Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:136701167..136703847-chr7:136709955..136712489,2	K562	blood:

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10954569	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11762896	0.88[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11971236	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11971309	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11982015	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12113365	0.89[ASN][1000 genomes]
rs12540615	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs13221430	0.91[ASN][1000 genomes]
rs1424548	0.87[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1424549	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs17500423	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs17506977	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1991115	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs34084423	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs34907276	0.81[ASN][1000 genomes]
rs35536027	0.87[ASN][1000 genomes]
rs62487072	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs67532040	0.86[ASN][1000 genomes]
rs6978427	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs73447194	0.86[ASN][1000 genomes]
rs7779506	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7779921	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7779999	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7780181	0.83[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 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
3	esv2753059	chr7:136633745-136893745	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 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	chr7:136700400-136717400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr7:136701000-136712000	Weak transcription	Left Ventricle	heart
3	chr7:136710200-136711800	Enhancers	Rectal Smooth Muscle	rectum
4	chr7:136710400-136711800	Enhancers	Fetal Heart	heart
5	chr7:136711000-136712000	Weak transcription	Stomach Smooth Muscle	stomach
6	chr7:136711400-136717400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr7:136711600-136711800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr7:136711600-136721400	Weak transcription	Colon Smooth Muscle	Colon

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