Variant report

Variant	rs10109744
Chromosome Location	chr8:130162530-130162531
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs10085924	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10096436	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10110179	0.94[AFR][1000 genomes]
rs28434686	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7814183	1.00[AFR][1000 genomes];0.80[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv891443	chr8:130016499-130220746	Weak transcription Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Active TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv891445	chr8:130152109-130224721	Enhancers ZNF genes & repeats Genic enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:130159800-130164200	Genic enhancers	Dnd41	blood
2	chr8:130161000-130174400	Weak transcription	Fetal Thymus	thymus
3	chr8:130162400-130162600	Enhancers	Fetal Muscle Leg	muscle
4	chr8:130162400-130163200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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