Variant report

Variant rs16964058
Chromosome Location chr18:30471456-30471457
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:8 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr18:30468400-30471600 Weak transcription Fetal Intestine Large intestine
2 chr18:30469800-30475200 Weak transcription Pancreas Pancrea
3 chr18:30470000-30471600 Weak transcription HepG2 liver
4 chr18:30470600-30473600 Weak transcription ES-I3 Cell Line embryonic stem cell
5 chr18:30470800-30471800 Weak transcription iPS-15b Cell Line embryonic stem cell
6 chr18:30471200-30472200 Enhancers Primary B cells from peripheral blood blood
7 chr18:30471200-30472600 Enhancers Primary B cells from cord blood blood
8 chr18:30471400-30471800 Flanking Active TSS Dnd41 blood

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