Variant report

Variant rs78272651
Chromosome Location chr1:147193969-147193970
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 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 chr1:147191000-147194800 Enhancers Placenta Placenta
4 chr1:147191600-147194200 Weak transcription H1 Cell Line embryonic stem cell
5 chr1:147192800-147194200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
6 chr1:147193000-147194200 Weak transcription Esophagus oesophagus
7 chr1:147193400-147194600 Enhancers Hela-S3 cervix
8 chr1:147193600-147194200 Enhancers NHEK skin
9 chr1:147193600-147194600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr1:147193600-147194600 Enhancers Primary neutrophils fromperipheralblood blood
11 chr1:147193600-147194600 Enhancers HMEC breast
12 chr1:147193800-147194000 Enhancers HUES6 Cell Line embryonic stem cell
13 chr1:147193800-147194000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
14 chr1:147193800-147194200 Enhancers Breast Myoepithelial Primary Cells Breast
15 chr1:147193800-147194200 Enhancers Pancreas Pancrea
16 chr1:147193800-147194400 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
17 chr1:147193800-147194400 Bivalent Enhancer Foreskin Melanocyte Primary Cells skin01 Skin
18 chr1:147193800-147194400 Enhancers Adipose Nuclei Adipose

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