Variant report

Variant rs12567184
Chromosome Location chr1:210162953-210162954
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:8 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:210159400-210163000 Weak transcription H1 Cell Line embryonic stem cell
2 chr1:210159400-210166600 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
3 chr1:210159600-210166200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
4 chr1:210159600-210168200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
5 chr1:210161600-210163400 Weak transcription HUES48 Cell Line embryonic stem cell
6 chr1:210162000-210163000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr1:210162000-210163600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
8 chr1:210162800-210189200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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