Variant report

Variant rs4709166
Chromosome Location chr6:167726526-167726527
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:167720400-167727600 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
2 chr6:167721800-167728000 Enhancers Fetal Brain Male brain
3 chr6:167722800-167727400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
4 chr6:167723800-167728400 Enhancers HepG2 liver
5 chr6:167724800-167726800 Strong transcription Fetal Intestine Small intestine
6 chr6:167725200-167730200 Weak transcription Duodenum Smooth Muscle Duodenum
7 chr6:167725400-167730600 Weak transcription Rectal Smooth Muscle rectum
8 chr6:167726000-167726600 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
9 chr6:167726200-167726800 Enhancers Brain Germinal Matrix brain
10 chr6:167726200-167726800 Enhancers Placenta Amnion Placenta Amnion
11 chr6:167726400-167726600 Enhancers HUES6 Cell Line embryonic stem cell
12 chr6:167726400-167728200 Enhancers Fetal Brain Female brain

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