Variant report

Variant rs371384331
Chromosome Location chr1:147192187-147192188
allele -/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:147189000-147192400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
2 chr1:147189400-147193000 Enhancers Esophagus oesophagus
3 chr1:147190200-147194200 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
4 chr1:147190200-147198800 Weak transcription Right Atrium heart
5 chr1:147190600-147193600 Weak transcription Primary neutrophils fromperipheralblood blood
6 chr1:147191000-147194800 Enhancers Placenta Placenta
7 chr1:147191200-147192200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr1:147191200-147192400 Weak transcription Fetal Muscle Leg muscle
9 chr1:147191600-147194200 Weak transcription H1 Cell Line embryonic stem cell
10 chr1:147191800-147192600 Weak transcription Left Ventricle heart
11 chr1:147191800-147193600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
12 chr1:147191800-147193600 Weak transcription HMEC breast
13 chr1:147191800-147193800 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
14 chr1:147191800-147193800 Weak transcription Pancreas Pancrea
15 chr1:147192000-147193600 Weak transcription NHEK skin
16 chr1:147192000-147193800 Weak transcription HUES6 Cell Line embryonic stem cell

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