Variant report

Variant rs28622347
Chromosome Location chr19:20179538-20179539
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:20177400-20180200 Enhancers ES-UCSF4 Cell Line embryonic stem cell
2 chr19:20177600-20180200 Active TSS hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
3 chr19:20178200-20180200 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
4 chr19:20178200-20180400 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
5 chr19:20178400-20179600 ZNF genes & repeats HUES6 Cell Line embryonic stem cell
6 chr19:20178600-20180000 Flanking Active TSS HUES48 Cell Line embryonic stem cell
7 chr19:20178600-20181600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
8 chr19:20178800-20180000 Weak transcription ES-I3 Cell Line embryonic stem cell
9 chr19:20179000-20179600 Active TSS Fetal Intestine Small intestine
10 chr19:20179200-20179600 Weak transcription H9 Cell Line embryonic stem cell
11 chr19:20179400-20179600 Flanking Active TSS iPS-15b Cell Line embryonic stem cell
12 chr19:20179400-20179600 Flanking Active TSS iPS-20b Cell Line embryonic stem cell
13 chr19:20179400-20179600 Flanking Active TSS Fetal Intestine Large intestine
14 chr19:20179400-20179800 Flanking Active TSS HUES64 Cell Line embryonic stem cell
15 chr19:20179400-20180200 Enhancers H1 Cell Line embryonic stem cell

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