Variant report

Variant rs4974624
Chromosome Location chr4:1409157-1409158
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:1399800-1411200 Weak transcription Right Atrium heart
2 chr4:1408600-1409200 Bivalent Enhancer Fetal Brain Male brain
3 chr4:1408800-1409200 Bivalent Enhancer H1 Cell Line embryonic stem cell
4 chr4:1408800-1409200 Bivalent/Poised TSS HUES6 Cell Line embryonic stem cell
5 chr4:1408800-1409200 Active TSS iPS-15b Cell Line embryonic stem cell
6 chr4:1408800-1409200 Transcr. at gene 5' and 3' iPS DF 19.11 Cell Line embryonic stem cell
7 chr4:1408800-1409200 Bivalent Enhancer Placenta Placenta
8 chr4:1408800-1409200 Bivalent Enhancer Fetal Stomach stomach
9 chr4:1408800-1409200 Enhancers Pancreas Pancrea
10 chr4:1408800-1409800 Flanking Active TSS K562 blood
11 chr4:1409000-1409200 Flanking Bivalent TSS/Enh H1 Derived Mesenchymal Stem Cells ES cell derived
12 chr4:1409000-1409200 Weak transcription H9 Cell Line embryonic stem cell
13 chr4:1409000-1409200 Genic enhancers iPS DF 6.9 Cell Line embryonic stem cell
14 chr4:1409000-1409200 Bivalent Enhancer Cortex derived primary cultured neurospheres brain
15 chr4:1409000-1409400 Bivalent Enhancer ES-UCSF4 Cell Line embryonic stem cell
16 chr4:1409000-1411000 Bivalent Enhancer Fetal Muscle Trunk muscle

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