Variant report

Variant	rs73781148
Chromosome Location	chr5:106978378-106978379
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs55712495	1.00[AMR][1000 genomes]
rs56387153	1.00[AMR][1000 genomes]
rs57235588	1.00[AMR][1000 genomes]
rs59056455	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59767200	1.00[AMR][1000 genomes]
rs61466405	1.00[AMR][1000 genomes]
rs61516790	1.00[AMR][1000 genomes]
rs61628334	1.00[AMR][1000 genomes]
rs73777707	1.00[AMR][1000 genomes]
rs73777721	1.00[AMR][1000 genomes]
rs73780413	1.00[AMR][1000 genomes]
rs73781124	1.00[AMR][1000 genomes]
rs73781143	1.00[AMR][1000 genomes]
rs73781144	1.00[AMR][1000 genomes]
rs73781146	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73781149	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73781153	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73781154	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv34018	chr5:106720912-107110506	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:106942400-106981600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr5:106966800-106979600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr5:106969400-106978800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr5:106969600-106988600	Weak transcription	Fetal Stomach	stomach
5	chr5:106970200-106985600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr5:106971600-106978800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr5:106972200-106986000	Weak transcription	HUES64 Cell Line	embryonic stem cell
8	chr5:106972600-106981800	Weak transcription	HMEC	breast
9	chr5:106972800-106983400	Weak transcription	Fetal Lung	lung
10	chr5:106973200-106978800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr5:106973200-106981600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
12	chr5:106973400-106982000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr5:106976600-106978800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr5:106976600-106981400	Weak transcription	Fetal Heart	heart
15	chr5:106976600-106981800	Weak transcription	HUES48 Cell Line	embryonic stem cell
16	chr5:106976600-106984600	Weak transcription	A549	lung
17	chr5:106976600-106987200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr5:106976600-106991600	Weak transcription	Left Ventricle	heart
19	chr5:106977800-106981200	Weak transcription	Pancreatic Islets	Pancreatic Islet

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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