Variant report

Variant rs7618197
Chromosome Location chr3:100370773-100370774
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:100366600-100372400 Weak transcription Fetal Intestine Small intestine
2 chr3:100369200-100371800 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
3 chr3:100369200-100374400 Weak transcription Primary neutrophils fromperipheralblood blood
4 chr3:100369400-100370800 Enhancers NHEK skin
5 chr3:100369800-100370800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr3:100370000-100370800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr3:100370000-100373800 Weak transcription Duodenum Mucosa Duodenum
8 chr3:100370200-100370800 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
9 chr3:100370200-100370800 Enhancers Muscle Satellite Cultured Cells --
10 chr3:100370200-100370800 Enhancers Osteobl bone
11 chr3:100370200-100371000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
12 chr3:100370200-100371000 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
13 chr3:100370200-100371000 Enhancers NHDF-Ad bronchial
14 chr3:100370200-100371800 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
15 chr3:100370200-100372600 Weak transcription ES-I3 Cell Line embryonic stem cell
16 chr3:100370200-100372600 Weak transcription K562 blood
17 chr3:100370200-100383800 Weak transcription Primary T helper memory cells from peripheral blood 1 blood
18 chr3:100370600-100371800 Strong transcription Liver Liver
19 chr3:100370600-100373800 Weak transcription Fetal Intestine Large intestine

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