Variant report

Variant rs454245
Chromosome Location chr1:153031979-153031980
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:153029800-153032400 Enhancers NHEK skin
2 chr1:153030000-153032400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
3 chr1:153030600-153032000 Weak transcription Esophagus oesophagus
4 chr1:153030800-153032200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
5 chr1:153031200-153032000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
6 chr1:153031400-153032000 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
7 chr1:153031400-153032000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
8 chr1:153031400-153032200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr1:153031400-153032200 Enhancers HMEC breast
10 chr1:153031600-153032200 Enhancers Placenta Placenta
11 chr1:153031600-153032200 Enhancers Pancreas Pancrea
12 chr1:153031600-153032200 Enhancers Placenta Amnion Placenta Amnion
13 chr1:153031600-153032400 Flanking Active TSS K562 blood
14 chr1:153031800-153032200 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
15 chr1:153031800-153032400 Enhancers Gastric stomach

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