Variant report

Variant rs10204733
Chromosome Location chr2:33218139-33218140
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 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 chr2:33215000-33219400 Enhancers Fetal Heart heart
3 chr2:33216600-33218400 Enhancers Breast Myoepithelial Primary Cells Breast
4 chr2:33216800-33219000 Enhancers Right Ventricle heart
5 chr2:33217000-33223800 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
6 chr2:33217200-33218400 Enhancers Right Atrium heart
7 chr2:33217200-33218400 Enhancers Stomach Smooth Muscle stomach
8 chr2:33217200-33219200 Enhancers Left Ventricle heart
9 chr2:33217400-33219000 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
10 chr2:33217400-33222600 Weak transcription K562 blood
11 chr2:33217600-33218200 Enhancers Colon Smooth Muscle Colon
12 chr2:33217600-33219000 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
13 chr2:33217600-33219000 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
14 chr2:33217800-33218200 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
15 chr2:33217800-33219000 Enhancers Fetal Stomach stomach
16 chr2:33217800-33219000 Enhancers Lung lung
17 chr2:33218000-33219000 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
18 chr2:33218000-33219000 Enhancers Fetal Muscle Leg muscle
19 chr2:33218000-33219200 Enhancers Cortex derived primary cultured neurospheres brain

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