Variant report

Variant rs58352100
Chromosome Location chr4:821240-821241
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:23 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:818200-822200 Weak transcription Pancreas Pancrea
2 chr4:819400-822200 Weak transcription Liver Liver
3 chr4:819400-822400 Weak transcription Gastric stomach
4 chr4:820200-822000 Weak transcription Hela-S3 cervix
5 chr4:820400-821400 Bivalent Enhancer Primary T cells fromperipheralblood blood
6 chr4:820400-821400 Bivalent Enhancer Fetal Stomach stomach
7 chr4:820600-821400 Bivalent Enhancer Esophagus oesophagus
8 chr4:820600-821400 Bivalent Enhancer Left Ventricle heart
9 chr4:820800-821400 Bivalent Enhancer H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
10 chr4:820800-821400 Bivalent/Poised TSS iPS-15b Cell Line embryonic stem cell
11 chr4:820800-821400 Bivalent/Poised TSS Ganglion Eminence derived primary cultured neurospheres brain
12 chr4:820800-822600 Weak transcription Right Ventricle heart
13 chr4:821000-821400 Bivalent Enhancer H9 Derived Neuron Cultured Cells ES cell derived
14 chr4:821000-821400 Bivalent Enhancer ES-UCSF4 Cell Line embryonic stem cell
15 chr4:821000-825600 Bivalent Enhancer Fetal Adrenal Gland Adrenal Gland
16 chr4:821000-828800 Weak transcription Right Atrium heart
17 chr4:821200-821400 Flanking Bivalent TSS/Enh ES-I3 Cell Line embryonic stem cell
18 chr4:821200-821400 Bivalent Enhancer HUES6 Cell Line embryonic stem cell
19 chr4:821200-821400 Bivalent/Poised TSS Foreskin Fibroblast Primary Cells skin01 Skin
20 chr4:821200-821400 Flanking Bivalent TSS/Enh Foreskin Fibroblast Primary Cells skin02 Skin
21 chr4:821200-821400 Bivalent/Poised TSS Foreskin Melanocyte Primary Cells skin01 Skin
22 chr4:821200-821800 Bivalent Enhancer H1 Derived Mesenchymal Stem Cells ES cell derived
23 chr4:821200-821800 Bivalent Enhancer iPS DF 19.11 Cell Line embryonic stem cell

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