Variant report

Variant rs62275576
Chromosome Location chr3:156343653-156343654
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:156336400-156345800 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
2 chr3:156338800-156345800 Weak transcription Fetal Intestine Small intestine
3 chr3:156339000-156343800 Weak transcription K562 blood
4 chr3:156339200-156343800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr3:156339200-156346000 Weak transcription HSMM muscle
6 chr3:156339200-156347800 Weak transcription Esophagus oesophagus
7 chr3:156342200-156345000 Weak transcription Fetal Heart heart
8 chr3:156343400-156344000 Enhancers Hela-S3 cervix
9 chr3:156343400-156344200 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
10 chr3:156343400-156344200 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
11 chr3:156343400-156344400 Enhancers Primary hematopoietic stem cells short term culture blood
12 chr3:156343600-156344000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr3:156343600-156344000 Enhancers Fetal Intestine Large intestine
14 chr3:156343600-156344200 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
15 chr3:156343600-156344200 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
16 chr3:156343600-156344400 Enhancers HMEC breast
17 chr3:156343600-156344600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
18 chr3:156343600-156349600 Enhancers NHEK skin

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