Variant report

Variant	rs73930274
Chromosome Location	chr19:39568008-39568009
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr19:39565899..39568671-chr3:161088109..161090760,2	MCF-7	breast:
2	chr19:39526693..39529184-chr19:39566725..39569356,2	K562	blood:
3	chr19:39566476..39569362-chr19:39573517..39575848,2	K562	blood:

Variant related genes	Relation type
ENSG00000196542	Chromatin interaction
ENSG00000183760	Chromatin interaction

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs17880870	1.00[AMR][1000 genomes]
rs17881574	1.00[AMR][1000 genomes]
rs17883178	1.00[AMR][1000 genomes]
rs56935544	1.00[AMR][1000 genomes]
rs57556122	1.00[AMR][1000 genomes]
rs58109066	1.00[AMR][1000 genomes]
rs59087858	1.00[AMR][1000 genomes]
rs73541565	1.00[AMR][1000 genomes]
rs73543539	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv458571	chr19:39533754-39628050	Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
2	nsv579508	chr19:39533754-39628050	Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
3	nsv522530	chr19:39552150-39573918	Bivalent Enhancer Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv1067028	chr19:39567228-39622846	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
5	nsv1060469	chr19:39567228-39624790	Enhancers Bivalent Enhancer Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:23 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:39562000-39570000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr19:39564600-39569200	Weak transcription	Brain Hippocampus Middle	brain
3	chr19:39564600-39569600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr19:39564600-39569600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr19:39565000-39571200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr19:39565200-39568400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr19:39565200-39568400	Weak transcription	NHDF-Ad	bronchial
8	chr19:39565200-39568400	Weak transcription	NHEK	skin
9	chr19:39565200-39568800	Weak transcription	Osteobl	bone
10	chr19:39565200-39569000	Weak transcription	Muscle Satellite Cultured Cells	--
11	chr19:39565200-39569000	Weak transcription	Hela-S3	cervix
12	chr19:39565400-39568200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr19:39565400-39568400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr19:39565400-39568600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr19:39565400-39573000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
16	chr19:39565400-39573200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr19:39565800-39569000	Weak transcription	HUVEC	blood vessel
18	chr19:39566000-39569000	Weak transcription	NH-A	brain
19	chr19:39567400-39574000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr19:39567800-39568200	Strong transcription	HMEC	breast
21	chr19:39567800-39569200	Enhancers	A549	lung
22	chr19:39568000-39568200	Bivalent Enhancer	Right Ventricle	heart
23	chr19:39568000-39570800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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