Variant report

Variant rs12214124
Chromosome Location chr6:13860822-13860823
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:13847800-13864000 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
2 chr6:13859800-13861000 Active TSS ES-I3 Cell Line embryonic stem cell
3 chr6:13859800-13861000 Bivalent/Poised TSS HUES64 Cell Line embryonic stem cell
4 chr6:13860000-13861000 Active TSS H1 Cell Line embryonic stem cell
5 chr6:13860000-13861000 Bivalent Enhancer Primary Natural Killer cells fromperipheralblood blood
6 chr6:13860000-13861000 Active TSS Fetal Brain Female brain
7 chr6:13860200-13861000 Active TSS HUES48 Cell Line embryonic stem cell
8 chr6:13860200-13861000 Active TSS iPS-15b Cell Line embryonic stem cell
9 chr6:13860200-13861000 Active TSS iPS-18 Cell Line embryonic stem cell
10 chr6:13860200-13861000 Bivalent/Poised TSS Primary T cells from cord blood blood
11 chr6:13860200-13861000 Active TSS Foreskin Melanocyte Primary Cells skin01 Skin
12 chr6:13860600-13861000 Active TSS HUES6 Cell Line embryonic stem cell
13 chr6:13860800-13861000 Enhancers Primary hematopoietic stem cells short term culture blood
14 chr6:13860800-13861000 Bivalent/Poised TSS Foreskin Keratinocyte Primary Cells skin02 Skin
15 chr6:13860800-13861000 Bivalent/Poised TSS Foreskin Keratinocyte Primary Cells skin03 Skin
16 chr6:13860800-13864000 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell

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