Variant report

Variant	rs55811739
Chromosome Location	chr22:27536861-27536862
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs16983778	0.91[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs73422331	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73422334	0.99[AFR][1000 genomes];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	nsv917333	chr22:26931825-27692024	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	142 gene(s)	inside rSNPs	diseases
2	esv34168	chr22:27289097-27678031	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
3	esv3413125	chr22:27404463-28121577	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Strong 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	31 gene(s)	inside rSNPs	diseases
4	nsv459860	chr22:27527005-28181436	Strong transcription Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
5	nsv588872	chr22:27527005-28181436	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:27533600-27537400	Enhancers	Brain Germinal Matrix	brain
2	chr22:27534400-27537000	Weak transcription	Fetal Brain Female	brain
3	chr22:27534600-27537200	Enhancers	NH-A	brain
4	chr22:27535200-27537200	Enhancers	Osteobl	bone
5	chr22:27535600-27538600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr22:27535800-27537000	Enhancers	Duodenum Smooth Muscle	Duodenum
7	chr22:27536000-27537000	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr22:27536000-27537000	Bivalent Enhancer	NHDF-Ad	bronchial
9	chr22:27536200-27537600	Enhancers	A549	lung
10	chr22:27536400-27538400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr22:27536400-27546000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr22:27536600-27537000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr22:27536600-27538000	Weak transcription	Colon Smooth Muscle	Colon
14	chr22:27536600-27555000	Weak transcription	Placenta Amnion	Placenta Amnion
15	chr22:27536800-27537200	Bivalent Enhancer	Muscle Satellite Cultured Cells	--
16	chr22:27536800-27540400	Weak transcription	Aorta	Aorta

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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