Variant report

Variant rs4709162
Chromosome Location chr6:167720325-167720326
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:167711600-167721600 Weak transcription Fetal Intestine Large intestine
2 chr6:167716200-167721200 Weak transcription Liver Liver
3 chr6:167717200-167721800 Strong transcription Fetal Intestine Small intestine
4 chr6:167717600-167720400 Enhancers Placenta Amnion Placenta Amnion
5 chr6:167717800-167724000 Weak transcription Fetal Brain Female brain
6 chr6:167718400-167720400 Enhancers HUES6 Cell Line embryonic stem cell
7 chr6:167718600-167720400 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
8 chr6:167719200-167720400 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
9 chr6:167719400-167720400 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
10 chr6:167719600-167720600 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
11 chr6:167719800-167720400 Bivalent Enhancer Foreskin Keratinocyte Primary Cells skin02 Skin
12 chr6:167720200-167720400 Flanking Active TSS iPS DF 19.11 Cell Line embryonic stem cell
13 chr6:167720200-167720800 Weak transcription HepG2 liver
14 chr6:167720200-167722200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
15 chr6:167720200-167723200 Weak transcription Rectal Smooth Muscle rectum
16 chr6:167720200-167723200 Weak transcription Stomach Mucosa stomach

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