Variant report

Variant rs16993830
Chromosome Location chr20:13181804-13181805
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr20:13180000-13182000 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
2 chr20:13180000-13182000 Enhancers HUES6 Cell Line embryonic stem cell
3 chr20:13180000-13182200 Enhancers HUES48 Cell Line embryonic stem cell
4 chr20:13180200-13182000 Enhancers H1 Cell Line embryonic stem cell
5 chr20:13180200-13182000 Enhancers iPS-15b Cell Line embryonic stem cell
6 chr20:13180200-13182000 Enhancers iPS-20b Cell Line embryonic stem cell
7 chr20:13180600-13182000 Enhancers iPS-18 Cell Line embryonic stem cell
8 chr20:13180600-13186000 Weak transcription NHEK skin
9 chr20:13181000-13182200 Enhancers HUES64 Cell Line embryonic stem cell
10 chr20:13181200-13182800 Bivalent Enhancer Brain Germinal Matrix brain
11 chr20:13181600-13182000 Enhancers Cortex derived primary cultured neurospheres brain
12 chr20:13181800-13182000 Active TSS ES-I3 Cell Line embryonic stem cell
13 chr20:13181800-13182000 Active TSS ES-WA7 Cell Line embryonic stem cell
14 chr20:13181800-13182000 Bivalent Enhancer Fetal Brain Male brain
15 chr20:13181800-13182000 Bivalent Enhancer Fetal Brain Female brain

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