Variant report

Variant	rs2929118
Chromosome Location	chr8:39893991-39893992
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10090043	1.00[AMR][1000 genomes]
rs13255021	1.00[AMR][1000 genomes]
rs13257182	1.00[AMR][1000 genomes]
rs2955894	1.00[AMR][1000 genomes]
rs2955896	1.00[AMR][1000 genomes]
rs2955897	1.00[AMR][1000 genomes]
rs2955898	1.00[AMR][1000 genomes]
rs2955900	1.00[AMR][1000 genomes]
rs2955901	1.00[AMR][1000 genomes]
rs2955904	1.00[AMR][1000 genomes]
rs2955905	1.00[AMR][1000 genomes]
rs2955906	1.00[AMR][1000 genomes]
rs2981159	1.00[AMR][1000 genomes]
rs2981160	1.00[AMR][1000 genomes]
rs2981161	1.00[AMR][1000 genomes]
rs2981162	1.00[AMR][1000 genomes]
rs4314635	1.00[AMR][1000 genomes]
rs4469437	1.00[AMR][1000 genomes]
rs4559228	1.00[AMR][1000 genomes]
rs4633046	1.00[AMR][1000 genomes]
rs56976900	1.00[AMR][1000 genomes]
rs59381479	1.00[AMR][1000 genomes]
rs6474203	1.00[AMR][1000 genomes]
rs7011669	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73605143	1.00[AMR][1000 genomes]
rs73605152	1.00[AMR][1000 genomes]
rs7826266	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv539555	chr8:39683857-40673606	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
2	nsv1033371	chr8:39749437-39899540	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv534582	chr8:39884590-40653224	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:39891200-39894200	Enhancers	Colon Smooth Muscle	Colon
2	chr8:39891200-39894400	Enhancers	Hela-S3	cervix
3	chr8:39891400-39895400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr8:39891400-39896800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr8:39891400-39898400	Weak transcription	Pancreas	Pancrea
6	chr8:39892600-39895200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr8:39892600-39895200	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr8:39892600-39896800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
9	chr8:39892600-39896800	Weak transcription	Fetal Lung	lung
10	chr8:39892600-39897800	Weak transcription	Rectal Smooth Muscle	rectum
11	chr8:39892600-39898200	Weak transcription	Sigmoid Colon	Sigmoid Colon
12	chr8:39893600-39895200	Weak transcription	Fetal Intestine Small	intestine
13	chr8:39893600-39895200	Weak transcription	A549	lung
14	chr8:39893600-39898400	Weak transcription	Liver	Liver
15	chr8:39893600-39898400	Weak transcription	Stomach Smooth Muscle	stomach
16	chr8:39893800-39895000	Weak transcription	Fetal Intestine Large	intestine
17	chr8:39893800-39897600	Weak transcription	HepG2	liver

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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