Variant report

Variant rs7048334
Chromosome Location chr9:139775023-139775024
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:139770800-139775800 Weak transcription K562 blood
2 chr9:139771200-139775200 Weak transcription Placenta Placenta
3 chr9:139771400-139775800 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
4 chr9:139774000-139776400 Weak transcription Right Atrium heart
5 chr9:139774800-139775200 ZNF genes & repeats iPS DF 19.11 Cell Line embryonic stem cell
6 chr9:139774800-139776000 Enhancers GM12878-XiMat blood
7 chr9:139774800-139776400 Enhancers Fetal Intestine Small intestine
8 chr9:139775000-139775200 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
9 chr9:139775000-139775200 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
10 chr9:139775000-139775200 Bivalent Enhancer Fetal Muscle Trunk muscle
11 chr9:139775000-139776000 Enhancers A549 lung
12 chr9:139775000-139776200 Enhancers Primary T cells fromperipheralblood blood
13 chr9:139775000-139776400 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
14 chr9:139775000-139776400 Enhancers Primary Natural Killer cells fromperipheralblood blood
15 chr9:139775000-139776400 Enhancers Fetal Intestine Large intestine
16 chr9:139775000-139778000 Enhancers Spleen Spleen

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