Variant report

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs4311117	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6048363	0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6048367	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6048369	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6082850	0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6082862	0.88[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6082866	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6106563	0.88[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6113817	0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6113818	0.85[ASN][1000 genomes]
rs6132547	0.84[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs6137756	0.90[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	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
2	nsv912816	chr20:22757960-23062927	Flanking Active TSS Bivalent/Poised TSS Enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
3	nsv3334	chr20:22773462-22818362	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:22776400-22785800	Weak transcription	Right Atrium	heart
2	chr20:22778600-22786200	Weak transcription	Gastric	stomach
3	chr20:22781800-22785400	Weak transcription	A549	lung
4	chr20:22781800-22786400	Enhancers	HSMMtube	muscle
5	chr20:22782000-22789000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr20:22782200-22790000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr20:22783200-22785400	Weak transcription	Placenta	Placenta
8	chr20:22783400-22785600	Weak transcription	Lung	lung
9	chr20:22783600-22785600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr20:22783600-22785600	Weak transcription	Esophagus	oesophagus
11	chr20:22783800-22785400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr20:22784000-22791400	Weak transcription	HMEC	breast
13	chr20:22784600-22785800	Weak transcription	Fetal Muscle Trunk	muscle
14	chr20:22784600-22786000	Enhancers	Spleen	Spleen
15	chr20:22784600-22786400	Enhancers	HSMM	muscle
16	chr20:22784800-22787000	Enhancers	Fetal Muscle Leg	muscle
17	chr20:22784800-22787000	Enhancers	Ovary	ovary
18	chr20:22785000-22785400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr20:22785000-22785800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr20:22785000-22786400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr20:22785200-22786000	Weak transcription	Aorta	Aorta

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