Variant report

Variant	rs1469179
Chromosome Location	chr7:136621677-136621678
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 93 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:91)

rs_ID	r²[population]
rs10243944	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10447876	0.97[ASN][1000 genomes]
rs10447877	1.00[ASN][1000 genomes]
rs10447878	0.97[ASN][1000 genomes]
rs10447879	1.00[ASN][1000 genomes]
rs10488598	1.00[CHD][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs10954567	0.86[JPT][hapmap]
rs11976272	1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs11981061	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs11982108	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs12532092	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs12532094	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs12533847	1.00[ASN][1000 genomes]
rs12535371	1.00[CHD][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs12536267	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs12536293	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs12536315	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs12536341	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs12537142	1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs12537962	1.00[CHD][hapmap];0.89[JPT][hapmap]
rs12539659	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs12539738	0.89[JPT][hapmap]
rs12540313	0.89[JPT][hapmap]
rs12707333	1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs12707334	0.85[ASN][1000 genomes]
rs13224113	0.85[ASN][1000 genomes]
rs13235468	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs13244595	0.89[JPT][hapmap]
rs13246516	1.00[CHD][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs1364404	0.85[ASN][1000 genomes]
rs1364405	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs1364409	1.00[YRI][hapmap];0.90[AFR][1000 genomes]
rs1424387	1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs17411478	1.00[CHD][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs17411561	1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs17412549	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs17412764	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs17412792	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs17495182	1.00[CHD][hapmap];0.89[JPT][hapmap]
rs17495548	1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs17495783	0.85[ASN][1000 genomes]
rs17496259	1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs17496363	1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs17496543	1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs17496575	1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs17496844	1.00[CHB][hapmap];0.89[JPT][hapmap];1.00[ASN][1000 genomes]
rs17496997	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs17497143	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs17497261	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs17497337	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs17497363	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs2278071	0.90[JPT][hapmap];0.82[ASN][1000 genomes]
rs2350781	1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs324640	1.00[CHB][hapmap]
rs324644	1.00[CHB][hapmap]
rs34777519	0.88[ASN][1000 genomes]
rs35458626	0.82[ASN][1000 genomes]
rs35850868	0.97[ASN][1000 genomes]
rs36210735	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4629799	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs55816133	0.85[ASN][1000 genomes]
rs55828513	1.00[ASN][1000 genomes]
rs55895689	1.00[ASN][1000 genomes]
rs62485228	0.85[ASN][1000 genomes]
rs62485229	0.85[ASN][1000 genomes]
rs62485234	1.00[ASN][1000 genomes]
rs62485236	1.00[ASN][1000 genomes]
rs62485237	1.00[ASN][1000 genomes]
rs62485238	1.00[ASN][1000 genomes]
rs62485239	1.00[ASN][1000 genomes]
rs62485240	1.00[ASN][1000 genomes]
rs62485241	1.00[ASN][1000 genomes]
rs62485242	1.00[ASN][1000 genomes]
rs62485243	0.97[ASN][1000 genomes]
rs62485244	1.00[ASN][1000 genomes]
rs62485245	1.00[ASN][1000 genomes]
rs62485246	1.00[ASN][1000 genomes]
rs62485247	1.00[ASN][1000 genomes]
rs62485248	1.00[ASN][1000 genomes]
rs62485254	1.00[ASN][1000 genomes]
rs6947206	0.88[ASW][hapmap];0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.86[MKK][hapmap];0.81[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73158708	0.85[ASN][1000 genomes]
rs73158738	1.00[ASN][1000 genomes]
rs7457321	1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs7458912	0.89[JPT][hapmap]
rs7790583	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs7792449	0.89[AFR][1000 genomes]
rs7799307	0.85[ASN][1000 genomes]
rs7800170	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7810473	1.00[CHD][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs7811061	1.00[CHD][hapmap];1.00[JPT][hapmap];0.85[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	nsv1029192	chr7:136433278-137147566	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv831147	chr7:136583444-136755741	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	8 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	chr7:136607800-136638000	Weak transcription	NHLF	lung
2	chr7:136610800-136623400	Weak transcription	Colon Smooth Muscle	Colon
3	chr7:136611000-136623200	Weak transcription	Left Ventricle	heart
4	chr7:136616600-136622600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr7:136620600-136624800	Enhancers	Fetal Heart	heart

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