Variant report

Variant rs60306368
Chromosome Location chr2:113562881-113562882
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:113553800-113563000 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
2 chr2:113555600-113563200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr2:113559000-113563000 Weak transcription Breast Myoepithelial Primary Cells Breast
4 chr2:113560600-113563600 Enhancers HMEC breast
5 chr2:113561200-113563600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr2:113561400-113563600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr2:113561600-113563600 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
8 chr2:113561800-113563600 Enhancers HepG2 liver
9 chr2:113562200-113563400 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
10 chr2:113562200-113563400 Weak transcription K562 blood
11 chr2:113562800-113563200 Flanking Active TSS Foreskin Keratinocyte Primary Cells skin02 Skin
12 chr2:113562800-113563400 Enhancers Placenta Amnion Placenta Amnion
13 chr2:113562800-113563600 Enhancers Primary B cells from peripheral blood blood
14 chr2:113562800-113563600 Enhancers Esophagus oesophagus
15 chr2:113562800-113563600 Flanking Active TSS GM12878-XiMat blood
16 chr2:113562800-113563600 Flanking Active TSS NHEK skin

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