Variant report

Variant rs536460490
Chromosome Location chr14:65602124-65602125
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:65596800-65602600 Enhancers Fetal Intestine Small intestine
2 chr14:65597800-65602600 Enhancers Fetal Intestine Large intestine
3 chr14:65598200-65602200 Enhancers Rectal Mucosa Donor 31 rectum
4 chr14:65598800-65604400 Weak transcription Colonic Mucosa Colon
5 chr14:65598800-65604400 Weak transcription Osteobl bone
6 chr14:65601400-65602400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
7 chr14:65601400-65602400 Enhancers Rectal Mucosa Donor 29 rectum
8 chr14:65601600-65602200 Enhancers Primary T cells fromperipheralblood blood
9 chr14:65601600-65602200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr14:65601600-65602400 Enhancers Fetal Thymus thymus
11 chr14:65601600-65602400 Enhancers Dnd41 blood
12 chr14:65601600-65605400 Enhancers Breast Myoepithelial Primary Cells Breast
13 chr14:65601800-65602200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
14 chr14:65601800-65602200 Enhancers Thymus Thymus
15 chr14:65601800-65602200 Enhancers NHEK skin
16 chr14:65602000-65604400 Weak transcription HMEC breast
17 chr14:65602000-65604600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived

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