Variant report

Variant rs58970858
Chromosome Location chr21:45769118-45769119
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr21:45760400-45769800 Weak transcription Right Atrium heart
2 chr21:45760600-45769200 Weak transcription Primary T helper naive cells fromperipheralblood blood
3 chr21:45760600-45772400 Weak transcription Primary T helper memory cells from peripheral blood 2 blood
4 chr21:45768200-45770000 Bivalent Enhancer Fetal Thymus thymus
5 chr21:45768400-45771200 Weak transcription Primary T helper naive cells from peripheral blood blood
6 chr21:45768400-45773200 Enhancers Primary hematopoietic stem cells blood
7 chr21:45768600-45769200 Bivalent Enhancer Rectal Mucosa Donor 31 rectum
8 chr21:45768600-45769400 Bivalent Enhancer Rectal Mucosa Donor 29 rectum
9 chr21:45768600-45769600 Bivalent Enhancer Colonic Mucosa Colon
10 chr21:45768600-45770000 Bivalent Enhancer Fetal Muscle Trunk muscle
11 chr21:45768800-45769800 Bivalent Enhancer Primary hematopoietic stem cells G-CSF-mobilized Male --
12 chr21:45769000-45769200 Flanking Bivalent TSS/Enh iPS DF 19.11 Cell Line embryonic stem cell
13 chr21:45769000-45769800 Bivalent Enhancer Primary neutrophils fromperipheralblood blood
14 chr21:45769000-45771400 Bivalent Enhancer Breast Myoepithelial Primary Cells Breast

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