Variant report

Variant rs12479173
Chromosome Location chr2:113649210-113649211
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:113647800-113649800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr2:113647800-113650200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
3 chr2:113647800-113650400 Enhancers Breast Myoepithelial Primary Cells Breast
4 chr2:113647800-113650600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
5 chr2:113647800-113651800 Enhancers Esophagus oesophagus
6 chr2:113648000-113650800 Enhancers HMEC breast
7 chr2:113648200-113652200 Enhancers Placenta Placenta
8 chr2:113648200-113655200 Weak transcription Sigmoid Colon Sigmoid Colon
9 chr2:113648400-113649600 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
10 chr2:113648600-113649600 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
11 chr2:113648800-113649600 Enhancers Monocytes-CD14+_RO01746 blood
12 chr2:113648800-113649800 Enhancers Primary monocytes fromperipheralblood blood
13 chr2:113648800-113650400 Enhancers Primary neutrophils fromperipheralblood blood
14 chr2:113649200-113649600 Enhancers Fetal Intestine Large intestine
15 chr2:113649200-113649600 Flanking Active TSS NHEK skin
16 chr2:113649200-113650200 Enhancers Placenta Amnion Placenta Amnion
17 chr2:113649200-113654800 Weak transcription K562 blood

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