Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:37568344..37572932-chr6:37584973..37589083,4	K562	blood:
2	chr6:37569357..37570973-chr6:37606772..37609640,2	K562	blood:

Variant related genes	Relation type
ENSG00000112139	Chromatin interaction

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs10947684	0.80[AFR][1000 genomes]
rs11751582	0.98[ASN][1000 genomes]
rs11752518	0.83[ASN][1000 genomes]
rs11752560	0.83[ASN][1000 genomes]
rs11753044	0.83[ASN][1000 genomes]
rs11753180	0.86[ASN][1000 genomes]
rs11754348	0.83[ASN][1000 genomes]
rs11755524	0.98[ASN][1000 genomes]
rs11755639	0.98[ASN][1000 genomes]
rs11758741	0.95[ASN][1000 genomes]
rs2051073	0.86[ASN][1000 genomes]
rs34388013	0.81[ASN][1000 genomes]
rs34529589	0.93[ASN][1000 genomes]
rs34989139	0.98[ASN][1000 genomes]
rs35084219	0.98[ASN][1000 genomes]
rs35288154	0.88[ASN][1000 genomes]
rs35416456	0.81[ASN][1000 genomes]
rs62398377	0.93[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6925759	0.86[ASN][1000 genomes]
rs71569382	0.88[ASN][1000 genomes]
rs71569383	0.88[ASN][1000 genomes]
rs71569384	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][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	esv2752124	chr6:37416219-37680622	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	22 gene(s)	inside rSNPs	diseases
2	nsv1028825	chr6:37495154-38278320	Enhancers Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Strong transcription 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	19 gene(s)	inside rSNPs	diseases
3	nsv1024016	chr6:37567651-37981590	Weak transcription Enhancers Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:37569800-37570200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr6:37569800-37571000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr6:37570000-37570200	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
4	chr6:37570000-37570200	Bivalent/Poised TSS	Placenta	Placenta
5	chr6:37570000-37571000	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr6:37570000-37571000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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