Variant report

Variant rs72942429
Chromosome Location chr2:113699446-113699447
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:113697000-113699800 Enhancers Liver Liver
2 chr2:113697400-113699600 Weak transcription Gastric stomach
3 chr2:113697600-113700400 Enhancers Colon Smooth Muscle Colon
4 chr2:113698200-113699800 Enhancers Rectal Smooth Muscle rectum
5 chr2:113698200-113700000 Enhancers Stomach Mucosa stomach
6 chr2:113699000-113699600 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
7 chr2:113699000-113699800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
8 chr2:113699000-113700800 Enhancers NHEK skin
9 chr2:113699000-113701000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr2:113699200-113699600 Enhancers Breast Myoepithelial Primary Cells Breast
11 chr2:113699200-113699600 Enhancers Primary monocytes fromperipheralblood blood
12 chr2:113699200-113700000 Enhancers Duodenum Smooth Muscle Duodenum
13 chr2:113699200-113700600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
14 chr2:113699200-113700600 Enhancers HMEC breast
15 chr2:113699400-113699800 Enhancers Primary T cells fromperipheralblood blood
16 chr2:113699400-113700400 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
17 chr2:113699400-113700400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin

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