Variant report

Variant rs2820584
Chromosome Location chr1:159924989-159924990
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:159916200-159930600 Weak transcription Right Atrium heart
2 chr1:159919800-159930400 Weak transcription Rectal Mucosa Donor 31 rectum
3 chr1:159923000-159926200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
4 chr1:159923400-159926400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
5 chr1:159923400-159926400 Enhancers NHEK skin
6 chr1:159923600-159925400 Enhancers HMEC breast
7 chr1:159923600-159925600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr1:159924000-159927800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
9 chr1:159924000-159928800 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
10 chr1:159924000-159928800 Weak transcription Esophagus oesophagus
11 chr1:159924200-159928400 Weak transcription Placenta Amnion Placenta Amnion
12 chr1:159924400-159927200 Weak transcription Fetal Intestine Small intestine
13 chr1:159924400-159927200 Weak transcription K562 blood
14 chr1:159924400-159929200 Weak transcription Osteobl bone

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