Variant report

Variant	rs57684217
Chromosome Location	chr20:24608918-24608919
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs56273983	1.00[AMR][1000 genomes]
rs57269062	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58113049	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58257276	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6036859	1.00[AMR][1000 genomes]
rs60918606	1.00[AMR][1000 genomes]
rs61313692	1.00[AMR][1000 genomes]
rs7354752	1.00[AMR][1000 genomes]
rs73902580	1.00[AMR][1000 genomes]
rs73902785	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73902786	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73902787	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73902788	1.00[AMR][1000 genomes]
rs73902790	1.00[AMR][1000 genomes]
rs73905125	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73905414	1.00[AMR][1000 genomes]
rs73905416	1.00[AMR][1000 genomes]
rs8119455	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv9793	chr20:23939613-24734850	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	esv3332519	chr20:24535099-24815615	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:24 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:24584400-24612600	Weak transcription	Aorta	Aorta
2	chr20:24591200-24609200	Weak transcription	Brain Anterior Caudate	brain
3	chr20:24600000-24609600	Weak transcription	Brain Angular Gyrus	brain
4	chr20:24602400-24610000	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr20:24607800-24611600	Enhancers	Brain Substantia Nigra	brain
6	chr20:24608200-24610000	Enhancers	Primary hematopoietic stem cells short term culture	blood
7	chr20:24608400-24609200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr20:24608400-24610600	Enhancers	Spleen	Spleen
9	chr20:24608400-24611000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr20:24608400-24611000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
11	chr20:24608400-24611400	Enhancers	Fetal Heart	heart
12	chr20:24608400-24613200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr20:24608600-24609000	Enhancers	Breast Myoepithelial Primary Cells	Breast
14	chr20:24608600-24609400	Weak transcription	Right Atrium	heart
15	chr20:24608600-24611400	Enhancers	Fetal Thymus	thymus
16	chr20:24608600-24615000	Weak transcription	H1 Cell Line	embryonic stem cell
17	chr20:24608800-24609000	Enhancers	Cortex derived primary cultured neurospheres	brain
18	chr20:24608800-24609400	Enhancers	Thymus	Thymus
19	chr20:24608800-24609800	Weak transcription	Primary monocytes fromperipheralblood	blood
20	chr20:24608800-24610400	Enhancers	Fetal Muscle Trunk	muscle
21	chr20:24608800-24610600	Enhancers	Primary T cells from cord blood	blood
22	chr20:24608800-24611000	Enhancers	Primary hematopoietic stem cells	blood
23	chr20:24608800-24611000	Enhancers	Brain Inferior Temporal Lobe	brain
24	chr20:24608800-24616800	Enhancers	Brain Hippocampus Middle	brain

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