Variant report

Variant rs3088147
Chromosome Location chr21:46792372-46792373
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr21:46779800-46792600 Weak transcription iPS-15b Cell Line embryonic stem cell
2 chr21:46782400-46798400 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
3 chr21:46785000-46793000 Weak transcription Esophagus oesophagus
4 chr21:46787600-46794000 Weak transcription Right Ventricle heart
5 chr21:46787600-46806800 Weak transcription Right Atrium heart
6 chr21:46787800-46796400 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
7 chr21:46788000-46792600 Weak transcription NH-A brain
8 chr21:46788000-46793200 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
9 chr21:46788000-46796400 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
10 chr21:46788800-46793000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
11 chr21:46788800-46794200 Weak transcription Adipose Nuclei Adipose
12 chr21:46789000-46792400 Weak transcription A549 lung
13 chr21:46789200-46793000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
14 chr21:46789800-46793000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
15 chr21:46791000-46792800 Enhancers Fetal Stomach stomach
16 chr21:46791400-46793600 Enhancers HepG2 liver
17 chr21:46792000-46793800 Enhancers NHEK skin
18 chr21:46792000-46794000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
19 chr21:46792000-46794000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
20 chr21:46792200-46792600 Weak transcription K562 blood
21 chr21:46792200-46794000 Enhancers HMEC breast

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