Variant report

Variant	rs74076804
Chromosome Location	chr14:97417694-97417695
allele	A/C
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:10)

rs_ID	r²[population]
rs10132099	1.00[AMR][1000 genomes]
rs10133651	1.00[AMR][1000 genomes]
rs10138391	1.00[AMR][1000 genomes]
rs10149054	1.00[AMR][1000 genomes]
rs13379383	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28404652	1.00[AMR][1000 genomes]
rs28415410	1.00[AMR][1000 genomes]
rs28718901	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74076808	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74076815	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1044202	chr14:97155291-97683983	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv542179	chr14:97155291-97683983	Weak transcription Strong transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
3	nsv948620	chr14:97334444-98133191	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	nsv832867	chr14:97365919-97541763	Bivalent/Poised TSS Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv902212	chr14:97413032-97474908	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Active TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:97408600-97428600	Weak transcription	Thymus	Thymus
2	chr14:97409600-97419000	Strong transcription	Dnd41	blood
3	chr14:97415000-97417800	Enhancers	Primary B cells from peripheral blood	blood
4	chr14:97416000-97420400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chr14:97416400-97425600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
6	chr14:97416600-97418000	Enhancers	Primary neutrophils fromperipheralblood	blood
7	chr14:97416600-97425000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
8	chr14:97417600-97418800	Enhancers	Fetal Brain Female	brain
9	chr14:97417600-97419000	Enhancers	Brain Germinal Matrix	brain

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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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