[EUR][1000 genomes]
rs12641197	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12641272	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12643881	0.81[CHD][hapmap]
rs13113384	0.91[EUR][1000 genomes]
rs13119700	0.91[EUR][1000 genomes]
rs13126829	0.95[EUR][1000 genomes]
rs13128445	1.00[MEX][hapmap]
rs13138833	0.91[EUR][1000 genomes]
rs1557804	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs17040454	0.84[CHD][hapmap]
rs17842269	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1859144	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1859145	0.82[ASN][1000 genomes]
rs1859146	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1859147	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1981540	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1981541	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2079108	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2214377	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2346014	0.91[EUR][1000 genomes]
rs28374470	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28463999	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs28542804	0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs28585579	0.91[EUR][1000 genomes]
rs28628718	0.91[EUR][1000 genomes]
rs28749845	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4524460	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6533426	0.91[EUR][1000 genomes]
rs6825928	1.00[CEU][hapmap];0.82[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap];0.93[TSI][hapmap]
rs6827985	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6841133	0.91[EUR][1000 genomes]
rs6841222	0.91[EUR][1000 genomes]
rs714586	1.00[MEX][hapmap]
rs7665024	0.95[EUR][1000 genomes]
rs7673595	1.00[CEU][hapmap]
rs7673867	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7675344	1.00[CEU][hapmap];0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7680752	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7680920	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7684744	0.91[EUR][1000 genomes]
rs7685787	0.91[EUR][1000 genomes]
rs7694523	0.95[EUR][1000 genomes]
rs7695754	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs7699247	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs876464	0.91[EUR][1000 genomes]
rs9307329	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9993228	0.91[EUR][1000 genomes]
rs9996165	1.00[CEU][hapmap];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9996432	0.91[EUR][1000 genomes]
rs9996537	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9996920	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9999270	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9999278	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9999751	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv461613	chr4:109922064-110593460	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
2	nsv595129	chr4:109922064-110593460	Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 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	chr4:110254400-110255800	Enhancers	HSMMtube	muscle
2	chr4:110254600-110255600	Weak transcription	Fetal Muscle Trunk	muscle
3	chr4:110254800-110255800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr4:110254800-110255800	Weak transcription	Fetal Muscle Leg	muscle
5	chr4:110254800-110256600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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