Variant report

Variant rs11899433
Chromosome Location chr2:33225360-33225361
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 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 chr2:33219000-33226400 Weak transcription Stomach Smooth Muscle stomach
4 chr2:33219000-33226800 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
5 chr2:33222600-33225600 Weak transcription NHLF lung
6 chr2:33223200-33238800 Weak transcription Fetal Intestine Small intestine
7 chr2:33223800-33227000 Enhancers Fetal Heart heart
8 chr2:33223800-33228800 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
9 chr2:33224400-33227400 Weak transcription Cortex derived primary cultured neurospheres brain
10 chr2:33224400-33228800 Enhancers Left Ventricle heart
11 chr2:33225000-33225600 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
12 chr2:33225000-33225800 Enhancers Right Ventricle heart
13 chr2:33225000-33226600 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
14 chr2:33225000-33233000 Enhancers Liver Liver

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