Variant report

Variant rs10129051
Chromosome Location chr12:72965387-72965388
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:6 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:72947600-72973600 Weak transcription Fetal Intestine Small intestine
2 chr12:72956400-72973800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
3 chr12:72958200-72984400 Weak transcription Pancreas Pancrea
4 chr12:72964400-72986800 Weak transcription Fetal Intestine Large intestine
5 chr12:72964800-72965400 Enhancers iPS-20b Cell Line embryonic stem cell
6 chr12:72965000-72965800 Enhancers HUES48 Cell Line embryonic stem cell

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