Variant report

Variant rs587625265
Chromosome Location chr1:147193131-147193132
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:147190200-147194200 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
2 chr1:147190200-147198800 Weak transcription Right Atrium heart
3 chr1:147190600-147193600 Weak transcription Primary neutrophils fromperipheralblood blood
4 chr1:147191000-147194800 Enhancers Placenta Placenta
5 chr1:147191600-147194200 Weak transcription H1 Cell Line embryonic stem cell
6 chr1:147191800-147193600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr1:147191800-147193600 Weak transcription HMEC breast
8 chr1:147191800-147193800 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
9 chr1:147191800-147193800 Weak transcription Pancreas Pancrea
10 chr1:147192000-147193600 Weak transcription NHEK skin
11 chr1:147192000-147193800 Weak transcription HUES6 Cell Line embryonic stem cell
12 chr1:147192200-147193600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr1:147192400-147193200 Enhancers Fetal Muscle Leg muscle
14 chr1:147192800-147194200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
15 chr1:147193000-147194200 Weak transcription Esophagus oesophagus

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