Variant report

Variant rs2140448
Chromosome Location chr18:30309442-30309443
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr18:30305600-30310000 Weak transcription Rectal Smooth Muscle rectum
2 chr18:30307000-30309600 Strong transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
3 chr18:30307200-30310000 Weak transcription Primary B cells from peripheral blood blood
4 chr18:30308200-30310000 Weak transcription Cortex derived primary cultured neurospheres brain
5 chr18:30308200-30310600 Enhancers ES-UCSF4 Cell Line embryonic stem cell
6 chr18:30308400-30310000 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
7 chr18:30308400-30310800 Enhancers HUES48 Cell Line embryonic stem cell
8 chr18:30308400-30310800 Enhancers iPS-18 Cell Line embryonic stem cell
9 chr18:30308800-30309800 Weak transcription iPS-15b Cell Line embryonic stem cell
10 chr18:30308800-30310000 Enhancers Dnd41 blood
11 chr18:30308800-30311400 Enhancers HUES64 Cell Line embryonic stem cell
12 chr18:30309200-30310400 Genic enhancers Primary B cells from cord blood blood
13 chr18:30309400-30311200 Enhancers iPS-20b Cell Line embryonic stem cell
14 chr18:30309400-30312400 Weak transcription HepG2 liver

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