Variant report

Variant rs59904938
Chromosome Location chr6:167618589-167618590
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:167613800-167622200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr6:167614400-167623200 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
3 chr6:167615800-167628800 Weak transcription Right Atrium heart
4 chr6:167617400-167618600 Weak transcription Fetal Brain Male brain
5 chr6:167617400-167619000 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
6 chr6:167617400-167620800 Enhancers HepG2 liver
7 chr6:167617400-167622400 Weak transcription Fetal Intestine Large intestine
8 chr6:167618000-167619000 Enhancers Fetal Intestine Small intestine
9 chr6:167618000-167619000 Enhancers Rectal Smooth Muscle rectum
10 chr6:167618400-167618600 Enhancers NH-A brain
11 chr6:167618400-167619000 Enhancers Placenta Amnion Placenta Amnion
12 chr6:167618400-167624400 Weak transcription Colon Smooth Muscle Colon

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