Variant report

Variant rs17497143
Chromosome Location chr7:136611501-136611502
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:136605200-136612200 Genic enhancers IMR90 fetal lung fibroblasts Cell Line lung
2 chr7:136607000-136612200 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
3 chr7:136607800-136638000 Weak transcription NHLF lung
4 chr7:136609000-136612000 Enhancers Primary hematopoietic stem cells short term culture blood
5 chr7:136609600-136613600 Weak transcription H9 Cell Line embryonic stem cell
6 chr7:136610400-136611600 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
7 chr7:136610400-136611800 Enhancers Stomach Smooth Muscle stomach
8 chr7:136610400-136612000 Enhancers HUVEC blood vessel
9 chr7:136610600-136611800 Enhancers Fetal Adrenal Gland Adrenal Gland
10 chr7:136610800-136611600 Weak transcription Primary hematopoietic stem cells blood
11 chr7:136610800-136612200 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
12 chr7:136610800-136623400 Weak transcription Colon Smooth Muscle Colon
13 chr7:136611000-136616400 Weak transcription Right Atrium heart
14 chr7:136611000-136623200 Weak transcription Left Ventricle heart
15 chr7:136611400-136611600 Enhancers Duodenum Smooth Muscle Duodenum
16 chr7:136611400-136611600 Enhancers Fetal Heart heart

Quick Search:


  
Input of quick search could be:

what's new

Quick links