Variant report

Variant	rs6036926
Chromosome Location	chr20:24819113-24819114
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs6036920	0.95[AFR][1000 genomes]
rs6050022	1.00[AMR][1000 genomes]
rs6050029	0.95[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1061412	chr20:24629468-24887869	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv544216	chr20:24629468-24887869	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv1061455	chr20:24733120-24861801	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv544218	chr20:24733120-24861801	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv1062140	chr20:24807962-25304054	Strong transcription Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
6	nsv544219	chr20:24807962-25304054	Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Active TSS Enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:24816800-24821400	Enhancers	Fetal Lung	lung
2	chr20:24817600-24821400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr20:24817800-24822600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr20:24817800-24822800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr20:24818000-24819400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr20:24818000-24820000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr20:24818200-24819200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr20:24818200-24819800	Enhancers	NH-A	brain
9	chr20:24818200-24820000	Enhancers	HSMM	muscle
10	chr20:24818400-24819400	Enhancers	NHEK	skin
11	chr20:24818400-24819800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr20:24818600-24823000	Weak transcription	Fetal Thymus	thymus
13	chr20:24818800-24819200	Enhancers	NHLF	lung
14	chr20:24818800-24822000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
15	chr20:24818800-24823400	Weak transcription	HUES6 Cell Line	embryonic stem cell
16	chr20:24819000-24819800	Enhancers	HSMMtube	muscle
17	chr20:24819000-24821000	Enhancers	GM12878-XiMat	blood
18	chr20:24819000-24821200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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

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