Variant report

Variant	rs149646998
Chromosome Location	chr20:24640242-24640243
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 0)

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	nsv9793	chr20:23939613-24734850	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	esv3332519	chr20:24535099-24815615	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv1061412	chr20:24629468-24887869	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv544216	chr20:24629468-24887869	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv524920	chr20:24639916-24683554	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Strong transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:24620000-24641200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr20:24629200-24642600	Weak transcription	Right Atrium	heart
3	chr20:24629400-24641000	Weak transcription	Right Ventricle	heart
4	chr20:24634600-24648800	Weak transcription	Gastric	stomach
5	chr20:24637200-24641200	Enhancers	Muscle Satellite Cultured Cells	--
6	chr20:24638600-24640400	Enhancers	Brain Hippocampus Middle	brain
7	chr20:24638600-24641600	Enhancers	Brain Substantia Nigra	brain
8	chr20:24638600-24643400	Weak transcription	Fetal Kidney	kidney
9	chr20:24639000-24650400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr20:24639200-24641400	Enhancers	Brain Anterior Caudate	brain
11	chr20:24639200-24648600	Weak transcription	Spleen	Spleen
12	chr20:24639400-24640600	Weak transcription	NH-A	brain
13	chr20:24639600-24641600	Enhancers	Brain Inferior Temporal Lobe	brain
14	chr20:24639600-24641800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr20:24639800-24641000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr20:24640000-24640400	Enhancers	Fetal Muscle Trunk	muscle
17	chr20:24640200-24640400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
18	chr20:24640200-24643200	Weak transcription	Brain Angular Gyrus	brain
19	chr20:24640200-24643200	Weak transcription	Brain Cingulate Gyrus	brain

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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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