Variant report

Variant rs11119382
Chromosome Location chr1:210159746-210159747
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:210146600-210160400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr1:210157800-210160200 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
3 chr1:210159400-210162000 Weak transcription NHEK skin
4 chr1:210159400-210163000 Weak transcription H1 Cell Line embryonic stem cell
5 chr1:210159400-210166600 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
6 chr1:210159600-210160400 Weak transcription iPS-15b Cell Line embryonic stem cell
7 chr1:210159600-210160600 Strong transcription Foreskin Melanocyte Primary Cells skin03 Skin
8 chr1:210159600-210160800 Weak transcription iPS-20b Cell Line embryonic stem cell
9 chr1:210159600-210166200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
10 chr1:210159600-210168200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell

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