Variant report

Variant	rs568842748
Chromosome Location	chr10:91286576-91286577
allele	-/A
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 4 )
Associated
traits (count: 0)

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	nsv1042848	chr10:90466032-91318474	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription 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 miRNA target site	66 gene(s)	inside rSNPs	diseases
2	nsv540741	chr10:90466032-91318474	Enhancers Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
3	nsv1041964	chr10:90861380-91378356	Flanking Active TSS Enhancers Weak transcription Genic enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
4	esv3385309	chr10:91286528-91286821	Enhancers Weak transcription	n/a	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:91279400-91294800	Weak transcription	HSMM	muscle
2	chr10:91279600-91292000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr10:91283600-91294600	Weak transcription	Muscle Satellite Cultured Cells	--
4	chr10:91284600-91287400	Weak transcription	Pancreas	Pancrea
5	chr10:91285200-91291400	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr10:91285400-91287600	Enhancers	Fetal Intestine Small	intestine
7	chr10:91285600-91286800	Enhancers	Fetal Intestine Large	intestine
8	chr10:91285800-91286600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr10:91285800-91286600	Enhancers	Adipose Nuclei	Adipose
10	chr10:91285800-91286600	Enhancers	Fetal Stomach	stomach
11	chr10:91285800-91286600	Enhancers	Gastric	stomach
12	chr10:91285800-91286600	Enhancers	Ovary	ovary
13	chr10:91286000-91286800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr10:91286200-91291400	Weak transcription	Fetal Heart	heart
15	chr10:91286400-91286600	Enhancers	Left Ventricle	heart
16	chr10:91286400-91286600	Enhancers	Lung	lung
17	chr10:91286400-91286600	Enhancers	Right Atrium	heart

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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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