Variant report

Variant rs7581496
Chromosome Location chr2:33930328-33930329
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:33928800-33930400 Enhancers HUES64 Cell Line embryonic stem cell
2 chr2:33929000-33930400 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
3 chr2:33929000-33931800 Enhancers Cortex derived primary cultured neurospheres brain
4 chr2:33929200-33930400 Enhancers iPS-20b Cell Line embryonic stem cell
5 chr2:33929200-33930600 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
6 chr2:33929400-33930400 Enhancers HUES6 Cell Line embryonic stem cell
7 chr2:33930000-33930600 Enhancers HUVEC blood vessel
8 chr2:33930000-33932000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
9 chr2:33930000-33937400 Weak transcription H9 Cell Line embryonic stem cell
10 chr2:33930200-33937000 Weak transcription ES-I3 Cell Line embryonic stem cell
11 chr2:33930200-33937000 Weak transcription iPS-15b Cell Line embryonic stem cell

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