Variant report

Variant	rs73932099
Chromosome Location	chr19:42290790-42290791
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs16975593	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs55989120	1.00[AFR][1000 genomes]
rs56064499	0.81[AFR][1000 genomes]
rs57872553	1.00[AFR][1000 genomes]
rs58364776	1.00[AFR][1000 genomes]
rs60395739	0.83[AFR][1000 genomes]
rs60561791	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61260704	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61479711	1.00[AFR][1000 genomes]
rs73932097	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73932101	1.00[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	nsv522854	chr19:42120283-42931004	Weak transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	104 gene(s)	inside rSNPs	diseases
2	nsv579615	chr19:42221434-42310388	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	esv3319044	chr19:42257039-42297123	Bivalent Enhancer Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	esv3319045	chr19:42257039-42297123	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:42288200-42292000	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr19:42289800-42291600	Weak transcription	Rectal Mucosa Donor 31	rectum
3	chr19:42290000-42290800	Enhancers	Primary B cells from cord blood	blood
4	chr19:42290000-42291200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
5	chr19:42290000-42292000	Enhancers	Monocytes-CD14+_RO01746	blood
6	chr19:42290200-42305200	Weak transcription	Fetal Thymus	thymus
7	chr19:42290400-42292000	Enhancers	Primary neutrophils fromperipheralblood	blood
8	chr19:42290600-42290800	Enhancers	Esophagus	oesophagus

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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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