Variant report

Variant rs117904954
Chromosome Location chr6:167626661-167626662
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:167615800-167628800 Weak transcription Right Atrium heart
2 chr6:167622400-167627200 Enhancers HepG2 liver
3 chr6:167623000-167629200 Enhancers Fetal Brain Male brain
4 chr6:167623600-167628200 Enhancers Fetal Brain Female brain
5 chr6:167624600-167632800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
6 chr6:167624800-167627800 Weak transcription Brain Germinal Matrix brain
7 chr6:167625600-167630000 Weak transcription Rectal Smooth Muscle rectum
8 chr6:167626000-167626800 Enhancers GM12878-XiMat blood
9 chr6:167626200-167627800 Weak transcription Brain Inferior Temporal Lobe brain
10 chr6:167626200-167635000 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
11 chr6:167626600-167631000 Weak transcription Placenta Amnion Placenta Amnion

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