Variant report

Variant rs72642324
Chromosome Location chr13:95654814-95654815
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:95649200-95655600 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
2 chr13:95650800-95655400 Weak transcription HUES48 Cell Line embryonic stem cell
3 chr13:95650800-95655400 Weak transcription iPS-18 Cell Line embryonic stem cell
4 chr13:95653000-95656600 Weak transcription Right Atrium heart
5 chr13:95654200-95656800 Enhancers H9 Cell Line embryonic stem cell
6 chr13:95654400-95655000 Enhancers Osteobl bone
7 chr13:95654400-95655200 Enhancers iPS-20b Cell Line embryonic stem cell
8 chr13:95654400-95655400 Enhancers HepG2 liver
9 chr13:95654400-95656200 Enhancers ES-I3 Cell Line embryonic stem cell
10 chr13:95654600-95655000 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
11 chr13:95654600-95655000 Bivalent Enhancer HUES6 Cell Line embryonic stem cell
12 chr13:95654600-95655000 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
13 chr13:95654600-95655000 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
14 chr13:95654600-95655000 Enhancers ES-UCSF4 Cell Line embryonic stem cell
15 chr13:95654600-95655000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
16 chr13:95654600-95655000 Enhancers Stomach Mucosa stomach
17 chr13:95654600-95655400 Bivalent Enhancer H1 Cell Line embryonic stem cell
18 chr13:95654800-95655000 Bivalent Enhancer Foreskin Keratinocyte Primary Cells skin03 Skin
19 chr13:95654800-95655800 Flanking Active TSS Primary hematopoietic stem cells G-CSF-mobilized Male --

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