Variant report

Variant rs10262964
Chromosome Location chr7:51050563-51050564
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:51049400-51052200 Enhancers HUES6 Cell Line embryonic stem cell
2 chr7:51049400-51052600 Enhancers HUES48 Cell Line embryonic stem cell
3 chr7:51049400-51052800 Enhancers H1 Cell Line embryonic stem cell
4 chr7:51049600-51050600 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
5 chr7:51049600-51052400 Enhancers iPS-18 Cell Line embryonic stem cell
6 chr7:51050000-51050600 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
7 chr7:51050000-51050800 Enhancers ES-UCSF4 Cell Line embryonic stem cell
8 chr7:51050000-51051400 Enhancers iPS-20b Cell Line embryonic stem cell
9 chr7:51050200-51050800 Enhancers H9 Cell Line embryonic stem cell
10 chr7:51050200-51050800 Enhancers HUES64 Cell Line embryonic stem cell
11 chr7:51050200-51050800 Bivalent Enhancer Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
12 chr7:51050200-51052000 Enhancers Cortex derived primary cultured neurospheres brain
13 chr7:51050400-51051400 Weak transcription iPS-15b Cell Line embryonic stem cell
14 chr7:51050400-51052000 Enhancers Ganglion Eminence derived primary cultured neurospheres brain

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