Variant report

Variant	rs74914237
Chromosome Location	chr3:133505193-133505194
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv877506	chr3:133423473-133569777	Weak transcription Active TSS Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
2	nsv933605	chr3:133425907-133680641	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
3	nsv829729	chr3:133444871-133620387	Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Strong transcription Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
4	nsv4018	chr3:133485867-133530668	Weak transcription Genic enhancers Enhancers Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
5	esv1005045	chr3:133501591-133510973	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	esv3421468	chr3:133503080-133505401	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv513074	chr3:133503208-133505438	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
8	esv3412696	chr3:133503460-133505322	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
9	esv8734	chr3:133503550-133505222	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
10	esv3892	chr3:133503658-133505216	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
11	nsv965212	chr3:133503735-133506316	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:133498600-133505800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr3:133498600-133510400	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr3:133498800-133508000	Weak transcription	Brain Cingulate Gyrus	brain
4	chr3:133499000-133505200	Weak transcription	Brain Anterior Caudate	brain
5	chr3:133499000-133510800	Weak transcription	Brain Hippocampus Middle	brain

Quick Search:

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

what's new

Quick links