Variant report

Variant	rs9672104
Chromosome Location	chr14:35168487-35168488
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs55807828	0.82[AFR][1000 genomes]
rs7156526	0.93[AFR][1000 genomes]
rs7159698	0.93[AFR][1000 genomes]
rs7160935	0.95[AFR][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	nsv1040980	chr14:34345018-35255592	Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	109 gene(s)	inside rSNPs	diseases
2	nsv1048408	chr14:34958352-35255592	Weak transcription Strong transcription Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
3	esv3392700	chr14:34989406-35365530	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	85 gene(s)	inside rSNPs	diseases
4	nsv1041857	chr14:35084889-35417180	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 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	chr14:35162800-35168800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr14:35162800-35169000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr14:35162800-35169000	Weak transcription	Psoas Muscle	Psoas
4	chr14:35163000-35168800	Weak transcription	Muscle Satellite Cultured Cells	--
5	chr14:35163000-35168800	Weak transcription	Brain Hippocampus Middle	brain
6	chr14:35163000-35168800	Weak transcription	Skeletal Muscle Male	skeletal muscle
7	chr14:35163000-35169000	Weak transcription	Skeletal Muscle Female	skeletal muscle
8	chr14:35163200-35171800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr14:35165600-35168800	Weak transcription	HepG2	liver
10	chr14:35166800-35169000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr14:35166800-35169400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr14:35167200-35168800	Enhancers	A549	lung
13	chr14:35167200-35169000	Enhancers	Hela-S3	cervix
14	chr14:35168000-35168800	Enhancers	NHDF-Ad	bronchial
15	chr14:35168200-35168800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr14:35168200-35169000	Enhancers	NHLF	lung
17	chr14:35168200-35169400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung

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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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