Variant report

Variant rs17010721
Chromosome Location chr2:31331103-31331104
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:31307400-31331600 Weak transcription Primary hematopoietic stem cells short term culture blood
2 chr2:31310600-31346800 Weak transcription Breast Myoepithelial Primary Cells Breast
3 chr2:31320600-31337800 Weak transcription Primary B cells from cord blood blood
4 chr2:31321400-31332000 Weak transcription Pancreatic Islets Pancreatic Islet
5 chr2:31328400-31335200 Enhancers Primary neutrophils fromperipheralblood blood
6 chr2:31329000-31336400 Weak transcription Spleen Spleen
7 chr2:31329200-31348200 Weak transcription A549 lung
8 chr2:31330200-31333400 Enhancers Fetal Brain Male brain
9 chr2:31330400-31331200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr2:31330400-31332400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr2:31330400-31332600 Enhancers HMEC breast
12 chr2:31330400-31332600 Enhancers NHEK skin
13 chr2:31330400-31332800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
14 chr2:31330400-31333200 Enhancers Fetal Brain Female brain
15 chr2:31330800-31331200 Enhancers Lung lung
16 chr2:31330800-31331200 Enhancers HSMM muscle
17 chr2:31330800-31332600 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
18 chr2:31330800-31334600 Enhancers Fetal Muscle Leg muscle
19 chr2:31331000-31332000 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
20 chr2:31331000-31332000 Enhancers Fetal Lung lung

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