Variant report

Variant rs1277752
Chromosome Location chr10:18522475-18522476
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:18514000-18522800 Weak transcription Esophagus oesophagus
2 chr10:18514400-18524400 Weak transcription Stomach Smooth Muscle stomach
3 chr10:18514400-18525600 Weak transcription Fetal Lung lung
4 chr10:18514400-18526600 Weak transcription Rectal Smooth Muscle rectum
5 chr10:18515800-18532000 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
6 chr10:18516800-18524800 Weak transcription Fetal Stomach stomach
7 chr10:18519600-18522600 Weak transcription Colon Smooth Muscle Colon
8 chr10:18520800-18525600 Weak transcription Cortex derived primary cultured neurospheres brain
9 chr10:18521800-18523400 Enhancers Fetal Adrenal Gland Adrenal Gland
10 chr10:18522000-18522600 Weak transcription Left Ventricle heart
11 chr10:18522000-18523600 Enhancers Ovary ovary
12 chr10:18522200-18522600 Enhancers iPS-18 Cell Line embryonic stem cell
13 chr10:18522200-18523600 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
14 chr10:18522400-18522800 Enhancers ES-I3 Cell Line embryonic stem cell
15 chr10:18522400-18523000 Enhancers iPS-20b Cell Line embryonic stem cell
16 chr10:18522400-18523200 Enhancers iPS-15b Cell Line embryonic stem cell
17 chr10:18522400-18523200 Enhancers Fetal Heart heart
18 chr10:18522400-18523600 Enhancers HUES48 Cell Line embryonic stem cell

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