Variant report

Variant	rs7253933
Chromosome Location	chr19:39569245-39569246
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr19:39526693..39529184-chr19:39566725..39569356,2	K562	blood:
2	chr19:39566476..39569362-chr19:39573517..39575848,2	K562	blood:

Variant related genes	Relation type
ENSG00000183760	Chromatin interaction

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs7250655	1.00[AFR][1000 genomes]
rs8112739	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:28 , 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	chr19:39564600-39569600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr19:39564600-39569600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr19:39565000-39571200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr19:39565400-39573000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
6	chr19:39565400-39573200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr19:39567400-39574000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr19:39568000-39570800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr19:39568200-39569400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr19:39568400-39570000	Enhancers	NHDF-Ad	bronchial
11	chr19:39568400-39570000	Enhancers	NHEK	skin
12	chr19:39568400-39570200	Enhancers	Brain Anterior Caudate	brain
13	chr19:39568400-39570600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr19:39568400-39571600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr19:39568600-39570200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr19:39568600-39570200	Enhancers	HMEC	breast
17	chr19:39568800-39570400	Enhancers	Osteobl	bone
18	chr19:39569000-39569800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr19:39569000-39569800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr19:39569000-39569800	Enhancers	Brain Substantia Nigra	brain
21	chr19:39569000-39569800	Enhancers	HUVEC	blood vessel
22	chr19:39569000-39569800	Enhancers	NH-A	brain
23	chr19:39569000-39570200	Enhancers	Muscle Satellite Cultured Cells	--
24	chr19:39569200-39569400	Bivalent Enhancer	Stomach Smooth Muscle	stomach
25	chr19:39569200-39569800	Flanking Active TSS	A549	lung
26	chr19:39569200-39569800	Flanking Active TSS	Hela-S3	cervix
27	chr19:39569200-39570200	Enhancers	Brain Hippocampus Middle	brain
28	chr19:39569200-39570200	Enhancers	Placenta	Placenta

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