Variant report

Variant	rs114155760
Chromosome Location	chr5:151818141-151818142
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1023828	chr5:151522149-151956217	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv883048	chr5:151682439-151846236	Enhancers Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv432814	chr5:151682807-151852807	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv432815	chr5:151682807-151875807	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv432816	chr5:151691807-151875807	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv969985	chr5:151817505-151821787	Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:151810800-151819000	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr5:151816200-151818600	Weak transcription	Fetal Intestine Small	intestine
3	chr5:151816400-151818800	Weak transcription	Fetal Intestine Large	intestine
4	chr5:151817000-151818200	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr5:151817000-151818200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr5:151817200-151818200	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr5:151817600-151818200	Enhancers	H1 Cell Line	embryonic stem cell
8	chr5:151817600-151818200	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr5:151817600-151818200	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr5:151818000-151818200	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr5:151818000-151819200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr5:151818000-151819200	Enhancers	Brain Substantia Nigra	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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