Variant report

Variant	rs74089925
Chromosome Location	chr1:76886622-76886623
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs17098940	1.00[AMR][1000 genomes]
rs17098975	0.84[AFR][1000 genomes]
rs6688867	0.85[AFR][1000 genomes]
rs74089923	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74089930	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7526631	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7546140	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	nsv870621	chr1:76620313-76997071	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv534168	chr1:76718950-77039352	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv1006776	chr1:76777323-76899975	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv462006	chr1:76826279-77042405	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
5	nsv546585	chr1:76826279-77042405	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:76876800-76888000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr1:76877000-76888000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr1:76878600-76898400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr1:76882200-76898000	Weak transcription	Primary B cells from cord blood	blood
5	chr1:76884600-76888200	Weak transcription	Ovary	ovary
6	chr1:76884800-76890800	Weak transcription	Fetal Lung	lung
7	chr1:76886200-76889800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr1:76886400-76886800	Flanking Active TSS	Fetal Heart	heart
9	chr1:76886600-76887000	Weak transcription	Aorta	Aorta

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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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