Variant report

Variant rs13404038
Chromosome Location chr2:151559187-151559188
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:151555000-151561600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
2 chr2:151558000-151562200 Weak transcription Osteobl bone
3 chr2:151558200-151559200 Enhancers H9 Cell Line embryonic stem cell
4 chr2:151558200-151559200 Enhancers Fetal Brain Male brain
5 chr2:151558400-151559200 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
6 chr2:151558600-151559400 Weak transcription HUES48 Cell Line embryonic stem cell
7 chr2:151558600-151564400 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
8 chr2:151558800-151563600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
9 chr2:151559000-151559400 Enhancers iPS-15b Cell Line embryonic stem cell
10 chr2:151559000-151560000 Enhancers iPS-18 Cell Line embryonic stem cell
11 chr2:151559000-151562200 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell

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