Variant report

Variant rs9957814
Chromosome Location chr18:30309040-30309041
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 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 chr18:30307800-30309400 Strong transcription HepG2 liver
5 chr18:30308200-30310000 Weak transcription Cortex derived primary cultured neurospheres brain
6 chr18:30308200-30310600 Enhancers ES-UCSF4 Cell Line embryonic stem cell
7 chr18:30308400-30309200 Strong transcription Primary B cells from cord blood blood
8 chr18:30308400-30310000 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
9 chr18:30308400-30310800 Enhancers HUES48 Cell Line embryonic stem cell
10 chr18:30308400-30310800 Enhancers iPS-18 Cell Line embryonic stem cell
11 chr18:30308800-30309200 Enhancers H1 Cell Line embryonic stem cell
12 chr18:30308800-30309200 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
13 chr18:30308800-30309400 Weak transcription iPS-20b Cell Line embryonic stem cell
14 chr18:30308800-30309800 Weak transcription iPS-15b Cell Line embryonic stem cell
15 chr18:30308800-30310000 Enhancers Dnd41 blood
16 chr18:30308800-30311400 Enhancers HUES64 Cell Line embryonic stem cell

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