Variant report

Variant rs11767606
Chromosome Location chr7:3220949-3220950
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:8 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:3205200-3221000 Weak transcription Right Atrium heart
2 chr7:3216800-3232600 Weak transcription H9 Cell Line embryonic stem cell
3 chr7:3219600-3223800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
4 chr7:3220200-3222800 Enhancers Fetal Brain Male brain
5 chr7:3220400-3221600 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
6 chr7:3220600-3221000 Weak transcription Pancreas Pancrea
7 chr7:3220600-3221000 Enhancers HepG2 liver
8 chr7:3220600-3228600 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived

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