Variant report

Variant rs143674975
Chromosome Location chr2:133280793-133280794
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:133268200-133282800 Weak transcription Fetal Intestine Small intestine
2 chr2:133274400-133283200 Weak transcription Pancreas Pancrea
3 chr2:133278400-133280800 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
4 chr2:133278600-133281000 Enhancers Breast Myoepithelial Primary Cells Breast
5 chr2:133279000-133280800 Enhancers Brain Germinal Matrix brain
6 chr2:133279000-133282600 Enhancers Fetal Brain Male brain
7 chr2:133279200-133281600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr2:133279200-133283000 Weak transcription Fetal Heart heart
9 chr2:133279800-133281200 Enhancers ES-WA7 Cell Line embryonic stem cell
10 chr2:133280000-133280800 Enhancers HUES64 Cell Line embryonic stem cell
11 chr2:133280000-133280800 Enhancers HMEC breast
12 chr2:133280200-133281000 Enhancers iPS-18 Cell Line embryonic stem cell
13 chr2:133280200-133281400 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
14 chr2:133280200-133281400 Enhancers Fetal Brain Female brain
15 chr2:133280400-133280800 Enhancers HUES48 Cell Line embryonic stem cell
16 chr2:133280400-133281200 Enhancers ES-I3 Cell Line embryonic stem cell
17 chr2:133280400-133281200 Enhancers iPS DF 19.11 Cell Line embryonic stem cell

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