Variant report

Variant	rs57154892
Chromosome Location	chr20:22746794-22746795
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs16984411	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16984435	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56896182	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58242823	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59207044	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60445726	1.00[AMR][1000 genomes]
rs61540052	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7261797	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7266128	1.00[AMR][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	nsv1061382	chr20:22706041-22763200	ZNF genes & repeats Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv544213	chr20:22722740-22791150	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv528221	chr20:22732749-22767280	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:22737800-22749000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr20:22743200-22751400	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr20:22744000-22748800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr20:22744600-22749000	Weak transcription	NH-A	brain
5	chr20:22744600-22749200	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr20:22744800-22748800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr20:22745200-22749400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr20:22745400-22750800	Weak transcription	Hela-S3	cervix
9	chr20:22745400-22752400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr20:22745400-22752400	Weak transcription	Gastric	stomach
11	chr20:22745600-22749000	Weak transcription	HSMMtube	muscle
12	chr20:22745800-22747000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr20:22745800-22748000	Weak transcription	Placenta Amnion	Placenta Amnion
14	chr20:22745800-22748200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr20:22745800-22748600	Weak transcription	HSMM	muscle
16	chr20:22745800-22749400	Weak transcription	Stomach Mucosa	stomach
17	chr20:22746000-22747800	Weak transcription	Placenta	Placenta
18	chr20:22746000-22748800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr20:22746000-22748800	Weak transcription	A549	lung
20	chr20:22746000-22749000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr20:22746000-22749000	Weak transcription	Ovary	ovary
22	chr20:22746000-22749000	Weak transcription	HMEC	breast
23	chr20:22746000-22749200	Weak transcription	NHEK	skin
24	chr20:22746000-22749400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr20:22746000-22751000	Weak transcription	Skeletal Muscle Male	skeletal muscle
26	chr20:22746000-22756000	Weak transcription	Spleen	Spleen

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