Variant report

Variant	rs6113803
Chromosome Location	chr20:22749362-22749363
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr20:22749168..22751913-chr20:22752671..22755024,2	K562	blood:

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs1761	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2092660	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2143902	1.00[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2179856	1.00[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap];0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2179859	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2404493	0.95[EUR][1000 genomes]
rs2424461	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2424464	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2424465	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2424466	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2424468	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2424469	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2424470	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2424473	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2424475	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2424476	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4331580	0.95[EUR][1000 genomes]
rs4516506	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4815144	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6075947	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6075948	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6082814	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6113810	0.95[EUR][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:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:22743200-22751400	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr20:22745200-22749400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr20:22745400-22750800	Weak transcription	Hela-S3	cervix
4	chr20:22745400-22752400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr20:22745400-22752400	Weak transcription	Gastric	stomach
6	chr20:22745800-22749400	Weak transcription	Stomach Mucosa	stomach
7	chr20:22746000-22749400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr20:22746000-22751000	Weak transcription	Skeletal Muscle Male	skeletal muscle
9	chr20:22746000-22756000	Weak transcription	Spleen	Spleen
10	chr20:22747800-22751400	Enhancers	Placenta	Placenta
11	chr20:22748000-22749600	Enhancers	Placenta Amnion	Placenta Amnion
12	chr20:22748200-22750400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr20:22748600-22750400	Enhancers	HSMM	muscle
14	chr20:22748800-22749400	Enhancers	A549	lung
15	chr20:22748800-22749600	Enhancers	Fetal Muscle Leg	muscle
16	chr20:22748800-22749800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr20:22748800-22750200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr20:22748800-22750400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr20:22748800-22750400	Enhancers	NHDF-Ad	bronchial
20	chr20:22748800-22751600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr20:22749000-22749600	Enhancers	Ovary	ovary
22	chr20:22749000-22749600	Enhancers	NH-A	brain
23	chr20:22749000-22749800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr20:22749000-22749800	Enhancers	HSMMtube	muscle
25	chr20:22749000-22750200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr20:22749000-22752000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr20:22749000-22752200	Enhancers	HMEC	breast
28	chr20:22749200-22749400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr20:22749200-22749600	Enhancers	Muscle Satellite Cultured Cells	--
30	chr20:22749200-22752000	Enhancers	NHEK	skin

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