Variant report

Variant rs34920948
Chromosome Location chr2:33224265-33224266
allele A/C/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:33202600-33225600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
2 chr2:33218200-33241000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
3 chr2:33219000-33225000 Weak transcription Right Ventricle heart
4 chr2:33219000-33226400 Weak transcription Stomach Smooth Muscle stomach
5 chr2:33219000-33226800 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
6 chr2:33219200-33224400 Weak transcription Left Ventricle heart
7 chr2:33222600-33225600 Weak transcription NHLF lung
8 chr2:33223200-33238800 Weak transcription Fetal Intestine Small intestine
9 chr2:33223800-33224400 Enhancers Cortex derived primary cultured neurospheres brain
10 chr2:33223800-33227000 Enhancers Fetal Heart heart
11 chr2:33223800-33228800 Enhancers IMR90 fetal lung fibroblasts Cell Line lung

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