Variant report

Variant rs587693572
Chromosome Location chr1:147192540-147192541
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:147189400-147193000 Enhancers Esophagus oesophagus
2 chr1:147190200-147194200 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
3 chr1:147190200-147198800 Weak transcription Right Atrium heart
4 chr1:147190600-147193600 Weak transcription Primary neutrophils fromperipheralblood blood
5 chr1:147191000-147194800 Enhancers Placenta Placenta
6 chr1:147191600-147194200 Weak transcription H1 Cell Line embryonic stem cell
7 chr1:147191800-147192600 Weak transcription Left Ventricle heart
8 chr1:147191800-147193600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr1:147191800-147193600 Weak transcription HMEC breast
10 chr1:147191800-147193800 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
11 chr1:147191800-147193800 Weak transcription Pancreas Pancrea
12 chr1:147192000-147193600 Weak transcription NHEK skin
13 chr1:147192000-147193800 Weak transcription HUES6 Cell Line embryonic stem cell
14 chr1:147192200-147193600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
15 chr1:147192400-147193200 Enhancers Fetal Muscle Leg muscle

Quick Search:


  
Input of quick search could be:

what's new

Quick links