Variant report

Variant rs17145249
Chromosome Location chr7:21794715-21794716
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:21782600-21798000 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
2 chr7:21789400-21804800 Weak transcription H9 Cell Line embryonic stem cell
3 chr7:21793400-21797600 Weak transcription Gastric stomach
4 chr7:21794200-21795000 Enhancers H1 Cell Line embryonic stem cell
5 chr7:21794200-21795000 Enhancers iPS-20b Cell Line embryonic stem cell
6 chr7:21794200-21797800 Enhancers HUES64 Cell Line embryonic stem cell
7 chr7:21794400-21795000 Enhancers HUES48 Cell Line embryonic stem cell
8 chr7:21794400-21795000 Enhancers HUES6 Cell Line embryonic stem cell
9 chr7:21794400-21795000 Enhancers iPS-18 Cell Line embryonic stem cell
10 chr7:21794400-21795600 Enhancers iPS-15b Cell Line embryonic stem cell
11 chr7:21794600-21795000 Enhancers ES-I3 Cell Line embryonic stem cell
12 chr7:21794600-21795000 Enhancers ES-WA7 Cell Line embryonic stem cell
13 chr7:21794600-21795000 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
14 chr7:21794600-21795000 Enhancers iPS DF 6.9 Cell Line embryonic stem cell

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