Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:32936100..32938638-chr14:32940941..32943770,2	K562	blood:

Variant related genes	Relation type
ENSG00000151320	Chromatin interaction

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs1951191	0.84[ASN][1000 genomes]
rs1957013	0.82[ASN][1000 genomes]
rs1957015	0.80[ASN][1000 genomes]
rs1957016	0.82[ASN][1000 genomes]
rs1957018	0.82[ASN][1000 genomes]
rs1957019	0.82[ASN][1000 genomes]
rs1957024	0.86[AFR][1000 genomes]
rs2224430	0.80[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2224431	0.90[ASN][1000 genomes]
rs4329831	0.92[ASN][1000 genomes]
rs56837786	0.97[ASN][1000 genomes]
rs6571518	0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7146377	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7147629	0.84[ASN][1000 genomes]
rs7149947	0.80[ASN][1000 genomes]
rs7493664	0.91[AFR][1000 genomes];0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs8013463	0.84[ASN][1000 genomes]
rs9285570	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs941746	0.82[ASN][1000 genomes]
rs9972147	0.90[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9972192	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[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	esv2758352	chr14:32858480-33016442	Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	esv2759978	chr14:32858480-33016442	Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv901595	chr14:32928634-32961434	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:32926800-32936800	Weak transcription	Brain Cingulate Gyrus	brain
2	chr14:32930600-32936800	Weak transcription	Aorta	Aorta
3	chr14:32930600-32937400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr14:32931000-32941400	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr14:32936200-32937400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
6	chr14:32936200-32937600	Enhancers	Fetal Heart	heart
7	chr14:32936200-32942800	Enhancers	Breast Myoepithelial Primary Cells	Breast
8	chr14:32936200-32942800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr14:32936400-32937000	Weak transcription	Brain Angular Gyrus	brain
10	chr14:32936400-32937000	Enhancers	Brain Inferior Temporal Lobe	brain
11	chr14:32936400-32938400	Enhancers	NHEK	skin
12	chr14:32936400-32943200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr14:32936400-32944800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr14:32936600-32939400	Enhancers	Colon Smooth Muscle	Colon
15	chr14:32936600-32941800	Enhancers	HMEC	breast

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