Variant report

Variant	rs73848204
Chromosome Location	chr4:130278576-130278577
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs17014617	1.00[AMR][1000 genomes]
rs17014625	1.00[AMR][1000 genomes]
rs55871533	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56015549	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57089329	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58918263	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60036541	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73848203	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73848205	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73851107	1.00[AMR][1000 genomes]
rs73851109	1.00[AMR][1000 genomes]
rs73851113	1.00[AMR][1000 genomes]
rs73851117	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73851118	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73851119	1.00[AMR][1000 genomes]
rs73851120	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73851121	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv534538	chr4:129799138-130431688	Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv830058	chr4:130136025-130315471	Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	esv1805721	chr4:130277165-130282466	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	inside rSNPs	diseases
4	esv1811943	chr4:130277165-130282466	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:130275400-130279600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr4:130276600-130279600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr4:130276800-130279600	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr4:130276800-130279800	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr4:130277000-130279800	Weak transcription	Fetal Lung	lung
6	chr4:130277200-130279600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr4:130277200-130279800	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr4:130277200-130284000	Weak transcription	Colon Smooth Muscle	Colon
9	chr4:130277400-130279000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr4:130277600-130284200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr4:130277800-130279200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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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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