Variant report

Variant	rs17152888
Chromosome Location	chr7:79410552-79410553
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 85 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:77)

rs_ID	r²[population]
rs11977110	1.00[ASN][1000 genomes]
rs1293091	0.86[ASN][1000 genomes]
rs1293109	0.86[ASN][1000 genomes]
rs1293110	0.85[ASN][1000 genomes]
rs1293111	0.84[ASN][1000 genomes]
rs1293112	0.86[ASN][1000 genomes]
rs1293113	0.86[ASN][1000 genomes]
rs1293115	0.86[ASN][1000 genomes]
rs1297413	0.86[ASN][1000 genomes]
rs1523834	0.92[ASN][1000 genomes]
rs1523842	0.80[ASN][1000 genomes]
rs1523843	0.83[ASN][1000 genomes]
rs16886625	0.97[ASN][1000 genomes]
rs17147916	0.97[ASN][1000 genomes]
rs17152857	1.00[ASN][1000 genomes]
rs17152858	1.00[ASN][1000 genomes]
rs17152859	1.00[ASN][1000 genomes]
rs17152860	1.00[ASN][1000 genomes]
rs17152864	1.00[ASN][1000 genomes]
rs17152926	0.92[ASN][1000 genomes]
rs17152944	0.89[ASN][1000 genomes]
rs1851752	1.00[ASN][1000 genomes]
rs1880167	0.92[ASN][1000 genomes]
rs1916732	0.95[ASN][1000 genomes]
rs1916740	0.95[ASN][1000 genomes]
rs1922725	0.86[ASN][1000 genomes]
rs1922726	0.86[ASN][1000 genomes]
rs1922728	0.85[ASN][1000 genomes]
rs1922734	0.95[ASN][1000 genomes]
rs1985747	0.81[ASN][1000 genomes]
rs2222904	0.95[ASN][1000 genomes]
rs2246996	0.85[ASN][1000 genomes]
rs2366248	0.95[ASN][1000 genomes]
rs2465515	0.89[ASN][1000 genomes]
rs2465517	0.83[ASN][1000 genomes]
rs2689797	0.83[ASN][1000 genomes]
rs2689804	0.95[ASN][1000 genomes]
rs2689805	0.95[ASN][1000 genomes]
rs2689810	0.95[ASN][1000 genomes]
rs2689811	0.88[ASN][1000 genomes]
rs2707858	0.89[ASN][1000 genomes]
rs2707886	0.86[ASN][1000 genomes]
rs2707887	0.86[ASN][1000 genomes]
rs2707897	0.92[ASN][1000 genomes]
rs2714640	0.85[ASN][1000 genomes]
rs2714642	0.95[ASN][1000 genomes]
rs2714652	0.83[ASN][1000 genomes]
rs2714653	0.86[ASN][1000 genomes]
rs2714655	0.86[ASN][1000 genomes]
rs2714656	0.85[ASN][1000 genomes]
rs2714661	0.85[ASN][1000 genomes]
rs2714662	0.86[ASN][1000 genomes]
rs2714664	0.85[ASN][1000 genomes]
rs2714695	0.86[ASN][1000 genomes]
rs2714696	0.86[ASN][1000 genomes]
rs4288313	0.83[ASN][1000 genomes]
rs4394329	0.92[ASN][1000 genomes]
rs55772364	1.00[ASN][1000 genomes]
rs56320258	1.00[ASN][1000 genomes]
rs56351881	1.00[ASN][1000 genomes]
rs57226669	1.00[ASN][1000 genomes]
rs57870645	0.88[ASN][1000 genomes]
rs57942274	1.00[ASN][1000 genomes]
rs59149988	0.85[ASN][1000 genomes]
rs59329952	0.97[ASN][1000 genomes]
rs60390345	1.00[ASN][1000 genomes]
rs60870507	1.00[ASN][1000 genomes]
rs6466768	0.83[ASN][1000 genomes]
rs724336	0.86[CHB][hapmap];0.85[JPT][hapmap]
rs73381226	1.00[ASN][1000 genomes]
rs73705067	1.00[ASN][1000 genomes]
rs7777781	0.89[ASN][1000 genomes]
rs7789978	0.97[ASN][1000 genomes]
rs7803517	0.85[JPT][hapmap]
rs7803852	0.85[JPT][hapmap]
rs886475	0.85[JPT][hapmap]
rs940308	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	nsv464598	chr7:78492642-79483480	Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
2	nsv607659	chr7:78492642-79483480	Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
3	esv2758121	chr7:79261464-79427646	Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	esv2759540	chr7:79261464-79427646	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv607670	chr7:79310586-79434743	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	esv2829876	chr7:79355196-79483480	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv888521	chr7:79371206-79483480	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv888522	chr7:79402551-79619012	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:79399400-79411000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr7:79407600-79410800	Weak transcription	Fetal Heart	heart
3	chr7:79409000-79411200	Weak transcription	Muscle Satellite Cultured Cells	--
4	chr7:79409000-79419400	Weak transcription	NHLF	lung
5	chr7:79409200-79411000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr7:79409200-79411000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr7:79409200-79416800	Weak transcription	Osteobl	bone
8	chr7:79410400-79411800	Enhancers	Fetal Lung	lung

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