Variant report

Variant rs578005370
Chromosome Location chr17:18283906-18283907
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr17:18267200-18288200 Weak transcription Right Atrium heart
2 chr17:18280400-18284200 Enhancers Stomach Mucosa stomach
3 chr17:18281400-18286400 Weak transcription Gastric stomach
4 chr17:18283000-18288200 Enhancers Fetal Thymus thymus
5 chr17:18283400-18287000 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
6 chr17:18283600-18284000 Enhancers ES-WA7 Cell Line embryonic stem cell
7 chr17:18283600-18284000 Enhancers ES-UCSF4 Cell Line embryonic stem cell
8 chr17:18283600-18284000 Bivalent Enhancer Primary monocytes fromperipheralblood blood
9 chr17:18283600-18284000 Bivalent Enhancer Monocytes-CD14+_RO01746 blood
10 chr17:18283800-18284000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
11 chr17:18283800-18284000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
12 chr17:18283800-18284000 Bivalent Enhancer Placenta Placenta
13 chr17:18283800-18284200 Weak transcription Esophagus oesophagus
14 chr17:18283800-18284800 Weak transcription Rectal Mucosa Donor 29 rectum
15 chr17:18283800-18286200 Weak transcription HUES6 Cell Line embryonic stem cell
16 chr17:18283800-18289400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin

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