Variant report

Variant rs3851166
Chromosome Location chr13:50409236-50409237
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:50396000-50414400 Weak transcription Right Atrium heart
2 chr13:50402200-50412800 Weak transcription Fetal Intestine Small intestine
3 chr13:50403000-50410200 Weak transcription HepG2 liver
4 chr13:50404000-50410600 Weak transcription ES-WA7 Cell Line embryonic stem cell
5 chr13:50405800-50414200 Weak transcription Primary hematopoietic stem cells blood
6 chr13:50406000-50410400 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
7 chr13:50407600-50409800 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
8 chr13:50407800-50410600 Weak transcription iPS-15b Cell Line embryonic stem cell
9 chr13:50407800-50410600 Weak transcription iPS-20b Cell Line embryonic stem cell
10 chr13:50407800-50410800 Weak transcription HUES6 Cell Line embryonic stem cell
11 chr13:50407800-50410800 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
12 chr13:50408000-50410200 Weak transcription Esophagus oesophagus
13 chr13:50408600-50410400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
14 chr13:50408800-50410200 Weak transcription HMEC breast
15 chr13:50408800-50410400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
16 chr13:50408800-50410400 Weak transcription NHEK skin

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