Variant report

Variant rs61866563
Chromosome Location chr10:119165113-119165114
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:119160000-119172400 Enhancers Primary neutrophils fromperipheralblood blood
2 chr10:119162200-119166200 Weak transcription Primary hematopoietic stem cells blood
3 chr10:119163000-119165800 Enhancers Liver Liver
4 chr10:119163800-119165200 Enhancers Fetal Adrenal Gland Adrenal Gland
5 chr10:119163800-119165200 Enhancers Fetal Intestine Large intestine
6 chr10:119163800-119165200 Enhancers Fetal Intestine Small intestine
7 chr10:119164000-119165200 Enhancers Duodenum Mucosa Duodenum
8 chr10:119164400-119170200 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
9 chr10:119164600-119170200 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
10 chr10:119164800-119166200 Weak transcription K562 blood
11 chr10:119164800-119167800 Weak transcription Monocytes-CD14+_RO01746 blood
12 chr10:119164800-119173400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr10:119165000-119166600 Enhancers HepG2 liver
14 chr10:119165000-119167600 Weak transcription Primary monocytes fromperipheralblood blood

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