Variant report

Variant	rs72951635
Chromosome Location	chr4:150879763-150879764
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:150874758..150877584-chr4:150877955..150879848,2	K562	blood:

Variant related genes	Relation type
ENSG00000250704	Chromatin interaction

Extended variants
information (count: 30 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs4464548	0.96[AFR][1000 genomes]
rs4482743	0.96[AFR][1000 genomes]
rs4493520	0.90[AFR][1000 genomes]
rs59305347	0.96[AFR][1000 genomes]
rs72951607	0.96[AFR][1000 genomes]
rs72951616	0.96[AFR][1000 genomes]
rs72951625	0.96[AFR][1000 genomes]
rs72951628	0.96[AFR][1000 genomes]
rs72951633	0.96[AFR][1000 genomes]
rs72951643	0.96[AFR][1000 genomes]
rs72951647	0.96[AFR][1000 genomes]
rs72955783	0.88[AFR][1000 genomes]
rs72955787	0.88[AFR][1000 genomes]
rs72957527	0.88[AFR][1000 genomes]
rs72969427	0.96[AFR][1000 genomes]
rs72969441	0.96[AFR][1000 genomes]
rs72969455	0.96[AFR][1000 genomes]
rs72969458	0.96[AFR][1000 genomes]
rs72969460	0.96[AFR][1000 genomes]
rs72969462	0.96[AFR][1000 genomes]
rs72969465	0.96[AFR][1000 genomes]
rs72969466	0.96[AFR][1000 genomes]
rs72969468	0.96[AFR][1000 genomes]
rs72969478	0.96[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1026797	chr4:150246932-151217137	Bivalent Enhancer Enhancers Strong transcription Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv1016169	chr4:150670127-150903827	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv537299	chr4:150670127-150903827	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv932022	chr4:150831733-151419552	Enhancers Weak transcription Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
5	nsv830111	chr4:150867357-151035556	Flanking Active TSS Enhancers Bivalent/Poised TSS ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv530158	chr4:150877557-151040992	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS 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	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:150877600-150885400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr4:150878800-150880600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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