Variant report

Variant rs563495145
Chromosome Location chr4:1407874-1407875
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:1399800-1411200 Weak transcription Right Atrium heart
2 chr4:1407000-1408000 Bivalent Enhancer H1 Cell Line embryonic stem cell
3 chr4:1407000-1408000 Bivalent Enhancer ES-UCSF4 Cell Line embryonic stem cell
4 chr4:1407200-1408000 Bivalent/Poised TSS iPS-15b Cell Line embryonic stem cell
5 chr4:1407200-1408000 Bivalent Enhancer Brain Germinal Matrix brain
6 chr4:1407400-1408400 Bivalent Enhancer Fetal Brain Male brain
7 chr4:1407600-1408000 Bivalent/Poised TSS HUES6 Cell Line embryonic stem cell
8 chr4:1407600-1408000 Flanking Bivalent TSS/Enh iPS DF 19.11 Cell Line embryonic stem cell
9 chr4:1407600-1408000 Bivalent Enhancer Breast Myoepithelial Primary Cells Breast
10 chr4:1407600-1408000 Bivalent Enhancer Primary Natural Killer cells fromperipheralblood blood
11 chr4:1407600-1408000 Bivalent Enhancer Primary hematopoietic stem cells G-CSF-mobilized Female --
12 chr4:1407600-1408000 Bivalent Enhancer Fetal Muscle Trunk muscle
13 chr4:1407800-1408000 Bivalent/Poised TSS ES-WA7 Cell Line embryonic stem cell
14 chr4:1407800-1408000 Bivalent/Poised TSS iPS DF 6.9 Cell Line embryonic stem cell
15 chr4:1407800-1408000 Bivalent Enhancer Cortex derived primary cultured neurospheres brain
16 chr4:1407800-1408000 Bivalent/Poised TSS Fetal Brain Female brain
17 chr4:1407800-1408000 Bivalent Enhancer Fetal Muscle Leg muscle
18 chr4:1407800-1408000 Bivalent Enhancer Fetal Stomach stomach
19 chr4:1407800-1408800 Weak transcription Pancreas Pancrea

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